Response to environmental flows in the Lower Tarim River, Xinjiang, China: an ecological interpretation of water-table dynamics

Increased water-dependent development and utilization have led to significant environmental and hydrological degradation of the Tarim River in western China and its dependent ecosystems. Between the 1950s and 1970s, 350 km of the lower reaches were drained and between 1960 and 1980 the water-table fell from between −2 and −3 m to between −8 and −10 m. Subsequently, riparian ecosystems were seriously degraded. In 2000, the Chinese government launched a program to restore the lower reaches of the river. Four environmental flows of 1034×10⁶ m³ were released from 2000 to 2002. This paper interprets and discusses the ecological significance of changes following the releases and identifies the relationship between water-table dynamics and vegetation responses. Short-term objectives for river restoration are proposed with possible monitoring parameters suggested.     

IFRP: a hybrid interval-parameter fuzzy robust programming approach for waste management planning under uncertainty

In this study, an interval-parameter fuzzy-robust programming (IFRP) model is developed and applied to the planning of solid waste management systems under uncertainty. As an extension of the existing fuzzy-robust programming and interval-parameter linear programming methods, the IFRP can explicitly address system uncertainties with complex presentations. Parameters in the IFRP model can be represented as interval numbers and/or fuzzy membership functions, such that the uncertainties can be directly communicated into the optimization process and resulting solution. Furthermore, highly uncertain information for the lower and upper bounds of interval parameters that exist due to the complexity of the real world can be effectively handled through introducing the concept of fuzzy boundary interval. Consequently, robustness of the optimization process and solution can be enhanced. Results of the case study indicate that useful solutions for planning municipal solid waste management practices can be generated. They reflect a compromise between optimality and stability of the study system. Willingness to pay higher costs will guarantee the system stability; however, a desire to reduce the costs will run the risk of potential instability of the system. The results also suggest that the proposed hybrid methodology is applicable to practical problems that are associated with highly complex and uncertain information.     

Phenanthrene degradation in Arthrobacter sp. P1-1: initial 1,2-, 3,4- and 9,10-dioxygenation, and meta- and ortho-cleavages of naphthalene-1,2-diol after its formation from naphthalene-1,2-dicarboxylic acid and hydroxyl naphthoic acids

Arthrobacter sp. P1-1, isolated from a polycyclic aromatic hydrocarbon (PAH)-contaminated site in Hilo, HI, USA, can decompose phenanthrene (40 mg l⁻¹) completely within 7 days. A detailed phenanthrene metabolism map was constructed based on metabolite analysis and replacement cultures. Initial dioxygenation occurs on 1,2-, 3,4-, and 9,10-C of phenanthrene, dominantly on 3,4-C positions. Rapid accumulation of 5,6- and 7,8-benzocoumarin suggests that phenanthrene-1,2- and -3,4-diols mainly undergo meta-cleavage. However, a trace amount of o-carboxyvinylnaphthoates and diphenic acid indicates a limited extent of ortho-cleavage of the diols. Naphthalene-1,2-diol, as a common and converged metabolite, was formed from 1-[(E)-2-carboxyvinyl]-2-naphthoic acid, naphthalene-1,2-dicarboxylic acid, and 1-hydroxy-2-naphthoic acid in separate culture tests. Naphthalene-1,2-diol is then degraded in a dominant phthalic acid pathway and a minor salicylic acid pathway. Several metabolites of phthalic acid were found, while no salicylic acid metabolites were detected. The strain P1-1 likely has a very diverse set of PAH-degrading enzymes or the enzymes having relaxed substrate-specificity.     

Heavy Metal Contamination and Distribution in the Urban Environment of Guangzhou, SE China

Ever-increasing heavy metal accumulation in the urban environment of Guangzhou, the largest light industrial production base and one of the most rapidly developing cities in China, poses a serious threat to environment as well as to human health in the region. As a sink or source, urban deposits are good indicators of the level and extent of heavy metal accumulation in the surface environment. The aim of this preliminary study was to examine the distribution of heavy metal contamination in the urban environment of Guangzhou. It was based on a systematic sampling of road dusts and corresponding gully sediments along major roads running mainly through commercial and residential to industrial districts of the city. In addition to road dusts and gully sediments, ceiling dusts from the Pearl River Tunnel were also collected to characterize anthropogenic emissions dominated by traffic-related activities. In general, the level of Cd, Cu, Pb and Zn contaminations were more severe on the industrialized side of Guangzhou than on the western side where heavy traffic and industrial activities were limited. The primary determinants of the level of heavy metal contamination and the distribution of this contamination in the urban environment of Guangzhou were the site-specific conditions of its urban setting, particularly the types of industries, the nature of the traffic flow, sample residence times and variations in grain size of the particulate contaminants. This study highlights the complexity of the urban system and indicates that in just such a system individual urban components should be interlinked to assess the long-term environmental and health effects of heavy metal contamination. Among the heavy metals tested – Cd, Cu, Pb and Zn – the level of Zn contamination was the most severe and widespread, and thus requires immediate attention.     

