Upscaling heterogeneity in aquifer reactivity via the exposure-time concept: inverse model

A novel inverse technique is proposed to quantitatively characterize macroscopic variability in aquifer reactivity in a Lagrangian representation. Reactivity heterogeneity is expressed in terms of distributions of flux over cumulative time of exposure of the solution to reactive surface area, termed here 'cumulative reactivity'. In cases involving single aqueous species the combined effects of physical and reactivity heterogeneity on reactive solute transport can often be established and further investigated through joint distributions of flux over travel time and cumulative reactivity. The inverse technique requires the breakthrough curve of a passive tracer to determine the distribution of flux over travel time, and additional breakthrough curves of reactive tracers provide additional moments of the distribution of flux over cumulative reactivity given travel time. Thus breakthroughs of one passive and two reactive tracers can provide the mean and variance of the distribution of flux over cumulative reactivity. This Lagrangian characterization is achieved with knowledge of the types of reactive surfaces present, but not their spatial locations. The distributions can subsequently be applied via forward modeling using the same technique to predict breakthrough curves of other solutes undergoing first-order reactions in similar physically and chemically heterogeneous configurations.     

Dynamic modeling of chemical fate and transport in multimedia environments at watershed scale-I: theoretical considerations and model implementation

A geo-referenced environmental fate model was developed for analyzing unsteady-state dispersion and distribution of chemicals in multimedia environmental systems. Chemical transport processes were formulated in seven environmental compartments of air, canopy, surface soil, root-zone soil, vadose-zone soil, surface water, and sediment. The model assumed that the compartments were completely mixed and chemical equilibrium was established instantaneously between the sub-compartments within each compartment. A fugacity approach was utilized to formulate the mechanisms of diffusion, advection, physical interfacial transport, and transformation reactions. The governing equations of chemical mass balances in the environmental compartments were solved simultaneously to reflect the interactions between the compartments. A geographic information system (GIS) database and geospatial analysis were integrated into the chemical transport simulation to provide spatially explicit estimations of model parameters at watershed scale. Temporal variations of the environmental properties and source emissions were also considered in the parameter estimations. The outputs of the model included time-dependent chemical concentrations in each compartment and its sub-compartments, and inter-media mass fluxes between adjacent compartments at daily time steps.     

Minimization of water use and wastewater contaminant load

This communication describes a project concerning the minimization of water use and wastewater contaminant load in an industrial setting. The location was a plant manufacturing cast aluminum parts for the automotive industry. The water used for industrial purposes was some 16 000 m³/yr with COD values sometimes higher than 5000 mg O₂/l. After a preliminary assessment, a global reduction in industrial water consumption of 33%, by means of re-circulation of the aqueous solution used for de-molding was achieved, implying a 95% reduction in de-molding solution. To minimize water use even further, recommendations to the company included a revision of the refrigeration closed-circuit and a better control of water used for general services.     

Chemical contamination and sediment toxicity along the coast of Corsica

Trace metals (Cd, Pb, Cu, Cr, Ni, Co, Zn, Hg, As, Mn, Al, Fe, and Li) and organic compounds (PCBs, PAHs, lindanes, and DDT and its degradation products) were measured in coastal sediment samples from 27 sites in lagoons and along coastal areas of Corsica. An oyster embryo bioassay evaluated the toxicity of sediments from sites in three coastal lagoons (Urbino, Diane, and Biguglia) and the west coast of Cape Corsica. Despite contamination levels generally lower than those in other Mediterranean coastal areas, contamination is found in specific sites in Corsica and includes natural arsenic contamination on the east coast, insecticide pollution (persistent lindane and DDT) in many areas, both cadmium and lead contamination around Sagone, general contamination of both main harbours (Bastia and Ajaccio) and their surrounding areas, and asbestos mining residues in western Cape Corsica. Monitoring development of Crassostrea gigas embryos showed toxic effects at sites near a factory on Cape Corsica, with up to 100% mortality of larvae, and lower levels of toxicity at Sagone (44% mortality) and in the three coastal lagoons (up to 28% mortality). Results of this regional study show the need for further monitoring to understand the environmental issues facing the Corsican coast.     

Species-specific attraction to pheromonal analogues in orchid bees

Male orchid bees (Euglossini) collect fragrances from flowers and other natural sources, a behaviour that has shaped the euglossine pollination syndrome. Males store such chemicals in hind leg pouches and later expose them during courtship display. In the present study, we show that complex bouquets of two sympatric species of Eulaema, E. meriana and E. bombiformis, are chemically distinct. When exposed during bioassays at display perches individual hind leg extracts rapidly and consistently attracted other males of the correct species, even if derived from males of disparate localities (French Guiana and Panama). Conspecific males as well as females of E. bombiformis arrived at natural perch sites only from downwind, and two copulations were observed. Our findings demonstrate that acquired odours mediate exclusive attraction within species and support the idea that such fragrances are pheromone analogues. Their role in acquiring matings and during male–male interaction is discussed.     

