Effects of porosity,dry unit weight,cement content and void/cement ratio on unconfined compressive strength of roof tile waste-silty soil mixtures

One of the conventional ways to improve the mechanical behavior of soils is to mix them with cementing agents such as cement, lime and fly ash. Recently, introduction to alternative materials or sub-products that can be adopted to improve the soil strength is of paramount importance. Therefore, the present study aims to investigate the effects of porosity (η), dry unit weight (γ_d) of molding, cement content (C) and porosity/volumetric cement content ratio (η/C_iv) or void/cement ratio on the unconfined compressive strength (q_u or UCS) of silty soil–roof tile waste (RT) mixtures. Soil samples are molded into four different dry unit weights (i.e. 13 kN/m³, 13.67 kN/m³, 14.33 kN/m³ and 15 kN/m³) using 3%, 6% and 9% cement and 5%, 15% and 30% RT. The results show that with the addition of cement, the strength of the RT–soil mixtures increases in a linear manner. On the other hand, the addition of RT decreases q_u of the samples at a constant percentage of cement, and the decrease in porosity can increase q_u. A dosage equation is derived from the experimental data using the porosity/volumetric cement content ratio (η/C_iv) where the control variables are the moisture content, crushed tile content, cement content and porosity.     

The application of an ether cleavage technique to a study of the biodegradation of a linear alcohol ethoxylate nonionic surfactant

The biodegradation of a linear alcohol ethoxylate nonionic surfactant (C₁₂-C₁₅, eo₉) was studied by gas chromatography of the alkyl bromides produced by acid cleavage of the surfactant ether linkages with hydrogen bromide. In laboratory cultures and in a lake environment, a conventional method showed rapid loss of surface activity. The gas chromatographic method revealed a rapid degradation of the surfactant alkyl moiety but a slow and incomplete removal of the polyethoxylate moiety.     

Determination of anionic surface-active substances in waters

We have studied sorption on the SDB-L polymer sorbent of anionic surface-active substances (ASAS) of the alkylsulfate class with a different length of a hydrocarbon radical and alkylarylsulfonates (sulfanol), methylene blue in the presence and absence of ASAS. We have developed the technique of sorption-photometric determination of the latter in waters with determination limit, which depends on ASAS hydrophobicity and constituting for C₁₀-0.046, C₁₂, C₁₆-0.020–0.024, and sulfanol-0.010 mg/dm³ at the sample volume 25 cm³.     

The inhibition of photochemical smog V. Products of the diethylhydroxylamine inhibited reaction

Mixtures of 1.6–26 mTorr C₂H₄ and about half as much NO and either O or $\text{1}\text{4}$ as much diethylhydroxylamine (DEHA) in 10 Torr N₂, ～ 160 Torr O₂ and 0 or 10 Torr H₂O were irradiated to determine the products of reaction. With DEHA present an initial product was HONO. After a short induction period, CH₃CHO, N₂O, and C₂H₅OH were produced. C₂H₅NO₂, NO₂, and some CO₂ were produced after a longer induction period. The CH₃CHO, HONO, N₂O, C₂H₅NO₂, C₂H₅ONO₂, and C₂H₅OH were not produced in the absence of DEHA. The relative maximum concentrations of CH₃CHO, N₂O, C₂H₅NO₂, C₂H₅ONO₂, and C₂H₅OH were 81, 27, 88, 15, and 1.1%, respectively, compared to the initial DEHA concentration.The reaction of NO₂ with DEHA in the absence of O₂ produced CH₃CHO and HONO as major products and C₂H₅OH and C₂H₅ONO₂ as minor products. In the presence of O₂, C₂H₅NO₂ was also produced.A mechanism for the reaction is suggested. Since the presence of DEHA markedly inhibits the reaction (initial rate of C₂H₄ removal reduced by a factor of 5 and initial rate of conversion of NO to NO₂ reduced by a factor of 20), and the only products of reaction not now found in urban atmospheres are the harmless compounds C₂H₅OH and C₂H₅NO₂, it is recommended that DEHA be considered for addition to urban atmospheres to inhibit photochemical smog production.     

