Pharmaceutical and personal care products in tile drainage following surface spreading and injection of dewatered municipal biosolids to an agricultural field

Land application of municipal biosolids can be a source of environmental contamination by pharmaceutical and personal care products (PPCPs). This study examined PPCP concentrations/temporally discrete mass loads in agricultural tile drainage systems where two applications of biosolids had previously taken place. The field plots received liquid municipal biosolids (LMB) in the fall of 2005 at an application rate of ∼ 93,500 L ha^− 1, and a second land application was conducted using dewatered municipal biosolids (DMB) applied at a rate of ∼ 8 Mt dw ha^− 1 in the summer of 2006. The DMB land application treatments consisted of direct injection (DI) of the DMB beneath the soil surface at a nominal depth of ∼ 0.11 m, and surface spreading (SS) plus subsequent tillage incorporation of DMB in the topsoil (∼ 0.10 m depth). The PPCPs examined included eight pharmaceuticals (acetaminophen, fluoxetine, ibuprofen, gemfibrozil, naproxen, carbamazepine, atenolol, sulfamethoxazole), the nicotine metabolite cotinine, and two antibacterial personal care products triclosan and triclocarban. Residues of naproxen, cotinine, atenolol and triclosan originating from the fall 2005 LMB application were detected in tile water nearly nine months after application (triclocarban was not measured in 2005). There were no significant differences (p > 0.05) in PPCP mass loads among the two DMB land application treatments (i.e., SS vs. DI); although, average PPCP mass loads late in the study season (> 100 days after application) were consistently higher for the DI treatment relative to the SS treatment. While the concentration of triclosan (∼ 14,000 ng g^− 1 dw) in DMB was about twice that of triclocarban (∼ 8000 ng g^− 1 dw), the average tile water concentrations for triclosan were much higher (43 ± 5 ng L^− 1) than they were for triclocarban (0.73 ± 0.14 ng L^− 1). Triclosan concentrations (maximum observed in 2006 ∼ 235 ng L^− 1) in tile water resulting from land applications may warrant attention from a toxicological perspective.     

Complementary methods to investigate the development of clogging within a horizontal sub-surface flow tertiary treatment wetland

A combination of experimental methods was applied at a clogged, horizontal subsurface flow (HSSF) municipal wastewater tertiary treatment wetland (TW) in the UK, to quantify the extent of surface and subsurface clogging which had resulted in undesirable surface flow. The three dimensional hydraulic conductivity profile was determined, using a purpose made device which recreates the constant head permeameter test in-situ. The hydrodynamic pathways were investigated by performing dye tracing tests with Rhodamine WT and a novel multi-channel, data-logging, flow through Fluorimeter which allows synchronous measurements to be taken from a matrix of sampling points. Hydraulic conductivity varied in all planes, with the lowest measurement of 0.1 m d⁻¹ corresponding to the surface layer at the inlet, and the maximum measurement of 1550 m d⁻¹ located at a 0.4 m depth at the outlet. According to dye tracing results, the region where the overland flow ceased received five times the average flow, which then vertically short-circuited below the rhizosphere. The tracer break-through curve obtained from the outlet showed that this preferential flow-path accounted for approximately 80% of the flow overall and arrived 8 h before a distinctly separate secondary flow-path. The overall volumetric efficiency of the clogged system was 71% and the hydrology was simulated using a dual-path, dead-zone storage model. It is concluded that uneven inlet distribution, continuous surface loading and high rhizosphere resistance is responsible for the clog formation observed in this system. The average inlet hydraulic conductivity was 2 m d⁻¹, suggesting that current European design guidelines, which predict that the system will reach an equilibrium hydraulic conductivity of 86 m d⁻¹, do not adequately describe the hydrology of mature systems.     

Adsorption, sedimentation, and inactivation of E. coli within wastewater treatment wetlands

