Models for the adsorption of organic compounds at gas-water interfaces

The solvation parameter model is used to characterize interactions responsible for adsorption at the gas-water interface for bulk water at 15 and 25 degrees C, snow at -6.8 degrees C, mineral-supported water films (alumina, calcium carbonate and quartz) at 15 degrees C, and dry soil at 15 degrees C. The mineral-supported water films and dry soil adsorption data are modeled at different relative humidities in the range 40-99%. The models produce satisfactory results with standard errors of the estimate of 0.12 to 0.17 for regression of the model predicted adsorption equilibrium constants against the experimental values (range for equilibrium constants -2 to -7 log units). The water surface is polar with a significant capacity for dipole-type and hydrogen-bonding interactions. In addition, it is strongly electron lone pair repulsive. Dispersion interactions favor adsorption at the water surface. Mineral-supported water films at relative humidities greater than 40% demonstrate adsorption properties similar to bulk water. The adsorption characteristics, however, depend on the relative humidity and the nature of the support. In the case of dry soil the adsorption properties at different relative humidities cannot simply be explained by adsorption of a water film covering the soil surface and the changes in adsorption characteristics with relative humidity are more complex than the mineral-supported water films.     

Stability and storage problems in organotin speciation in environmental samples

The stability of both tributyltin (TBT) and triphenyltin (TPT) in water, sediment, oysters and cockles was studied over a period of 18 months using several storage conditions. Butyltins were stable in unacidified sea-water stored in polycarbonate bottles in the dark at 4 degrees C for 7 months, but half of the TBT concentration was lost after 540 d. A comparable preservation time was achieved for butyltins stored on C18 cartridges at room temperature. However, phenyltins extracted from sea-water were stable for only 60 d stored on cartridges and even more pronounced losses (about 90% after 540 d) occurred when they were stored in either polycarbonate or Pyrex glass bottles. Losses of organotins were observed in sediments after air drying and pasteurization treatments using a freeze-dried sediment as a comparator, whereas both butyltin and phenyltin species remained stable in sediments stored at -20 degrees C for the 18 months tested, irrespective of the treatment used for stabilization. Air drying followed by pasteurization was shown to be superior to other treatments for the stabilization of organotin compounds in sediments stored at higher temperatures, but 30% of TBT was lost after 540 d at 25 degrees C. Finally, butyltins were stable in both frozen cockles and oysters in the dark over a 7 month period and in freeze-dried samples stored at 4 degrees C for 5 months, but TBT losses of about 70% were observed after 540 d.     

Effects of temperature parameters on thermal-optical analysis of organic and elemental carbon in aerosol

Thermal-optical analysis (TOA) is a popular method to determine aerosol elemental carbon (EC) and organic carbon (OC) collected on quartz fiber filter. However, temperature protocol adopted in TOA has great effects on OC and EC results. The purpose of this study is to investigate and quantify the effects of maximum temperature (T(max)) and residence time (RT) for each step in helium stage on ECOC measurements. Fourteen typical source samples and 20 ambient samples were collected and six temperature programs were designed for this study. It was found that EC value decreases regularly as T(max ) ascends, i.e., EC results from T(max) of 650 degrees C, 750 degrees C and 850 degrees C are 0.89 +/- 0.06, 0.76 +/- 0.10, 0.62 +/- 0.13 times EC value from T( max) of 550 degrees C, respectively, and the magnitude of EC drop (EC(d), percent) is significantly correlated with OC abundance in total carbon (R(OC/TC)), expressed as EC(d) = 66.8R(OC/TC)-14.4 (r = 0.87); pyrolized OC(POC) values are also sensitive to T(max), but there are various trends for samples with different OC constituents. On average of the samples studied here, prolonged RT reduces EC values by only 3%, almost negligible compared to the effect of T(max), and reduces POC by 9%, much less than that by previous report.     

