京津冀产业碳排放强度变化及驱动因素研究

为探讨京津冀地区温室气体排放强度变化的影响因素,采用对数平均迪式分解模型及归因分析(LMDI-Attribution)方法,基于1996—2014年数据从细分行业角度进行研究。针对温室气体排放强度作产业结构、能源强度和排放因子三因素LMDI乘法分解,对温室气体排放强度变化的影响效应作归因分析,量化4个行业对分解因素影响效应的贡献,得到以下主要结论:1996—2014年京津冀地区温室气体排放强度主要呈现下降趋势,累计下降23.05%。其中,能源强度是温室气体排放强度下降的主导因素,其影响效应为-61.18%,对这一影响效应贡献最大的是工业,并且四大经济部门均通过能源强度在不同程度上使得温室气体排放强度有所减小,可见"阶梯电价"、"千家企业节能项目"、"十大重点节能项目"等相关政策在工业发展中对提高能源效率的作用明显。产业结构使得温室气体排放强度增加23.53%,其主要贡献者是工业,说明"工业产品出口退税率调整"等一系列政策的效果不明显;然而农业则使得温室气体排放强度降低,贡献值为3.09%。碳排放因子在1996—2014年间对温室气体排放强度的影响为60.47%,是京津冀地区温室气体排放强度增加的主要因素,说明京津冀地区的能源结构不合理。工业对这一效应的贡献最大为55.97%。可见,工业在京津冀地区的温室气体减排工作中起到最为关键的作用。     

基于卫星夜间灯光数据的中国分省碳排放时空模拟

中国能源统计数据"横向不可比,纵向不可加"现象依然突出,尤其是分省能源消费统计千差万别,给分省碳排放评估带来了较大困难,如何利用卫星遥感数据科学合理地估算中国分省碳排放是当前亟须研究的问题。本文运用DMSP/OLS全球稳定夜间灯光数据,在通过相互校正、年内融合和年际间校正等系列处理得到中国分省稳定夜间灯光数据的基础上,首先分别构建中国分省稳定夜间灯光亮度DN值与人均碳排放和单位面积碳排放之间的时空地理加权回归模型,两个模型整体效果均较好,拟合优度分别高达96.74%和99.24%;其次运用稳定夜间灯光亮度DN值对分省人均碳排放和单位面积碳排放进行时空模拟;最后运用人口规模和土地面积对分省碳排放进行估算。估算结果显示:(1)整体来看,2000—2013年年均碳排放模拟值与实际值6.3349×109t较为接近,两个模型的相对误差均在0.5%以内。(2)分年度来看,所有年份的相对误差均在5%以内,2006年分省加总碳排放模拟值与实际碳排放6.2036×109t最为接近,绝对误差和相对误差均较小,两个模型模拟值的相对误差均为0.04%。(3)分省域来看,2000—2013年年均碳排放模拟值与实际碳排放均非常接近,除海南和宁夏外,其余28个省区市的相对误差均在1%以内。(4)分年度分省域来看,以2013年为例,40%省份的相对误差在2%以内,70%省份的相对误差在5%以内。从整体、分年度、分省域、分年度分省域的估算结果来看,基于稳定夜间灯光数据的中国分省碳排放时空模拟效果良好。因此,运用卫星夜间灯光数据可以较为准确地对中国分省碳排放进行估算和预测,为卫星遥感影像数据服务分省碳排放监测和评估提供一种补充性参考。     

Polychlorinated dibenzo-p-dioxins/furans and dioxin-like polychlorinated biphenyls in food and feed in the Lithuanian market

Foods and feeds were analyzed during the period of 2007–2014 employing validated and accredited methods based on gas chromatography–high-resolution mass spectrometry. Sampling has been carried out in-line with national monitoring programs as well as during import controls into Lithuania. Food samples such as eggs, milk, beef, pork, poultry, fats of plant and animal origin, fish, cod liver, and feed samples such as premixes, feeds of plant origin, compound feed, mineral feed, vegetable oil, and fish meals were analyzed. Most of the samples exhibited concentrations below maximum limits, except cod liver. Health impacts were assessed in respect to human daily intakes. Data between groups are compared.     

