Understanding the impact of waste disposal sites on soil quality for agricultural production: A case study of the Kiteezi landfill,Uganda

Leachate from waste disposal sites (WDS) can significantly affect the soil physical, chemical and biological qualities, reducing soil health and agricultural productivity. However, there is a paucity of data on soil quality for understanding soil health impact due to WDS in Uganda. This study's aim was to understand, using the Kiteezi landfill site, how WDS impact soil properties. Soil samples were collected over 4 months in and around the landfill from three locations, and the soil quality data of the nearby area were used as baseline data for assessing the impact on soil due to WDS in the area. There were significant increases in the concentration of all studied parameters at the landfill except total N. The concentrations of ammonium (14.84 ± 1.76 mg/kg), nitrate (127.96 ± 18.36 mg/kg), and pH (7.8) were above the optimum levels. The levels of available P (181.4 ± 28.9 mg/kg) and exchangeable bases; K (2.23 ± 0.24 mg/kg), Na (1.17 ± 0.14 mg/kg), Mg (3.35 ± 0.3 mg/kg) and Ca (14 ± 1.1 mg/kg) cmol (+)/kg were optimal for plant growth. The calculated CEC of 20.75 cmol (+)/kg) showed that soils have a good potential to supply plant nutrients. Heavy metal levels were still below the permissible limit. Hence, the study shows that although WDS may contribute to the increase of soil fertility, they can potentially reduce the overall productivity of soil by increasing nutrient levels beyond optimum levels.     

浅谈串联四极杆质谱（GC—QqQ-MS／MS）在土壤样品有机污染物分析中的应用

建立了ASE-GPC—GC-QqQ—MS／MS测定土壤中17种有机氯农药和19种多氯联苯以及MAE-SPE—GC-QqQ—MS／MS测定土壤中16种多环芳烃和18种邻苯二甲酸酯的方法。多环芳烃和邻苯二甲酸酯定量限在0．02～2．81μg／kg之间，有机氯农药和多氯联苯定量限在0．01～0．51μg/kg之间。样品加标浓度在5μg/kg时多环芳烃和邻苯二甲酸酯的平均回收率在66．6％～122．1％之间，相对标准偏差均小于20％；有机氯农药和多氯联苯平均回收率在79．6％～93．2％之间，相对标准偏差均小于15％。     

Attenuation of methane and volatile organic compounds in landfill soil covers

The potential for natural attenuation of volatile organic compounds (VOCs) in landfill covers was investigated in soil microcosms incubated with methane and air, simulating the gas composition in landfill soil covers. Soil was sampled at Skellingsted Landfill at a location emitting methane. In total, 26 VOCs were investigated, including chlorinated methanes, ethanes, ethenes, fluorinated hydrocarbons, and aromatic hydrocarbons. The soil showed a high capacity for methane oxidation resulting in very high oxidation rates of between 24 and 112 microg CH4 g(-1) h(-1). All lower chlorinated compounds were shown degradable, and the degradation occurred in parallel with the oxidation of methane. In general, the degradation rates of the chlorinated aliphatics were inversely related to the chlorine to carbon ratios. For example, in batch experiments with chlorinated ethylenes, the highest rates were observed for vinyl chloride (VC) and lowest rates for trichloroethylene (TCE), while tetrachloroethylene (PCE) was not degraded. Maximal oxidation rates for the halogenated aliphatic compounds varied between 0.03 and 1.7 microg g(-1) h(-1). Fully halogenated hydrocarbons (PCE, tetrachloromethane [TeCM], chlorofluorocarbon [CFC]-11, CFC-12, and CFC-113) were not degraded in the presence of methane and oxygen. Aromatic hydrocarbons were rapidly degraded giving high maximal oxidation rates (0.17-1.4 microg g(-1) h(-1)). The capacity for methane oxidation was related to the depth of oxygen penetration. The methane oxidizers were very active in oxidizing methane and the selected trace components down to a depth of 50 cm below the surface. Maximal oxidation activity occurred in a zone between 15 and 20 cm below the surface, as this depth allowed sufficient supply of both methane and oxygen. Mass balance calculations using the maximal oxidation rates obtained demonstrated that landfill soil covers have a significant potential for not only methane oxidation but also cometabolic degradation of selected volatile organics, thereby reducing emissions to the atmosphere.     