Laboratory and field validation of a combined NO2-SO2 Radiello passive sampler

A combined NO2-SO2 Radiello radial-type diffusive sampler was validated under controlled laboratory conditions and compared with NO2-SO2 results of 3 other type of samplers in a field comparison at two locations Ghent-Mariakerke and Borgerhout in Flanders. Laboratory exposures at different temperatures (-5, 10 and 30 degrees C) and relative humidities (0, 50 and 80% RH) in combination with varying concentration levels and exposure times were carried out, with a focus on extreme conditions. Concentration level and exposure time were changed together following suppliers linear working range of samplers and assuring absolute amounts of compounds on the sampler corresponding to those of environmental levels. The average uptake rate for NO2 for 24 hour exposures at 10 degrees C and 50% RH and tested concentration levels (+/-73, 146 and 293 ppb NO2) was 0.076 +/- 0.011 ng ppb(-1) min(-1). Uptake rates during all experiments were lower than the uptake rate given in the instruction manual of the sampler. A significant effect of temperature and relative humidity on NO2 uptake rate was observed. The temperature effect from 10 to 30 degrees C corresponds to the temperature effect given by the supplier of the samplers. High relative humidity (70 to 80%) caused a strong non-reproducible decrease of uptake rate for NO2 at 24 hour experiments but this effect was not observed at longer exposures except for the tests at -5 degrees C. At the tested temperature below zero in combination with high relative humidity the sampler showed anomalous behaviour for NO2. The possible effect of concentration level and exposure time for NO2 needs further research. The average uptake rate for SO2 calculated from all exposures is 0.478 +/- 0.075 ng of sulfate ion each ppb min of SO2 and accords to suppliers uptake rate. No clear effects of temperature, relative humidity or concentration level/exposure time on the uptake rate for SO2 were found, partly due to the large scatter of results. Although NO2 accuracy of Radiello samplers was better during field campaigns than during laboratory validation, IVL and OGAWA samplers gave better results for NO2. In the field, IVL samplers showed best agreement with the continuous analyzers for both NO2 and SO2.     

Effects of temperature on the acute toxicity of cadmium to Corophium Insidiosum

This study aimed to optimise the methodology for the use of Corophium insidiosum in a bioassay. Taking into account that it would be suitable to execute the bioassay with organisms having a good sensitivity during the year and low mortality in control sediment, the influence of different temperatures (10–15–20 and 25°C) has been examined. C. insidiosum was collected during August, November 2005 and January 2006, in Mar Piccolo basin (Ionian sea). The results obtained show that this species mortality in the negative control sediment, ranged from 2.6 ± 0.6% at 10°C in August to 17 ± 2.2% at 20°C in November, at different temperatures tested. At 20°C there were significant differences in mortality among different months examined. Indeed no relationship among months was found at 15°C. Significant differences between August and November at 25°C, between November and January were not found at 10°C. The 96-h LC50 values found for cadmium at all temperature experimental conditions ranged from 2.11 mg/l (1.57–2.82) to 0.70 mg/l (0.54–0.93). The highest values were found at 10°C in November and January. The results showed that the optimal temperature for the bioassay seems to be between 15°C and 20°C. Even if, at 20°C the mortality differs significantly among organisms sampled.     

Study of summer heat exposure at the ground services operations of a main international airport in Saudi Arabia

