碱/超声预处理对头孢菌素菌渣破壁效果的影响

为提高头孢菌素菌渣的厌氧消化利用率,采用碱解与超声波破碎联合处理方法对头孢菌素菌渣进行细胞破壁,并通过正交实验和单因素实验研究pH值、含水率、声能密度和反应时间对破壁效果的影响。结果表明,最佳处理条件为:pH值为11.5、含水率为94%、声能密度为2 W/mL、反应时间为30 min,处理后SCOD溶解率为265.26%,总氮溶解率为155.28%,破壁效果明显。     

Residue levels of fenitrothion and aminocarb in the air samples collected from experimental spray blocks in New Brunswick in 1982

Abstract

Fenitrothion and aminocarb formulations were aerially sprayed over mixed coniferous forests near Fredericton and Bathurst, New Brunswick, Canada. Insecticide concentrations inside the spray blocks were measured at intervals of time by trapping the airborne toxicants in a fritted‐glass bubbler containing dimethylformamide (DMF). The residues in DMF were analysed by gas chromatography. Concentrations of the insecticides in the air sampled decreased rapidly with time from peak levels of 1997 ng/m³ (fenitrothion) and 1201 ng/m³ (aminocarb). Concentrations of the two insecticides in the air samplers were dependent upon the nature of the chemicals, type of formulation used, spray timings and other environmental factors.     

Book Reviews

CARCINOGENESIS AND MUTAGENESIS, by Myron A. Mehlman, Morris F. Cranmer and Raymond E. Shapiro, from the Journal of Environmental Pathology and Toxicology (Official Organ of the American College of Toxicology), 388 pages and 135 tables and figures, 1977, linen, format 261 × 178 mm, ISBN 0–930376–02–1, printed by Pathotox Publishers, Inc., Park Forest South, Illinois 60466, $23.00

WASTE TREATMENT AND UTILIZATION (Theory and Practice of Waste Management) by Murray Moo‐Young and Grahame J. Farquhar, University of Waterloo, Ontario, Canada; 574 pages, 211 illustrations and 513 literature references, linen, format 256 × 182mm, ISBN 0–08–023831–9, printed by Pergamon Press Ltd., Oxford OX3 OBW, England 1979, US$ 70.00 or £32.00.

HANDBOOK ON THE TOXICOLOGY OF METALS by Lars Friberg (S‐10401 Stockholm), Gunnar F. Nordberg (DK‐5000 Odense) and Velimir B. Vouk (WHO, CH‐1211 Geneva), and sponsored by the U.S. Environmental Protection Agency 1979, 709 pages, linen, format 246 × 173 mm, ISBN 0–444–80075–1, printed by Elsevier/North‐Holland Biomedical Press, Amsterdam NL, $117.00/Dfl. 240.00     

The veterinary drug ivermectin influences immune response in the yellow dung fly (Scathophaga stercoraria)

Phenoloxidase (PO) is a key enzyme involved in the immune response of insects. We show that egg-to-adult exposure to residues of 0.001, but not 0.0005 mg kg⁻¹ ivermectin elevated PO activity in yellow dung flies (Scathophaga stercoraria) developing in cattle dung. Fly fat content was unaffected by the treatments. Therefore, the response of PO was a direct effect of ivermectin and not an indirect one caused by an alteration in body ‘condition’. This supports the non-intuitive conclusion that flies surviving exposure to faecal residues may have enhanced immune function. To our knowledge, this is the first study to assess the effects on PO activity of insecticidal residues in livestock dung. The non-target effects of such residues are of wide interest, given the global use of veterinary products.     

Determination of pendimethalin (PROWL®480 EC) spray drift from ground applications

Abstract

Pendimethalin herbicide (PROWL^®480 EC) spray drift was determined from ground applications representing the highest rate applied to corn in eastern Canada. A novel drift collector pattern was laid out on the ground immediately before herbicide application. Most of the drift collectors were located downwind of the application target area. The maximum labelled rate of 1.68 kg ai/Ha was applied on 2 occasions on separate sites. In both applications, drift collector cards indicated that concentrations of pendimethalin were not detectable outside the target zone (<0.01 μg/cm²) at or beyond the 10 metre drift collector stations. Risk assessment calculations indicated that non‐target organisms would not be at significant risk from off‐site movement of pendimethalin.     

Persistence of fensulfothion in a sandy‐loam soil and uptake by rutabagas,carrots and radishes using microplots

Abstract

Field microplots were treated with 141 and 282 ppm fensulfothion and 37.1 and 74.2 ppm fensulfothion sulfone. These concentrations are equivalent to field treatment rates of 8.48 and 16.96 kg Al/ha, fensulfothion, and 2.23 and 4.47 kg Al/ha, fensulfothion sulfone, respectively, for banded application (10 cm wide, rows 80 cm apart). The half‐lives in a sandy loam soil were 30–39 and 14–23 days, respectively. Fensulfothion sulfone and sulfide were the main derivatives found in fensulfothion treated soil.

The maximum levels of these derivatives were 21.22 and 22.95 ppm, respectively for the 8.48 kg/ha treatment and 33.90 and 42.45 ppm, respectively, for the higher treatment, which occurred between 30–60 days.