Bacteria fate and transport within constructed wetlands must be understood if engineered wetlands are to become a reliable form of wastewater treatment. This study investigated the relative importance of microbial treatment mechanisms in constructed wetlands treating both domestic and agricultural wastewater. Escherichia coli (E. coli) inactivation, adsorption, and settling rates were measured in the lab within two types of wastewater (dairy wastewater lagoon effluent and domestic septic tank effluent). In situ E. coli inactivation was also measured within a domestic wastewater treatment wetland and the adsorption of E. coli was also measured within the wetland effluent.Inactivation of E. coli appears to be the most significant contributor to E. coli removal within the wastewaters and wetland environments examined in this study. E. coli survived longer within the dairy wastewater (DW) compared to the domestic wastewater treatment wetland water (WW). First order rate constants for E. coli inactivation within the WW in the lab ranged from 0.09 day⁻¹ (d⁻¹) at 7.6 °C to 0.18 d⁻¹ at 22.8 °C. The average in situ rate constant observed within the domestic wetland ranged from 0.02 d⁻¹ to 0.03 d⁻¹ at an average water temperature of 17 °C. First order rate constants for E. coli inactivation within the DW ranged from 0.01 d⁻¹ at 7.7 °C to 0.04 d⁻¹ at 24.6 °C. Calculated distribution coefficients (K_d) were 19,000 mL g⁻¹, 324,000 mL g⁻¹, and 293 mL g⁻¹ for E. coli with domestic septic tank effluent (STE), treated wetland effluent (WLE), and DW, respectively. Approximately 50%, 20%, and 90% of E. coli were “free floating” or associated with particles <5 μm in size within the STE, WLE, and DW respectively. Although 10-50% of E. coli were found to associate with particles >5 μm within both the STE and DW, settling did not appear to contribute to E. coli removal within sedimentation experiments, indicating that the particles the bacteria were associated with had very small settling velocities.The results of this study highlight the importance of wastewater characterization when designing a treatment wetland system for bacterial removal. This study illustrated the level of variability in E. coli removal processes that can be observed within different wastewater, and wetland environments.     

Elemental and organic carbon in aerosols over urbanized coastal region (southern Baltic Sea, Gdynia)

Studies on PM 10, total particulate matter (TSP), elemental carbon (EC) and organic carbon (OC) concentrations were carried out in the Polish coastal zone of the Baltic Sea, in urbanized Gdynia. The interaction between the land, the air and the sea was clearly observed. The highest concentrations of PM 10, TSP and both carbon fractions were noted in the air masses moving from southern and western Poland and Europe. The EC was generally of primary origin and its contribution to TSP and PM 10 mass was on average 2.3% and 3.7% respectively. Under low wind speed conditions local sources (traffic and industry) influenced increases in elemental carbon and PM 10 concentrations in Gdynia. Elemental carbon demonstrated a pronounced weekly cycle, yielding minimum values at the weekend and maximum values on Thursdays. The role of harbors and ship yards in creating high EC concentrations was clearly observed. Concentration of organic carbon was ten times higher than that of elemental carbon, and the average OC contribution to PM 10 mass was very high (31.6%). An inverse situation was observed when air masses were transported from over the Atlantic Ocean, the North Sea and the Baltic Sea. These clean air masses were characterized by the lowest concentrations of all analysed compounds.Obtained results for organic and elemental carbon fluxes showed that atmospheric aerosols can be treated, along with water run-off, as a carbon source for the coastal waters of the Baltic Sea. The enrichment of surface water was more effective in the case of organic carbon (0.27 ± 0.19 mmol m⁻² d⁻¹). Elemental carbon fluxes were one order of magnitude smaller, on average 0.03 ± 0.04 mmol m⁻² d⁻¹. We suggest that in some situations atmospheric carbon input can explain up to 18% of total carbon fluxes into the Baltic coastal waters.     

The occurrence of antibiotics in an urban watershed: From wastewater to drinking water

The presence of 28 antibiotics in three hospital effluents, five wastewater treatment plants (WWTPs), six rivers and a drinking water storage catchment were investigated within watersheds of South-East Queensland, Australia. All antibiotics were detected at least once, with the exception of the polypeptide bacitracin which was not detected at all. Antibiotics were found in hospital effluent ranging from 0.01-14.5 μg L^− 1, dominated by the β-lactam, quinolone and sulphonamide groups. Antibiotics were found in WWTP influent up to 64 μg L^− 1, dominated by the β-lactam, quinolone and sulphonamide groups. Investigated WWTPs were highly effective in removing antibiotics from the water phase, with an average removal rate of greater than 80% for all targeted antibiotics. However, antibiotics were still detected in WWTP effluents in the low ng L^− 1 range up to a maximum of 3.4 μg L^− 1, with the macrolide, quinolone and sulphonamide antibiotics most prevalent. Similarly, antibiotics were detected quite frequently in the low ng L^− 1 range, up to 2 μg L^− 1 in the surface waters of six investigated rivers including freshwater, estuarine and marine samples. The total investigated antibiotic concentration (TIAC) within the Nerang River was significantly lower (p < 0.05) than all other rivers sampled. The absence of WWTP discharge to this river is a likely explanation for the significantly lower TIAC and suggests that WWTP discharges are a dominant source of antibiotics to investigated surface waters. A significant difference (p < 0.001) was identified between TIACs at surface water sites with WWTP discharge compared to sites with no WWTP discharge, providing further evidence that WWTPs are an important source of antibiotics to streams. Despite the presence of antibiotics in surface waters used for drinking water extraction, no targeted antibiotics were detected in any drinking water samples.     

