Plant uptake of atmospheric brominated flame retardants at an E-waste site in southern China

Brominated flame retardants (BFRs) were measured in eucalyptus leaves and pine needles as well as the leaf surface particles (LSPs) of the two species at an e-waste site in southern China in 2007-2008. The monthly concentrations of total BFRs in the eucalyptus leaves and pine needles were in range of 30.6-154 and 15.1-236 ng/g dry weight, respectively, and relatively higher concentrations were observed in winter and spring. Correlation analysis of BFR concentrations and comparison of PBDE compositions between the plants and LSPs, air (gaseous and particle-bound phases), and ambient variables were conducted. The results revealed that BFRs in the plants, especially for less brominated BFRs, showed positive relationships with BFRs in the LSPs and negative relationships with the gaseous BFRs and ambient temperature. The PBDE profiles in the plants were similar to the gaseous profile for low brominated BDEs (di- through hexa-BDEs) and to the LSP profiles for highly brominated BDEs (hepta- through deca-BDEs). Applying McLachlan's framework to our data suggests that the uptake of BFRs was controlled primarily by gaseous partitioning equilibrium for compounds with log octanol-air partition coefficients (K(OA)) < 12 and by particle-bound deposition for compounds with log K(OA) > 13. Different relationships between the plant/air partition coefficient (K(PA)) and K(OA), which depend on the uptake mechanisms, were observed for polybrominated diphenyl ethers (PBDEs). This paper adds to the current knowledge of the factors and mechanisms governing plant uptake of semivolatile organic compounds with relatively high K(OA) in the environment.     

Variation in saponin content during the growing season of spotted medic [Medicago arabica (L.) Huds.]

BACKGROUND: Spotted medic [Medicago arabica (L.) Huds.] is a minor forage species containing saponins which are reported to be biologically active. This study assessed the concentration and composition pattern of spotted medic saponins during the growing season and at senescence. The pattern of saponins was based on identification and quantification of their constituent sapogenins. At senescence, individual saponin concentrations of aerial and subterranean plant organs were also determined. RESULTS: Leaf total saponin content did not vary during the growing season and decreased remarkably at senescence. Seven sapogenins were identified and quantified during the season, bayogenin and hederagenin being the most abundant ones throughout. Total saponin content varied among plant organs at senescence, with the highest concentration in roots. A variable number of saponins from one (in seeds) to 19 (in leaves) were quantified. A clear relationship between leaf concentrations of sapogenins and those of their derivative saponins was revealed by correlation analysis. CONCLUSION: The species displayed a sapogenins/saponins pattern markedly different from those of other perennial or annual Medicago species. Saponins of queretaroic acid and 2β‐hydroxy queretaroic acid had no precedent in the Leguminosae. The high concentration of biologically active hederagenin suggested further assessment of possible effects on feeding animals. Copyright © 2010 Society of Chemical Industry     

Uptake and storage of PCBs by plant cuticles

The uptake kinetics and storage of PCBs by isolated cuticles and cuticular waxes from Hedera helix, Prunus laurocerasus, and Ilex aquifolium were studied. Small chambers were used, allowing variation in plant uptake parameters to be studied by having the same air boundary layer in each chamber. During the 64 day study tri- and tetrachlorinated biphenyls generally reached equilibrium in waxes but not in whole cuticles. Differences between species were observed. Higher chlorinated PCB congeners did not approach equilibrium in either sample type. Although PCBs showed higher affinity for waxes than whole cuticles, the latter dominated the total uptake capacity on a surface area basis, because of the large amount of nonwax cuticular components. Mass transfer coefficients (MTCs) for PCB uptake (into both cuticles and waxes) indicated partition dependence up to log octanol/air partition coefficients (K(OA)) of 8.5-10, depending on species and sample type. For cuticles, higher MTCs occurred at the beginning of the experiment than later. This was not seen in reconstituted waxes, a difference which may be explained by the dispersion of intracuticular waxes within cuticles. For more lipophilic compounds, uptake appeared to be limited by diffusion processes, which may be influenced by plant physiology. Leaf surface area is, therefore, likely to control the ability of vegetation to scavenge these compounds from the air in many field situations.     

