Production,respiration and net ecosystem metabolism in U.S. estuaries

Primary production, respiration, and net ecosystem metabolism (NEM) are useful indicators of ecosystem level trophic conditions within estuaries. In this study, dissolved oxygen data collected every half hour between January 1996 to December 1998 by the National Estuarine Research Reserve System Wide Monitoring Program were used to calculate primary production, respiration, and net ecosystem metabolism. Data from two sites at each of 14 Reserves were analyzed. On average, three quarters of the data available could be used to calculate metabolic rates. Data from two of the Reserves were used to evaluate the assumption of homogeneity of water masses moving past the oxygen sensor. Temperature was the single most important factor controlling metabolic rates at individual sites, although salinity was also important at about half the sites. On an annual basis, respiration exceeded gross primary production demonstrating that all but 4 of the 28 sites were heterotrophic.     

Community metabolism in a deep (stratified) tropical reservoir during a period of high water-level fluctuations

As long as lakes and reservoirs are an important component of the global carbon cycle, monitoring of their metabolism is required, especially in the tropics. In particular, the response of deep reservoirs to water-level fluctuations (WLF) is an understudied field. Here, we study community metabolism through oxygen dynamics in a deep monomictic reservoir where high WLF (~10 m) have recently occurred. Simultaneous monitoring of environmental variables and zooplankton dynamics was used to assess the effects of WLF on the metabolism of the eutrophic Valle de Bravo (VB) reservoir, where cyanobacteria blooms are frequent. Mean gross primary production (P _g) was high (2.2 g C m^?2 day^?1), but temporal variation of P _g was low except for a drastic reduction during circulation attributed to zooplankton grazing. The trophogenic layer showed net autotrophy on an annual basis, but turned to net heterotrophy during mixing, and furthermore when the whole water-column oxygen balance was calculated, considering the aphotic respiration (R _aphotic). The high total respiration resulting (3.1 g C m^?2 day^?1) is considered to be partly due to mixing enhanced by WLF. Net ecosystem production was equivalent to a net export of 3.4 mg CO₂?m^?2 day^?1 to the atmosphere. Low water levels are posed to intensify boundary-mixing events driven by the wind during the stratification in VB. Long-term monitoring showed changes in the planktonic community and a strong silicon decrease that matched with low water-level periods. The effects of low water-level on metabolism and planktonic community in VB suggest that water-level manipulation could be a useful management tool to promote phytoplankton groups other than cyanobacteria.     

Seasonal effects on the air-water carbon dioxide exchange in the Hooghly estuary,NE coast of Bay of Bengal,India

Monthly variation of CO2 fugacity (fCO2) in surface water and related atmospheric exchanges were measured in the Hooghly estuary which is one of the most important estuaries, since it is fed by one of the world's largest rivers, the Ganges with a flow of 15,646 m3 s-1 (1.6% of the world's combined river flow). Carbon dioxide fluxes averaged over the entire estuary are in the range of -2.78 to 84.4 mmol m-2 d-1. This estuary acts as a sink for CO2 during monsoon months and seasonal variation of its flux is controlled by dilution of seawater by river water. Since the solubility of CO2 and the disassociation of carbonic acid in estuarine water are controlled by temperature and salinity, the observed variations of CO2 fluxes are compared with those predicted from seasonal changes in temperature, salinity and the ratio of gross primary production to community respiration using empirical equations with an explained variability of 55%.     

The relative influence of nutrients and habitat on stream metabolism in agricultural streams

Stream metabolism was measured in 33 streams across a gradient of nutrient concentrations in four agricultural areas of the USA to determine the relative influence of nutrient concentrations and habitat on primary production (GPP) and respiration (CR-24). In conjunction with the stream metabolism estimates, water quality and algal biomass samples were collected, as was an assessment of habitat in the sampling reach. When data for all study areas were combined, there were no statistically significant relations between gross primary production or community respiration and any of the independent variables. However, significant regression models were developed for three study areas for GPP (r ² = 0.79–0.91) and CR-24 (r ² = 0.76–0.77). Various forms of nutrients (total phosphorus and area-weighted total nitrogen loading) were significant for predicting GPP in two study areas, with habitat variables important in seven significant models. Important physical variables included light availability, precipitation, basin area, and in-stream habitat cover. Both benthic and seston chlorophyll were not found to be important explanatory variables in any of the models; however, benthic ash-free dry weight was important in two models for GPP.     

