Elevated concentrations of endotoxin in indoor air due to cigarette smoking

Exposure to environmental tobacco smoke (ETS) is an important worldwide public health issue. The present study demonstrates that cigarette smoke can be a major source of endotoxin (lipopolysaccharide, LPS) in indoor environments. Gas-chromatography/mass-spectrometry was used to determine 3-hydroxy fatty acids as markers of endotoxin in air-borne house dust in homes of smokers and non-smokers. Air concentrations of endotoxin were 4-63 times higher in rooms of smoking students than in identical rooms of non-smoking students. The fact that cigarette smoke contains large amounts of endotoxin may partly explain the high prevalence of respiratory disorders among smokers and may also draw attention to a hitherto neglected risk factor of ETS.     

Cost-effective monitoring for a soil vapor extraction (SVE) system: a simplified modeling and gas sensor test

In order to establish cost-effective monitoring strategies for soil vapor extraction (SVE), a simplified model for multi-component mass transfer of a complex liquid mixture in porous media and gas sensor are proposed and experimentally evaluated. The basic task for the cost-effective monitoring of SVE is to decide how to predict the performances of venting systems in terms of the contaminant vapor removal rate and the time required to accomplish the clean-up specification. The method includes classifying of individual components of a complex mixture on the basis of gas chromatographic (GC) profile and treating each resulting group as a pseudo-single compound. BTEX components of gasoline were selected for model input and the remainders were divided into 4 groups based on their GC retention times. The model proposed in this study is capable of predicting with accuracy volatilization behaviors of gasoline components in soil and the gas sensor (FIGARO TGS 823) was tested by GC-FID to toluene and TPH-GRO(Total Petroleum Hydrocarbon-Gasoline Range Organics) gas samples. A VOC gas sensor was developed which recognizes TPH-GRO concentrations between 250 and 50 ppm. The developed gas sensor test and proposed model can be used as a valuable tool for the cost-effective monitoring for SVE systems.     

Evaluation of the methyl ester O-methyl acetate derivative of muramic acid for the determination of peptidoglycan in environmental samples by ion-trap GC-MS-MS

Muramic acid (MA) is a unique amino sugar that is a constituent of the peptidoglycan (PG) present in prokaryotic cell walls. MA can serve as a marker for quantifying bacterial load, e.g. in indoor environments, by using gas chromatography-tandem mass spectrometry (GC-MS-MS). We demonstrated recently that the methyl ester O-methyl acetate (MMA) derivative can be used to detect MA in house dust by ion-trap GC-MS-MS. However, since the MMA derivative is not formed from free MA quantification was not optimal. Here we report 1) significant improvements in sample preparation of the MMA derivative and 2) an evaluation of the performance of derivative, using for comparison the alditol acetate derivative, the gold standard in quantitative trace analysis of MA in complex matrices. The MMA derivative was analysed using an MS instrument with internal ionization and the alditol acetate derivative was analysed using an instrument with external ionization. 13C-labelled cyanobacteria, containing MA in their PG, were used as the internal standard. A linear relationship was found between the two methods in studies on 27 parallel samples of airborne dust from school classes collected on filters. Although the analytical sensitivity of the MMA derivatives was somewhat slightly lower than of the alditol acetate derivative, this may be due to differences in yield of derivative, sample clean-up efficiency, or different performance of the GC columns or MS instruments. However preparation of the MMA derivative is quick and compatible with preparation of methyl esters of 3-hydroxy fatty acids (used as markers of Gram negative endotoxin) allowing the levels of both markers to be determined in the same dust sample. In conclusion, the MMA procedure can be used to determine MA in environmental samples with good reproducibility provided the concentration of the 13C-labelled MA internal standard in the cyanobacteria is first determined with an alternative method.     