Carrots appeared to take up more fensulfothion from soil than rutabagas or radishes. The residue levels at harvest decreased in the order carrot peel > pulp > rutabagas root > peel > pulp. Residue levels of fensulfothion and sulfone in radishes were similar to those found in rutabagas. The ratio sulfoxide/sulfone in rutabagas ranged from 0.4–1.5 and in carrots from 1.7–7.6. This phenomenon is thought to be due to oxidative enzyme systems present in rutabagas. Dimethyl phosphorothioic acid, but not dimethyl phosphoric acid was detected (max. 1.33 ppm) in some rutabagas samples but not in carrots.     

Fate of the veterinary antibiotic 14C-difloxacin in soil including simultaneous amendment of pig manure with the focus on non-extractable residues

The fate of ¹⁴C-labeled difloxacin (¹⁴C-DIF) was studied in time course experiments after application on soil (Ap horizon of silt loam) and amendment of authentic DIF containing pig manure (146 mL kg^?1; 4.17 MBq kg^?1; 0.85 mg kg^?1) or water (124 mL kg^?1; 0.42 MBq kg^?1; 0.09 mg kg^?1) for 56 and 120 days of incubation, respectively.

Mineralization of ¹⁴C-DIF was below 0.2% in both experiments after 56 days or 120 days. In the course of the experiments, portions of extractable radioactivity (Accelerated Solvent Extraction (ASE); acetonitrile-water) decreased to 19–21% depending only little on manure amendment. Non-extractable residues of ¹⁴C-DIF increased to 70–74% after 56 days and 120 days, respectively, and therefore were the main route of ¹⁴C-DIF in soil. According to radioanalytical HPLC and LC-MS/MS, only the parent compound was found in all extracts over the whole time of the experiment. According to fractionation of the non-extractable residues (NER) into particle size fractions, ¹⁴C portions were associated to the water used for fractionation, the silt and clay fractions, whereas no radioactivity was detected in the sand fraction. The majority of ¹⁴C was found within the clay fractions.

Fractionation of humic components showed that radioactivity derived from ¹⁴C-DIF was associated with humic acids, fulvic acids, humins and minerals and very little with soluble, non-humic HCl fraction. The highest portions of radioactivity were found in the fulvic acid fraction. Results obtained by size exclusion chromatography (SEC) of the purified fulvic acids were similar for every sample analyzed. One large portion of ¹⁴C co-eluted with fulvic acids of a molecular weight below 910 g mol^?1. Both fractionation methods demonstrated that the parent compound DIF or initial metabolites were rapidly integrated into humic materials and, thus, were major components of NER.     

Residues of carbofuran and its two carbamate metabolites in field‐treated rutabaga 1

Abstract

Carbofuran was applied over seeded rutabaga cv. York and residues (corrected for recovery) of carbofuran, 3‐hydroxy‐ and 3‐ketocarbofuran in the harvested roots averaged 0.15, 0.23 and 0.07 ppm in peel and 0.09, 0.14 and 0.05 ppm in pulp, respectively. Samples were extracted by hot acid digestion, partitioned in methylene chloride and cleaned up on Florisil. The 3‐hydroxy‐carbofuran was ethoxylated and the compounds were converted into their dinitrophenyl ethers and analysed by electron capture gas chromatography using 3% OV‐3 column.     

超临界水气化处理对脱水污泥中重金属环境风险的影响

为探究超临界水气化前后脱水污泥中重金属的变化及生态风险,从重金属(Ni、Cu、Zn、Pb、Cr)的含量、化学形态分布及浸出毒性等多方面出发,利用地层累积指数(Igeo)、潜在生态风险指数(RI)和风险评估指数法(RAC)对江苏地区10种不同种脱水污泥超临界水气化前后重金属的环境生态风险进行综合评价.结果表明:不同污水厂脱水污泥经超临界水气化处理后,绝大部分污泥中重金属浸出毒性和生物可利用组分重金属含量明显降低,即处理后重金属的直接环境风险大大降低.不同重金属含量的脱水污泥经超临界水气化处理后,重金属环境污染程度及潜在生态风险程度显著降低,环境风险值被降至相对安全水平,对环境表现出低风险或无风险.p H值在一定程度上影响处理后污泥中重金属的环境风险.超临界处理时,污泥的p H呈现酸性时会引起反应釜腐蚀,从而导致固相残渣中Ni、Cr的生物可利用组分含量增加,当p H呈现碱性时则更利于重金属以稳定形态富集到固相产物中.     

Organochlorine levels in human blood from residents in areas of limited pesticide use in Sudan

Ninety-nine human blood samples were collected from the riverine region of northern Sudan and the traditional and mechanized rain-fed areas of western and eastern Sudan, representing areas of limited pesticide use in Sudan. Blood samples were analyzed for organochlorine pesticides by gas liquid chromatography (GLC) followed by electron-capture detection (ECD). p,p′-DDE (a metabolite of DDT), heptachlor epoxide, β-hexachlorocyclohexane (β-HCH), and dieldrin were detected in all locations surveyed. The level of total organochlorine burden was highest in the traditional rain-fed area, followed by the mechanized rain-fed area, and the riverine area. A highly significant correlation was observed between total organochlorine blood burden and the age of the donors (r = 0.608**).