组合人工湿地工艺微生物群落结构及脱氮效果研究

将复合垂直流、表面流、潜流3种不同类型的人工湿地串联起来,研究每种人工湿地的脱氮微生物及其脱氮效果.结果表明,各种人工湿地池填料表面微生物数量丰富,组合人工湿地系统形成两个串联的A/O单元,脱氮效果良好,其中总氮去除率达82.61%.     

潮汐流-潜流组合人工湿地污水净化效率

构建了潮汐流-潜流组合和潜流-潮汐流组合人工湿地对污水进行处理，分别研究2种组合人工湿地对污水的净化效果。结果表明，在平均进水COD浓度为214．28mg／L、NH4＋-N浓度为10．57mg／L、PO34--P浓度为5．44mg／L、TN浓度为10．25mg／L，水力负荷为o．2m3／（m2·d）的条件下，潮汐流-潜流组合人工湿地对COD、PO34--P的去除率分别为58．28％和46．99％，与潜流-潮汐流组合人工湿地处理效果相近；对NH4＋-N、TN，潮汐流-潜流组合人工湿地的去除率分别为69．93％和71．03％，比潜流-潮汐流组合人工湿地分别高15％和33％。潮汐流-潜流人工湿地的组合，在系统内实现了硝化-反硝化的组合，强化了系统对TN的净化效果，其对TN的净化效果比-般的潜流和表面流人工湿地组合提高20％～30％。总体上，潮汐流-潜流组合人工湿地具有更好的净化效果。     

曝气对两种人工湿地污水净化效果的影响

采用复合垂直流和水平潜流2种人工湿地处理混合污水,研究了在气水比(曝气体积/湿地进水体积)为2、4、6、8和10时2种人工湿地对污水的净化效果.结果显示:(1)复合垂直流人工湿地以气水比为2进行曝气时,对污水的净化效果最好,上行池出水的COD、TN、NH4+-N、NO3--N平均去除率比不曝气时分别提高了16.47%、...     

不同复合人工湿地对高污染河流有机污染物的去除

为了研究复合人工湿地对高污染河流污水中有机污染物的去除效果及规律,实验构建了不同水力负荷下的潜流+潜流、潜流+表面流、潜流+潜流+表面流、表面流+表面流等人工湿地单元组合成的5个复合人工湿地.连续运行一年以来,各复合人工湿地对BOD5、COD和SS的去除效果分别为91.9％ ～94.7％、69.3％ ～75.8％和92.3％ ～ 93.9％,相对于多级表流湿地,多级潜流湿地更利于有机污染物和悬浮物的去除;BOD5、COD和SS主要在各复合湿地的第一级湿地单元内得到去除;复合人工湿地对COD去除效果秋夏季两季好,春冬两季差;复合人工湿地能有效去除悬浮态BOD5和COD,出水中部分溶解态有机物难以有效降解.     

预曝气+垂直潜流人工湿地处理农村生活污水工程应用

传统无动力垂直潜流人工湿地,由于内部溶解氧的不足,存在除污能力下降、填料堵塞等问题。本研究采用预曝气的人工增氧方式,设计预曝气+垂直潜流人工湿地模式,以厌氧池+微曝气生物接触池+两级复合垂直流人工湿地的组合工艺,建设晋城市巴公镇农村生活污水治理项目中试端和应用示范端,探讨了实际工程应用对农村生活污水的治理效果,以及预曝气对复合垂直流人工湿地的影响。结果表明,经过8个月的运行,应用示范端出水中TN、NH₄⁺-N和COD值均满足设计出水水质要求,平均去除率分别为88.3%、93.7%和77.4%,且抗冲击能力较强、不易受冬季低温影响;对TP的去除效果较不稳定,对比中试端对TP的平均去除率94.3%,应用示范端对TP的平均去除率仅为17%;预曝气的人工增氧方式,使得系统中一级复合垂直流人工湿地对污水中TN、NH₄⁺-N、TP和COD的平均去除率分别提高了14.9%、6.8%、4.6%和10.1%。     

垂直流微电解耦合人工湿地强化处理生活污水的研究

比较了普通垂直流人工湿地、上升垂直流微电解耦合人工湿地和复合垂直流微电解耦合人工湿地处理生活污水的效果。结果表明,两种微电解耦合人工湿地的启动时间比普通垂直流人工湿地缩短近一半。3种人工湿地对氨氮的去除率无显著差异。对COD和总磷的去除率大小均表现为:复合垂直流微电解耦合人工湿地上升垂直流微电解耦合人工湿地普通垂直流人工湿地。3种人工湿地对COD和总磷的去除率随水力停留时间(HRT)的延长而升高。HRT为3d时,上升垂直流微电解耦合人工湿地和复合垂直流微电解耦合人工湿地的出水COD平均质量浓度分别为29.06、19.86mg/L,总磷分别为0.46、0.39mg/L,均达到《城镇污水处理厂污染物排放标准》(GB 18918—2002)的一级A排放要求。由于复合垂直流微电解耦合人工湿地结构复杂、造价高,相比上升垂直流微电解耦合人工湿地对COD和总磷的去除率提高又不明显,故推荐使用上升垂直流微电解耦合人工湿地。     