Evaluation and validation of two different chromatographic methods (HPLC and LC-MS/MS) for the determination and confirmation of ochratoxin A in pig tissues

This study was undertaken to compare two different analytical methods for the determination and confirmation of ochratoxin A (OTA) in blood serum, kidney and liver of pigs. Sample clean-up was based on liquid-liquid phase extraction. The detection of OTA was accomplished with high-performance liquid chromatography (HPLC) combined either with fluorescence detection (FL) or electro spray ionization (ESI+) tandem mass spectrometry (MS–MS). Comparative method evaluation was based on the investigation of 90 samples of blood serum, kidney and liver per animal originating from different regions of Serbia. The analytical results are discussed in view of the respective method validation data and the corresponding experimental protocols. In general, analytical data obtained with (LC–MS–MS) liquid chromatography electro spray tandem mass spectro metry detection offered comparable good results at the sub-ppb concentration level. The results indicate that the liquid chromatography electro spray tandem mass spectrometric (LC-MS/MS) method was more specific and sensitive for the analysis and confirmation of ochratoxin A in pig tissues then high pressure liquid chromatography (HPLC) method after methylation of OTA.     

Fate of azadirachtin A and related azadirachtoids on tomatoes after greenhouse treatment

The degradation of the main azadirachtoids on tomatoes was studied after greenhouse treatment. These experiments were carried out at 1 and 5× the concentration recommended by the manufacturer. In all experiments the deposition of azadirachtin A (AZA-A) was below the maximum residue level (MRL). Even if at the highest dose, AZA-A half-life time calculated as pseudo first order kinetic was 1.2 days in agreement with the recommended preharvest interval (PHI) of 3 days. Experiments with a model system showed that sunlight photodegradation is the main factor influencing the rate of disappearance of AZA-A after greenhouse treatment while tomato epicuticular waxes doubled the photodegradation rate of AZA-A in a commercial formulation.     

Pesticide dissipation curves in peach,pear and tomato crops in Uruguay*

Dissipation curves of azoxystrobin and of the neonicotinoids acetamiprid and thiacloprid in peach; azinphos-methyl and carbaryl in pear and azoxystrobin, chlorfenapyr and chlorpyrifos in high-tunnel tomato crops were studied in the Southern region of Uruguay. An analytical methodology based on solid phase extraction (SPE) and detection by High Performance Liquid Chromatography with Diode Array Detector (HPLC/DAD) was used for acetamiprid and thiacloprid. Coupled SPE and detection by Gas Chromatography with Mass Selective Detector (GC/MSD) was used for the detection of azinphos-methyl, azoxystrobin, carbaryl, chlorfenapyr and chlorpyrifos residues. Curves were modeled mathematically with Solver program of Microsoft Excel®. The best fit for acetamiprid and thiacloprid in peach was achieved with the exponential model (r²=0.961 and 0.944, respectively). In the case of peach fruits there is not a Maximum Residue Limit (MRL) for acetamiprid in the Codex Alimentarius, while 0.5 mg/kg is the value rated for thiacloprid. The MRLs accepted by the European Union (EU) are 0.1 mg/kg for acetamiprid and 0.3 mg/kg for thiacloprid. According to the curves determined in these experiments, thiacloprid residues 10 to 12 days after application (daa) were below the MRLs established by both sources. In the case of acetamiprid, 25 daa would be required, according to the exponential mathematical model, to get residues levels below the MRL values established by the EU. For azinphos methyl in pear, the residues detected were mathematically fitted to an exponential model (r²=0.999). According to it, residue levels under the MRL established by the EU (0.05 mg/kg) are gotten in our conditions in 20 daa. In plastic tunnel tomato chlorfenapyr residues were not detected from 16 daa, having the dissipation curve an exponential trend. In the same condition, there was not a decay of the azoxystrobin concentration during a 24-day trial, being it around 0.40 ± 0.05 mg/kg.     