Impacts of polycyclic aromatic hydrocarbons from vehicular activities on the ambient air quality of Lagos mega city

In response to the growing concern about the contribution of polycyclic aromatic hydrocarbons (PAHs) from vehicular activities in Lagos mega city and their effect on air quality, PAH emissions were estimated using the emission factors approach. To make these estimates, PAH emission factors were calculated from the profile ratio of four PAHs emitted from vehicle sources obtained from the European Environment Agency's emission inventory guidebook, whereas the total number of registered vehicles based on the type of fuel they use for a period of 10 years was obtained from Lagos State Bureau of Statistics. Vehicle emissions were estimated using a combination of individual emission factors, the total number of vehicles in use based on fuel type, and the average mileage covered. The average highest level of emission of PAHs of 3.542 kilograms (kg) for gasoline‐powered vehicles was obtained in 2013, whereas the average lowest level of emission of 2.679 kg was recorded for diesel‐powered vehicles in 2007. In the same manner, 2013 had highest annual average total emission of 6.384 kg, whereas the lowest annual total PAHs emission of 5.727 kg was recorded in 2007. It is therefore advised that effective control measure should be put in place by regulatory agency to prevent personnel exposure to these hazardous substances.     

便携式GC-MS在石油污染土壤应急监测中的应用

针对石油污染土壤中VOCs含量的应急监测,便携式气相色谱-质谱联用仪适用于土壤中甲苯、乙苯、二甲苯、三氯苯等13种苯系物的快速定量检测,通过对某废弃炼油厂土壤样品测定,该方法在快速定性的同时,定量测定5~20411μg/kg土壤样品具有很高的可靠性。     

Evaluation of groundwater and soil pollution in a landfill area using electrical resistivity imaging survey

Landfills are sources of groundwater and soil pollution due to the production of leachate and its migration through refuse. This study was conducted in order to determine the extent of groundwater and soil pollution within and around the landfill of Seri Petaling located in the State of Selangor, Malaysia. The condition of nearby surface water was also determined. An electrical resistivity imaging survey was used to investigate the leachate production within the landfill. Groundwater geochemistry was carried out and chemical analysis of water samples was conducted upstream and downstream of the landfill. Surface water was also analyzed in order to determine its quality. Soil chemical analysis was performed on soil samples taken from different locations within and around the landfill in the vadose zone (unsaturated zone) and below the water table (in the soil saturated zone). The resistivity image along line L–L₁ indicated the presence of large zones of decomposed waste bodies saturated with highly conducting leachate. Analysis of trace elements indicated their presence in very low concentrations and did not reflect any sign of heavy metal pollution of ground and surface water or of soil. Major ions represented by Na, K, and Cl were found in anomalous concentrations in the groundwater of the downstream bore hole, where they are 99.1%, 99.2%, and 99.4%, respectively, higher compared to the upstream bore hole. Electrical conductivity (EC) was also found in anomalous concentration downstream. Ca and Mg ions represent the water hardness (which is comparatively high downstream). There is a general trend of pollution towards the downstream area. Sulfates (SO₄) and nitrates (NO₃) are found in the area in low concentrations, even below the WHO standards for drinking water, but are significantly higher in the surface water compared to the groundwater. Phosphate (PO₄) and nitrite (NO₂), although present in low levels, are significantly higher at the downstream. There is no significant difference in the amount of fluoride (F) in the different locations. In the soil vadose zone, heavy metals were found to be in their typical normal ranges and within the background concentrations. Soil exchangeable bases were significantly higher in the soil saturated zone compared to the vadose zone, and no significant difference was obtained in the levels of inorganic pollutants. With the exception of Cd, the concentration ranges of all trace elements (Cu, Zn, Cr, Pb, and Ni) of Seri Petaling landfill soils were below the upper limits of baseline concentrations published from different sources.     