Effects of temperature and soil moisture on methyl halide and chloroform fluxes from drained peatland pasture soils

A series of laboratory-based incubations using a stable isotope tracer technique was applied to measure the net and gross fluxes of CH(3)Cl and CH(3)Br as well as the net fluxes of CHCl(3) from surface soils of the Sacramento-San Joaquin Delta of California. Annually averaged flux measurements show that these mineral/oxidized peat soils are a net source of CH(3)Cl (140 ± 266 nmol m(-2) d(-1)) and CHCl(3) (258 ± 288 nmol m(-2) d(-1)), and a net sink of CH(3)Br (-2.3 ± 4.5 nmol m(-2) d(-1)). Gross CH(3)Cl and CH(3)Br fluxes are strongly influenced by both soil moisture and temperature: gross production rates of CH(3)Cl and CH(3)Br are linearly correlated with temperature, whereas gross consumption rates exhibit Gaussian relationships with maximum consumption at soil moisture levels between 20 and 30% volumetric water content (VWC) and a temperature range of 25 to 35 °C. Although soil moisture and soil temperature strongly affect consumption rates, the range of gross consumption rates overall is limited (-506 ± 176 nmol m(-2) d(-1) for CH(3)Cl and -12 ± 4 nmol m(-2) d(-1) for CH(3)Br) and is similar to rates reported in previous studies. CHCl(3) fluxes are not correlated with methyl halide fluxes, temperature, or soil moisture. The annual emission rates of CHCl(3) from the Sacramento-San Joaquin Delta are found to be a potentially significant local source of this compound.     

Aerosol size distribution and mass concentration measurements in various cities of Pakistan

During March and April 2010 aerosol inventories from four large cities in Pakistan were assessed in terms of particle size distributions (N), mass (M) concentrations, and particulate matter (PM) concentrations. These M and PM concentrations were obtained for Karachi, Lahore, Rawalpindi, and Peshawar from N concentrations using a native algorithm based on the Grimm model 1.109 dust monitor. The results have confirmed high N, M and PM concentrations in all four cities. They also revealed major contributions to the aerosol concentrations from the re-suspension of road dust, from sea salt aerosols, and from vehicular and industrial emissions. During the study period the 24 hour average PM(10) concentrations for three sites in Karachi were found to be 461 μg m(-3), 270 μg m(-3), and 88 μg m(-3), while the average values for Lahore, Rawalpindi and Peshawar were 198 μg m(-3), 448 μg m(-3), and 540 μg m(-3), respectively. The corresponding 24 hour average PM(2.5) concentrations were 185 μg m(-3), 151 μg m(-3), and 60 μg m(-3) for the three sites in Karachi, and 91 μg m(-3), 140 μg m(-3), and 160 μg m(-3) for Lahore, Rawalpindi and Peshawar, respectively. The low PM(2.5)/PM(10) ratios revealed a high proportion of coarser particles, which are likely to have originated from (a) traffic, (b) other combustion sources, and (c) the re-suspension of road dust. Our calculated 24 hour averaged PM(10) and PM(2.5) concentrations at all sampling points were between 2 and 10 times higher than the maximum PM concentrations recommended by the WHO guidelines. The aerosol samples collected were analyzed for crustal elements (Al, Fe, Si, Mg, Ca) and trace elements (B, Ba, Cr, Cu, K, Na, Mn, Ni, P, Pb, S, Sr, Cd, Ti, Zn and Zr). The averaged concentrations for crustal elements ranged from 1.02 ± 0.76 μg m(-3) for Si at the Sea View location in Karachi to 74.96 ± 7.39 μg m(-3) for Ca in Rawalpindi, and averaged concentrations for trace elements varied from 7.0 ± 0.75 ng m(-3) for B from the SUPARCO location in Karachi to 17.84 ± 0.30 μg m(-3) for Na at the M. A. Jinnah Road location, also in Karachi.     