Effect of corona discharge on the gas composition of the sample flow in a Gas Particle Partitioner

A Gas Particle Partitioner (GPP) that allows highly efficient separation of gas and particles with no effect on the thermodynamic conditions and substantially no change of the gas composition has been developed. The GPP is a coaxial arrangement with inner and outer electrodes and utilizes a corona discharge to electrically charge the particles and a strong electric field to remove them from the sample flow. Several measures were taken to avoid an influence of the corona discharge on the gas composition. The GPP can be applied for various applications. This paper focuses on the use of the GPP as a pre-filter for gas analyzers, where zero pressure drop and a minimization of the influence of the corona discharge on the gas composition are the main objective. Due to its design, the GPP introduces no changes to the thermodynamic conditions. However, corona discharge is known to produce significant amounts of ozone and oxides of nitrogen. The effect of the corona on the gas composition of the sample flow was determined under various conditions. The gas concentrations strongly depended on several aspects, such as material and diameter of the corona wire and polarity of the corona voltage. Due to the measures taken to minimize an effect on the gas composition, the concentrations of these gases could effectively be reduced. Along with the maximum gas-particle separation efficiency of near 100%, the additional O3 concentration was 42 ppbV and the additional NO2 concentration 15 ppbV. If an efficiency of 95% is acceptable, the added concentrations can be as low as 2.5 ppbV (O3) and 0.5 ppbV (NO2), respectively.     

Paramagnetic antibody-modified microparticles coupled with voltammetry as a tool for isolation and detection of metallothionen as a bioindicator of metal pollution

Low-molecular mass proteins rich in cysteines called metallothioneins (MT) can be considered as markers for the pollution of the environment by metals. Here, we report on suggestion for an automated procedure for the isolation of MT followed by voltammetric analysis. Primarily, we optimized the automated detection of MT using an electrochemical analyser. It was found that the most sensitive and repeatable analyses are obtained at a temperature of 4 °C for the supporting electrolyte. Further, we optimized experimental conditions for the isolation of MT by using antibody-linked paramagnetic microparticles. Under the optimal conditions (4 h long interaction between the microparticles and MT), the microparticles were tested on isolation of various amounts of MT. The lowest isolated amount of MT by antibody-linked paramagnetic microparticles was 5 μg ml(-1) of MT (50 ng). The automated procedure of MT isolation was further tested on isolation of MT from guppy fish (Poecilia reticulata) treated with silver(i) ions (50 μM AgNO(3)). The whole process lasted less than five hours and was fully automated. We attempted to correlate these results with the standard method for MT isolation. The correlation coefficient is 0.9901, which confirms that results are in good agreement. Moreover, the concentration of silver ions in tissues of fish treated with Ag(i) ions was determined by high performance liquid chromatography with electrochemical detection.     

The Effects of Application of Poultry Manure to Crude Oil Polluted Soils on Maize (Zea Mays) Growth and Soil Properties

A Figaro-type gas sensor system was investigated for the monitoring of volatile organic contaminants (VOC) in the exhaust gas from a soil vapor extraction (SVE) process. Benzene, toluene, ethyl benzene and xylene (BTEX), and their mixtures, were tested as representative contaminants. Reasonably good correlation factors >0.98 were obtained between the GC analyses and the sensor responses for each component, and for the total gas concentrations. Although the composition of the exhaust gas from SVE process, as well as the amount of each component, change with time, the sensor can be used to estimate the residual amount of contaminants by measuring the total concentrations in the exhaust gas. The sensor can be utilized as a valuable tool for the monitoring of SVE process by indicating when the operation to remediate a contaminated site should be stopped. The proposed ceramic gas sensor system may be a good alternative to existing methods, because it can satisfy the essential monitoring necessities of SVE processes, and has many advantages over other fully equipped instrumentation, as a cost-effective device, with long-term monitoring stability.     

Methane emission from naturally ventilated livestock buildings can be determined from gas concentration measurements

Determination of emission of contaminant gases as ammonia, methane, or laughing gas from natural ventilated livestock buildings with large opening is a challenge due to the large variations in gas concentration and air velocity in the openings. The close relation between calculated animal heat production and the carbon dioxide production from the animals have in several cases been utilized for estimation of the ventilation air exchange rate for the estimation of ammonia and greenhouse gas emissions. Using this method, the problem of the complicated air velocity and concentration distribution in the openings is avoided; however, there are still some important issues remained unanswered: (1) the precision of the estimations, (2) the requirement for the length of measuring periods, and (3) the required measuring point number and location. The purpose of this work was to investigate how estimated average gas emission and the precision of the estimation are influenced by different calculation procedures, measuring period length, measure point locations, measure point numbers, and criteria for excluding measuring data. The analyses were based on existing data from a 6-day measuring period in a naturally ventilated, 150 milking cow building. The results showed that the methane emission can be determined with much higher precision than ammonia or laughing gas emissions, and, for methane, relatively precise estimations can be based on measure periods as short as 3 h. This result makes it feasible to investigate the influence of feed composition on methane emission in a relative large number of operating cattle buildings and consequently it can support a development towards reduced greenhouse gas emission from cattle production.     

