Spatial Variation of the Precipitation Chemistry in the Thrace Region of Turkey

Pollutants affect not only the environment in which they originate since they are also transported by air currents to other locations. For this reason, air pollution is a global problem for all countries and the air and water quality need to be monitored carefully. More information on precipitation chemistry is required to determine the source of pollution as well as its effects on the ecosystems. In this study, precipitation chemistry has been analyzed for the first time by using simple bulk collectors located at four different sites in Northwest Turkey for a period of two years. About 650 sequential rainwater samples were collected and analyzed for pH, electrical conductivity, anions such as , , Cl^?, and cations such as Na⁺, K⁺, Mg²⁺, Ca²⁺, and . The selected sites were under the effect of different environmental factors. Our results showed that the highest and concentrations were measured in the Northwest of the research area. Additionally, it has been found that Ca²⁺ ions are abundant within all rainwater samples.     

Mineral Content of Bottled and Desalinated Household Drinking Water in Kuwait

Three hundred and twenty‐two samples of desalinated household water were collected from 99 sampling locations that covered 95% of Kuwaiti's residential areas. Seventy‐one brands of bottled water were collected from Kuwaiti markets. The water quality parameters that were studied included pH, electrical conductivity (EC), total dissolved solids (TDS), F^?, Cl^?, Br^?, , , , , , , , and the major macronutrients Na⁺, K⁺, Ca²⁺, and Mg²⁺. The analysis yielded a large range of results for most of these parameters, with differences in some cases exceeding 10‐fold. With a few exceptions, the results were found to comply with US‐EPA and WHO standards. Only the water in two brands of bottled water was acidic (pH < 6.5). The TDS was found to be higher than the US‐EPA regulated value in 4 and 3% of the household samples and bottled water brands, respectively. The fluoride levels were generally higher in bottled water than in household water. However, the household water that was produced by the Doha desalination plant and some of the European brands of bottled water were the best samples studied in terms of their quantity of Ca²⁺, Mg²⁺, and Na⁺ compared with the DRI values for those substances. EC and TDS were positively correlated with , , Na⁺, K⁺, Ca²⁺, and Mg²⁺ for household water but only with Ca²⁺ and Mg²⁺ for bottled water.     

Spatial and temporal variations in summer precipitation in Japanese mountain areas

We examined spatial and temporal variations in precipitation measured during summer season between 1976 and 2007 for 28 stations located in mountain areas across Japan using the amount of precipitation (Pr), the mean depth of precipitation events (η), and the inverse of the mean interval times (λ). We obtained positive correlations between the period mean Pr (Pr ) and the period mean η ( ) and between Pr and the period mean λ ( ) for the 28 stations. Pr was more strongly related to than to , indicating the spatial variations in Pr that are primarily related to the variations in . In addition, Pr was more strongly related to η than to λ for most stations on the basis of data for 1976–2007, indicating that the year‐to‐year variations in Pr are primarily related to η. We also examined temporal trends in Pr, η and λ for 1976–2007 and found no systematic trends for 23 of the 28 stations, suggesting long‐term trends that are not common in mountain areas of Japan. The relationships between Pr and and between Pr and η presented in this study enable us to generate a temporal precipitation distribution pattern based on only Pr and Pr data, respectively. Furthermore, probabilistic stochastic hydrological models require precipitation characteristics as input; thus, this study contributes to the determination of hydrological cycles and their possible future changes in Japanese mountain areas and therefore to water resource management. Copyright © 2010 John Wiley & Sons, Ltd.     

Factors controlling groundwater chemistry in an agricultural area with complex topographic and land use patterns in mid‐western South Korea

