The structure of the fire fighting foam surfactant Forafac®1157 and its biological and photolytic transformation products

For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by ¹H, ¹³C and ¹⁹F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility.     

纤维素降解细菌筛选及降解特性分析

基于获得高效纤维素降解细菌的目的,通过LB培养基的培养以及刚果红培养基的筛选,从牛粪堆肥中筛选获得2株高效纤维素降解细菌。经鉴定,分别为枯草芽胞杆菌(Bacillus subtilis)和地衣芽胞杆菌(Bacillus licheniformis)。所筛选得到的菌种具有很高的滤纸降解能力,可在6d内使滤纸剧烈崩溃,振摇成均匀糊状;其中,地衣芽胞杆菌的羧甲基纤维素钠酶活峰值在发酵第4天达到峰值(237U/g)。     

壬基酚降解菌产酶条件的优化

通过单因素试验和正交试验确定了实验室保藏的壬基酚降解菌株沙雷氏菌(Serratiasp.LJ)的最佳产酶条件:以壬基酚、硫酸铵为碳源、氮源,培养基初始pH为6.8,培养温度为30℃,种子活化时间为24h,接种量为3%(体积分数)。在此条件下培养72h后,最高酶活力为1.314IU/mL,是优化前的1.77倍。     

人工湿地构筑根孔作用下土壤物质分布状况

嘉兴市石臼漾湿地应用人工构筑根孔技术,以玉米秸秆和油菜秸秆按比例混合埋植于土壤亚表层,作为湿地的基质/填料。在湿地运行一年半后,按照正交设计表,以埋植秸秆的种类(S)、填埋的土壤层次(L)、距离秸秆外环的远近(D)和秸秆周围土壤的表观颜色(C)作为实验因素,对秸秆周围养分物质浓度、土壤酶活性以及铁含量进行采样分析。实验结果显示:玉米秸秆和油菜秸秆腐烂较充分,分别形成较发达的粗根孔和细根孔;根孔周围土壤呈中度还原状态;粗根孔具有较强的优先流效应,其周围土壤具有较高的养分物质含量和较低的Fe2+/Fe3+比。粗根孔周围土壤具有较高的磷酸酶活性,而细根孔周围具有较高的β-葡糖苷酶活性和脲酶活性。综合比较,人工湿地构建初期,径级较大秸秆腐烂后形成的粗根孔发挥着更高的水分传导效率和更强的物质截留效应。     

湿地生态系统基质重金属积累与酶活性的研究现状

湿地生态系统具有净化污水的功能,因其具有高效低耗等优点,在污水处理方面极具开发应用前景,而基质作为湿地生态系统重要组成部分,已成为众多学者的研究热点。本文综合分析了湿地生态系统基质中重金属积累和酶活性的时空分布及影响因素的研究现状,并对相关研究提出了新的认识与展望,以期为湿地生态系统基质去除废水中重金属的深入研究和应用提供综合分析资料。     

腐熟蓝藻与厌氧污泥混合厌氧发酵特性

采用批次小试实验对不同腐熟程度的蓝藻进行厌氧发酵产沼气实验研究。结果表明,新鲜蓝藻在30-35℃时腐熟7 d后,可在35℃的厌氧温度下获得最高的产气速率和246 mL/g COD的产气量,产气潜力为354 mL/g（VS）。厌氧反应15 d后,累计产气量、COD和VFA浓度趋于稳定。淀粉酶和脱氢酶的活性在厌氧反应初期受到抑制,蛋白酶活性和辅酶F420浓度在厌氧系统中逐渐增加,分别在第6天达到27.66μmol/（g VS·min）和第15天达到0.62μmol/g（VS）。15-18d是腐熟蓝藻适宜的中温厌氧发酵时间,少于以新鲜蓝藻为基质的厌氧消化时间。蓝藻腐熟过程促进了厌氧反应,腐熟7 d的蓝藻厌氧系统具有更高的微生物活性和产甲烷能力。     