Volatile chlorinated hydrocarbons in a coastal urban atmosphere

Ambient airborne C₁- and C₂-chlorocarbons (CHCl₃, CCl₄, CH₃ CCl₃, C₂HCl₃ and C₂Cl₄) were measured by means of gas-liquid chromatography with electron capture detection. Concentrations of up to 50 μg m^?3 were found, indicating emission sources for CHCl₃, CH₃ CCl₃, C₂ HCl₃ and C₂Cl₄. No specific source could be revealed for CCl₄ in the area of a typical North German city. The ambient concentrations were found to be strongly influenced by wind direction. Except for CCl₄ the concentrations were significantly higher than those in remote atlantic air.     

A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury

Mercury (Hg) exposure causes health problems including cardiovascular diseases. Although precise mechanisms have not been precisely defined yet, matrix metalloproteinases (MMPs) may be involved. The gene encoding MMP-9 presents genetic polymorphisms which affect the expression and activity level of this enzyme. Two polymorphisms in the promoter region [C^− 1562T and (CA)_n] are functionally relevant, and are implicated in several diseases. This study aimed at examining how these polymorphisms affect the circulating MMP-9 levels and its endogenous inhibitor, the tissue inhibitor of metalloproteinase-1 (TIMP-1) in 266 subjects environmentally exposed to Hg. Blood and plasma Hg concentrations were determined by inductively coupled plasma-mass spectrometry (ICP-MS). MMP-9 and TIMP-1 concentrations were measured in plasma samples by gelatin zymography and ELISA, respectively. Genotypes for the C^− 1562T and the microsatellite (CA)_n polymorphisms were determined. We found a positive association (P < 0.05) between plasma Hg concentrations and MMP-9/TIMP-1 ratio (an index of net MMP-9 activity). When the subjects were divided into tertiles with basis on their plasma Hg concentrations, we found that the (CA)_n polymorphism modified MMP-9 concentrations and MMP-9/TIMP-1 ratio in subjects with the lowest Hg concentrations (first tertile), with the highest MMP-9 levels being found in subjects with genotypes including alleles with 21 or more CA repeats (H alleles) (P < 0.05). Conversely, this polymorphism had no effects on subjects with intermediate or high plasma Hg levels (second and third tertiles, respectively). The C^− 1562T polymorphism had no effects on MMP-9 levels. These findings suggest a significant interaction between the (CA)_n polymorphism and low levels of Hg exposure, possibly increasing the risk of developing diseases in subjects with H alleles.     

Contribution from the primary and secondary sources to the atmospheric formaldehyde in Kolkata, India

A novel and straight forward method is adopted to segregate the contribution of primary and secondary sources of formaldehyde based on the rates of its formation and removal at different times in the urban atmosphere of Kolkata. To achieve the above objective, the diurnal and seasonal mixing ratios of formaldehyde were measured during dry season at two busy roadside locations. The maximal secondary formation fluxes of formaldehyde during summer and winter were found to be 6.63 × 10⁷ and 1.23 × 10⁷ molecules cm^− 3 s^− 1, respectively. Apart from formaldehyde (C₁), several other carbonyls were quantified in this study. An overall good correlation between acetaldehyde (C₂) and propanal (C₃) indicates the contribution of vehicular emission to the carbonyl budget. The secondary formaldehyde contributions in summer and winter were about 71% and 32%, respectively. The relative mean contributions of C₁, C₂ and ozone towards generation of OH fluxes in summer were found to be 1.56 × 10⁷, 6.96 × 10⁵, and 1.29 × 10⁷ molecules cm^− 3 s^− 1, respectively, which were 3.2, 3.4 and 1.6 times higher than those in winter.     