Shallow and bedrock groundwater from granitic aquifers were investigated for the hydrogeochemistry of major and minor constituents in an agricultural area. Nitrate concentrations were observed up to 49 mg/l as NO₃‐N, with 22% of samples exceeding the drinking water standard, which could pose a significant threat because most residents rely on groundwater as their drinking water source. Principal component analysis revealed three principal components (PCs): (1) nitrate contamination, contributed by major cations, Cl^?, SO and NO , (2) reduction processes positively involving Fe, Mn and B, and negatively involving dissolved oxygen and NO and (3) natural mineralization, involving HCO and F^?. Cluster analysis, performed on the PC scores, resulted in seven sample groups, which were successfully identified by total depth, elevation and land use. The nitrate‐contaminated groups had mixed land uses, with locally concentrated residential areas. Uncontaminated groundwater groups were found in the natural environment, including high‐altitude spring water and bedrock groundwater with a higher degree of natural mineralization. Shallow groundwater groups in paddy fields in lowlands were affected by reducing environments, of which one group was characterized by high Fe, Mn and B, and negligible nitrate. Groundwater with intermediate nitrate and lower Cl^? and SO was found primarily in hilly terrains with orchards and vegetable gardens, indicating lower contaminant loadings than lowland areas. Higher concentrations of F^? and nitrate were observed in the nitrate‐contaminated water, which seemed unlikely to be explained by groundwater mixing. The strong acidity generated from nitrification may infiltrate deeper into the aquifer, induce accelerated weathering of bedrock and result in the coexistence of F^? and nitrate, which may be an evidence of intense nitrate loading, leading to soil acidification. Multivariate statistical analysis successfully delineated hydrochemical characteristics of groundwater attained by natural and anthropogenic processes in an agriculturally stressed area with complex topographic land use patterns. Copyright © 2009 John Wiley & Sons, Ltd.     

Experimental Designs Applied to Desorption of Dichromate Ions after Separation and Preconcentration from Natural and Industrial Water by Modified Nano‐Alumina

Nano‐alumina modified by 9‐aminoacridine was used as a sorbent for separation and determination of dichromate ions from water. Statistical method, based on surface response design, has been used for the optimization of dichromate ions elution from 9‐aminoacridine nano‐alumina. The adsorbed dichromate ions were found to be eluted quantitatively with 0.8 mol L^?1 KCl in 1.6 mol L^?1 NaOH which optimized by response surface design. Under optimum conditions, the accuracy, precision (relative standard deviation, RSD%) and R‐square of the method were calculated as >98, <3, and >94%, respectively. Remarkable agreement between experimental and theoretical data was confirmed the predicted assumption. The method was applied to the simultaneous determination of dichromate in natural and industrial water samples. We also examined the retention of dichromate anions in the presence of Cl^?, , and anions at pH 3.     

Adsorption–Reduction Behavior of Co(NH3) on Activated Carbon

A novel method has been put forward to retrofit the wet ammonia desulfurization process to realize the combined removal of sulfur dioxide and nitric oxide by introducing soluble cobalt(II) salt into aqueous ammonia solution. The active constituent of scrubbing NO from the flue gases is the produced by ammonia coordinating with Co²⁺. The regeneration of can be realized under the catalysis of activated carbon so as to sustain a high NO removal efficiency for a long time. In this paper, the adsorption–reduction behavior of on activated carbon has been researched using scanning electron microscopy, X‐ray diffraction, and X‐ray photoelectron spectroscopy. A conclusion can be drawn from the results that cobalt ions in the aqueous solution are adsorbed by activated carbon and most of them are reduced to Co²⁺ ions, and some of the Co²⁺ ions are further reduced into metallic cobalt. The results also demonstrate that the functional groups on the surface of carbon take part in this redox reaction. The C? H groups on the carbon surface are oxidized into C? OH, and then some of the hydroxyl groups are further oxidized into carbonyl or carboxyl groups.     

Atmospheric and Surface Water Pollution Interpretation in the Gdańsk Beltway Impact Range by the Use of Multivariate Analysis

The present study deals with the application of the hierarchical cluster analysis and non‐parametric tests in order to interpret the Gdańsk Beltway impact range. The data set represents concentration values for major inorganic ions (Na⁺, NH, K⁺, Mg²⁺, Ca²⁺, F⁻, Cl⁻, NO, and SO) as well as electrolytic conductivity and pH measured in various water samples [precipitation, throughfall water, road runoff, and surface water (drainage ditches, surface water reservoirs, and spring water)] collected in the vicinity of the beltway. Several similarity groups were discovered both in the objects and in the variables modes according to the water sample. In the majority of cases clear anthropogenic (fertilizers usage and transport, road salting in winter) and semi‐natural (sea salt aerosols, erosion of construction materials) impacts were discovered. Spatial variation was discovered for road runoff samples and samples collected from surface water reservoirs and springs. Surprisingly no clear seasonal variability was discovered for precipitation chemistry, while some evidences for existing of summer and winter specific chemical profile was discovered for road runoff samples. In general, limited range of the Gdańsk Beltway impact was proven.     