Summer heat in coastal subtropical Jeddah, augmented by heat from operating ground servicing equipment in King Abdul-Aziz International Airport (KAAIA), presents a major occupational problem to ground service operators, particularly the air traffic control coordinator (ATCC), that hinders their work efficiency and induces health disorders to them. The present study was conducted to assess the magnitude of this problem and propose heat control strategy and remedial actions for the Saudi Arabian Airlines (SAUDIA). Heat parameters including air temperature (T (a)), wet bulb temperature (T (w)), globe temperature (T (g)) and air velocity were measured around serviced planes and in other locations used by ATCC, and the WBGT and the ATCC-WBGT-TWAs were computed. Mostly all the T (a) measurements, and many T (w) measurements, were higher than T (a) and T (w) forecasted by the Presidency of Meteorology and Environment (PME) due to heat dissipated from operating vehicles and equipment in service. The measured and PME forecasted parameters have good and medium linear correlations (T (a): r (2) = 0.74 and T (w): r (2) = 0.64). The computed WBGT in the service stations around planes are considerably higher than the 25 and 27.5 degrees C recommended TLV(R) for non-acclimatized and acclimatized operators. However, the computed ATCC- WBGT-TWA levels indicate that the shift-work-schedule which was recommended to be implemented by SAUDIA has successfully reduced their heat exposure to acceptable levels, except for a very few operators (6.7% exceeding WBGT-TLV(R) of 25 degrees C and 2.2% exceeding TLV(R) of 27.5 degrees C) for whom the shift-work schedules might be corrected to achieve safe heat exposure.     

Development and validation of methods for environmental monitoring of cyclophosphamide in workplaces

Methods to monitor contamination of workplaces with antineoplastic drugs have been developed and validated. Cyclophosphamide (CP) was used as a model compound as it is one of the most commonly used antineoplastic drugs. A wipe sampling method to detect contamination with CP at surfaces was developed. A personal air sampling method to sample gas and vapour on solid sorbent tubes and particles with filters was also developed. Wipe and filter samples were extracted and sorbent samples were eluted, all with ethyl acetate. The samples were analysed with liquid chromatography tandem mass spectrometry. (2)H(6)-labelled cyclophosphamide was used as an internal standard. The between-day precision was 2-5% for wipe samples, 4-6% for sorbent samples and 3-8% for filter samples. The limit of detection was 0.02 ng CP per sample for the wipe and filter methods and 0.03 ng CP per sample for the solid sorbent method. Wipe sampling on surfaces made of different materials resulted in mean recoveries between 78-106%. The desorption recovery was between 97-102% for the wipe samples, 97% for the sorbent samples and 101% for the filter samples. Samples were stable for up to 2 months at 5 degrees C and -20 degrees C and for about 2 d at room temperature. The developed methods were applied to the measurement of contamination with CP in a hospital pharmacy. Trace amounts of CP, 1.3 and 1.4 ng, were detected on surfaces in the pharmacy.     

Compartment modeling of MTBE in the generic environment and estimations of the aquatic MTBE input in Germany using the EQC model

The use of the gasoline additive methyl tert-butyl ether (MTBE) has caused serious concern about groundwater and surface water contamination. The behavior of MTBE in the two most relevant compartments, surface water and air in a generic environment and in a simulated German environment is investigated using the equilibrium criterion (EQC) model. Due to lack of literature data, the half-life time of MTBE in river water is estimated to about 80-120 d (105 d) at 18 degrees C and roughly 1.5 a (year)(533 d) at 4 degrees C from a batch experiment. The EQC model considers four compartments, air, surface water, soil and sediment in an environment of typically 100,000 km2 with about 10% of the area covered with water. The user can progress through the tiered sequence of Level I to III with increasing complexity which reveals more information about the the fate of the considered chemical. The equilibrium mass distribution of MTBE calculated with the Level I model shows that 87% partitions into air and 13% into surface water at 10 degrees C. The results of the Level II calculations indicate that 50% of MTBE in the air is transported from the system and 38% in the air is degraded at 10 degrees C. The resulting total persistence time of 3 d for MTBE in the generic environment of the Level II model can be compared to the calculated value for chlorobenzene. The MTBE input into water is significantly more sensitive to the 'mode of entry' than input into air. The MTBE concentration in surface water is almost exclusively the result of direct emission into water, whereas the atmosphere can additionally be loaded by volatilization from water. The total aquatic MTBE emission in Germany and the average MTBE concentration in German surface waters were roughly estimated to 20-80 t a(-1) (tons per year)(50 t a(-1)) and 50 ng L(-1), respectively. Surface water concentrations calculated with the underlying assumptions of the model can neither be explained by exposure through waste water and industrial effluents nor with an estimated loss of industrially used MTBE in Germany. For the year-round scenario at 10 degrees C, MTBE concentrations of 19 ng L(-1) (surface water) and 167 ng m(-3) (air) result. However, it remains unclear whether the assumptions of the model, the lack of analyses from industrial effluents or both are responsible for the difference. Additional aquatic emission sources could result from gasoline transport on and storage near rivers. The comparison of winter and summer scenarios shows that in summer, atmospheric (25%) and aqueous (50%) concentrations are lower than in winter due to higher degradation rates.     