Characterization of the burning behavior and gaseous emissions of pine needles in a cone calorimeter – FTIR apparatus

The paper presents flammability studies related with the combustion of Maritime pine needles (pinus pinaster, representative of Mediterranean vegetation) in a cone calorimeter (CC) under air atmosphere with piloted ignition and self-ignition for different heat fluxes, from 10 to 50 kW m⁻². The Main objective is to measure the yields of the gaseous emissions released during the experiments because one of the major risks during the fire is from the smoke and products of combustion. Identification of exhaust gaseous compounds and concentration measurements have been done by FTIR, NDIR, chemiluminescence and paramagnetism gas analyzers for assessing the fire behavior and identifying the decomposition chemistry. Among the 15 different compounds simultaneously analyzed, the yields of CH₄, CO₂, CO, H₂O, NO and O₂ have been quantified. HCN and light-weight hydrocarbons (C₂H₂, C₂H₄, C₃H₆ and C₃H₈) have been observed at low concentrations.The results show that carbon dioxide and water are the main emissions during the experiments. Also, the carbon balance shows that about 5% of the carbon released as carbon monoxide and hydrocarbon whatever the external heat flux chosen. Moreover, flammability parameters such as Mass Loss, Mass Loss Rate (MLR) and Time to Ignition (t_ig) have been determined for each condition during the experiments. Pine needles is considered often as a thermally thin material. However, the bed of pine needles behaves as a thermally thick material in the conditions tested.     

Electrochemical disinfection of Escherichia coli in the presence and absence of primary sludge particulates

Electrochemical (EC) residual disinfection of Escherichia coli (E. coli) in the presence and absence of primary sludge particulates (PSPs) was studied. The kinetics followed a first-order rate law. When PSPs were absent, the EC residual disinfection rate coefficient (k) increased linearly with EC pretreatment energy (E_C, 0–0.63 kWh/m³). However, with 143 mg PSPs/L, k first increased linearly with E_C (0–0.28 kWh/m³) and then decreased linearly with E_C (0.28–0.42 kWh/m³). H₂O₂ was detected during EC pretreatment in PSPs-free samples and the H₂O₂ concentration (C_H) increased with E_C (0–0.83 kWh/m³) linearly. Chloride was detected in PSPs aqueous samples (143 mg PSPs/L) and its concentration (C_C) changed during EC pretreatment: initially, a decrease of C_C was observed when E_C increased from 0 to 0.28 kWh/m³, followed by an increase of C_C when E_C increased 0.28–0.42 kWh/m³. In both cases, k correlated to the initial post-EC chloride concentration (C_CI) in an inverse linear relationship. This two-stage change of C_C and k was caused by a combination of two reactions: anodic oxidation of chloride and the reaction of chloramines with excess chlorine. This paper explains the mechanisms underlying EC residual disinfection in the presence and absence of PSPs, and proposes a feasible strategy for EC disinfection when PSPs are present, an approach that could be useful in the treatment of combined sewage overflow (CSO).     

Characterization of thermal properties and analysis of combustion behavior of PMMA in a cone calorimeter

This paper deals with the thermal degradation of a black poly(methyl)methacrylate (PMMA) in a cone calorimeter (CC) in air with a piloted ignition. The influence of several heat fluxes (11 kW m⁻² and 12 kW m⁻², and ten values from 15 to 60 kW m⁻² in steps of 5 kW m⁻²) on PMMA sample degradation and the decomposition chemistry has been studied. Thus, thermal properties have been deduced and calculated from ignition time and mass loss rate (MLR) curves. During our experiments, among compounds quantified simultaneously by a Fourier transformed infrared (FTIR) or gas analyzer, five main species (CO₂, CO, H₂O, NO and O₂) have been encountered, regardless of the external heat flux considered. The main product concentrations allow calculation of the corresponding emission yields. Thus, mass balances of C and H atoms contained in these exhaust gases were able to be compared with those included in the initial PMMA sample. Using the standard oxygen consumption method, heat release rate (HRR), total heat release (THR) and effective heat of combustion (EHC) have been calculated for each irradiance level. Therefore, these different results (thermal properties, emission yields, HRR, THR and EHC) are in quite good accordance (same order of magnitude) with those found in previous studies.     