Biotic landfill cover treatments for mitigating methane emissions

Landfill methane (CH₄) emissions have been cited as one ofthe anthropogenic gas releases that can and should be controlledto reduce global climate change. This article reviews recent research that identifies ways to enhance microbial consumptionof the gas in the aerobic portion of a landfill cover. Use of these methods can augment CH₄ emission reductions achievedby gas collection or provide a sole means to consume CH₄ atsmall landfills that do not have active gas collection systems.Field studies indicate that high levels of CH₄ removal can be achieved by optimizing natural soil microbial processes. Further, during biotic conversion, not all of the CH₄ carbonis converted to carbon dioxide (CO₂) gas and released to theatmosphere; some of it will be sequestered in microbial biomass.Because biotic covers can employ residuals from other municipalprocesses, financial benefits can also accrue from avoided costsfor residuals disposal.     

Determination of estrogenic activity in landfill leachate by simplified yeast two-hybrid assay

We previously developed a simplified yeast two-hybrid assay of estrogenic activity. In the present study, the optimal conditions for sensitivity and stability of this assay were decided. The assay could determine the estrogenic activity of 4 x 10(-11) mol dm(-1) 17beta-estradiol and also anti-estrogenic activity by using 4-hydroxytamoxifen as a control. The assay was used to test various chemicals suspected of estrogenicity. Many kinds of chemical, including alkylphenols, naphthols, xylenols, methoxychlor, phthalates, and bisphenol-A, showed estrogenic activity, and several, such as 2,5-xylenol and di-iso-octyl phthalate, showed anti-estrogenic but no estrogenic activity. Copresence of two estrogenic chemicals produced additive activity. The assay was also used to test leachate and water samples from the sea-based landfill of Osaka North Port in Japan. Estrogenic activity was detected in leachate from a municipal waste-dumping site, but not in that from a dredged soil-dumping site, which did however cause inhibition of cell growth.     

Determination of Ni(CO)4, Fe(CO)5, Mo(CO)6, and W(CO)6 in sewage gas by using cryotrapping gas chromatography inductively coupled plasma mass spectrometry

Evidence for the occurrence of Ni(CO)4 in addition to Mo(CO)6 and W(CO)6 in fermentation gases from a municipal sewage treatment plant is presented for the first time. The gases were sampled at the top of the sewage sludge digester using Tedlar bags, and were analysed using cryotrapping followed by gas chromatography coupled with inductively coupled mass spectrometry (GC-ICP-MS). The use of an ICP-MS as an element-specific detector gives sufficiently low detection limits for metals and was coupled to a packed column gas chromatograph. This method provides information about the speciation of volatile transition metals in contrast to previously used methods for the determination of Ni(CO)4 in gas samples. The element-specific detection of three different isotopes (m/z 58, 60, 62) and the correspondence of the samples' retention times with those of the standard provided convincing evidence that Ni(CO)4 is present in the fermentation gas. The concentrations found were in the sub-ppb level, which is at least one order of magnitude lower than the threshold level of 1 ppb (v/v). In addition, Mo(CO)6 and W(CO)6 were also measured in the sub-ppb range in contrast to the absence of Fe(CO)5. The stabilities of Ni(CO)4, Fe(CO)5, and Mo(CO)6 were tested in a carbon monoxide atmosphere. In the presence of distilled water, the following order of stability was found after 11 weeks: Fe(CO)5 < Ni(CO)4 < Mo(CO)6. In the presence of an aqueous solution containing nickel, molybdenum, tungsten and iron, however, only Fe(CO)5 was significantly decomposed (< 0.3% recovery); Ni(CO)4 and Mo(CO)6 were stable after 11 weeks. No W(CO)6 was formed. The low stability of Fe(CO)5 in the presence of water could be the reason why no volatile iron compound was found in sewage gas. This study showed that GC-ICP-MS can be employed to identify species-specific traces of metal carbonyls in process gases such as sewage gas.     