吹扫捕集／毛细管气相色谱一质谱法同时测定生活饮用水中12种氧苯类化合物的研究

建立了吹扫捕集法浓缩样品中的氯苯类化合物,气相色谱一质谱法测定生活饮用水中12种氧苯类的方法。经色谱分离后用质谱检测器测定,外标法定量。利用中等极性毛细管柱（DB624,30m×0．25mm×0．25μm）程序升温。达到12种氯苯的分离效果。该方法的检出限范围为0．031～0．78μg／L,标准曲线相关系数为0．997～0．999,相对标准偏差为3％～11％,实际水样加标回收率为75％～107％。本文建立的方法简单,重现性好、检出限低,适用于水中氧代苯类化合物的测定。     

Monitoring Water Quality and Quantity of National Watersheds in Turkey

National data from the hydrological network for 38 rivers out of 25 watersheds were used to detect spatial and temporal trends in water quality and quantity characteristics between 1995 and 2002. Assessment of water quality and quantity included flow rate, water temperature, pH, electrical conductivity, sodium adsorption rate, Na, K, Ca+Mg, CO₃, HCO₃, Cl, SO₄, and boron. Among the major ions assessed on a watershed basis, Turkish river waters are relatively high in Ca+Mg, Na and HCO₃, and low in K and CO₃. The watersheds in Turkey experienced a general trend of 16% decrease in flow rates between 1995 and 2002 at a mean annual rate of about 4 m³ s^?1, with a considerable spatial variation. Similarly, there appeared to be an increasing trend in river water temperature, at a mean annual rate of about 0.2°C. A substantial proportion of watersheds experienced an increase in pH, in particular, after 1997, with a maximum increase from 8.1 to 8.4 observed in Euphrates (P?R ² values in accounting for variations of pH and water temperature only. The findings of the study can provide a useful assessment of controls over water quality and quantity and assist in devising integrated and sustainable management practices for watersheds at the regional scale in Turkey.     

Measurement of total antimony and antimony species in mine contaminated soils by ICPMS and HPLC-ICPMS

This paper describes the measurement of total antimony and antimony species in "real world" mine contaminated sediments using ICPMS and HPLC-ICPMS. Low and high temperature microwave extraction procedures (90 degrees C and 150 degrees C, respectively) using a range of nitric-hydrochloric acid combinations were examined as to their efficacy to extract antimony from six mine contaminated soils and a certified reference material. The use of the higher temperature with nitric-hydrochloric acid (1:2 (v/v)) was suitable to release antimony from sediments and the certified reference material, NIST 2710 Montana soil. Antimony concentrations obtained using this acid mixture were similar to those obtained using a more aggressive extraction with nitric, hydrochloric, perchloric and hydrofluoric acid mixture. A 25 mM citric acid solution at 90 degrees C for 15 min extracted 47-78% of antimony from soils. A Hamilton PRP X-100 anion exchange column with 20 mM EDTA mobile phase, pH 4.5, flow rate 1.5 mL min(-1) and column temperature of 50 degrees C was used to separate antimony species. Column recoveries ranged from 78-104%. The predominant form of antimony was Sb(5+). Little conversion of Sb(5+) occurred (<5%) during extraction, however, significant conversion of Sb(3+) occurred (approximately 36%). The extraction of antimony species with citric acid should be useful in the determination of inorganic antimony available to plants, as plants commonly excrete carboxylic acids, including citric acid, into their rhizospheres to mobilise trace elements for nutritional purposes.     