Environmental occurrence and degradation of the herbicide n-chloridazon

A sampling campaign was carried out for n-chloridazon (n-CLZ) and its degradation product desphenyl-chloridazon (DPC) in the Hesse region (Germany) during the year 2007: a total of 548 environmental samples including groundwater, surface water and wastewater treatment plant (WWTP) effluent were analysed. Furthermore, aerobic degradation of n-CLZ has been studied utilising a fixed bed bioreactor (FBBR).In surface water, n-CLZ was detected at low concentrations (average 0.01 ± 0.06 μg L⁻¹; maximum 0.89 μg L⁻¹) with a seasonal peak, whereas DPC was present throughout the year at much higher concentrations (average 0.72 ± 0.81 μg L⁻¹; maximum 7.4 μg L⁻¹). Higher n-CLZ concentrations were observed in the North compared with South Hesse, which is ascribed to a higher density of agricultural areas. Furthermore, methylated DPC (Me-DPC), another degradation product, was detected in surface water.In the degradation test, n-CLZ was completely converted to DPC at all concentrations tested (Me-DPC was not formed under the test conditions). DPC was resistant to further degradation during the whole experimental period of 98 days. The results obtained suggest persistence and high dispersion of DPC in the aquatic environment.     

An experimental study on ventilation efficiency of isolation room

This paper presents an experimental modeling of contaminant dispersion in a mock-up isolation room with different negative pressure differentials and ventilation rates. A hypothetical contaminant (sulfur hexafluoride, SF₆) is emitted from a patient lying on a bed in the mock-up isolation room. The impacts of ventilation rates 12 and 24 h⁻¹ and pressure differentials −2.5, −5.0, −8.0, and −15.0 Pa on the ventilation effectiveness in the room are evaluated quantitatively. A local air quality index and an exposure index for healthcare workers are introduced in the research to evaluate the ventilation efficiency of the isolation room. Based on the results of our experiment, the ventilation efficiency of the isolation room ranks the highest at −15.0 Pa/24 h⁻¹, followed, respectively, by −15.0 Pa/12 h⁻¹, −8.0 Pa/24 h⁻¹, −5.0 Pa/24 h⁻¹, −2.5 Pa/24 h⁻¹, −8.0 Pa/12 h⁻¹, −5.0 Pa/12 h⁻¹, and −2.5 Pa/12 h⁻¹.     

Changes in water quality of the River Frome (UK) from 1965 to 2009: is phosphorus mitigation finally working?

The water quality of the River Frome, Dorset, southern England, was monitored at weekly intervals from 1965 until 2009. Determinands included phosphorus, nitrogen, silicon, potassium, calcium, sodium, magnesium, pH, alkalinity and temperature. Nitrate-N concentrations increased from an annual average of 2.4 mg l^− 1 in the mid to late 1960s to 6.0 mg l^− 1 in 2008-2009, but the rate of increase was beginning to slow. Annual soluble reactive phosphorus (SRP) concentrations increased from 101 μg l^− 1 in the mid 1960s to a maximum of 190 μg l^− 1 in 1989. In 2002, there was a step reduction in SRP concentration (average = 88 μg l^− 1 in 2002-2005), with further improvement in 2007-2009 (average = 49 μg l^− 1), due to the introduction of phosphorus stripping at sewage treatment works. Phosphorus and nitrate concentrations showed clear annual cycles, related to the timing of inputs from the catchment, and within-stream bioaccumulation and release. Annual depressions in silicon concentration each spring (due to diatom proliferation) reached a maximum between 1980 and 1991, (the period of maximum SRP concentration) indicating that algal biomass had increased within the river. The timing of these silicon depressions was closely related to temperature. Excess carbon dioxide partial pressures (EpCO₂) of 60 times atmospheric CO₂ were also observed through the winter periods from 1980 to 1992, when phosphorus concentration was greatest, indicating very high respiration rates due to microbial decomposition of this enhanced biomass. Declining phosphorus concentrations since 2002 reduced productivity and algal biomass in the summer, and EpCO₂ through the winter, indicating that sewage treatment improvements had improved riverine ecology. Algal blooms were limited by phosphorus, rather than silicon concentration. The value of long-term water quality data sets is discussed. The data from this monitoring programme are made freely available to the wider science community through the CEH data portal (http://gateway.ceh.ac.uk/).     