Elemental Composition of Urban Aerosol Collected in Florence, Italy

An extensive investigation is in progress aiming at the characterisation of the air particulate composition in Florence. For our investigation, we use the external PIXE-PIGE beam facility of the I.N.F.N. Van de Graaff accelerator at the Physics Department of the Florence University. In order to gather information on both the longer- and shorter-time trends of the aerosol elemental composition, we are analysing both long temporal series (about 1 year) of 24-h Millipore filters collected by the health authorities in 3 different sites, and filters collected simultaneously in two of the above sites for about one month, by two streakers with one-hour resolution, providing size fractionation between particle size smaller than 2.5 µm and from 2.5 µm to 10 µm. The streakers sampling period includes two days during which the Municipality of Florence has banned the circulation of non-catalytic cars, due to the increase of NO₂ above the "recommended safety values". We present here the first obtained results for the sampling site located near a heavy traffic road.     

The evaluation of a low resolution fourier transform infrared (FTIR) gas analyser for monitoring of solvent emission rates under field conditions

The applicability of a low resolution (8 cm-1) Fourier transform infrared (FTIR) gas analyser with an absorption path length of 3 m was evaluated for the on-line monitoring of organic solvent mixture emissions in a flexographic ink manufacturing plant. The on-line monitoring revealed that the highest variations of solvent concentrations, up to three decades, occurred in the exhaust air. The FTIR analyser with a dynamic range of four decades covers well the concentration ranges typically found in the exhaust air and in the workroom air of ink manufacturing plants. The average emission rate of solvent mixture based on a sampling period of two days was 1.8 kg h-1 consisting of mainly ethanol (70%), ethyl acetate (15%) and propan-2-ol (11%). The detection limits of the analyser for the solvent compounds ranged from 0.3 to 4.3 mg m-3 and the measurement uncertainty was less than 10% in the concentration range of 8-15,000 mg m-3. These characteristics make the apparatus appropriate for most industrial hygiene applications. An FTIR spectrophotometer, equipped with an multipoint sampling unit, facilitates rapid identification of solvent components, real-time display of concentration data relevant to workroom air and environment monitoring as well as process control. Furthermore, the on-line concentration information enabled a rapid selection of representative sampling locations. The spectrophotometer is transportable, rugged and relatively simple to calibrate even in a hostile industrial environment.     

A study of ground-level ozone pollution, ozone precursors and subtropical meteorological conditions in central Taiwan

Hourly concentrations of ozone (O(3)), 55 volatile organic compounds (VOCs, ozone precursors) and nitrogen oxides (NOx) were measured at an upwind urban site, a downwind suburban site, and a rural site in central Taiwan, from January 2003 to December 2006. VOC and NOx mean concentrations showed a gradient from high to low across the urban (56 ppb and 34 ppb), suburban (38 ppb and 27 ppb) and rural sites (25 ppb and 21 ppb) but a reverse gradient in ozone across these sites (24, 27, and 29 ppb, respectively). Although there was about twice the difference in VOC concentrations between the urban and rural sites, nearly 65% ozone formation potential was contributed to by the same 9 VOCs. Seasonal patterns showed peak ozone levels in autumn and minima in summer at the urban site, but minima in winter at the downwind suburban and rural sites. Ozone precursor levels, on the other hand, were lowest in summer and highest in winter. The diurnal pattern showed that ozone levels peaked one hour later at the rural site than at the urban site. The ethylbenzene to m,p-xylene ratio, an indicator of the age of the air mass, increased from 0.4 at the urban site to 0.6 at the suburban site and 0.8 at the rural site during daily peak ozone times. This finding suggests the transport of ozone and precursors from upwind to downwind producing elevated ozone levels in the suburban and rural areas. Ozone episodes occurred mostly in days with a mean midday UV index of 6.5 (1 UV index=100 J m(-2)) and wind speed at 1.3 m s(-1) at all three sites.     