Optimized enrichment and purification of ferrocyanide for C and N isotope analysis of aqueous solutions

The occurrence of ferrocyanide, Fe(CN)₆⁴⁻, in aqueous environments is of concern, since it is potentially hazardous. For tracing the source of ferrocyanide in contaminated water we developed a method that relies on the determination of the stable isotope ratios of ¹³C/¹²C and ¹⁵N/¹⁴N of this complexed cyanide (CN) after precipitating it as cupric ferrocyanide, Cu₂[Fe(CN)₆]·7H₂O. The precipitate was combusted and the isotope ratios were determined by continuous flow isotope ratio mass spectrometry.At first, ferrocyanide enrichment from synthetic water containing cyanide with known isotopic composition was studied by using six commercial anion-exchange resins. Five resins revealed a quick and complete sorption of ferrocyanide. A nearly quantitative desorption was achieved using NaCl solutions of 5 and 10% by weight for four resins. Subsequent determination of the δ¹³C_CN and δ¹⁵N_CN values of the ferrocyanide revealed that no significant isotope fractionation occurred during this procedure. These results were reproduced even in column experiments using larger water volumes.Potential interferences were also addressed. Sulfate in excess competes for exchange sites but can be precipitated as BaSO₄ prior to ferrocyanide enrichment. Non-cyanide carbon compounds may co-precipitate with cupric ferrocyanide, thus possibly modifying the isotope ratios. However, neither dissolved inorganic carbon nor highly soluble organic compounds did interfere with the method. Poorly soluble organics like BTEX and PAH can be eliminated by passing the samples through appropriate adsorber resins in a prior step.The proposed method is an excellent way of precise determination of the stable cyanide-carbon and cyanide-nitrogen isotope ratios in ferrocyanide-containing aqueous samples, which was successfully applied to four contaminated groundwater samples since measured aqueous isotopes ratios match those of corresponding cyanide-bearing solid wastes.     

Comparative study on organic constituents in polluted and unpolluted inland aquatic environments-I features of hydrocarbons for polluted and unpolluted waters

The constituents of hydrocarbons between highly polluted river waters collected from the Tokyo area and unpolluted river, brook, reservoir and pond waters obtained from the Ogasawara (Bonin) Islands were compared to characterize their features for polluted and unpolluted waters. n-Alkanes between the carbon chain length of C₁₂ and C₃₆, squalane and unresolved complex mixture of hydrocarbons (UCMH) were found in most of the river waters of the Tokyo area at the contents ranging from 0.026 to 14 μg 1⁻¹, from 0.004 to 1.7 μg 1⁻¹ and from less than 5 to 290 μg 1⁻¹, respectively, whereas in the waters of the Ogasawara Islands, only n-alkanes ranging from C₁₃ to C₃₇ were found with the great predominance of odd-carbon numbers at the contents varying from 0.042 to 4.0 μg 1⁻¹.It was indicated that the presence of squalane, UCMH and even-carbon numbered n-alkanes as the major constituents are intimately correlated with artificial hydrocarbon sources (fossil fuels and their products and both combustion products, and industrial products), while the great predominance of odd-carbon numbered n-alkanes for the unpolluted areas are mainly due to algae and higher plants. Besides, the major portion of n-alkanes, squalane and UCMH are thought to be present in polluted and unpolluted waters associated with particulate materials.     