Assessment of in-stream phosphorus dynamics in agricultural drainage ditches

The intensive agricultural systems in the Midwestern United States can enrich surface waters with nutrients. Agricultural drainage ditches serve as the first and second order streams throughout much of this region, as well as other highly productive agricultural areas in humid regions throughout the world. This project was conducted to evaluate in-stream processing of soluble P (SP) in agricultural drainage ditches. Soluble P injection studies were conducted at seven sites along three drainage ditches (298 to 4300 ha drainage area), and one site on a third-order stream that receives the discharge from the agricultural ditches (19,000 ha drainage area) by increasing the SP concentration in the ditch water by approximately 0.25 mg L^− 1. Sediments collected from smaller watersheds contained greater amounts of Mehlich 3 and exchangeable P (ExP), silt and clay size particles, and organic matter. Phosphorus uptake lengths (S_net) ranged from 40 to 1900 m, and SP uptake rates (U) ranged from 0.4 to 52 mg m^− 2 h^− 1. Phosphorus S_net was correlated with ditch geomorphological (i.e. width) and sediment properties (i.e. organic matter, ExP, and equilibrium P concentration; r² = 1.00, P < 0.001), indirect drainage in the watershed (r² = 0.92, P < 0.001), and the amount of small grains, forest, urban area, alfalfa and corn (r² = 1.00, P < 0.0001). Agricultural drainage ditches actively process nutrients and could potentially be managed to optimize this processing to minimize SP export from these landscapes.     

Indoor/outdoor relationship of fine particles less than 2.5 μm (PM2.5) in residential homes locations in central Indian region

The high levels in developing countries and the apparent scale of its impact on the global burden of disease underline the importance of particulate as an environmental health risk and the consequence need for monitoring them particularly in indoor microenvironment. PM2.5 μm, 1.0 μm, 0.5 μm and 0.25 μm were measured inside and outside 14 residential homes located in different microenvironment during a six-month period (October 2007–March 2008) in Agra located in the central region of India. Particulate mass concentrations were measured using Grimm aerosol spectrometer for 24 h inside and outside the homes located in roadside, rural and urban area, along with the field survey study done in the same region. The indoor average concentrations recorded for PM_2.5, PM_1.0, PM_0.5 and PM_0.25 were maximum for the rural homes (173.03 μgm⁻³, 133.26 μgm⁻³, 96.02 μgm⁻³, 8.56 μgm⁻³) followed by roadside homes (137.93 μgm⁻³, 117.09 μgm⁻³, 68.17 μgm⁻³, 8.55 μgm⁻³) and then by urban homes (135.55 μgm⁻³, 102.92 μgm⁻³, 38.38 μgm⁻³, 6.35 μgm⁻³). The average I/O ratios for PM_2.5, PM_1.0, PM_0.5 and PM_0.25 in roadside and rural areas were close to or above 1.00 and less than 1.00 for urban areas. The I/O ratios obtained were linked to the indoor activities using occupant's diary entries. The positive values of correlation coefficient (r) also indicated the indoor concentrations of particulate matter were correlated with the corresponding outdoor concentrations.     

An improved system for the control of dissolved oxygen in freshwater aquaria

A system for the removal and control of dissolved oxygen (DO) from freshwater was designed and constructed with aquarium-type fish studies in mind. Degassed water was obtained using a partial vacuum of −14 psi, and DO regulated at an aquarium scale using electronically controlled aeration with timed partial water renewal. The degassing system was capable of producing water with ∼1.7 mg L⁻¹ DO within 10 min of operation, and 0.55 mg L⁻¹ after 2 h. The control system was capable of maintaining DO levels of ca 0.8 mg L⁻¹ over 48 h in the absence of aeration and further capable of precisely controlling DO levels as low as 1.16±0.002 mg L⁻¹ (mean±SEM) with aeration over a 48 h period.     