北京市垃圾填埋场地下水中砷、汞含量分析

生活垃圾的处置一直以填埋为主,垃圾填埋承载着巨大的环境压力,尤其是垃圾填埋产生的渗滤液会对地下水造成砷、汞污染。为了解北京市生活垃圾填埋场地下水砷、汞污染水平,在北京市5座生活垃圾填埋场布设采样点,采集36个地下水样品,采用氢化物发生-原子荧光法,分析了地下水砷、汞含量特征。结果表明,36个地下水样品砷浓度范围0.41~4.82μg/L,汞浓度范围0.024~0.121μg/L,北京市典型垃圾填埋场地下水样品不存在砷、汞污染问题。     

土壤锑污染对桑树的影响初探

运用盆栽实验和实验分析方法,研究了土壤锑(Sb)污染对桑叶品质的影响,揭示了桑树对土壤锑的耐性机制。在土壤中分别添加三价锑15mg/kg、40mg/kg、80mg/kg、120mg/kg、160mg/kg和300mg/kg,以植物生长指标及生理指标为测试指标,实验周期60d。实验结果表明,低浓度Sb处理(<40mg/kg)对桑树生长有促进作用;随着土壤Sb浓度增高(40—300mg/kg),它对桑树产生抑制效应。但当土壤锑浓度不超过160mg/kg时,桑树对土壤锑污染有一定的耐性,其耐性指数>0.8。土壤锑污染对桑叶叶绿素含量、淀粉含量和可溶性糖含量影响不显著,桑叶中的锑含量随土壤锑含量的增加而增多。     

Convenience improves composting and recycling rates in high-density residential buildings

Increasing volumes of solid waste, implicated in environmental pollution and health problems, are central to the current environmental crisis. In two randomized field experiments, we demonstrate that convenience dramatically boosts recycling and composting rates in multi-family dwellings and university residences. When compost bins were placed on each floor in a multi-family residence, instead of on the ground floor, composting rates increased by 70%, diverting 27 kilograms of compost from the landfill per unit per year. When recycling stations were placed just meters from suites in student residences, instead of in the basement, recycling increased by 147% (container), and 137% (paper), and composting increased by 139%, diverting 23, 22, and 14 kilograms of containers, paper, and compost, respectively, from the landfill per person per year. Simply making recycling and composting convenient can significantly increase waste diversion, and as such this single intervention has important implications for waste management and environmental policy.     

镇江东部地区土壤中多环芳烃的污染特征及来源解析

分析了镇江东部扬中地区土壤中16种优先控制的多环芳烃（PAHs）污染物的含量特征及污染水平。结果表明，该地区土壤的多环芳烃总量为2．4～49．9μg／Kg，其中荧蒽的含量最高，同我国其他地区相比，其污染水平比较低。5个采样点PAHs含量表明有两个点受工业企业影响，其他3个点具有类似的面源污染即地质成因来源。     

Analysis of volatile and semivolatile hydrocarbons recovered from steam-classified municipal solid waste

Hazardous household wastes comprise a significant proportion of municipal solid waste (MSW), and therefore serve as the source of many toxic or carcinogenic organic chemicals that are released in the environment through landfill gases or leachates. In the present study, we demonstrate the utility of the steam classification process in removing hazardous semivolatile organic compounds (SVOCs) and volatile organic compounds (VOCs) from MSW. Steam classification is a patented technology that involves the treatment of MSW with steam under pressure to yield a cellulosic biomass product that can be used as a fuel or in building materials. The SVOCs and VOCs from the waste off-gases are collected in the steam condensate and in an effluent charcoal filter. The results of this study show that at least two SVOCs and at least 17 VOCs can be removed from the waste. The most commonly identified compounds were diethylphthalate, styrene, 1,4-dichlorobenzene, and toluene in the condensates, and styrene, 1,1,1-trichloroethane, and toluene in the charcoal filters. On a weight basis, aromatic hydrocarbons were primarily recovered in the condensates, while the chloroaliphatic hydrocarbons were recovered almost exclusively from the charcoal filters. 1,3-Dichlorobenzene, 1,4-dichlorobenzene, and chloroform together comprised nearly 50% of the 4470 micrograms kg(-1) average mass of SVOCs and VOCs recovered from about 454 kg of MSW in these experiments. Toxicity characteristic leaching procedure (TCLP) analyses showed that steam classification recovered at least 75 to 91% of tested analytes. Overall, these results suggest that steam classification represents an effective technology for a significant reduction or the removal of hazardous organics from the waste stream, and, consequently, in reducing the extent of environmental contamination associated with landfill leachates and gases.     