空气质量AQI实时发布的改进探讨

针对《环境空气质量指数(AQI)技术规定(试行)》(HJ 633-2012)中对空气质量AQI实时发布存在的欠缺,从增加颗粒物1 h浓度的AQI分级浓度限值及颗粒物24 h滑动平均值计算方法改进着手,解决PM2.5和PM10的24 h滑动平均值实时延迟、1 h平均值代替24 h滑动平均值偏高等问题。     

Uranium bioassay and radioactive dust measurements at some uranium processing sites in Egypt--health effects

The safety of radiation workers in the uranium mining industry requires close and continuous monitoring of their working conditions. In this study, external radiation surveillance, radioactive dust monitoring and the bioassay of uranium were carried out in some processing sites. As dust represents one of the most important sources of radiation exposure in mills and mines, dust monitoring and bioassays were performed for a sample of workers on the production lines. The concentration of uranium in air ranged from 22.6 x 10(-7) to 11.1 x 10(-5) Bq cm-3, and the exposure levels ranged from 1 to 80 microSv h-1. Laser fluorimetric determination of uranium in urine samples showed concentrations in the range 8.4-29.2 micrograms L-1. Renal function parameters, such as serum creatinine and urea, and hematological parameters were determined in an attempt to correlate them with radiation exposure and the health status of the workers. Urine specimens collected from workers at the ore crushing and separation site showed elevated concentrations of uranium (up to 29.2 micrograms L-1) and a strong correlation between these concentrations and the registered serum creatinine. The mean uranium excretion in the investigated group was more than 20 times the occupational exposure decision level for urine uranium of 0.8 microgram L-1.     

Evaluation of acoustical particle counter for the sizing of fog droplets

An acoustical particle counter (or acoustical particle sizing device) was evaluated for counting and sizing of fog droplets. Fog droplets were generated under controlled conditions in the laboratory. Fog droplet sizes were measured by an optical and an electron microscope and compared to results from the acoustical particle counter. Most of the droplets were found to be in the size range of 5–30 µm. The mean diameters estimated from the acoustical particle counter were in agreement with the microscope values of mean droplet diameter. A Rich 100 condensation nuclei monitor was also operated simultaneously during the fog droplet counting to monitor the condensation nuclei counts in the laboratory. The results indicate that condensation nuclei count is inversely correlated with the fog droplet threshold diameter. Aerosols of uniform size (35 µm) were generated by the vibrating orifice monodisperse aerosol generator and counted at three different flow rates by the acoustical particle counter. The counts/liter/minute were similar, indicating the reliability of the acoustical particle counter.     

A two-column method for long-term monitoring of non-methane hydrocarbons (NMHCs) and oxygenated volatile organic compounds (o-VOCs)

A method has been developed for concurrent analysis of C2-C7 hydrocarbons and C2-C5 oxygenated volatile organic compounds (o-VOCs) including alcohols, aldehydes, ketones and ethers. A multi-bed, Peltier-cooled adsorbent trap, consisting of Carboxen 1000 and Carbopack B, was used to acquire one sample per hour. Upon injection the sample was split in an approximately 50:50 ratio between a 50 m aluminium oxide (Al2O3) porous layer open tubular (PLOT) column and a 10 m LOWOX column. Eluents from each column were then analysed using flame ionisation detection (FID). Regular calibration of the system was performed using a standard cylinder mixture at the parts per billion by volume (ppbV) level for non-methane hydrocarbons (NMHCs) and a permeation tube method for the oxygenated species. The system is fully automated with NMHC detection limits between 1 and 10 parts per trillion by volume (pptV) and o-VOC detection limits between 10 and 40 pptV.     

In-situ measurement of photosynthetic oxygen production in the water column

A novel hardware device is described to determine photosynthetic and respiratory oxygen uptake and release, respectively, in organisms in their natural habitat even under the rough conditions of their marine environment. Both macroalgae and phytoplankton can be utilized and oxygen exchange can be determined in solar radiation. The chamber can be used at or above the water surface or can be lowered into the water column. The data of oxygen concentration, irradiance and temperature are constantly monitored by a laptop computer and stored in disk files. The experimental data measured in some macroalgae as well as in phytoplankton indicate that the irradiance window for positive net photosynthetic oxygen production is fairly limited under natural conditions; at too low irradiances respiration exceeds photosynthesis and at too high irradiances photosynthesis is shut down by photoinhibition, at least in species not adapted to unattenuated solar radiation.     