Temporal variability of nitrate transport through hydrological response during flood events within a large agricultural catchment in south-west France

The temporal variability of nitrate transport was monitored continuously in a large agricultural catchment, the 1110 km² Save catchment in south-west France, from January 2007 to June 2009. The overall aim was to analyse the temporal transport of nitrate through hydrological response during flood events in the catchment. Nitrate loads and hysteresis were also analysed and the relationships between nitrate and hydro-climatological variables within flood events were determined. During the study period, 19 flood events were analysed using extensive datasets obtained by manual and automatic sampling. The maximum NO₃⁻ concentration during flood varied from 8.2 mg l⁻¹ to 41.1 mg l⁻¹ with flood discharge from 6.75 m³ s⁻¹ to 112.60 m³ s⁻¹. The annual NO₃⁻ loads in 2007 and 2008 amounted to 2514 t and 3047 t, respectively, with average specific yield of 2.5 t km⁻¹² yr⁻¹. The temporal transport of nitrate loads during different seasonal flood events varied from 12 t to 909 t. Nitrate transport during flood events amounted to 1600 t (64% of annual load; 16% of annual duration) in 2007 and 1872 t (62% of annual load; 20% of annual duration) in 2008. The level of peak discharge during flood events did not control peak nitrate concentrations, since similar nitrate peaks were produced by different peak discharges. Statistically strong correlations were found between nitrate transport and total precipitation, flood duration, peak discharge and total water yield. These four variables may be the main factors controlling nitrate export from the Save catchment. The relationship between nitrate and discharge (hysteresis patterns) investigated through flood events in this study was mainly dominated by anticlockwise behaviour.     

Mercury contamination in the vicinity of a chlor-alkali plant and potential risks to local population

A mercury-cell chlor-alkali plant operated in Estarreja (North-western Portugal) for 50 years causing widespread environmental contamination. Although production by this process ceased in 2002, mercury contamination from the plant remains significant. The main objective of this study was to investigate mercury impact on the nearby environment and potential risks to local population. To assess the level of contamination soil samples were collected from agricultural fields in the vicinity of the plant, extending the study by taking samples of the predominant vegetation suitable for animal and human consumption, water samples, and fish species from a nearby coastal lagoon, to gain a preliminary insight into the potential for contamination of the terrestrial and aquatic food web. To determine population exposure to mercury, hair samples were collected from local residents. Total mercury concentration in the 0-15 cm layer of soil was found to be highly variable, ranging between 0.010 and 91 mg kg^− 1, although mercury contamination of soils was found to be restricted to a confined area. Lolium perenne roots contained between 0.0070 and 2.0 mg kg^− 1, and there is evidence that root systems uptake mercury from the soil. Levels of mercury in the aerial parts of plants ranged between 0.018 and 0.98 mg kg^− 1. It appears that plants with higher mercury concentration in soils and roots also display higher mercury concentration in leaves.Total mercury concentration in water samples ranged between 12 and 846 ng L^− 1, all samples presenting concentrations below the maximum level allowable for drinking water defined in the Portuguese law (1.0 μg L^− 1).Mercury levels in fish samples were below the maximum limit defined in the Portuguese law (0.5 mg kg^− 1), ranging from 0.0040 to 0.24 mg kg^− 1. Vegetables collected presented maximum mercury concentration of 0.17 mg kg^− 1. In general, food is not contaminated and should not be responsible for major human exposure to the metal.Mercury determined in human hair samples (0.090-4.2 mg kg^− 1; mean 1.5 mg kg^− 1) can be considered within normal limits, according to WHO guidelines suggesting that it is not affecting the local population. Despite being subject to decades of mercury emissions, nowadays this pollutant is only found in limited small areas and must not constitute a risk for human health, should these areas be restricted and monitored.Considering the present data, it appears that the population from Estarreja is currently not being affected by mercury levels that still remain in the environment.     