Capturing temporal variability for estimates of annual hydrochemical export from a first‐order agricultural catchment in southern Ontario,Canada

This 2‐year study (2000, 2001) reports annual nutrient (phosphorus, nitrate) export from a first‐order agricultural watershed in southern Ontario based on an intensive monitoring programme. The importance of storm and melt events in annual export estimates is demonstrated and the temporal variability in nutrient loading during events is related to processes occurring within the catchment. The feasibility of predicting event‐related nutrient export from hydrometric data is explored. The importance of sampling frequency throughout events is also shown. Export of total phosphorus (TP), soluble reactive phosphorus (SRP) and nitrate ( ) for 2000 and 2001 averaged 0·35 kg ha^?1 year^?1, 0·09 kg ha^?1 year^?1, and 35 kg ha^?1 year^?1 (as N) respectively. Approximately 75% of annual TP export, 80% of annual SRP export and 70% of annual export occurred during 28 events per year. A small number of large‐magnitude events (>34 mm) accounted for 18–42% of annual TP export, 0–61% of annual SRP export and 13–33% of annual NO export. Our results show that temporal variability in nutrient export is largely governed by discharge in this basin, and export can be predicted from discharge. SRP and TP export can also be predicted from discharge, but only for events that are not large in magnitude. The sampling interval throughout events is important in obtaining precise estimates of nutrient export, as infrequent sampling intervals may over‐ or under‐estimate nutrient export by ± 45% per event for P. This study improves our understanding of and P export patterns and our ability to predict or model them by relating temporal variability in event nutrient export to discharge and processes occurring within the basin, and also by exploring the significance of sampling interval in the context of the importance of individual events, season and temporal variability during events. Copyright © 2006 John Wiley & Sons, Ltd.     

Water Quality Management Based on Division of Dry and Wet Seasons in Pearl River Delta,China

In the Pearl River Delta (PRD), river water quality deteriorates continually due to the population increase and ongoing industrialization and urbanization. In this study, a water quality management paradigm based on the seasonal variation is proposed. For better exploring the seasonal change of water quality, wavelet analysis was used to analyze the division of dry and wet seasons in the PRD during 1952–2009. Then water quality seasonal variation in 2008 and relevant impact factors were analyzed by multivariate statistic methods as a case to make some management measures. The results show that there are some differences of dry and wet seasons division among different years. Wet season mainly appear from April to September, which occupy the largest proportion among the 58 years (about 70%) and then followed by the wet season from May to October (about 13.8% of the total years). As to the water quality of 2008, significant differences exist between dry and wet seasons for 17 water quality parameters except TP, , Fe²⁺, and Zn²⁺. Levels of parameters pH, EC, COD_Mn, BOD₅, , , and Cl^? in dry season are much higher than those in wet season. In dry season the variations of river water quality are mainly influenced by domestic sewage, industrial effluents, and salt water intrusion. While in wet season, except the aforementioned pollution sources, drainages from cultivated land and livestock farm are also the main factors influencing water pollution. Thus, water quality management measures are proposed in dry and wet seasons, respectively. The results obtained from this study would further facilitate water quality protection and water resources management in the PRD.     

Factors Affecting UV/H2O2 Oxidation of 17α‐Ethynyestradiol in Water

In this study, bench‐scale experiments were conducted to examine the UV/H₂O₂ oxidation of 17α‐ethynyestradiol (EE2) in water in a batch operation mode. The EE2 degradation exhibited pseudo‐first‐order kinetics, and the removal was ascribed to the production of hydroxyl radicals (^?OH) by the UV/H₂O₂ system. Typically, the EE2 oxidation rate increased with increasing UV intensity and H₂O₂ dose, and with deceasing initial EE2 levels and solution pH. At EE2₀ = 650 µg/L, UV intensity = 154 µW/cm², H₂O₂ = 5 mg/L, and neutral pH, the UV/H₂O₂ treatment was able to remove 90% of the EE2 content within 30 min. Four anions commonly present in water were found to inhibit EE2 degradation to varying degrees: > > Cl^? > . Our results demonstrate that the described UV/H₂O₂ process is an effective method to control EE2 pollution in water.     