Estimating the influence of forests on the overall fate of semivolatile organic compounds using a multimedia fate model

On the basis of recently reported measurements of semivolatile organic compound (SOC) uptake in forest canopies, simple expressions are derived that allow the inclusion of a canopy compartment into existing non-steady-state multimedia fate models based on the fugacity approach. One such model is used to assess how the inclusion of the canopy compartment in the model affects the calculated overall behavior of SOCs with specific physical--chemical properties. The primary effect of the forest is an increase in the net atmospheric deposition to the terrestrial environment, reducing atmospheric concentrations and accordingly the extent of deposition to the agricultural and aquatic environments. This effect was most pronounced for chemicals with log KOA around 9-10 and log KAW -2 to -3; their average air concentrations during the growing season decreased by a factor of 5 when the canopy compartment was included. Concentration levels in virtually all compartments are decreased at the expense of increased concentrations in the forest soil. The effect of the forest lies not in a large capacity for these chemicals but in the efficiency of pumping the chemicals from the atmosphere to the forest soil, a storage reservoir with high capacity from which the chemicals can return to the atmosphere only with difficulty. Because of seasonal variability of canopy size and atmospheric stability, uptake into forests is higher during spring and summer than in winter. The model suggests that this may dampen temperature-driven seasonal fluctuations of air concentrations and in regions with large deciduous forests may lead to a temporary, yet notable dip in air concentrations during leaf development in spring. A sensitivity analysis revealed a strong effect of forest cover, forest composition, and degradation half-lives. A high degradation loss on the plant surface has the effect of preventing the saturation of the small plant reservoir and can cause very significant reductions in atmospheric concentrations of those SOCs for which uptake in the canopy is limited by the size of the reservoir.     

Deposition of polybrominated diphenyl ethers, polychlorinated biphenyls, and polycyclic aromatic hydrocarbons to a boreal deciduous forest

The atmospheric deposition of several groups of semi-volatile organic compounds to a deciduous forest in Canada was determined using an indirect technique based on ratios of measured canopy interception and air concentrations. Air (gas and particle phase) and bulk deposition were sampled for 14 months from October 2001 to December 2002 at both a forest and a nearby clearing, and extracts were quantified for polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and polycyclic aromatic hydrocarbons (PAHs). Long-term average dry deposition velocities for vapors and particle-bound species were then derived for the canopy growing period. The mean dry gaseous deposition velocity for PBDEs and PCBs to the Canadian deciduous forest was 2.7 +/- 0.52 cm x s(-1), which is similar to the only other measured value for a deciduous canopy. Particle-bound deposition velocities to the canopy due to diffusion and impaction were 0.8 cm x s(-1) for the PBDEs and 0.11 cm x s(-1) for the PAHs. Differences in the particle-bound deposition velocities between PBDEs and PAHs and between deciduous canopies in Canada and Germany are explainable by differences in particle size distribution. The interception/concentration ratios for several PAHs were too low to be interpretable as dry gaseous deposition velocities. This is likely because the measured deposition flux under the canopy was less than the deposition flux to the canopy, possibly as a result of photodegradation in the canopy. From the ratio of canopy interception and average gas-phase concentration of less chlorinated PCBs, a predictive relationship between the canopy/air partition coefficient KPA and the octanol/air partition coefficient KOA was derived (KPA = 110 KOA0.67). Despite differences in local climate and canopy composition and structure, the deposition velocities and the canopy uptake capacity measured in Canada were remarkably similar to those reported in Germany, lending credibility to the suggestion that high gaseous deposition velocities are common throughout boreal and temperate deciduous forests. These extraordinarily high deposition velocities of semi-volatile organic compounds to deciduous forest canopies are at the core of the hypothesis of a significant filter effect of forests on a regional and global scale.     