Accumulation of oxytetracycline and norfloxacin from saline soil by soybeans

Soil of former shrimp aquaculture facilities in Thailand may be contaminated by antibiotics (e.g. oxytetracycline and norfloxacin) and have elevated salinity. Therefore, reuse of this land can be problematic. The utility of soybean (Glycine max (L.) Merr.) for phytoremediation was investigated. The rate of germination and seedling emergence in prepared contaminated soil (conductivity 17.7 dS m^− 1 from adding 70 mg sodium chloride g^− 1 dry weight, 105 mg kg^− 1 dry weight oxytetracycline and 55 mg kg^− 1 dry weight norfloxacin) in sunlight was approximately 80% that of uncontaminated soil. This reduction was largely due to the high salinity. The antibiotics of interest degraded relatively rapidly in soil (half-life < 10 h for both) but loss was slower in deionised water. Accumulation of the antibiotics from deionised water by soybean resulted in little effect on growth rate and maximum levels in plants were observed after two days exposure, followed by declining concentrations. For soybean plants grown in saline soil, 90% removal of NaCl from soil adjacent to plant roots was observed, most within two days. Wilting and defoliation occurred, but plants recovered after 10 days and maximum salt levels in plants exceeded 20,000 mg g^− 1 dry weight with translocation from root to shoot tissue noted. Soybean plants also accumulated the antibiotics from prepared contaminated saline soil, but translocation from the roots was not observed. The results showed that soybean can be valuable for phytoremediation in these situations.     

Internal loading of phosphorus in a sedimentation pond of a treatment wetland: effect of a phytoplankton crash

Sedimentation ponds are widely believed to act as a primary removal process for phosphorus (P) in nutrient treatment wetlands. High frequency in-situ P, ammonium (NH₄⁺) and dissolved oxygen measurements, alongside occasional water quality measurements, assessed changes in nutrient concentrations and productivity in the sedimentation pond of a treatment wetland between March and June. Diffusive equilibrium in thin films (DET) probes were used to measure in-situ nutrient and chemistry pore-water profiles. Diffusive fluxes across the sediment-water interface were calculated from the pore-water profiles, and dissolved oxygen was used to calculate rates of primary productivity and respiration. The sedimentation pond was a net sink for total P (TP), soluble reactive P (SRP) and NH₄⁺ in March, but became subject to a net internal loading of TP, SRP and NH₄⁺ in May, with SRP concentrations increasing by up to 41 μM (1300 μl^− 1). Reductions in chlorophyll a and dissolved oxygen concentrations also occurred at this time. The sediment changed from a small net sink of SRP in March (average diffusive flux: − 8.2 μmol m^− 2 day^− 1) to a net source of SRP in June (average diffusive flux: + 1324 μmol m^− 2 day^− 1). A diurnal pattern in water column P concentrations, with maxima in the early hours of the morning, and minima in the afternoon, occurred during May. The diurnal pattern and release of SRP from the sediment were attributed to microbial degradation of diatom biomass, causing reduction of the dissolved oxygen concentration and leading to redox-dependent release of P from the sediment. In June, 2.7 mol-P day^− 1 were removed by photosynthesis and 23 mol-P day^− 1 were supplied by respiration in the lake volume. SRP was also released through microbial respiration within the water column, including the decomposition of algal matter. It is imperative that consideration to internal recycling is given when maintaining sedimentation ponds, and before the installation of new ponds designed to treat nutrient waste.     

Characterisation of atmospheric deposition as a source of contaminants in urban rainwater tanks

To characterise atmospheric input of chemical contaminants to urban rainwater tanks, bulk deposition (wet + dry deposition) was collected at sixteen sites in Brisbane, Queensland, Australia on a monthly basis during April 2007-March 2008 (N = 175). Water from rainwater tanks (22 sites, 26 tanks) was also sampled concurrently. The deposition/tank water was analysed for metals, soluble anions and selected samples were additionally analysed for PAHs, pesticides, phenols, organic & inorganic carbon. Flux (mg/m²/d) of total solids mass was found to correlate with average daily rainfall (R² = 0.49) indicating the dominance of the wet deposition contribution to total solids mass. On average 97% of the total mass of analysed components was accounted for by Cl⁻ (25.0%), Na (22.6%), organic carbon (20.5%), NO₃⁻ (10.5%), SO₄²⁻ (9.8%), inorganic carbon (5.7%), PO₄³⁻ (1.6%) and NO₂⁻ (1.5%). For other minor elements the average flux from highest to lowest was in the order of Fe > Al > Zn > Mn > Sr > Pb > Ba > Cu > Se. There was a significant effect of location on flux of K, Sb, Sn, Li, Mn, Fe, Cu, Zn, Ba, Pb and SO₄²⁻ but not other metals or anions. Overall the water quality resulting from the deposition (wet + dry) was good but 10.3%, 1.7% and 17.7% of samples had concentrations of Pb, Cd and Fe respectively greater than the Australian Drinking Water Guidelines (ADWG). This generally occurred in the drier months. In comparison 14.2% and 6.1% of tank samples had total Pb and Zn concentrations exceeding the guidelines. The cumulative mean concentration of lead in deposition was on average only 1/4 of that in tank water over the year at a site with high concentrations of Pb in tank water. This is an indication that deposition from the atmosphere is not the major contributor to high lead concentrations in urban rainwater tanks in a city with reasonable air quality, though it is still a significant portion.     