Detection of sulfur-free odorants in natural gas using ion mobility spectrometry

Beside the primary motivation of the public gas suppliers for odorizing natural gas with a sulfur-free odorant, which relates to the image of the environment-friendly fuel, natural gas, competing with low-sulfur heating fuel and diesel, a question of crucial importance of how to detect such sulfur-free odorants comes up. Concerning the replacement of sulfur-containing by sulfur-free odorization, the availability of a fast and sensitive detection method that can, further, be used on-site plays a key role. The minimum concentration of the new sulfur-free odorant Gasodor S-Free (S-Free) in natural gas should be added at a level of at least 8.8 mg m(-3) to assure a significant warning smell. Therefore, a dynamic range between 0 and approx. 25 mg m(-3) must be realised in the rather complex matrix of natural gas. By means of a handheld ion mobility spectrometer, the odorant content in natural gas is determined within less than 80 s total analysis time directly at the gas pipe. The concentration of S-Free is monitored between 4 and 23 mg m(-3) respecting the quality of the natural gas (high- and low-caloric gas). Results of the validation using a gas chromatograph as a reference standard will be discussed in detail.     

Review of PSR framework and development of a DPSIR model to assess greenhouse effect in Taiwan

In dealing with the complex issues of greenhouse gas (GHG) emission and climate change mitigation, many interrelated factors such as cost, level of technology development, supply and demand of energy, structure of industry, and expenditures on research and development exist. Using indicators to monitor environmental impacts and evaluate the efficacies of policies and regulations has been practiced for a long time, and it can serve as a useful tool for decision making and for comparison between different countries. Although numerous indicators have been developed for relevant subjects, integrated approaches that consider individual changes, dynamic interaction, and multi-dimensions of indicators are scarce. This paper aimed to develop a Driving Force-Pressure-State-Impact-Response (DPSIR) framework to assess the problems. This DPSIR model is mainly related to energy consumption, environmental impacts, and policy responses. The objectives of the paper were: (1) conduct a literature review on the indicators that have been used in GHG-related studies; (2) develop a DPSIR model that incorporates GHG-related indicators and evaluate their relationships using a cause?Ceffect chain of GHG emission; and (3) develop a calculative method that can be used to explain the dynamic correlation among the interdependent indicators. Taiwan is a significant source of global GHG emissions. A case study, using the developed framework and Taiwan??s actual data of the past two decades, was conducted. The results indicate that regulatory strategies for pollution control are inadequate in terms of ensuring environmental quality, and the nature does not have the capability to revert the impacts from the existing level of pollution.     

Fuel characteristics and emissions from biomass burning and land-use change in Nigeria

Nigeria is one of the 13 low-latitude countries that have significant biomass burning activities. Biomass burning occurs in moist savanna, dry forests, and forest plantations. Fires in the forest zone are associated with slash-and-burn agriculture; the areal extent of burning is estimated to be 80% of the natural savanna. In forest plantations, close to 100% of litter is burned. Current estimates of emissions from land-use change are based on a 1976 national study and extrapolations from it. The following non-carbon dioxide (CO₂) trace gas emissions were calculated from savanna burning: methane (CH₄), 145 gigagrams (Gg); carbon monoxide (CO), 3831 Gg; nitrous oxide (N₂O), 2 Gg; and nitrogen oxides (NO_x), 49 Gg. Deforestation rates in forests and woodlands are 300 × 10³ ha (kilohectare, or kha) and 200 × kha per year, respectively. Trace gas emissions from deforestation were estimated to be 300 Gg CH₄, 2.4 Gg N₂O, and 24 Gg NO_x. CO₂ emissions from burning, decay of biomass, and long-term emissions from soil totaled 125 561 Gg. These estimates should be viewed as preliminary, because greenhouse gas emission inventories from burning, deforestation, and land-use change require two components: fuel load and emission factors. Fuel load is dependent on the areal extent of various land uses, and the biomass stocking and some of these data in Nigeria are highly uncertain.     