四种稳定剂对霞多丽葡萄酒稳定性的影响研究

为研究稳定剂对白葡萄酒的稳定效果,以前人报道冷稳定效果较好的80 mg/L偏酒石酸(metatartaric acid,MTA)和空白组(CK)为对照,向霞多丽葡萄酒中添加不同浓度梯度的聚天冬氨酸钾(potassium polyaspartate,KPA)、羧甲基纤维素(carboxylmethylcellulose,CMC)、阿拉伯树胶(gum Arabic,GA)和甘露糖蛋白(mannoprotein,MP),以冷处理前、后电导率下降值为判定酒石酸盐稳定的主要指标,浊度和冷、热处理后沉淀量等为辅助指标,研究四种稳定剂在不同浓度下的稳定效果,筛选出每种稳定剂的最佳浓度,同时比较四种稳定剂之间的作用效果。结果表明:KPA的最佳浓度是100 mg/L,电导率变化量小(27 μs/cm),浊度、酒石酸和钾离子含量与CK差异不显著(P>0.05),冷、热处理后沉淀产生量明显少于80 mg/L的MTA处理和CK。四个浓度的CMC都能起到很好的冷稳定效果,其中150 mg/L的CMC的综合效果最佳。GA最佳浓度是50 mg/L,经处理后酒样非常稳定,浊度有少量升高,冷、热处理后有少量沉淀产生。MP的最佳浓度为50 mg/L,四个浓度MP虽能起到稳定葡萄酒的作用,但随浓度升高会增加酒样浊度。结论:100 mg/L的KPA综合作用效果最好,其次为50 mg/L GA、50 mg/L MP和150 mg/L CMC。本研究结果为新型稳定剂KPA在葡萄酒中的应用提供一定的理论依据。     

Accumulation of trifluoroacetate in seasonal wetlands in California

Trifluoroacetate (TFA, CF3COO-) is a stable and mildly phytotoxic breakdown product of several fluorinated organic compounds including the hydro(chloro)fluorocarbons (HFC/HCFCs) that have largely replaced the stratospheric ozone-depleting chlorofluorocarbons (CFCs). TFA enters aquatic ecosystems primarily through precipitation and has the potential to accumulate in water bodies with little or no outflow to the point where toxic concentrations could be achieved. This study demonstrated that seasonal wetlands lacking outflow concentrated TFA as they evaporated during the dry season. In addition, the TFA within the pools was retained between years, which may result in long-term TFA accumulation. Since plants acquire TFA from their growing media, the plants exposed to high aqueous concentrations of TFA within the pools had elevated TFA concentrations with a median concentration of 279 ng/g dry weight in their tissues as compared to 33 ng/g for species growing outside the pools. The highest TFA concentrations in water, which occurred just prior to the pools drying up, were in the 2-10 micrograms/L range. These concentrations are approximately 190 or less than reported toxic concentrations for the most sensitive species tested, but our evidence suggests that these concentrations will increase with continued TFA deposition into the pools.     

Variable air temperature response of gas-phase atmospheric polychlorinated biphenyls near a former manufacturing facility

Many investigations of gas-phase atmospheric PCB show a strong relationship between concentration and air temperature, especially near PCB sources. Comparative gas-phase atmospheric PCB trends during an annual temperature regime at two sites near a former PCB manufacturing plant and nearby PCB landfills in Anniston, AL, indicate a departure from this trend. The Mars Hill sampling site, located closest to the plant and landfills, shows an annual average sigmaPCB concentration of 27 ng m(-3) (ranging from 8.7 to 82 ng m(-3)) three times the average at Carter, 1.5 km away (9 ng m(-3), ranging from 1.1 to 39). However, total PCB and congener concentrations vary more with air temperature at Carter where PCB are evaporating from surfaces during warmer weather. The slopes of the Clausius-Clapeyron plots of 18 of the most concentrated congeners representing dichloro- through heptachlorobiphenyl homologues are significantly higher at the Carter site. While some of the atmospheric PCB at Mars Hill is derived from ground surface evaporation, the source of much of it apparently is the material buried in the landfills, which has different thermal properties than surface materials and is not in equilibrium with air temperature.     