The anaerobic degradation of detergent range fatty alcohol ethoxylates. Studies with C-labelled model surfactants

The anaerobic degradation of fatty alcohol polyglycol ethers was studied in a model sludge digester employing stearyl alcohol ethoxylate which was ¹⁴C-labelled either in the alkyl or in the heptaglycol chain. After 4-weeks' incubation of the ¹⁴C-compounds at 35°C in the presence of raw sludge as additional digestible substrate more than 80% of the initial radioactivity was found as methane and carbon dioxide. In addition, the major part of radioactivity in the digested sludge, corresponding to nearly 10% of added ¹⁴C, was attributable to biomass so that ultimate degradation of the two model surfactants amounted to more than 90%. Analysis of the small fraction of radiolabelled metabolites in the sludge supernatant allowed conclusions with regard to the anaerobic degradation route of linear alcohol ethoxylates. After primary biodegradation of the surfactant molecule by scission into the alkyl and poly(ethylene glycol) moieties the further biodegradation of the latter seems to proceed as under aerobic conditions, i.e. via oxidative or hydrolytic depolymerization steps. Eventually, ultimate biodegradation of the obtained monomers (C₂-units) leads to the formation of the gaseous end products.     

Indoor air quality in new and renovated low-income apartments with mechanical ventilation and natural gas cooking in California

This paper presents pollutant concentrations and performance data for code-required mechanical ventilation equipment in 23 low-income apartments at 4 properties constructed or renovated 2013-2017. All apartments had natural gas cooking burners. Occupants pledged to not use windows for ventilation during the study but several did. Measured airflows of range hoods and bathroom exhaust fans were lower than product specifications. Only eight apartments operationally met all ventilation code requirements. Pollutants measured over one week in each apartment included time-resolved fine particulate matter (PM_2.5), nitrogen dioxide (NO₂), formaldehyde and carbon dioxide (CO₂) and time-integrated formaldehyde, NO₂ and nitrogen oxides (NO_X). Compared to a recent study of California houses with code-compliant ventilation, apartments were smaller, had fewer occupants, higher densities, and higher mechanical ventilation rates. Mean PM_2.5, formaldehyde, NO₂, and CO₂ were 7.7 µg/m³, 14.1, 18.8, and 741 ppm in apartments; these are 4% lower, 25% lower, 165% higher, and 18% higher compared to houses with similar cooking frequency. Four apartments had weekly PM_2.5 above the California annual outdoor standard of 12 µg/m³ and also discrete days above the World Health Organization 24-hour guideline of 25 µg/m³. Two apartments had weekly NO₂ above the California annual outdoor standard of 30 ppb.     

Comparative study on organic constituents in polluted and unpolluted inland aquatic environments—V: Organic carbons and hydrocarbons in sediments

Organic carbons and hydrocarbons were analysed for polluted sediments from Tama River and sludges from night soil and sewage treatment plants in the Tokyo area and unpolluted sediments from river and reservoirs from Chichi-jima Island in the Ogasawara (Bonin) Islands to characterize their features for polluted and unpolluted aquatic environments. In addition the relationships of the features of organic constituents between waters and sediments were given. The contents of n-alkanes (C₁₄-C₃₆). squalane and unresolved complex mixture of hydrocarbons (UCMH) for the sediments from Tama River ranged from 16 to 94, 0.86–15 and 250–1100 μ g⁻¹ dry base, which are much higher than those of the sediments from Chichi-jima Island. The major constituents of hydrocarbons in the sediments and sludges from the Tokyo area were mainly odd-carbon numbered n-alkanes and squalane, whereas those of the island were only odd-carbon numbered n-alkanes. Hydrocarbons as carbon (total content × 0.851. as C₂₀H₄₂, HCC)/total organic carbon (TOC), HCC/extractable organic carbon with ethyl acetate (EOC), squalane as carbon (SqC)/TOC. SqC/EOC and UCMH/n-Alkane (C₁₅-C₃₃) values for the sediments from Tama River were much higher than those of the sediments from the island, while carbon preference index (CPI_H) values for the sediments of Tama River were considerably lower than those of the island. It was thus indicated that HCC/TOC, HCC/EOC, UCMH/n-Alkane and CPI^H values should be the important indicators of hydrocarbon pollution for aquatic environments. In addition SqC/TOC and SqC/EOC ratios are apparently useful measures of urban-industrial activities on aquatic environments.The similarity of the nature of hydrocarbons of sediments and sludges from the Tokyo area indicated that the sewage contributed considerably to urban river sediments. Further it was also indicated that hydrocarbons were concentrated in sedimentary environments, although the features of hydrocarbons in sediments are generally similar to those of waters.     