Relationship between CH₄ and N₂O flux from soil and their ambient mixing ratio in a riparian rice-based agroecosystem of tropical region

Temporal variations of the ambient mixing ratio of greenhouse gas (CH(4) and N(2)O) in a riparian rice-based agro-ecosystem of tropical region were studied during 2005-2006 in coastal Odisha. The endeavour was made with the hypothesis that the ambient mixing ratio of CH(4) and N(2)O depends on the changes in the flux of CH(4) and N(2)O from the rice fields in the riparian rice ecosystems. A higher ambient mixing ratio of CH(4) was recorded during the tillering to grain filling stages of the rice crop, during both dry and wet seasons. The higher ambient mixing ratio of CH(4) during the wet season may attribute to the higher CH(4) emission from the rice field. The average mixing ratio of CH(4) was recorded as 1.84 ± 0.05 ppmv and 1.85 ± 0.06 ppmv during 2005 and 2006, respectively. The ambient CH(4) mixing ratio was recorded negatively correlated with the average ambient temperature. The N(2)O mixing ratio ranged from 261.57 to 399.44 ppbv with an average of 330.57 ppbv during 2005. However, the average mixing ratio of N(2)O was recorded as 318.83 ± 20.00 ppbv during 2006. The N(2)O mixing ratio was recorded to be negatively correlated with rainfall and average ambient temperature. Significant negative correlation (r = -0.209) of N(2)O with sunshine hours may attribute to the photochemical break down of N(2)O. The temporal variation of N(2)O flux from the rice field does not affect the ambient mixing ratio of N(2)O in the same way as in the case of the ambient mixing ratio of CH(4). However, the higher mixing ratio of N(2)O during the fallow period of the post monsoon period may attribute to the N(2)O flux from soil. Results indicate that intensively cultivated coastal ecosystems can be a major source of ambient greenhouse gas.     

Degradation of chlortoluron in water disinfection processes: a kinetic study

The kinetics of the reaction between chlortoluron, a phenylurea herbicide [N'-(2-hydroxy-4-methyl-5-chlorophenyl)-N,N-dimethylurea], and hypochlorite, the active species in water disinfection processes involving chlorine, were investigated by HPLC-UV and HPLC-electrospray ionisation mass spectrometry (HPLC-ESI-MS). In particular, the concentrations of the main chlortoluron by-products were monitored as a function of time by HPLC-ESI-MS and a kinetic model was developed to fit the relevant curves. The results showed that chlortoluron degradation starts with two parallel pathways, namely, chlorination and hydroxylation of the aromatic ring, which are then followed by consecutive chlorination reactions, and after almost 2 weeks by ring opening and partial mineralisation, as confirmed by head-space solid-phase microextraction gas chromatography-MS (SPME-GC-MS) and total organic carbon (TOC) measurements. Kinetic constants for the first reactions of the overall process, under pseudo-first-order conditions (hypochlorite excess), were estimated by a fitting procedure.     

Organochlorine pesticide residues in sediments from coastal environment of Cantabria (northern Spain) and evaluation of the Atlantic Ocean

This paper documents levels of organochlorine pesticides (OCs) in coastal surface sediments from selected reference sites on the northern Atlantic Spanish coast. One hundred eight samples covering three estuaries in the Cantabrian Coast were sampled in 2006 and analyzed in the finer fraction (<63 ??m) for 19 OCs by gas chromatography with electron capture detector after confirmation by mass spectrometry. Detected organochlorine pesticides were endosulfan ??, endosulfan ??, endosulfan sulfate, hexachlorobenzene (HCB), aldrin, dieldrin, methoxychlor, 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene (4,4??-DDE) and 1,1-dichloro-2,2-bis(4-chlorophenyl)ethane (4,4??-DDD). Total OCs concentrations ranged from 1.8 ng g^???1 dry weight (dw) to 3.9 ng g^???1 dw, showing a uniform distribution along the studied area, and being consistent with recorded levels in the literature for coastal sediments in other reference sites with low levels of pollution by OCs along the Atlantic Ocean. Endosulfan, 4,4??-DDD, HCB, aldrin, and dieldrin seemed to be ubiquitous as the legacy of past uses and deposition. OCs concentrations were significantly correlated to organic matter content and particle size distribution. No adverse biological effects derived from these pollutants are expected to take place as it can be concluded from the comparison with the existent marine sediment quality guidelines.     