Multiresidue determination of carbamate,organochlorine, organophosphorus,and dicarboximide pesticides in lettuce by GC/MS

An extraction method based on matrix solid-phase dispersion was developed to determine pirimicarb, methyl parathion, malathion, procymidone, α -endosulfan and β -endosulfan in lettuce using gas chromatography-mass spectrometry. The best results were obtained using 4.0 g of lettuce, 2.0 g of silica as dispersant sorbent, 0.1 g of activated carbon as clean up sorbent and acetonitrile as eluting solvent. The method was validated using lettuce samples fortified with pesticides at six different concentration levels (0.1 to 2.0 mg/kg). Average recoveries (7 replicates) ranged from 50 to 120 %, with relative standard deviations between 0.6 and 8.0 %. Detection and quantification limits for lettuce ranged from 0.01 to 0.02 mg/kg and 0.04 to 0.10 mg/kg, respectively.     

Age-dating Diesel Fuel Spills: Using the European Empirical Time-based Model in the U.S.A.

In 1993, a paper was published by Christensen and Larsen that offered a method for determining the age of diesel oil spills in soil (Christensen and Larsen, 1993 Ground Water Mount. R . Fall , 142-149). It presented an empirical time-based model of the degradation of diesel fuel in soils using chemical data gathered at petroleum release sites in Denmark and the Netherlands. Now, evaluation of the validity of the application of this work to subsurface petroleum releases in other countries remains. In the U.S.A., investigations assessing date(s) of release of diesel fuel in soils, e.g. age dating of subsurface petroleum contamination, have considerable interest. Litigation-driven scientific investigations with accompanying expert testimony in a court of law are underway. The number of instances where application of the Christensen and Larsen empirical time-based model to petroleum-contaminated properties is growing in the U.S.A. This paper presents two case studies which evaluate the applicability of the Christensen and Larsen empirical time-based model to petroleum-contaminated properties in general. It illustrates the approach using gas chromatographic data from two recently-completed projects evaluating the applicability of the Christensen and Larsen model to a No. 2 fuel oil/diesel fuel surface spill in the U.S.A. Results showed that the application of the model to petroleum-contaminated soils was scientifically valid, provided its applicability was evaluated using hypothesis testing for specific changes in the characteristics of the petroleum hydrocarbon distribution in a number of soil samples collected over time at one site. The paper offers observations on the application of the Christensen and Larsen model to petroleum found in the light non-aqueous phase liquid (LNAPL) phase and groundwater.     

碳源及反硝化芽孢杆菌强化低C/N比景观水体的生物脱氮

实验探讨了添加碳源及投加反硝化细菌对低碳氮比景观水体生物脱氮的影响。结果表明,有机碳源及B.subtilis FS05均能显著促进实验水体的生物脱氮作用,实验水体在28℃静置72 h后,乙醇添加组的TN、氨氮、硝酸盐及亚硝酸盐的去除率分别达到了62.7%、67.0%、69.8%和29.4%,而同样条件下,B.subtilis FS05投加组的去除率分别达到了66.9%、73.4%、66.0%和82.2%。从水质变化趋势可以看出,投加B.subtilis FS05能在更短时间内完成生物脱氮过程,其中,硝酸盐和亚硝酸盐去除速率最快,分别仅需要18 h和12 h。     

不同流量分配比对多级A/O工艺去除有机物及脱氮的影响

采用三级A/O工艺分段进水工艺处理低碳源生活污水,考察了进水流量分配比对系统去除有机物、硝化反硝化能力以及去除TN的影响。通过对水质指标沿程监测结果表明,不同流量分配比(4∶3∶3,5∶3∶2,6∶3∶1)对系统去除有机物及硝化效率影响不大,出水COD、氨氮分别均在30 mg/L、1 mg/L以下。但反硝化效果受流量分配比的影响较大,在流量比为5∶3∶2时,有效利用原水中碳源进行反硝化,反硝化效果最好。在流量比为5∶3∶2的情况下,TN出水为5.7 mg/L去除率为82.9%,优于流量分配比为6∶3∶1和4∶3∶3时的脱氮效果。总体而言,分段进水工艺在对碳源的有效利用及能耗节省方面优于单点进水。