Ultraviolet spectrophotometric characterization and bactericidal properties of electrolyzed oxidizing water as influenced by amperage and pH

To identify the primary component responsible in electrolyzed oxidizing (EO) water for inactivation, this study determined the concentrations of hypochlorous acid (HOCl) and hypochlorite ions (OCl-) and related those concentrations to the microbicidal activity of the water. The ultraviolet absorption spectra were used to determine the concentrations of HOCl and OCl- in EO water and the chemical equilibrium of these species with change in pH and amperage. EO water generated at higher amperage contained a higher chlorine concentration. The maximum concentration of HOCl was observed around pH 4 where the maximum log reduction (2.3 log10 CFU/ml) of Bacillus cereus F4431/73 vegetative cells also occurred. The high correlation (r = 0.95) between HOCl concentrations and bactericidal effectiveness of EO water supports HOCl's role as the primary inactivation agent. Caution should be taken with standard titrimetric methods for measurement of chlorine as they cannot differentiate the levels of HOCl present in EO water of varying pHs.     

The effect of slaughter operations on the contamination of chicken carcasses with thermotolerant Campylobacter

To evaluate the effect of specific slaughter operations on the contamination of broiler carcasses with naturally occurring thermotolerant Campylobacter, experiments were carried out in two Danish commercial slaughter plants (Plant I and Plant II). Six broiler flocks determined Campylobacter positive prior to slaughter were investigated at four sampling locations within each slaughter plant. Quantification of thermotolerant Campylobacter in 30 neck skin samples per flock per sampling location showed that the evisceration operation in Plant I led to a significant increase in the Campylobacter concentration of 0.5 log(10) cfu/g in average, whereas no significant changes were observed during this operation in Plant II. Air chilling (Plant I) and water chilling (Plant II), both including a carcass wash prior to the chilling operation, caused similar, but significant reductions of 0.83 and 0.97 log(10) cfu/g, respectively. In packed frozen chickens (Plant II) an additional reduction of 1.38 log(10) cfu/g in average was obtained due to the freezing operation. In packed chilled chickens (Plant I), however, the number of thermotolerant Campylobacter per gram remained at the same level as after air chilling. Enumeration of thermotolerant Campylobacter in 30 intestinal samples per flock showed that in two of the six flocks examined the within flock colonization was very low (<3% and 27% positive samples). The remaining four flocks were colonized at percentages of 100 (three flocks) and 97 (one flock) and had intestinal mean counts ranging from 6.65 to 8.20 log(10) cfu/g. A correlation between Campylobacter concentrations in intestinal content and on chicken carcasses after the defeathering operation was documented. This finding indicates that a reduction in the Campylobacter concentration on chicken carcasses may also be obtained by interventions aimed at reducing the concentration of Campylobacter in the intestines of the living birds.     

Influence of rooting medium pH and shoot and root temperature on the nitrate reductase activity of winter barley

In three separate experiments, the effects of rooting medium pH (pH 4.0, 5.3 and 6.5), root temperature (5, 10 and 15 C) and shoot temperature (6 and 17 C) on the growth, in-vivo nitrate reductase activity and nitrogen status of winter barley were investigated. Except where temperature was specifically studied, air and/or root temperatures were maintained at 10 C to simulate the typically cool conditions which prevail during the early growing season for cereals in northern Europe. Although growth, nitrate uptake and nitrate reductase activity were markedly affected by variations in temperature and pH. the Nitrogen Response Index, which is the quotient of in-vivo induced and endogenous nitrate reductase activities in shoot or root material, was unaffected and uniquely reflected the N status of the plant.     

Distribution and air-sea exchange of current-use pesticides (CUPs) from East Asia to the high Arctic Ocean

Surface seawater and marine boundary layer air samples were collected on the ice-breaker R/V Xuelong (Snow Dragon) from the East China Sea to the high Arctic (33.23-84.5° N) in July to September 2010 and have been analyzed for six current-use pesticides (CUPs): trifluralin, endosulfan, chlorothalonil, chlorpyrifos, dacthal, and dicofol. In all oceanic air samples, the six CUPs were detected, showing highest level (>100 pg/m(3)) in the Sea of Japan. Gaseous CUPs basically decreased from East Asia (between 36.6 and 45.1° N) toward Bering and Chukchi Seas. The dissolved CUPs in ocean water ranged widely from 相似文献   