Polybrominated diphenyl ethers, perfluorinated alkylated substances, and metals in tile drainage and groundwater following applications of municipal biosolids to agricultural fields

Polybrominated diphenyl ethers (PBDEs), perfluorinated alkylated substances (PFAS), and metals were monitored in tile drainage and groundwater following liquid (LMB) and dewatered municipal biosolid (DMB) applications to silty-clay loam agricultural field plots. LMB was applied (93,500 L ha^− 1) in late fall 2005 via surface spreading on un-tilled soil (SS_LMB), and a one-pass aerator-based pre-tillage prior to surface spreading (AerWay SSD) (A). The DMB was applied (8 Mg dw ha^− 1) in early summer 2006 on the same plots by injecting DMB beneath the soil surface (DI), and surface spreading on un-tilled soil (SS_DMB). Key PBDE congeners (BDE-47, -99, -100, -153, -154, -183, -209) comprising 97% of total PBDE in LMB, had maximum tile effluent concentrations ranging from 6 to 320 ng L^− 1 during application-induced tile flow. SS_LMB application-induced tile mass loads for these PBDE congeners were significantly higher than those for control (C) plots (no LMB) (p < 0.05), but not A plots (p > 0.05). PBDE mass loss via tile (0-2 h post-application) as a percent of mass applied was ~ 0.04-0.1% and ~ 0.8-1.7% for A and SS_LMB, respectively. Total PBDE loading to soil via LMB and DMB application was 0.0018 and 0.02 kg total PBDE ha^− 1 yr^− 1, respectively. Total PBDE concentration in soil (0-0.2 m) after both applications was 115 ng g^− 1 dw, (sampled 599 days and 340 days post LMB and DMB applications respectively). Of all the PFAS compounds, only PFOS (max concentration = 17 ng L^− 1) and PFOA (12 ng L^− 1) were found above detectable limits in tile drainage from the application plots. Mass loads of metals in tile for the LMB application-induced tile hydrograph event, and post-application concentrations of metals in groundwater, showed significant (p < 0.05) land application treatment effects (SS_LMB > A > C for tile and SS_LMB and A > C for groundwater for most results). Following DMB application, no significant differences in metal mass loads in tile were found between SS_DMB and DI treatments (PBDE/PFAS were not measured). But for many metals (Cu, Se, Cd, Mo, Hg and Pb) both SS_DMB and DI loads were significantly higher than those from C, but only during < 100 days post DMB application. Clearly, pre-tilling the soil (e.g., A) prior to surface application of LMB will reduce application-based PBDE and metal contamination to tile drainage and shallow groundwater. Directly injecting DMB in soil does not significantly increase metal loading to tile drains relative to SS_DMB, thus, DI should be considered a DMB land application option.     

Seasonality of diffusive exchange of polychlorinated biphenyls and hexachlorobenzene across the air-sea interface of Kaohsiung Harbor, Taiwan

Gaseous and dissolved concentrations of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) were measured in the ambient air and water of Kaohsiung Harbor lagoon, Taiwan, from December 2003 to January 2005. During the rainy season (April to September), gaseous PCB and HCB concentrations were low due to both scavenging by precipitation and dilution by prevailing southwesterly winds blown from the atmosphere of the South China Sea. In contrast, trace precipitation and prevailing northeasterly winds during the dry season (October to March) resulted in higher gaseous PCB and HCB concentrations. Instantaneous air-water exchange fluxes of PCB homologues and HCB were calculated from 22 pairs of air and water samples from Kaohsiung Harbor lagoon. All net fluxes of PCB homologues and HCB in this study are from water to air (net volatilization). The highest net volatile flux observed was + 172 ng m^− 2 day^− 1 (dichlorobiphenyls) in December, 2003 due to the high wind speed and high dissolved concentration. The PCB homologues and HCB fluxes were significantly governed by dissolved concentrations in Kaohsiung Harbor lagoon. For low molecular weight PCBs (LMW PCBs), their fluxes were also significantly correlated with wind speed. The net PCB and HCB fluxes suggest that the annual sums of 69 PCBs and HCB measured in this study were mainly volatile (57.4 × 10³ and 28.3 × 10³ ng m^− 2 yr^− 1, respectively) and estimated yearly, 1.5 kg and 0.76 kg of PCBs and HCB were emitted from the harbor lagoon surface waters to the ambient atmosphere. The average tPCB flux in this study was about one-tenth of tPCB fluxes seen in New York Harbor and in the Delaware River, which are reported to be greatly impacted by PCBs.     