农户庭院型人工湿地对农村生活污水的净化效果

为了探讨人工湿地在农村生活污水处理应用中的可行性,通过在广东省珠海市上洲村建立农户型水平潜流和垂直流人工湿地系统各一套,比较2种人工湿地对农村生活污水净化效果的差异。在运行稳定阶段,2套系统处理出水中COD、BOD5、TP、NH4+-N和TN的平均浓度均达到了城镇污水处理厂排放标准(GB18918-2002)一级A标准。2套系统对农村生活污水的各污染物都具有很好的去除效果。其中,垂直流湿地对COD、BOD5、TP、TN和NH4+-N平均去除率分别为96.10%、96.01%、85.32%、91.18%和82.44%;水平潜流湿地则分别为93.29%、94.41%、86.52%、85.95%和77.46%。统计分析结果表明,垂直流湿地对NH4+-N的去除率高于水平潜流湿地,且其差异达到显著水平;水平潜流湿地对TP的去除率高于垂直流湿地,但其差异未达到显著水平。     

2种人工湿地的水力停留时间及净化效果

以复合垂直流人工湿地(IVCW)和水平潜流人工湿地(HSCW)为研究对象,研究了2种湿地运行的季节性最佳水力停留时间(HRT)参数,并监测了2种湿地在最佳HRT参数下运行时对污水的净化效果。结果显示:(1)在IVCW中,最佳HRT在春、秋季为8～10 h;夏季为6 h;冬季为12 h。在HSCW中,最佳HRT在春、秋季为10～12 h;夏季为6～8h;冬季为24～36 h。(2)2种湿地对COD的去除率均无显著的季节性差异;湿地进水中NH4+-N/TN比值与TN去除率显著负相关;不同季节下IVCW对TN的去除效果均高于HSCW。(3)水温对TN、TP去除率的影响在IVCW中比HSCW中的明显;水温高时,2种湿地中的TN去除率较高,IVCW中的TP去除率也较高,但HSCW中的TP去除率则较低,它们间均未达到显著的相关性。     

表流-水平流复合人工湿地对高污染河水的净化

为了研究表流-水平流复合人工湿地对高污染河水的净化效果及植物对复合湿地中二级潜流湿地的影响作用,实验构建了表流+芦苇水平潜流和表流+无植物水平潜流复合人工湿地。在相同的水力负荷下连续运行一年的结果表明,复合人工湿地对高污染河水中TN、NH3-N、TP、COD、BOD5和SS的去除率分别为57.3%~63.1%、65.7%~68.1%、69.4%~82.7%、85.3%~86.3%、96.7%~96.9%和97.9%~98.2%,种有植物的二级潜流湿地具有更好的脱氮和除磷效果;表流湿地作为复合湿地的第一级能够有效去除大部分的有机污染物和悬浮物,进而避免二级潜流湿地的堵塞,并利于二级潜流湿地的脱氮除磷的进行;复合湿地对有机物和悬浮物的去除不受季节性波动的影响,但是其脱氮效果受季节波动的影响较大。     

复合人工湿地对城市受污染河水的净化效果

采用2种复合人工湿地系统处理昆明市城市河流污水,为期1年的运行结果表明:2种复合人工湿地系统对城市河流污水具有良好的污染物去除性能,TN、TP、COD和SS的月平均去除率分别达到50%、85%、85%和80%以上;2种复合人工湿地系统具有良好的耐冲击性,季节变化对出水水质不存在显著影响。其中,垂直上行流复合人工湿地系统性能更优于垂直上行流与水平流复合人工湿地系统;强降雨会对复合人工湿地出水水质造成一定的影响。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.     

Biochemical interaction of six op delayed neurotoxicants with several neurotargets

Abstract

Five organophosphorous insecticides: Leptophos, EPN, Cyano‐fenphos, trichloronate and salithion proved to cause irreversible ataxia not only to chicken but also to mice and sheep. TOCP was included as a reference. Cyanofenphos blocked the catecholamine B‐receptor binding activity with ³H‐norepinephrine at a level similar to that of the specific inhibitor propranolol in the mouse heart preparation. In the lamb heart preparation, the B‐receptor was more sensitive to Leptophos, salithion and TOCP than to propranolol. The six compounds and their oxons were screened for their in‐vitro inhibition to monamine oxidase (MAO), acetyl cholinesterase (AChE) and neurotoxic esterase (NTE) in the brain of either mouse, lamb or chicken. It is believed that their AChE inhibition stands for their acute toxicity, while NTE inhibition is responsible for their paralytic ataxia.