Evaluation of heavy metal contamination in Phaeozem of northeast China

Surface and profile Phaeozem soil samples from 31 locations affected by various anthropogenic activities such as mining, chemical manufacturing, traffic emission and pesticide application were collected in Heilongjiang Province and Jilin Province, northeast China. The range of total concentrations of four heavy metals Cd, Pb, Cu and Zn in the soil was 0.011–3.137, 10.31–62.34, 9.74–51.21 and 39.54–247.59 mg kg⁻¹, respectively, determined using the acidic digestion procedure. Four methods including single contamination evaluation, background concentration comparison, surface/subsurface concentration comparison and exchangeable fraction evaluation were used to evaluate the extent of metal contamination in Phaeozem. The results indicated that different activities increased the concentrations of the heavy metals in surface soils, where high concentrations of cadmium and lead were found close to chemical plants and in the suburbs of the investigated cities. The four methods showed a general trend of increased soil contamination with heavy metals. Cadmium was of the most concern compared with the other contaminated elements in the study area, due to the long-term phosphatic fertilizer utilization and industrial activities. The proper evaluation method for cadmium contamination was the background concentration comparison, while for zinc and copper was the single contaminative index evaluation. Cadmium and lead could be the potential environmental risk in the Phaeozem area based on the different evaluations.     

Travel time and trajectory moments of conservative solutes in two-dimensional convergent flows

We address advective transport of a solute traveling toward a single pumping well in a two-dimensional randomly heterogeneous aquifer. The two random variables of interest are the trajectory followed by an individual particle from the injection point to the well location and the particle travel time under steady-state conditions. Our main objective is to derive the predictors of trajectory and travel time and the associated uncertainty, in terms of their first two statistical moments (mean and variance). We consider a solute that undergoes mass transfer between a mobile and an immobile zone. Based on Lawrence et al. [Lawrence, A.E., Sánchez-Vila, X., Rubin, Y., 2002. Conditional moments of the breakthrough curves of kinetically sorbing solute in heterogeneous porous media using multirate mass transfer models for sorption and desorption. Water Resour. Res. 38 (11), 1248, doi:10.1029/2001WR001006.], travel time moments can be written in terms of those of a conservative solute times a deterministic quantity. Moreover, the moments of solute particles trajectory do not depend on mass transfer processes. The resulting mean and variance of travel time and trajectory for a conservative species can be written as functions of the first, second moments and cross-moments of trajectory and velocity components. The equations are developed from a consistent second order expansion in sigmaY (standard deviation of the natural logarithm of hydraulic conductivity). Our solution can be completely integrated with the moment equations of groundwater flow of Guadagnini and Neuman [Guadagnini, A., Neuman, S.P., 1999a. Nonlocal and localized analyses of conditional mean steady state flow in bounded, randomly non uniform domains 1. Theory and computational approach. Water Resour. Res. 35(10), 2999-3018.,Guadagnini, A., Neuman, S.P., 1999b. Nonlocal and localized analyses of conditional mean steady state flow in bounded, randomly non uniform domains 2. Computational examples. Water Resour. Res. 35(10), 3019-3039.], it is free of distributional assumptions regarding the log conductivity field, and formally includes conditioning. We present analytical expressions for the unconditional case by making use of the results of Riva et al. [Riva, M., Guadagnini, A., Neuman, S.P., Franzetti, S., 2001. Radial flow in a bounded randomly heterogeneous aquifer. Transport in Porous Media 45, 139-193.]. The quality of the solution is supported by numerical Monte Carlo simulations. Potential uses of this work include the determination of aquifer reclamation time by means of a single pumping well, and the demarcation of the region potentially affected by the presence of a contaminant in the proximity of a well, whenever the aquifer is very thin and Dupuit-Forchheimer assumption holds.     

Effects of pH, organic acids, and inorganic ions on lead desorption from soils

The desorption characteristics of lead in two variable charge soils (one developed from Arenaceous rock (RAR) and the other derived from Quaternary red earths (REQ)) were studied, and the effects of pH value, organic acid, and competitive ions were examined. Desorption of Pb(2+) decreased from nearly 100.0 to 20.0% within pH 1.0-4.0 in both soils, and then the decrease diminished at pH > 4.0. Organic ligands at relatively low concentrations (< or =10(-3) mol L(-1)) slightly inhibited Pb(2+) desorption, but enhanced Pb(2+) desorption at higher concentrations. In this study, citric acid or acetic acid at higher concentrations (>10(-3) mol L(-1)) had the greatest improvement of Pb(2+) desorption, followed by malic acid; and the smallest was oxalic acid. Desorption of the adsorbed Pb(2+) increased greatly with increasing concentrations of added Cu(2+) or Zn(2+). Applied Cu(2+) increased Pb(2+) desorption more than Zn(2+) at the same loading.     