Statistical approaches for hydrogeochemical characterization of groundwater in West Delhi, India

Parametric statistical approaches, correlations and multiple linear regressions were used to develop models for the interpretation of hydrogeochemical parameters in the Western part of Delhi state, India. The hydrogeochemical parameters indicated that the groundwater quality is not safe for consumption. The water is moderately saline and the salinity level is increasing over time. There is also the problem of nitrate pollution. The correlation between electrical conductivity (EC) and other water quality parameters except potassium (K(+)), nitrate (NO(3)(-)) and bicarbonate (HCO(3)(-)) is significantly positive and Ca(++)+ Mg(++)/Na(+)+ K(+) is significantly negative. In predicting EC, the multiple R(2) values of 0.996 and 0.985 indicate that 99.6% and 98.5% variability in the observed EC could be ascribed to the combined effect of Na(+), HCO(3)(-), Cl(-), SO(4)(--), NO(3)(-) and Ca(++)+ Mg(++) for the year of 2005 and 2006 respectively. Out of 99.6% of the variability in EC in 2005, 51.2% was due to Cl(-) alone, and 8.5%, 12.5%, 6.1%, 14.7% and 6.7% were due to Na(+), HCO(3)(-), SO(4)(--), NO(3)(-) and Ca(++) + Mg(++). Similarly in 2006, out of 98.5% of the variability in EC, 48.5% was due to Cl(-) alone, and 10.4%, 12.7%, 5.3%, 17.2% and 4.4% were due to Na(+), HCO(3)(-), SO(4)(--), NO(3)(-) and Ca(++)+ Mg(++). The analysis shows that a good correlation exists between EC, Cl(-) and SO(4)(--) either individually or in combination with other ions and the multiple regression models can predict EC at 5% level of significance.     

The effect of temperature and NaCl concentration on the kinetic method of toxicity determination using Vibrio fischeri

In this paper the effect of temperature and NaCl concentration on the kinetic method of toxicity determination using Vibrio fischeri was studied for 50 ppm Zn(2+). This work shows that both NaCl concentration and temperature affect the kinetics of toxicity as well as the luminescence of the bacteria, and hence these are important factors that need to be considered in the development of a miniaturised portable instrument. Furthermore, this work shows that the conditions for which the kinetic test was most sensitive, i.e. exhibited the greatest response, were 23 degrees C and 2% NaCl. However, at these conditions small variations in temperature and NaCl concentration could lead to great errors in the results. Thus 12.5 degrees C and 2% NaCl are preferred as at these conditions the obtained results are more robust. Although at the latter conditions the toxicity rate constant was found to be 5.5 times less than that for 23 degrees C, the value is comparable to that obtained for 15 degrees C. From the data available it was also found that the temperature dependence of the toxicity rate fits the Arrhenius equation, in a behaviour similar to that of simpler chemical reactions.     

荧光法快速测定水中粪大肠菌群

为研究荧光法测定水中粪大肠菌群的适用性,在6家实验室使用荧光法对粪大肠菌群的标准菌株和实际水样进行测定,并与多管发酵法进行比对。结果表明:6家实验室对标准菌株的监测结果均在误差范围内,实验室内相对误差为-2. 75%～1. 71%,准确度较高;对3个不同浓度实际水样进行精密度测定,实验室内相对标准偏差分别为1. 30%～3. 93%、1. 94%～4. 72%、1. 88%～4. 54%,实验室间的相对标准偏差分别为1. 14%、1. 59%、1. 72%,精密度较高;用荧光法与多管发酵法同时测定实际水样,2种方法测试结果线性相关性良好且变化趋势相同,对测试数据进行t检验,2种方法测试结果无显著差异。     