PAHs in air and seawater along a North-South Atlantic transect: trends, processes and possible sources

Polycyclic aromatic hydrocarbons (PAHs) were simultaneously measured in air and surface seawater between 49 degrees N and 25 degrees S in the open Atlantic Ocean. Elevated concentrations of PAHs (sigma10 PAHs approximately 1.4-2.5 ng m(-3) air, and 0.7-1 ng L(-1) seawater) occurred in the Biscay Bay and off the northwest coast of Africa. The unexpectedly high concentrations off NW Africa were discussed assessing the possible contribution of the emerging oil industry along the African shore, the role of biomass burning and natural sources of PAHs. In the southern Atlantic, concentrations of PAHs were close to detection limits (sigma10 PAHs approximately 0.02-0.5 ng m(-3) air, and 0.06-0.5 ng L(-1) seawater) and showed decreasing trends with increasing latitudes. Correlations of PAHs' partial pressures versus inverse temperature were not significant in contrast to results for polychlorinated biphenyls from the same transect. This could have been due to the importance of ongoing primary sources and the shorter atmospheric life-times of PAHs. Air-water fugacity ratios (fa/fw) were calculated for selected compounds. They were close to 1 for fluoranthene and pyrene in remote open ocean areas suggesting air-water partitioning near equilibrium. Ratios for anthracene and phenanthrene were < 0.3 in the remote tropical Atlantic, suggesting net volatilization.     

PA、H103及XAD-4树脂在茶多酚吸附工艺中的特性研究

本文主要研究了PA、H103及XAD-4树脂在茶多酚吸附分离体系中的吸附热力学特性及吸附动力学特性。热力学研究表明,三种吸附剂的吸附等温线都属于优惠型的吸附等温线,并可以用Langmiur 方程来描述,且与Langmiur方程高度相关;动力学特性研究表明,PA和H103树脂为中速吸附型的吸附剂,XAD-4为慢速吸附型的吸附剂。PA、H103及XAD-4树脂的吸附平衡速率常数依次为KPA=1.461h-1,KH103=1.198h-1,KXAD-4=0.498h-1。     

Solid-phase microextraction to predict bioavailability and accumulation of organic micropollutants in terrestrial organisms after exposure to a field-contaminated soil

The risk posed by soil contaminants strongly depends on their bioavailability. In this study, a partition-based sampling method was applied as a tool to estimate bioavailability in soil. The accumulation of organic micropollutants was measured in two earthworm species (Eisenia andrei and Aporrectodea caliginosa) and in 30-microm poly(dimethylsiloxane) (PDMS)-coated solid-phase micro extraction (SPME) fibers after exposure to two field-contaminated soils. Within 10 days, steady state in earthworms was reached, and within 20 days in the SPME fibers. Steady-state concentrations in both earthworm species were linearly related to concentrations in fibers over a 10,000-fold range of concentrations. Measured concentrations in earthworms were compared to levels calculated via equilibrium partitioning theory and total concentrations of contaminants in soil. In addition, freely dissolved concentrations of contaminants in pore water, derived from SPME measurements, were used to calculate concentrations in earthworms. Measured concentrations in earthworms were close to estimated concentrations from the SPME fiber measurements. Freely dissolved concentrations of contaminants in pore water, derived from SPME measurements, were used to calculate bioconcentration factors (BCF) in earthworms. A plot of log BCFs against the octanol-water partition coefficient (log Kow) was linear up to a log Kow of 8. These results show that measuring concentrations of hydrophobic chemicals in a PDMS-coated fiber represents a simple tool to estimate internal concentrations of chemicals in biota exposed to soil.     