Temporal variations of airborne particle concentration in an arid region

Airborne particle concentration (APC) measurements were carried out at the Sede Boker experimental station located in the northern Negev Desert, about 50 km south of Beer Sheva, during the years 1987--1997. The basic sampling period used in 1987--1993 was 12 h (day and night) and in 1994--1997 the sampling period was 24 h. For the entire study period, the average airborne particle concentration (APC) was 123.8 microg/m3, the highest value was 4204.2 microg/m3; and the lowest, near 5 microg/m3. For the 24 h average, about 90% of the cases were defined as normal situations (APC between 0-200 microg/m3) about, 8.5%, hazy periods (APC between 200-500 microg/m3), 1.4% dusty periods (APC between 500-1000 microg/m3) and about 0.7% were intense dusty periods (APC above 1000 microg/m3). Statistical analysis of the data showed significant seasonal and monthly fluctuations. The seasonal variation of the APC was further examined using different definitions of the seasons (astronomical, meteorological, and synoptic).     

Air Quality and Monitoring Strategy in the Helsinki Metropolitan Area, Finland

The Helsinki Metropolitan Area Council (YTV) is responsible for air quality monitoring in the Helsinki area. Air quality has been monitored periodically since the late 1950s. An automatic SO2 monitoring network was constructed in 1975 and TSP measurements were added in 1978. Since then the network has been expanded and currently five automatic multicomponent stations form the basis of the network monitoring SO2, NO, NO2, CO, PM10 and O3 concentrations. Manual TSP and PM10 measurements are also conducted. Mobile monitoring units are also being used as well as special measurement campaigns. The effects of air pollution on nature are studied in bioindicator monitoring. An air quality index is used in order to inform the public of the current air quality situation. Changes in air quality are reflected in monitoring strategy. SO2 concentrations have decreased in the past two decades. Annual averages in 1995 were at or below 5 µg/m3. Traffic is the major source for pollutants even though catalytic converters have lowered traffic emissions somewhat. The highest annual average NO2 concentration at an urban site was 49 µg/m3 in 1995, and there has been no clear change in NO2 levels. There has been a decreasing trend in CO concentrations. Maximum annual TSP and PM10 averages in 1995 were 92 and 32 µg/m3, respectively. The highest average lead concentration was 0.01 µg/m3. Elevated concentrations are experienced from time to time. During the spring daily TSP and PM10 concentrations can go up to around 300 and 150 µg/m3, respectively. This is caused by resuspension mainly due to street sanding. Also a major winter NO2 episode occurred in December 1995. The highest hourly NO2 concentrations reached 400 µg/m3.     

Anthropogenic emissions of methane and nitrous oxide in the Federal Republic of Germany

The anthropogenic emission sources of methane (CH₄) and nitrous oxide (N₂O) in the Federal Republic of Germany were investigated. The object of the recently completed first phase of this research project was to summarize the present knowledge about the emission sources, make a first rough estimate of the emissions, identify the need for further research in the field, and - as far as possible - discuss the existing possibilities to reduce emissions. The main CH₄ emission sources identified are the landfills, stock farming and pit mining, the main N₂O sources are agriculture (including a minor contribution from animal wastes) and the production of adipic acid, the latter possibly being reducible by means of a new catalytic process. The total anthropogenic emissions of CH₄ from Germany are estimated at 5.4 – 7.7 million tonnes per year, contributing a share of roughly 2 % to the world-wide anthropogenic emissions (350 million t/a). Those of N₂O are estimated at 200 000 – 280 000 tonnes per year (world-wide 1.4 – 6.5 million t/a).     