Two fish bile reference materials certified for PAH metabolites

Environmental pollution with polycyclic aromatic hydrocarbons (PAHs) from pyrogenic or petrochemical sources is a matter of concern in many aquatic ecosystems. For field monitoring purposes, PAH metabolite levels in fish bile samples can be used as biomarkers of exposure, but previously there were no reference materials for analytical method validation or quality control. In this paper we describe the preparation and certification of two fish bile materials. BCR 720 is a pure bile material from sediment-exposed flounder (Platichthys flesus) and BCR 721 is a pure bile material from oil-exposed plaice (Pleuronectes platessa). Homogeneity and stability tests were carried out and a group of 12 expert laboratories was assembled for the certification measurements. The methods applied were liquid chromatography with fluorescence detection or gas chromatography with mass spectrometric detection. In BCR 720 three PAH metabolites were certified: 1-hydroxyphenanthrene, 1-hydroxypyrene and 3-hydroxybenzo[a]pyrene. In BCR 721 1-hydroxypyrene was certified. The fourth target compound, 2-hydroxynaphthalene, could not be certified, but the results obtained are listed. The major findings from earlier feasibility studies and recommendations for the optimal use of the reference materials are also included.     

Large particles are responsible for elevated bacterial marker levels in school air upon occupation

Muramic acid (Mur) is found in bacterial peptidoglycan (PG) whereas 3-hydroxy fatty acids (3-OH FAs) are found in Gram-negative bacterial lipopolysaccharide (LPS). Thus Mur and 3-OH FAs serve as markers to assess bacterial levels in indoor air. An initial survey, in a school, demonstrated that the levels of dust, PG and LPS (pmol m(-3)) were each much higher in occupied rooms than in the same rooms when unoccupied. In each instance, the Mur content of dust was increased and the hydroxy fatty acid distribution changed similarly suggesting an alteration in the bacterial population. Here, findings are compared with results from two additional schools. Follow-up aerosol monitoring by particle size was also performed for the first time for all 3 schools. The particle size distribution was shown to be quite different in occupied versus unoccupied schoolrooms. Within individual classrooms, concentrations of airborne particles [greater-than-or-equal]0.8 [micro sign]m in diameter, and CO(2) were correlated. This suggests that the increased levels of larger particles are responsible for elevation of bacterial markers during occupation. Release of culturable and non-culturable bacteria or bacterial aggregates from children (e.g. from flaking skin) might explain this phenomenon.     

Modelling-tracer study for risk assessment of a proposed sour gas facility

As an integral part of a risk assessment of a sour gas pipeline proposed for a recreational area in the Rocky Mountain foothills, the dispersion of hydrogen sulphide was assessed using meteorological monitoring, tracer gas concentration measurement and a complex terrain diffusion model. Sulphur hexafluoride was released into the nocturnal drainage winds of two valleys in the eastern slopes of the Alberta Rockies southwest of Calgary. The resulting concentrations were measured at several points on transects at various distances from the source. The NUVAL version of the dispersion model IMPACT (Integrated Model for Plumes and Atmospherics in Complex Terrain) was site tuned using the measured concentrations and concurrent meteorological data. Relative mean absolute errors of 24–50% were obtained. The Gaussian model (PLUMES) with modified stability classes gave relative mean absolute errors of 42–64% in predicting transect maxima. Dilution rates were found to be much larger than would be experienced under similar conditions over flat terrain.     

一种快速便捷的温室气体本底浓度采样方法初探

引入生态和气象研究领域的本底大气观测技术,提出一种便捷快速的温室气体本底浓度采样方法。该方法需要的设备简单,便于携带,能够快速完成采样。2011年5—7月,利用该方法,自西向东分别在处于我国三大阶梯的青藏高原东北缘、秦巴山区、长江中下游平原,选择不同类型的土地覆盖下垫面开展了地面采样实验,获得了33组以CO2和CH4为主的温室气体浓度数据。根据获得的采样结果,分别开展了人工采样数据分析及其与器测本底数据、卫星反演同期数据产品的对比分析,结果显示,几类数据趋势相符,数值相对偏差较低。总体认为,该方法获得的采样数据可靠、采样效率高,且成本低廉,这在我国温室气体自动监测站还比较少的现实情况下,不失为一种可选的快速便捷监测技术手段。