Magnesium Ammonium Phosphate Production from Wastewater through Box–Behnken Design and Its Effect on Nutrient Element Uptake in Plants

This study examined ${\rm NH}_{{\rm 4}}^{{\rm + }} $ , ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ recovery and the concentration of residual ions from anaerobic effluent of the potato processing industry through magnesium ammonium phosphate (MAP) precipitation using a Box–Behnken design. The regression model was statistically significant in terms of ${\rm NH}_{{\rm 4}}^{{\rm + }} $ and ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ removal efficiency and residual ion concentrations. Optimum ${\rm NH}_{{\rm 4}}^{{\rm + }} $ and ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ removal was obtained at pH 9.50 and at Mg²⁺/${\rm NH}_{{\rm 4}}^{{\rm + }} $ /${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ molar ratio of 1.8:1:1.8. Under these conditions, Mg, Ca, K, Fe, and Cl concentrations required for plant growth significantly decreased with MAP precipitation, which was supported by EDX analysis of dry MAP precipitate. The fertilizer effect of MAP on the growth of corn and tomato plants was compared with chemical fertilizers through pot trials. Nutrient element uptake levels of plants were examined in different fertilizer sources. While Mg, Fe, Cu, Mn, and Zn nutrient element uptake levels were sufficient in MAP pots, Ca uptake exceeded sufficient level. Average levels of N, P, K, Mg, Cu, and Mn of corn plant were higher in MAP than other pots. The average N, P, and Mg levels of tomato plant in MAP pots were higher than other pots. N/K ratio, which is important in tomato plants, was better optimized in MAP pots. Only Ni, Cr, and Pb heavy metals were found in plants.     

Chemical dynamics of N-containing ionic species in a boreal forest snowcover during the spring melt period

A study of the changes in the ionic loads of NO, NH, SO and H⁺ in a boreal forest snowpack at Lake Laflamme, Québec was carried out using hydrological and chemical data from field lysimeters. The results showed that depletion of the N-containing species occurs periodically in the snowpack during meltwater discharge. Rain-on-snow events led to in-pack losses of NO and NH at a rate of 130 μeq m^?2 day^?1 and 101·3 μeq m^?2day^?1 respectively. On dry days, however, dry deposition and deposition of organic debris from the canopy resulted in increases of 183·3 μeq m^?2day^?1 for NO and 4·5 μeq m^?2day^?1 for NH in the pack. In contrast, SO₄^2? showed continual in-pack increases due to deposition of 5·0 μeq m^?2day^?1 for wet days and 92·6 μeq m^?2day^?1 for dry days. The depletion of NO and NH is due to microbiological uptake of these nutrients during periods when the free water content of the pack is high. Controlled melts in a laboratory snowmelt simulator containing snow and organic matter from the forest canopy at Lake Laflamme showed losses of NO and NH similar to those observed in the field. As the microbiological uptake proceeds at a rate comparable to that of ionic load increases in the pack by dry deposition, models of the chemical dynamics of snowmelt should take the former into account in any system where organic content of the snowpack is appreciable.     

Regulating Environmental Factors of Nutrients Release from Wheat Straw Biochar for Sustainable Agriculture

One mechanism by which biochar application enhances soil nutrient availability is through direct nutrients release from biochar. However, factors controlling the release processes are poorly understood. In this study, the effects of pH, biochar to water ratio, temperature, ionic strength, and equilibration time on the release of PO, NO, NH, K⁺, Na⁺, Ca²⁺, and Mg²⁺ from biochar were evaluated in simulated experiments. The release of PO, K⁺, Ca²⁺, and Mg²⁺ was significantly affected by extraction pH, suggesting that their release from biochar was pH dependent or an H⁺‐consuming process. Correlation analysis indicated that PO and Ca²⁺, PO and Mg²⁺, and Ca²⁺ and Mg²⁺ were co‐solubilized with increasing soil acidity. To a lesser extent, the recovery of the nutrients was also affected by the ratio of biochar to water: more nutrients were soluble with more water supply. In contrast, the release of Na was not affected by pH while the concentration increased with decreasing biochar to water ratio. Meanwhile, other factors (temperature, ionic strength, and equilibration time) had less effect on nutrient release from biochar. Under the influence of pH, the patterns of NO and PO release from biochar were different: extractable NO concentration was not affected by the pH but more PO was released in strongly acidic conditions. Our data suggested that P was mainly retained in inorganic forms while N was in organic forms in biochar. We conclude that environmental factors have marked influences on nutrients release from biochar.     