Using passive air samplers to assess urban-rural trends for persistent organic pollutants and polycyclic aromatic hydrocarbons. 2. Seasonal trends for PAHs, PCBs, and organochlorine pesticides

This is the second of two papers demonstrating the feasibility of using passive air samplers to investigate persistent organic pollutants along an urban-rural transect in Toronto. The first paper investigated spatial trends for polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). This second paper investigates the seasonality of air concentrations for polycyclic aromatic hydrocarbons (PAHs), PCBs, and OCPs along this transect. Air samplers, consisting of polyurethane foam (PUF) disks housed in stainless steel domed chambers, were deployed for three 4-month integration periods from June 2000 to July 2001. The seasonal variations of derived air concentrations for PAHs, PCBs, and OCPs reflected the different source characteristics for these compounds. PAHs showed a strong urban-rural gradient with maximum concentrations at urban sites during the summer period (July-October). These high summer values in Toronto were attributed to increases in evaporative emissions from petroleum products such as asphalt. PCBs also exhibited a strong urban-rural gradient with maximum air concentrations (approximately 2-3 times higher) during the spring period (April-June). This was attributed to increased surface-air exchange of PCBs that had accumulated in the surface layer over the winter. alpha-HCH was fairly uniformly distributed, spatially and temporally, as expected. This pattern and the derived air concentration of approximately 35 to approximately 100 pg m(-3) agreed well with high volume air data from this region, adding confidence to the operation of the passive samplers and showing that site-to-site differences in sampling rates was not an issue. For other OCPs, highest concentrations were observed during the spring period. This was associated with either (i) their local and/or regional application (gamma-HCH, endosulfan) and (ii) their revolatilization (chlordanes, DDT isomers, dieldrin, and toxaphene). Principal component analysis resulted in clusters for the different target chemicals according to their chemical class/source type. The results of this study demonstrate how such a simple sampling technique can provide both spatial and seasonal information. These data, integrated over seasons, can be used to evaluate contaminant trends and the potential role of large urban centers as sources of some semivolatile compounds to the regional environment, including the Great Lakes ecosystem.     

Altitudinal and seasonal variations of persistent organic pollutants in the Bolivian Andes Mountains

Polyurethane foam disk passive air samplers were deployed over four periods of approximately 3 months along an altitudinal gradient (1820, 2600, 4650, and 5200 masl) on the east side of the Andean mountain range in Bolivia. The purpose of the study was to assess the gas-phase concentration and the altitudinal and seasonal trends of organochlorine pesticides and polychlorinated biphenyls (PCBs). Target compounds that were regularly detected included alpha- and gamma-hexachlorocyclohexane (HCH), endosulfans, and select PCB congeners. Endosulfans and HCH concentrations increased with altitude. Enrichment factors (concentration at the highest altitude divided by concentration at the lowest altitude) ranged from 10 to 20 for HCHs and 3 to 10 for endosulfans. Air parcel back trajectory analysis indicated that, in general, the high-altitude sites were exposed to a larger airshed and hence susceptible to long-range atmospheric transport from more distant regions. Seasonal differences were also observed with SigmaHCH concentrations peaking during periods 2 and 3 (March-September 2005). Airsheds (derived from the analysis of back trajectories) for periods 2 and 3 were less oriented along the Andes range (mountain air) with greater input from coastal regions. Endosulfans peaked during periods 1 and 2 (February-June 2005) and also exhibited the highest air concentrations of the target compounds, reaching approximately 1500 pg/m3 at the two highest elevation sites. PCB air concentrations at all sites were generally typical of global background values (<12 pg/m3) and showed no increase with altitude. This is the first study to measure air concentrations of persistent organic pollutants (POPs) in Bolivia and one of only a few studies to investigate altitudinal gradients of POPs.     

Brominated flame retardants in the atmosphere of E-waste and rural sites in southern China: seasonal variation, temperature dependence, and gas-particle partitioning