Characterization of aerosol optical properties, chemical composition and mixing states in the winter season in Shanghai, China

Physical and chemical properties of ambient aerosols at the single particle level were studied in Shanghai from December 22 to 28, 2009. A Cavity-Ring-Down Aerosol Extinction Spectrometer（CRD-AES） and a nephelometer were deployed to measure aerosol light extinction and scattering properties, respectively. An Aerosol Time-of-Flight Mass Spectrometer（ATOFMS）was used to detect single particle sizes and chemical composition. Seven particle types were detected. Air parcels arrived at the sampling site from the vicinity of Shanghai until mid-day of December 25, when they started to originate from North China. The aerosol extinction,scattering, and absorption coefficients all dropped sharply when this cold, clean air arrived.Aerosol particles changed from a highly aged type before this meteorological shift to a relatively fresh type afterwards. The aerosol optical properties were dependent on the wind direction.Aerosols with high extinction coefficient and scattering Angstrom exponent（SAE） were observed when the wind blew from the west and northwest, indicating that they were predominantly fine particles. Nitrate and ammonium correlated most strongly with the change in aerosol optical properties. In the elemental carbon/organic carbon（ECOC） particle type, the diurnal trends of single scattering albedo（SSA） and elemental carbon（EC） signal intensity had a negative correlation. We also found a negative correlation（r =-0.87） between high mass-OC particle number fraction and the SSA in a relatively clean period, suggesting that particulate aromatic components might play an important role in light absorption in urban areas.     

Particle number concentration, size distribution and chemical composition during haze and photochemical smog episodes in Shanghai

The aerosol number concentration and size distribution as well as size-resolved particle chemical composition were measured during haze and photochemical smog episodes in Shanghai in 2009. The number of haze days accounted for 43%, of which 30% was severe （visibility 〈 2 km） and moderate （2 km 〈 visibility 〈 3 km） haze, mainly distributed in winter and spring. The mean particle number concentration was about 17,000/cm3 in haze, more than 2 times that in clean days. The greatest increase of particle number concentration was in 0.5-1μm and 1-10 μm size fractions during haze events, about 17.78 times and 8.78 times those of clean days. The largest increase of particle number concentration was within 50-100 nm and 100-200 nm fractions during photochemical smog episodes, about 5.89 times and 4.29 times those of clean days. The particle volume concentration and surface concentration in haze, photochemical smog and clean days were 102, 49, 15 μm3/cm3 and 949, 649, 206 μm2/cm3, respectively. As haze events got more severe, the number concentration of particles smaller than 50 nm decreased, but the particles of 50-200 nm and 0.5-1μm increased. The diurnal variation of particle number concentration showed a bimodal pattern in haze days. All soluble ions were increased during haze events, of which NH4, SO24- and NO3 increased great/y, followed by Na＋, IC, Ca2＋ and CI-. These ions were very different in size-resolved particles during haze and photochemical smog episodes.     

Chemical characteristics of size-resolved aerosols in winter in Beijing

Size-resolved aerosols were continuously collected by a Nano Sampler for 13 days at an urban site in Beijing during winter 2012 to measure the chemical composition of ambient aerosol particles. Data collected by the Nano Sampler and an ACSM(Aerodyne Aerosol Chemical Speciation Monitor) were compared. Between the data sets,similar trends and strong correlations were observed,demonstrating the validity of the Nano Sampler. PM10 and PM2.5concentrations during the measurement were 150.5 ± 96.0 μg/m3(mean ± standard variation)and 106.9 ± 71.6 μg/m3,respectively. The PM2.5/PM10 ratio was 0.70 ± 0.10,indicating that PM2.5dominated PM10. The aerosol size distributions showed that three size bins of 0.5–1,1–2.5 and 2.5–10 μm contributed 21.8%,23.3% and 26.0% to the total mass concentration(TMC),respectively. OM(organic matter) and SIA(secondary ionic aerosol,mainly SO42-,NO3-and NH4+) were major components of PM2.5. Secondary compounds(SIA and secondary organic carbon) accounted for half of TMC(about 49.8%) in PM2.5,and suggested that secondary aerosols significantly contributed to the serious particulate matter pollution observed in winter. Coal burning,biomass combustion,vehicle emissions and SIA were found to be the main sources of PM2.5. Mass concentrations of water-soluble ions and undetected materials,as well as their fractions in TMC,strikingly increased with deteriorating particle pollution conditions,while OM and EC(elemental carbon) exhibited different variations,with mass concentrations slightly increasing but fractions in TMC decreasing.     

化学沉淀法处理模拟含铜废水的研究

采用化学沉淀法对模拟含铜废水进行处理,分别考察了反应pH值、温度、沉淀时间、絮凝剂(PAM)用量以及PAM作用下沉淀时间等因素对模拟含铜废水处理的影响,并在最佳条件下对实际含铜废水进行了处理研究。结果表明,采用化学沉淀法处理200 mg/L的模拟含铜废水时,1‰聚丙烯酰胺(PAM)的最佳加入比例为30 mg/L,在25℃下,合适的pH值为7.12左右,沉淀时间13 min。在此条件下对来自葫芦岛锌厂的酸性平均含铜为167 mg/L的实际废水继续处理,处理后废水中铜离子浓度平均值为0.87 mg/L,可以实现实际废水中铜离子的有效去除。