The anaerobic degradation of detergent range fatty alcohol ethoxylates. Studies with 14C-labelled model surfactants

The anaerobic degradation of fatty alcohol polyglycol ethers was studied in a model sludge digester employing stearyl alcohol ethoxylate which was ¹⁴C-labelled either in the alkyl or in the heptaglycol chain. After 4-weeks' incubation of the ¹⁴C-compounds at 35°C in the presence of raw sludge as additional digestible substrate more than 80% of the initial radioactivity was found as methane and carbon dioxide. In addition, the major part of radioactivity in the digested sludge, corresponding to nearly 10% of added ¹⁴C, was attributable to biomass so that ultimate degradation of the two model surfactants amounted to more than 90%. Analysis of the small fraction of radiolabelled metabolites in the sludge supernatant allowed conclusions with regard to the anaerobic degradation route of linear alcohol ethoxylates. After primary biodegradation of the surfactant molecule by scission into the alkyl and poly(ethylene glycol) moieties the further biodegradation of the latter seems to proceed as under aerobic conditions, i.e. via oxidative or hydrolytic depolymerization steps. Eventually, ultimate biodegradation of the obtained monomers (C₂-units) leads to the formation of the gaseous end products.     

Uptake and release of zinc by aquatic bryophytes (Fontinalis antipyretica L. ex. Hedw.)

The zinc uptake and posterior release by an aquatic bryophyte—Fontinalis antipyretica L. Ex Hedw.—was experimentally studied in laboratory exposing the plants to different zinc concentrations in the range, 1.0–5.0 mg l⁻¹, for a 144 h contamination period, and then exposed to metal-free water for a 120 h decontamination period. The experiments were carried out in perfectly mixed contactors at controlled illumination, using mosses picked out in February 1997, with a background initial zinc concentration of 263 mg g⁻¹ (dry wt.). A first-order mass transfer kinetic model was fitted to the experimental data to determine the uptake and release constants, k₁ and k₂, the zinc concentration in mosses at the end of the uptake period, C_mu, and at the equilibrium, for the contamination and decontamination stages, C_me and C_mr, respectively. A bioconcentration factor, BCF=k₁/k₂ (zinc concentration in the plant, dry wt./zinc concentration in the water) was determined. A biological elimination factor defined as BEF=1−C_mr/C_mu was also calculated. BCF decreases from about 4500 to 2950 as Zn concentration in water increases from 1.05 to 3.80 mg l⁻¹. BEF is approximately constant and equal to 0.80. Comparing Zn and Cu accumulation by Fontinalis antipyretica, it was concluded that the uptake rate for Zn (145 h⁻¹) is much lower than for Cu (628 h⁻¹) and the amount retained by the plant decreased by a factor of about seven.     

Ultrafine,fine, and black carbon particle concentrations in California child‐care facilities