The recycling of electrical and electronic waste(e-waste) in developing countries has attracted much attention as a significant source of brominated flame retardants (BFRs).Gaseous and particle-bound BFRs were measured in the atmosphere at e-waste and rural sites in southern China during 2007-2008. The annual average concentrations in the air were 3260 ± 3370 and 219 ± 192 pg/m3 for polybrominated diphenyl ethers (PBDEs) and were 546 ± 547 and 165 ± 144 pg/m3 for non-PBDE BFRs at the e-waste and rural sites,respectively. PBDEs had unusually high relative concentrations of di- and tribrominated congeners at the e-waste site. The Clausius-Clapeyron (CC) plots showed that the gaseous concentrations of less brominated BFRs (di- through hexa-BFRs) were strongly controlled by temperature-driven evaporation from contaminated surfaces (e.g., e-waste, soils, and recycled e-waste remains) except for winter. However, weak temperature dependence at the rural site suggests that regional or long-range atmospheric transport was largely responsible for the air concentrations. Gas-particle partitioning (KP) of PBDEs correlated well with the subcooled liquid vapor pressure (PL(o)) for most sampling events. The varied slopes of log KP versus log PL(o) plots for the e-waste site (-0.59 to -1.29) indicated an influence of ambient temperature and atmospheric particle properties on the partitioning behavior of BFRs. The flat slopes (-0.23 to -0.80) for the rural site implied an absorption-dominant partitioning. This paper suggests that e-waste recycling in Asian low-latitude regions is a significant source of less brominated BFRs and has important implications for their global transport from warm to colder climate     

Distribution of airborne microorganisms in commercial pork slaughter processes

The objective of this research was to determine the prevalence and distribution of airborne bacterial contamination, with particular reference to Escherichia coli and Salmonella, at a number of stages in a pork slaughtering plant. Air samples (impaction and sedimentation) were recovered from seven locations before and during operations in a commercial pork processing plant. Aerobic mesophilic bacteria, E. coli counts and the incidence of Salmonella in the air were determined. Most sample locations which provided high impaction counts also provided high sedimentation counts. Before commencement of operations, there were no significant differences in aerobic mesophilic bacteria obtained from the sample locations. However, within 2 h of the commencement of operations, aerobic mesophilic bacteria in the wet room (3.14 log10 cfu/m3) were significantly higher (P < 0.05) than those in the clean room (2.66 log10 cfu/m3) and chiller (2.34 log10 cfu/m3). By the afternoon, similar aerobic mesophilic bacteria counts were recovered in the wet and clean rooms, although counts in both of these areas were significantly higher (P > 0.05) than in the chiller. In general there were no significant differences in E. coli counts between rooms (wet room, clean room and chiller) and these did not increase during the production day. Salmonella were detected at the locations of the dehairing and evisceration operations. Aerobic mesophilic bacteria in the air within the abattoir increased as production proceeded. In addition the air within the abattoir contained organisms such as Salmonella and E. coli. Positive correlations (P < 0.05-P < 0.001) between impaction and sedimentation samples were found suggesting that air may be an important source of carcass contamination.     

Automated measurements of ammonia and nitric acid in indoor and outdoor air

Simultaneous temporally resolved indoor and outdoor measurements of ammonia and nitric acid are valuable for determining the gas-particle equilibrium conditions governing concentrations of ammonium nitrate aerosol. We report the results of simultaneous automated indoor and outdoor measurements of ammonia and nitric acid concentrations made at an unoccupied, single-story residence in Clovis, CA during three periods from October 2000 to January 2001. The measurements were conducted as part of a controlled study to explore mechanisms governing indoor concentrations of fine aerosols of outdoor origin. The gas-phase measurements were performed using diffusion denuders and ion chromatography with 30 min temporal resolution and detection limits below 1 ppb. The conditions of the field experiment span a wide range of outdoor climate as well as natural and forced indoor conditions. During all periods ammonia concentrations were generally slightly higher indoors than out, with both outdoor and indoor concentrations varying in a range from approximately 5 to 30 ppb. Nitric acid was only detected in outdoor air in October 2000, at concentrations up to 3 ppb. During the October period, the product of outdoor nitric acid and ammonia concentrations sometimes deviated from that expected for equilibrium between gas and ammonium nitrate particulate phases and the degree and direction of disequilibrium were correlated with trends in air temperature. The consistently low indoor concentrations of nitric acid were not consistent with equilibrium between gas and particle phases and suggest that a combination of low penetration into the building and a high loss rate for nitric acid reduce indoor concentrations significantly below those outdoors.