Respirometric Evaluation by Graphical Analysis for Microbial Systems

Analysis of respirometric graphs for system diagnosis has recently drawn much attention due to the nature of the test being a fast method with reliable oxygen uptake (Ou) data. In this study, a new graphical analysis procedure is proposed, using the oxygen uptake rate (OUR) vs. Ou respirogram because of its distinct characteristics that provides easy visual inspection. The OUR plot is typically divided into two respiration phases, and each one of these phases can be simulated by a previously derived analytical equation. Based on the 2-phase model, five characteristic parameters (CPs) were derived for the OUR respirogram. Mathematically the 5 CPs can be related to the system parameters (SPs), including the four Monod kinetic parameters and two operating conditions (initial substrate and biomass concentration). Sensitivity analyses were then conducted to assess the 5 CPs for the level of effect caused by system parameters (SPs). This study also conducted respirometric tests under batch operation to evaluate the applicability of the graphical analysis method. Based on the 5 CPs estimated from the OUR respirogram of the tests, it can be concluded that respirometric tests normally experience the problems associated with initial lag, non-uniform seeding, and inadequate mixing.     

Mixing ratios of carbonyls and BTEX in ambient air of Kolkata, India and their associated health risk

Mixing ratios of 15 carbonyls and BTEX (benzene, toluene, ethyl benzene, xylenes) were measured for the first time in ambient air of Kolkata, India at three sites from March to June 2006 and their photochemical reactivity was evaluated. Day and nighttime samples were collected on weekly basis. Formaldehyde was the most abundant carbonyl (mean concentration ranging between 14.07 microg m(-3) to 26.12 microg m(-3) over the three sites) followed by acetaldehyde (7.60-18.67 microg m(-3)) and acetone (4.43-10.34 microg m(-3)). Among the high molecular weight aldehydes, nonanal showed the highest concentration. Among the mono-aromatic VOCs, mean concentration of toluene (27.65-103.31 microg m(-3)) was maximum, closely followed by benzene (24.97-79.18 microg m(-3)). Mean formaldehyde to acetaldehyde (1.4) and acetaldehyde to propanal ratios (5.0) were typical of urban air. Based on their photochemical reactivity towards OH. radical, the concentrations of the VOCs were scaled to formaldehyde equivalent, which showed that the high molecular weight carbonyls and xylenes contribute significantly to the total OH-reactive mass of the VOCs. Due to the toxic effect of the VOCs studied, an assessment for both cancer risk and non-cancer hazard due to exposure to the population were calculated. Integrated life time cancer risk (ILTCR) due to four carcinogens (benzene, ethyl benzene, formaldehyde and acetaldehyde) and non-cancer hazard index for the VOCs at their prevailing level were estimated to be 1.42E-04 and 5.6 respectively.     

Antimony: a traffic-related element in the atmosphere of Buenos Aires, Argentina

Vehicular traffic is one of the main sources of antimony in highly populated urban areas like Buenos Aires where an overall traffic density of 1 500 000 vehicles per day (corresponding to 7500 vehicles km(-2)) is estimated. In this context, a study was undertaken to ascertain the levels of Sb and other traffic-related elements (TRE) in the atmosphere of this city. To this end, sixty-seven samples of PM-10 particulate matter were collected during eight days in nine representative sampling sites located downtown Buenos Aires and spread over an area of about 30 km2. The collection of particulate matter was performed on ash-free glass-fibre filters using high volume samplers with PM-10 sampling heads. A combination of aqua regia and perchloric acid was used for leaching metals from filters. The resulting solutions were evaporated and then diluted with 0.1 mol l(-1) HCl. Antimony was determined by inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS) at ng g(-1) levels. Concentrations of Sb varied from 12.9 +/- 0.9 to 375 +/- 23 microg g(-1)(equivalent to 0.87 +/- 0.06 to 15.3 +/- 0.8 ng m(-3)). Statistical analysis was performed on the data set including the measured PM-10 mass and Sb concentrations for the monitored period. Correlations of Sb with other TRE namely, Cu and Mo were also assessed. The highest concentrations of Sb were detected at two sites (Hospital Alemán and Casa Rapallini) located in streets with traffic consisting mostly of passenger cars and showing a "stop-and-go" pattern in peak hours. Antimony levels in the Buenos Aires PM-10 are by far below the level of 0.5 mg m(-3)(for an 8 hour workday, 40 hour work week) set by the US Occupational Safety and Health Administration (OSHA) for occupational exposure. However, monitoring of Sb and other TRE should be carried out in a systematic fashion to detect the possibility of increases in from the present levels.