Dissolution of trace element contaminants from two coastal plain soils as affected by pH

Trace element mobility in soils depends on contaminant concentration, chemical speciation, water movement, and soil matrix properties such as mineralogy, pH, and redox potential. Our objective was to characterize trace element dissolution in response to acidification of soil samples from two abandoned incinerators in the North Carolina Coastal Plain. Trace element concentrations in 11 soil samples from both sites ranged from 2 to 46 mg Cu kg(-1), 3 to 105 mg Pb kg(-1), 1 to 102 mg Zn kg(-1), 3 to 11 mg Cr kg(-1), < 0.1 to 10 mg As kg(-1), and < 0.01 to 0.9 mg Cd kg(-1). Acidified CaCl2 solutions were passed through soil columns to bring the effluent solution to approximately pH 4 during a 280-h flow period. Maximum concentrations of dissolved Cu, Pb, and Zn at the lowest pH of an experiment (pH 3.8-4.1) were 0.32 mg Cu L(-1), 0.11 mg Pb L(-1), and 1.3 mg Zn L(-1) for samples from the site with well-drained soils, and 0.25 mg Cu L(-1), 1.2 mg Pb L(-1), and 1.4 mg Zn L(-1) for samples from the site with more poorly drained soils. Dissolved Cu concentration at pH 4 increased linearly with increasing soil Cu concentration, but no such relationship was found for Zn. Dissolved concentrations of other trace elements were below our analytical detection limits. Synchrotron X-ray absorption near edge structure (XANES) spectroscopy showed that Cr and As were in their less mobile Cr(III) and As(V) oxidation states. XANES analysis of Cu and Zn on selected samples indicated an association of Cu(II) with soil organic matter and Zn(II) with Al- and Fe-oxides or franklinite.     

Characterization of pollutants in Florida street sweepings for management and reuse

Disposal and beneficial-use options for street sweeping residuals collected as part of routine roadway maintenance activities in Florida, USA, were assessed by characterizing approximately 200 samples collected from 20 municipalities. Total concentrations (mg/kg or μg/kg) and leachable concentrations (mg/L or μg/L) of 11 metals and a number of organic pollutant groups (volatile organics, semi-volatile organics, pesticides, herbicides, carbamates) in the samples were measured. The synthetic precipitation leaching procedure (SPLP) was performed to evaluate the leachability of the pollutants. From the total metal analysis, several metals (e.g., arsenic, barium, chromium, copper, nickel, lead, and zinc) were commonly found above their detection limits. Zinc was found to have the highest mean concentration of all metals measured (46.7 mg/kg), followed by copper (10.7 mg/kg) and barium (10.5 mg/kg). The metal with the smallest mean concentration was arsenic (0.48 mg/kg). A small fraction of the total arsenic, barium, lead, and zinc leached in some samples using the SPLP; leached concentrations were relatively low. A few organic compounds (e.g., 4,4′-DDT, endrin, and endosulfan II) were detected in a limited number of samples. When the total and leaching results were compared to risk-based Florida soil cleanup target levels and groundwater cleanup target levels, the street sweepings were not found to pose a significant human-health risk via direct exposure or groundwater contamination.     

Soil and plant characteristics of landfill sites near Merseyside,England

An ecological survey of the plant and soil characteristics was carried out on three landfill sites near Merseyside, England. It was discovered that bare ground at two of the landfill areas had high levels of methane contained in the soil air (Sefton Meadows landfill: 6–8% at 35 cm and 16–35% at 65 cm below soil surface; Coalgate Lane landfill: 1–24% at 35 cm and 39–45% at 40 cm below soils surface), causing the appearance of dark grey reduced regions in the soil, a phenomenon similar to flooded soil. The wellvegetated areas at the two sites had lower levels of methane (under 7%).In areas relatively free of methane, the concentrations of mineralized N and NO₃ ^– had significant correlations with the dry weights of vegetation (r = 0.71 withp<0.01;r=0.61 withp<0.02 accordingly), indicating the necessity of applying available nitrogen fertilizer.     