Monitoring of Impact of Ferti‐irrigation by Post‐methanated Distillery Effluent on Groundwater Quality

The impact assessment of molasses‐based distillery‐effluent irrigation on groundwater quality around village Gajraula in the district of Jyotiba Phule Nagar, Uttar Pradesh, India was studied by sampling groundwater on monthly intervals consecutively for summer, winter and monsoon seasons during 2006–2007 and water quality parameters, viz. pH, electrical conductivity (EC), chloride (Cl^?), sulphate (SO), nitrate (NO), chemical oxygen demand (COD), total solids (TS), total dissolved solids (TDS), sodium (Na⁺), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), zinc (Zn²⁺), iron (Fe³⁺), and total coliforms (TC) were monitored. Results depicted that the values of all parameters decreased with increasing depth of water table. Sulphate, nitrate and potassium contents were maximal in agricultural site during monsoon while EC, Cl^?, TS, TDS, Na⁺, Ca²⁺, Mg²⁺, Zn, and Fe were maximal in industrial sites during summer. Groundwater samples of residential site harboured maximum coliforms especially during monsoon, highlighting threat to groundwater. Significant positive correlation matrix between coliforms with nitrate, sulphate and potassium ions explained their survival on these nutrients. To overcome this, important measures emphasizing improvement in effluent treatment technology matching site‐specific characteristics are recommended for eco‐friendly ferti‐irrigation.     

Carbamazepine Removal from Groundwater: Effectiveness of the TiO2/UV,Nanoparticulate Zero‐Valent Iron,and Fenton (NZVI/H2O2) Processes

Pharmaceutical compounds, widely produced and used all around the world, are partly responsible for the widespread water pollution in the environment. Carbamazepine (CBZ) is an antiepileptic drug that persists in the environment for many years. In the present study, we used the TiO₂/UV, nanoparticulate zero‐valent iron (NZVI), and NZVI/H₂O₂ treatment processes to compare efficiency of CBZ removal from water. Influence of NZVI loading, H₂O₂ concentration, TiO₂ loading, UV lamp power, and the matrix (distilled water and groundwater) on CBZ removal efficiency was evaluated using full factorial design. Results indicated that the NZVI/H₂O₂ process oxidized CBZ within 5 min. On the other hand, the NZVI process alone did not reduce CBZ concentration after 120 min of process time. The NZVI/H₂O₂ process was equally effective in CBZ removal from both distilled water and groundwater whereas the TiO₂/UV process was less effective due to the presence of ions in groundwater. CBZ removal efficiency of the TiO₂/UV process declined 30% when the matrix was changed from distilled water to groundwater. Negative divalent ions, i.e., and , were the main cause of reduction of CBZ removal efficiency from groundwater. It is likely that these two ions adsorb onto, and consequently prevent the superoxide anion and hydroxyl radical OH^? from being generated on, the surface of the TiO₂.     

Floodplain catastrophes in the UK Holocene: messages for managing climate change

Floodplains may be transformed when environmental changes or human activity causes alluvial systems to cross channel pattern thresholds. Thresholds between pattern states based on occurrence fields are only available for some pattern distinctions, and these may not encompass the alluvial contexts and range of dynamic factors involved. Pattern changes now known from the UK Holocene are reviewed as a basis for appreciating the potential for future transformations in a changing environment. These involved episodic boulder and gravel spreads in upland environments, and braiding meandering, anastomosing → meandering and active inactive transformations in more lowland contexts. Concern for possible impacts of climatic change need to be grounded in an appreciation of the nature and scale of these past changes. Some potential future changes may be relatively predictable in location (braiding meandering); others are more difficult given both present knowledge and the varying, modified and inheritance‐rich ‘contexts of vulnerability’ that floodplains now represent. Implications for management are discussed. Copyright © 2010 John Wiley & Sons, Ltd.     