Modeling trihalomethane formation for Jabal Amman water supply in Jordan

A mathematical model that expresses Total trihalomethane (TTHM) concentration in terms of initial chlorine concentration, total organic carbon, bromide ion concentration, contact time, and pH is developed for Zai water treatment plant which supplies water to Jabal Amman. The developed mathematical model is for constant temperature of 20°C. To adjust model calculated TTHM concentrations for temperatures other than 20°C, another mathematical model that expresses TTHM growth rate as function of temperature is also developed. To test the ability of the two developed models in predicting TTHM concentrations throughout water supplies, a sampling program that aimed at measuring TTHM concentrations in addition to the predictors in the two developed mathematical models namely; chlorine concentration, bromide ion concentration, total organic carbon, temperature and pH throughout Jabal Amman water supply was conducted. The two developed mathematical models and WaterCad, which was used to determine water age, were used to predict TTHM concentrations throughout Jabal Amman water supply. Predicted TTHM concentrations were compared to actual TTHM concentrations measured during the sampling program. Results showed that there is good agreement between measured and, calculated TTHM concentrations, which means that the method presented in this paper, can be used to obtain good estimates of TTHM concentrations throughout networks.     

Radiological aspects of some Egyptian thermo-mineral springs

In Egypt, nineteen water springs with temperatures exceeding 35 degrees C, which can be considered thermal waters, were reported. The radiological aspects of thermal water in three northern regions of Egypt (Gulf of Suez, Cairo, and Bahariya Oasis) were investigated. The activity concentrations of natural radionuclides of 226Ra, 40K, total uranium and 210Pb (210Po) in water samples were determined using gamma spectrometry, laser fluorimetry and alpha spectrometry after chemical separation, respectively. The highest concentrations are detected in two locations, namely Sudr and Hammam Faroun springs, which are the hottest waters in Egypt (89 and 72 degrees C respectively). It seems that the presence of 226Ra is correlated to the water mineralization and the depth and the temperature of the reservoir's base. Also, these results seem evidence of uranium accumulation at depth in the mother bedrock and/or uranium immobilization due to uranium reduction to the immobile 4+-oxidation state in the reservoir base. The average activity concentrations of 40K are dependent on the water's origin, i.e. meteoric water mixed with sea water (Gulf of Suez springs) and meteoric water (Bahariya Oasis wells). There is no prescribed dose limit for short term and temporary exposure to thermal water. Workers at the thermal springs should be regularly monitored because of their continuous exposure to enhanced radiation levels over a long period of time. The hydrochemical characteristics, environmental isotopes aspects and water origin are briefly discussed based on published data.     

Occurrence of Giardia and Cryptosporidium in Italian water supplies

A total of 21 samples: raw water (RW) samples; water samples after coagulation with aluminium sulfate (clarified water: CW); and water after chlorination (treated water: TW) from a water purification plant that treats river surface water from the neighbourhood of Foggia (Italy), were analysed for the presence of Giardia cysts and Cryptosporidium oocysts. Bacteriological indicator of faecal contamination (total and faecal coliforms, faecal streptococci,), total bacterial count at 22 and 36 degrees C and physicochemical parameters (turbidity, temperature, pH) were evaluated. Cryptosporidium oocysts were not found in any samples examined, while Giardia cysts were found only in RW samples, with the maximal concentration of 8 cysts/100 l. A positive correlation was found between the Giardia densities and quality parameters such as TC, FC and TBC at 22 degrees C. Giardia levels in raw water samples correlated (p < 0.05) with TC, FC and with temperature. No other water quality parameters was consistently correlated with cysts level.     

Potential application of recycled rubber in oil pollution control

The abundance and indiscriminate disposal of scrap tyres inurban areas in Nigeria create serious health and environmentalproblems. The potential of using rubber recycled from scraptyres as an absorbent in crude oil clean up was investigated.Rubber particles of mesh sizes within the range of 0.15 to2.36 mm were used to absorb crude oil at different temperatures(5 to 40 °C). The rapid increase in oil absorption withinthe first 20 min was followed by a much slower rate, with theequilibrium absorption being attained after 30 min. Theequilibrium absorption increased with decreasing particle sizeand decreasing temperature of absorption. At 30 °C, the oil absorption for the 0.15 mm rubber particles was more than twice that of the 2.36 mm particle size. When regenerated recycledrubber was used, the equilibrium absorption decreased by about15–40%. The extent of reduction was higher for the largerparticles and at lower temperature of absorption.     