Sydney tar ponds: some problems in quantifying toxic waste

Information on the type and amount of hazardous and toxic waste is required to develop a meaningful strategy and estimate a realistic cost for clean up of the Sydney Tar Pond site which is located on Cape Breton, in the province of Nova Scotia, Canada. The site covers the area of the decommissioned Sysco (Sydney Steel Corporation) plant. The materials of concern include BTEX (benzene, toluene, ethylbenzene, and xylenes), PAH (polycyclic aromatic hydrocarbons), PCB (polychlorinated biphenyl), and particulates laden with toxic metals, such as arsenic, lead, and others. The originally nontoxic materials such as soil, blast furnace slag, and vegetation, as well as surface and ground waters, which were subsequently contaminated, must also be included if they fail tests prescribed by environmental regulations. An extensive sampling program must be undertaken to obtain data for an accurate estimate of the waste to be cleaned and disposed of. Apparently, 700,000 tons of toxic waste, which is believed to be present on the site, may represent only a fraction of the actual amount. The clean-up of the site is only part of the solution. Toxic waste has to be disposed of in accordance with environmental regulations.     

In situ bioremediation of an underground diesel fuel spill: A case history

In the winter months of 1983, approximately 1000 gallons of diesel fuel had flowed along an asphalt parking lot of a commercial establishment towards a surface drain near an open creek. Investigations led to the discovery of an underground storage tank leaking diesel fuel. Exploratory borings showed that contamination was near the surface horizon and the capillary zone of the water table. Hydrocarbon quantities ranged up to 1500 mg/kg of soil. The plume continued to move in an eastward direction toward the surface water of the creek. A laboratory study indicated relatively high numbers of hydrocarbon-oxidizing organisms relative to glucose-utilizing microorganisms in the unsaturated vadose zone. Bioreclamation was initiated in April 1984 by injecting nutrients (nitrogen and phosphorus) and hydrogen peroxide and terminated in October 1984 upon no detection (<1 mg/kg) of hydrocarbons. A verification boring within the vicinity of the contaminated plume confirmed that residual contamination had attained background levels. The monitoring program was terminated in January 1987.     

UPLC-DAD-FLD测定土壤中多环芳烃

本文建立了以加速溶剂萃取（ASE）和固相萃取为提取和净化手段，采用超速液相色谱-二极管阵列-荧光检测器（UPLC-DAD-FLD）串联捡测土壤中16种多环芳烃的方法。通过色谱柱的比较，选择更小粒径和内径的分析柱（Supelco SILTMLC．PAH，100×3．0mm，3μm），缩短了分析时间，也节省了溶剂（乙腈），满足大量样品的快速灵敏分析的需要。在保留时间定性的基础上，利用PDA获取的紫外扫描光谱图与目标化合物的特征吸收标准谱图比较，提高了定性分析的准确性。在优化的实验条件下，该方法显示出良好的线性关系（r〉0．999）和精密度（RSD〈10％），16种多环芳烃的检出限在0．005—1．33μg／kg之间，并成功应用于样品分析，样品加标回收率为71．4％～120％。实验中为了确保整个分析过程的可靠性，替代物的加标回收率控制在50％-150％之间；土壤标准参考物的测定结果都在预测值范围内，验证了该方法的准确性。     

Case study: examining the contribution of historical sources of lead in urban soils in Portland,Maine, USA