Anthropogenic acidification effects in primeval forests in the Transcarpathian Mts., western Ukraine

The precipitation chemistry, deposition, nutrient pools and composition of soils and soil water, as well as an estimate of historical deposition of sulphur (S) and inorganic nitrogen (N) for the period 1860-2008, were determined in primeval deciduous and coniferous forests at the sites Javornik and Pop Ivan, respectively. Measured S throughfall inputs of 10 kg ha^− 1 year^− 1 in 2008 were similar to those estimated for the period 1900-1950 at both sites. The highest estimated S inputs were in the 1980s. Measured bulk deposition of N in 2008 was lower at Pop Ivan (5.6 kg ha^− 1 year^− 1) compared to Javornik (12 kg ha^− 1 year^− 1). Significantly lower NO₃ deposition was both estimated and measured at Pop Ivan. Higher soil base cation concentrations were observed at well-buffered Javornik underlain by flysch (Ca pool of 2046 kg ha^− 1 and base saturation of 29%) compared to Pop Ivan underlain by crystalline schist (Ca pool of 186 kg ha^− 1 and base saturation of 6.5%). The soil pool of organic carbon (C) was higher at Pop Ivan (212 t ha^− 1) compared to Javornik (127 t ha^− 1). The C concentration was positively correlated with organic N in the soil (p < 0.001) at both sites, but the mass average C/N ratio in the forest floor was lower at Javornik (22) than at Pop Ivan (26). High N leaching of 17 kg ha^− 1 year^− 1 at the 90 cm depth was measured in the soil water at Javornik, suggesting high mineralization and nitrification rates in old growth deciduous forests in the area. Despite relatively low Al concentrations in the soil water, a low soil water Bc/Al ratio (0.9) (Bc = Ca + Mg + K) was found in the upper mineral soil at Pop Ivan. This suggests that the spruce forest ecosystems in the area are vulnerable to anthropogenic acidification and to the adverse effects of Al on forest root systems.     

DDT contamination from indoor residual spraying for malaria control

The insecticide DDT is still used in specific areas of South Africa for indoor residual spray (IRS) to control malaria vectors. Local residents could be exposed to residues of DDT through various pathways including indoor air, dust, soil, food and water. The aims of this study were to determine the levels of DDT contamination, as a result of IRS, in representative homesteads, and to evaluate the possible routes of human exposure. Two villages, exposed (DV) and reference (TV) were selected. Sampling was done two months after the IRS process was completed. Twelve homesteads were selected in DV and nine in TV. Human serum, indoor air, floor dust, outside soil, potable water, leafy vegetables, and chicken samples (muscle, fat and liver) were collected and analyzed for both the o,p′- and p,p′-isomers of DDT, DDD and DDE. DDT was detected in all the media analyzed indicating a combination of potential dietary and non-dietary pathways of uptake. DV had the most samples with detectable levels of DDT and its metabolites, and with the exception of chicken muscle samples, DV also had higher mean levels for all the components analyzed compared to TV. Seventy-nine percent of participants from DV had serum levels of DDT (mean ∑ DDT 7.3 µg g⁻¹ lipid). These residues constituted mainly of p,p′-DDD and p,p′-DDE. ∑ DDT levels were detected in all indoor air (mean ∑ DDT 3900.0 ng m^− 3) and floor dust (mean ∑ DDT 1200.0 µg m^− 2) samples. Levels were also detected in outside soil (mean ∑ DDT 25.0 µg kg^− 1) and potable water (mean ∑ DDT 2.0 µg L^− 1). Vegetable sample composition (mean ∑ DDT 43.0 µg kg^− 1) constituted mainly p,p′-DDT and p,p′-DDD. Chicken samples were highly contaminated with DDT (muscle mean ∑ DDT 700.0 µg kg^− 1, fat mean ∑ DDT 240,000.0 µg kg^− 1, liver mean ∑ DDT 1600.0 µg kg^− 1). The results of the current study raise concerns regarding the potential health effects in residents living in the immediate environment following DDT IRS.