Nitrous Oxide Emission from <Emphasis Type="Italic">Deyeuxia angustifolia</Emphasis> Freshwater Marsh in Northeast China

Here we report N₂O emission results for freshwater marshes isolated from human activities at the Sanjiang Experimental Station of Marsh Wetland Ecology in northeastern China. These results are important for us to understand N₂O emission in natural processes in undisturbed freshwater marsh. Two adjacent plots of Deyeuxia angustifolia freshwater marsh with different water regimes, i.e., seasonally waterlogged (SW) and not- waterlogged (NW), were chosen for gas sampling, and soil and biomass studies. Emissions of N₂O from NW plots were obviously higher than from the SW plots. Daily maximum N₂O flux was observed at 13 o′clock and the seasonal maximum occurred in end July to early August. The annual average N₂O emissions from the NW marsh were 4.45 μg m⁻² h⁻¹ in 2002 and 6.85 μg m⁻² h⁻¹ in 2003 during growing season. The SW marsh was overall a sink for N₂O with corresponding annual emissions of −1.00 μg m⁻² h⁻¹ for 2002 and −0.76 μg m⁻² h⁻¹ for 2003. There were significant correlations between N₂O fluxes and temperatures of both air and 5-cm-depth soil. The range of soil redox potential 200–400 mV appeared to be optimum for N₂O flux. Besides temperature and plant biomass, the freeze–thaw process is also an important factor for N₂O emission burst. Our results show that the freshwater marsh isolated from human activity in northeastern China is not a major source of N₂O.     

Field demonstration of in situ immobilization of soil Pb using P amendments

A long-term field-scale demonstration project on the feasibility of using P to immobilize Pb in a Pb-contaminated urban soil was conducted. Phosphate was applied at an average rate of 3040 mg P/kg soil based on a P/Pb molar ration of 4.0, with four treatments: T₀, no P application; T₁, H₃PO₄ only; T₂, 1/2 H₃PO₄+1/2 CaH₂PO₄; and T₃, 1/2 H₃PO₄+1/2 phosphate rock. Soil samples were collected and analyzed 220 days after the P applications. For all P treatments, toxicity characteristic leaching procedure (TCLP) extractable Pb levels in surface soils (0-10 cm) were reduced to below 5.0 mg Pb/l, with T₂ also effective in reducing the TCLP Pb level in subsurface soils (10-30 cm, <4.63 mg/l). Sequential extraction analysis indicates that P was effective in transforming soil Pb from non-residual fractions to a residual fraction. Such a transformation was mainly through dissolution of Pb associated with carbonate fraction and precipitation of pyromorphite-like minerals, which were confirmed using X-ray diffraction (XRD). Among these three treatments, T₃ was the most effective in reducing Pb mobility and minimizing P and Pb leaching in the soil. Our research clearly demonstrates that P amendments were effective in immobilizing Pb in contaminated soil.     

Ions in motor vehicle exhaust and their dispersion near busy roads

Measurements in the exhaust plume of a petrol-driven motor car showed that molecular cluster ions of both signs were present in approximately equal amounts. The emission rate increased sharply with engine speed while the charge symmetry remained unchanged. Measurements at the kerbside of nine motorways and five city roads showed that the mean total cluster ion concentration near city roads (603 cm^?3) was about one-half of that near motorways (1211 cm^?3) and about twice as high as that in the urban background (269 cm^?3). Both positive and negative ion concentrations near a motorway showed a significant linear increase with traffic density (R² = 0.3 at p < 0.05) and correlated well with each other in real time (R² = 0.87 at p < 0.01). Heavy duty diesel vehicles comprised the main source of ions near busy roads. Measurements were conducted as a function of downwind distance from two motorways carrying around 120–150 vehicles per minute. Total traffic-related cluster ion concentrations decreased rapidly with distance, falling by one-half from the closest approach of 2 m to 5 m of the kerb. Measured concentrations decreased to background at about 15 m from the kerb when the wind speed was 1.3 m s^?1, this distance being greater at higher wind speed. The number and net charge concentrations of aerosol particles were also measured. Unlike particles that were carried downwind to distances of a few hundred metres, cluster ions emitted by motor vehicles were not present at more than a few tens of metres from the road.