While the presence of lead in urban soils from residential lead paint and leaded gasoline is well documented, the relative contribution of lead from area historical industrial activities is not. This study examined the connection between historical industrial sources of lead in Portland, Maine, USA from 1860 to 1970 to current, spatial distributions of soil lead. Collecting 1859 surface and 122 sub-surface soil samples in accordance with USEPA's Lead Safe Yard Protocols, lead concentrations varied from 9 mg/kg to >100,000 mg/kg with most of the samples greater than USEPA's critical value for lead (400 mg/kg). Using historical documents, probable sources of lead were mapped. In comparing two datasets, no clear relationship emerged. Findings were hampered by inability to sample under large areas of impervious surfaces and private properties. Because of lead's immobility in soil, one would expect decreasing concentration with depth, but lead concentrations varied with depth and location. The haphazard dumping of lead-contaminated industrial waste and the relocation of contaminated fill are likely factors. These findings suggest that in urban areas where multiple historical sources of lead existed, surface sampling to determine presence of lead may not be sufficient to protect public health.     

Linking Soil Erosion to Instream Dissolved Phosphorus Cycling and Periphyton Growth

Phosphorus (P) is a limiting nutrient in freshwater systems and when present in runoff from agricultural lands or urban centers may contribute to excessive periphyton growth. In this study, we examined the link between soil erosion and delivery of eroded soil to streams during flow events, and the impact of that freshly deposited soil on dissolved reactive P (DRP) concentrations and periphyton growth under baseflow conditions when the risk of stream eutrophication is greatest. A microcosm experiment was designed to simulate the release of P from soil which had been amended with different amounts of P fertilizer to overlying water during baseflow conditions. Unglazed tiles, inoculated for five days in a second order stream, were incubated for seven days in microcosms containing soil with eight levels of soil Mehlich‐3 plant available phosphorus (M3P) ranging from 20 to 679 mg/kg M3P. Microcosm DRP was monitored. Following incubation tiles were scraped and the periphyton analyzed for chlorophyll a. Microcosm DRP concentrations increased with increasing soil M3P and equilibrium phosphorus concentration (EPC₀). Relationships between M3P, EPC₀, and DRP were nonlinear and increases in soil M3P and/or DRP had a greater impact on biomass accumulation when these parameters were above threshold values of 30 mg/kg M3P and 0.125 mg/L DRP. Significantly, this ecological threshold corresponds to the agronomic thresholds above which increased soil M3P does not increase plant response.     

Hydrologic and Phosphorus Export Behavior of Small Streams in Commercial Poultry‐Pasture Watersheds1

Romeis, J. Joshua, C. Rhett Jackson, L. Mark Risse, Andrew N. Sharpley, and David E. Radcliffe, 2011. Hydrologic and Phosphorus Export Behavior of Small Streams in Commercial Poultry‐Pasture Watersheds. Journal of the American Water Resources Association (JAWRA) 1‐19. DOI: 10.1111/j.1752‐1688.2011.00521.x Abstract: Few watershed‐scale studies have evaluated phosphorus export in streamflow from commercial poultry‐pasture operations. Continuous streamflow and mixed‐frequency water quality datasets were collected from nine commercial poultry‐pasture (AG) and three forested (FORS) headwater streams (2.4‐44 ha) in the upper Etowah River basin of Georgia to estimate total P (TP) loads and examine variability of hydrologic response and water quality of storm and nonstorm‐flow regimes. Data collection duration ranged from 18 to 22 months, and approximately 1,600 water quality samples were collected. Significant (p < 0.1) inverse relationships were detected between peak flow response variables and both drainage area and fraction of forest cover. Order‐of‐magnitude differences in TP and dissolved reactive P (DRP) concentration were observed between AG and FORS sites and among AG sites. TP yields of FORS sites ranged from 0.01 to 0.1 kg P/ha. Yields of AG sites ranged from 0.031 to 3.17 kg P/ha (median = 0.354 kg P/ha). With 95% confidence intervals, AG yields ranged from 0.025 to 13.1 kg P/ha. These small‐watershed‐scale yields were similar to field‐scale yields measured in other studies in other regions. TP yields were significantly related to area‐weighted Mehlich‐1 soil test P concentrations (p = 0.0073) and base‐flow water sample P concentrations (p ≤ 0.0005). Water quality sampling during base‐flow conditions may be a useful screening tool for P risk‐based management programs.