Although many U.S. children spend time in child care, little information exists on exposures to airborne particulate matter (PM) in this environment, even though PM may be associated with asthma and other respiratory illness, which is a key concern for young children. To address this data gap, we measured ultrafine particles (UFP), PM_2.5, PM₁₀, and black carbon in 40 California child‐care facilities and examined associations with potential determinants. We also tested a low‐cost optical particle measuring device (Dylos monitor). Median (interquartile range) concentrations for indoor UFP, gravimetric PM_2.5, real‐time PM_2.5, gravimetric PM₁₀, and black carbon over the course of a child‐care day were 14 000 (11 000‐29 000) particles/cm³, 15 (9.6‐21) μg/m³, 15 (11‐23) μg/m³, 48 (33‐73) μg/m³, and 0.43 (0.25‐0.65) ng/m³, respectively. Indoor black carbon concentrations were inversely associated with air exchange rate (Spearman's rho = ?.36) and positively associated with the sum of all Gaussian‐adjusted traffic volume within a one‐kilometer radius (Spearman's rho = .45) (P‐values <.05). Finally, the Dylos may be a valid low‐cost alternative to monitor PM levels indoors in future studies. Overall, results indicate the need for additional studies examining particle levels, potential health risks, and mitigation strategies in child‐care facilities.     

The toxic effects of trinitrotoluene (TNT) and its primary degradation products on two species of algae and the fathead minnow

The effects of alpha trinitrotoluene (alpha TNT) and its primary degradation product (TNTcc), commonly referred to as “pink water”, were determined on members of two trophic levels. The growth responses of the algae Selenastrum capricornutum and Microcystis aeruginosa were examined through static bioassays. Death and behavioral responses of the fathead minnow (Pimephales promelas) were determined using a proportional diluter. Alpha TNT and TNTcc were both more toxic to the fathead minnow than to either species of alga. Five and 15 mg l⁻¹ alpha TNT inhibited S. capricornutum and M. aeruginosa growth, respectively. TNTcc inhibited S. capricornutum growth at concentrations above 9 mg l⁻¹; it was lethal to M. aeruginosa at 50 mg l⁻¹, but stimulated growth at lower concentrations. The 96-h lc₅₀ values based on the death response of the fathead minnow to alpha TNT and TNTcc were 2.58 and 1.60 mg l⁻¹, respectively. The 96-h ec₅₀ values based on the behavioral responses were 0.46 and 0.64 mg l⁻¹, respectively. There was no response to concentrations of 0.05 mg l⁻¹ alpha TNT and 0.07 mg l⁻¹ TNTcc.     

Evaluation of wastewater nitrogen transformation in a natural wetland (Ulaanbaatar, Mongolia) using dual-isotope analysis of nitrate

The Tuul River, which provides water for the daily needs of many residents of Ulaanbaatar, Mongolia, has been increasingly polluted by wastewater from the city's sewage treatment plant. Information on water movement and the transformation of water-borne materials is required to alleviate the deterioration of water quality. We conducted a synoptic survey of general water movement, water quality including inorganic nitrogen concentrations, and isotopic composition of nitrogen (δ¹⁵N-NO₃⁻, δ¹⁸O-NO₃⁻, and δ¹⁵N-NH₄⁺) and water (δ¹⁸O-H₂O) in a wetland area that receives wastewater before it enters the Tuul River. We sampled surface water, groundwater, and spring water along the two major water routes in the wetland that flow from the drain of the sewage treatment plant to the Tuul River: a continuous tributary and a discontinuous tributary. The continuous tributary had high ammonium (NH₄⁺) concentrations and nearly stable δ¹⁵N-NH₄⁺, δ¹⁵N-NO₃⁻, and δ¹⁸O-NO₃⁻ concentrations throughout its length, indicating that nitrogen transformation (i.e., nitrification and denitrification) during transit was small. In contrast, NH₄⁺ concentrations decreased along the discontinuous tributary and nitrate (NO₃⁻) concentrations were low at many points. Values of δ¹⁵N-NH₄⁺, δ¹⁵N-NO₃⁻, and δ¹⁸O-NO₃⁻ increased with flow along the discontinuous route. Our results indicate that nitrification and denitrification contribute to nitrogen removal in the wetland area along the discontinuous tributary with slow water transport. Differences in hydrological pathways and the velocity of wastewater transport through the wetland area greatly affect the extent of nitrogen removal.