A comparison of X-ray fluorescence and wet chemical analysis of air filter samples from a scrap lead smelting operation

Personal and area air samples were taken at a scrap lead smelter operation in a bullet manufacturing facility. Samples were taken using the 37-mm styrene-acrylonitrile closed-face filter cassette (CFC, the current US standard device for lead sampling), the 37-mm GSP or "cone" sampler, the 25-mm Institute of Occupational Medicine (IOM) inhalable sampler, and the 25-mm Button sampler (developed at the University of Cincinnati). Polyvinylchloride filters were used for sampling. The filters were pre- and post-weighed, and analyzed for lead content using a field-portable X-ray fluorescence (XRF) analyzer. The filters were then extracted with dilute nitric acid in an ultrasonic extraction bath and the solutions were analyzed by inductively coupled plasma optical emission spectroscopy. The 25-mm filters were analyzed using a single XRF reading, while three readings on different parts of the filter were taken from the 37-mm filters. The single reading from the 25-mm filters was adjusted for the nominal area of the filter to obtain the mass loading, while the three readings from the 37-mm filters were inserted into two different algorithms for calculating the mass loadings, and the algorithms were compared. The IOM sampler was designed for material collected in the body of the sampler to be part of the collected sample as well as that on the filter. Therefore, the IOM sampler cassettes were rinsed separately to determine if wall-loss corrections were necessary. All four samplers gave very good correlations between the two analytical methods above the limit of detection of the XRF procedure. The limit of detection for the 25-mm filters (5 microg) was lower than for the 37-mm filters (10 microg). The percentage of XRF results that were within 25% of the corresponding ICP results was evaluated. In addition, the bias from linear regression was estimated. Linear regression for the Button sampler and the IOM sampler using single readings and the GSP using all tested techniques for total filter loading gave acceptable XRF readings at loadings equivalent to sampling at the OSHA 8-hour Action Level and Permissible Exposure Limit. However, the CFC only had acceptable results when the center reading corrected for filter area was used, which was surprising, and may be a result of a limited data set. In addition to linear regression, simple estimation of bias indicated reasonable agreements between XRF and ICP results for single XRF readings on the Button sampler filters, (82% of the individual results within criterion), and on the IOM sampler filters (77% or 61%--see text), and on the GSP sampler filters using the OSHA algorithm (78%). As a result of this pilot project, all three samplers were considered suitable for inclusion in further field research studies.     

Interaction effects of elevated CO2 and temperature on microbial biomass and enzyme activities in tropical rice soils

The impacts of elevated CO(2) and temperature on microbial biomass and soil enzyme activities in four physicochemically different types of tropical rice soils (Aeric Endoaquept, Aeric Tropoaquept, Ultic Haplustalf and Udic Rhodostalf) were investigated in a laboratory incubation study. Soil samples were incubated under 400, 500 and 600 μmol mol(-1) CO(2) concentration at 25°C, 35°C and 45°C for 2 months. Elevated CO(2) significantly increased the mean microbial biomass carbon (MBC) content, across the soils, over control by 6.2%, 38.0% and 49.2% at 400, 500 and 600 μmol mol(-1) CO(2) concentration, respectively. Soil enzyme activities (fluorescein diacetate hydrolase, dehydrogenase, β-glucosidase, urease, alkaline and acid phosphatases) also increased significantly ranging from 1.3% (urease) to 53.2% (alkaline phosphatase) under high CO(2) in the soils studied. Both MBC and soil enzyme activities were further stimulated at high temperatures suggesting elevated CO(2) and high temperature interaction accelerated the general turnover of the organic C fractions of the soil and through increase in microbially mediated processes.