Groundwater quality in Mesogea basin in eastern Attica (Greece)

Studies on the hydrogeological conditions of the Mesogea basin in east Attica reveal that the aquifers developed on the post‐alpine formations at the inner part of the coastal brackish zone exhibit positive hydraulic head. These Neogene and Quaternary deposits present high salt concentrations. Selected points were sampled (total 85: 51 wells and 34 boreholes) in order to obtain hydrogeological and hydrochemical data for a better understanding of the structure, operation and dynamics of the aquifer of the area. Statistical methods, R‐mode factor analysis and scatter‐plot diagrams were used for the hydrochemical analysis and presentation of the data. The groundwater resources are relatively weak and there is significant quality degradation due to the geological structure of the greater area, as well as the bad management of the aquifer and anthropogenic activities. Groundwater is characterized by high salt concentrations. Electrical conductivity values range between 260 and 6970 µS cm^?1. High salt concentrations at the coastal aquifers are due to sea intrusion, whereas they are attributed to the dissolution of minerals of the geological environment in the inland area. The groundwaters of the study area can be classified into five water types: Ca–HCO₃, Mg–HCO₃, Na–HCO₃, Na–Cl and Mg–Cl. They are saturated in dolomite and calcite, whereas they are unsaturated in anhydrite. High ion concentrations, e.g. ] (0‐221 mg l^?1), ] (0·01‐1·88 mg l^?1), ] (0·01‐6·75 mg l^?1), as well as high heavy metals concentrations are attributed to anthropogenic impacts. Copyright © 2006 John Wiley & Sons, Ltd.     

Temporal trends of bulk precipitation and stream water chemistry (1977–1997) in a small forested area,Krusné hory,northern Bohemia,Czech Republic

The Krusné hory (Erzgebirge or Ore Mountains) has been heavily affected by high atmospheric pollutant deposition caused by fossil fuel combustion in an adjacent Tertiary coal basin. Long‐term routine sampling of bulk precipitation (1977–1996) and stream water (1977–1998) in a forested area on the south‐eastern slope of the mountains were used to evaluate trends and patterns in solute concentration and flux with respect to controlling processes. From 1977 to 1996, the annual volume‐weighted Ca²⁺ and SOconcentrations decreased in bulk precipitation. However, after 1989, when a pronounced and continuous decrease occurred in coal production, annual volume‐weighted concentrations decreased for most solutes, except H⁺. The concentration decreases were marked, with 1996 levels at or below 50% of those in 1989. The lack of a trend in H⁺ is attributed to similar decreases in both acid anions and neutralizing base cations. Stream water concentrations of most solutes, i.e. H⁺, Ca²⁺, Mg²⁺, SONOwere highest at the onset of sampling in 1977, decreased markedly from 1977 to 1983 and decreased more gradually from 1983 to 1998. The spruce forest die‐back and removal reduced dry deposition of these solutes by reducing the filtering action, which was provided by the forest canopy. A notable decrease in stream water Ca²⁺ concentrations occurred after 1995 and may be due to the depletion of Ca²⁺, which was provided by catchment liming in 1986, 1988 and 1989. Solute flux trends in bulk atmospheric deposition and stream water generally were not significant and the lack of trend is attributed to the large interannual variability in precipitation quantity and runoff, respectively. All solutes except Na⁺ varied seasonally. The average seasonal concentrations varied between the solutes, but for most solutes were highest in winter and spring and lowest in summer, correlating with the seasonal trend in runoff. For Ca²⁺, Mg²⁺ and SOthe concentration minimum occurs in September and the maximum occurs in February or March, correlating with the seasonal baseflow. These solutes are primarily controlled by the contribution of soil water and groundwater to stream flow. During snowmelt, the meltwater generally causes concentrations to decrease as soil water and groundwater are diluted. For NO₃ , average minimum concentrations occur in August at the end of the growing season concurrent with the lowest stream flow, and the maximum occurs in February and March with high stream flow during snowmelt. Seasonal stream water NOconcentration variations are large compared with the long‐term decrease. Copyright © 1999 John Wiley & Sons, Ltd.     

H2S Emissions from a Submerged Pilot‐Scale Fixed Bed Biofilm Reactor

A study was performed in two submerged, pilot‐scale biofilm bioreactors operated under different conditions to determine the relationship between the operating parameters and H₂S emission. H₂S was always detected in the exhaust air at concentrations varying from 1 to 353 ppm_v. The specific aeration rate was the most influencing parameter, with As < 30 kg COD (dissolved oxygen concentrations <4 mg L^?1) increasing noticeably the H₂S production. The periodical removal of the accumulated sludge reduced H₂S emissions by ～14%.