蒽醌染料中间体溴氨酸降解酶的特性

从污染地分离筛选出的菌株BX26对蒽醌染料中间体溴氨酸有显著的降解脱色作用,降解过程受降解酶的控制,试验结果表明,降解酶为溴氨酸诱导的胞外酶,该酶在温度高于50℃处理后失活,盐度对该酶失活有影响,盐度高于1%会显著降低该酶活力,酶对溴氨酸的催化脱色要有氧参加,氮气气氛中酶活受抑制。     

浸水冷应激对雏鸡某些酶活性及消化道粘膜充血的影响

以海兰雄性雏鸡为试验对象,研究急性浸水冷应激对健康雏鸡某些酶活性消化道粘膜充血的影响。结果表明：雏鸡在浸水冷应激后血清肌酸激酶（CrK）呈一致性升高趋势;而丙氨酸氨基转肽酶（ALT）的活性则在冷应激后15min明显升高（P＞0.05）,而后降低,至120min时又恢复致冷应激前水平,雏鸡血清乳酸脱氢酶（LDH）在冷应激后15－60min呈渐进性升高,而后降低;血清γ－谷氨酰转肽酶（γ－GT）的变化趋势为,在冷应激后15min稍升高,而后则逐渐下降;血清尿素氮（BUN)的变化无是,在冷应激后60min降低,浸水应激后不同时间对海兰雏鸡消化道粘膜充血的结果表明：雏鸡在浸水应激后即刻观察造成消化道充血现象并不严重;而浸水应激后不同时间却对雏鸡消化道产生相对较强的影响,特别是冷应激后1－2h胃肠道充血比较严重。     

Effect of some herbicides on activities of microorganisms and enzymes in soil

Abstract

Laboratory tests were conducted with eight herbicides, atrazine, butylate, ethalfluralin, imazethapyr, linuron, metolachlor, metribuzin and trifluralin, applied to a loamy sand at rate of 10 μg/g to determine if these materials caused any serious effects on microbial and enzymatic activities related to soil fertility. Some herbicides showed an effect on bacteria and fungi for the first week of incubation, but, subsequently, the populations returned to levels similar to those obtained in the controls. After several herbicide treatments there appeared to cause a slight depression of nitrification. Sulfur oxidation was better than that obtained with untreated soil in all treatments. Oxygen consumption was increased significantly after 96 hr incubation with atrazine. The soil dehydrogenase and amylase activities were inhibited by ethalfluralin treatment respectively for 1 wk and 1 day, and p‐nitrophenol liberation was inhibited for 2 hrs by all herbicide treatments. Results indicated that the herbicidal treatments at the level tested were not drastic enough to be considered deleterious to soil microbial and enzymatic activities which are important to soil fertility.     

Effect of tracer dyes on initial deposits and persistence of bacillus thuringiensis subsp. kurstaki toxin after application of two commercial formulations onto spruce trees

Abstract

The effect of two tracer dyes [Erio Acid Red (EAR) and Acid Black 48 (AB‐48)] on initial deposits and persistence of Bacillus thuringiensis subsp. kurstaki (Btk) toxin (delta‐endotoxin) was studied after spraying two commercial formulations, Foray® 48B and Foray® 76B, over potted white spruce [Picea glauca (Moench) Voss] seedlings, at a dosage rate of 30 billion international units (BIU) per ha. Spray was applied using a spinning disc atomizer calibrated to deliver droplet sizes similar to those utilized in ultra‐low‐volume (ULV) treatments in operational insect control programs. The sprayed seedlings were left outdoors at the Sault Ste. Marie laboratory for 18 days under natural conditions of sunlight, wind and rainfall. Initial deposits and persistence of delta‐endotoxin protein in spruce foliage were determined by immunoassay [enzyme linked immunosorbent assay (ELISA)] quantification of the delta‐endotoxin. The total protein (inactive plus active) and delta‐endotoxin (active protein) concentrations in the two formulations were determined by a gravimetric procedure and by ELISA respectively.

The initial deposit levels of the toxin on foliage were not markedly affected by the addition of either of the two tracer dyes, and showed only a narrow range of 1521 to 1625 ng/g foliage (fresh weight) for Foray 48B, and 1789 to 2056 ng/g for Foray 76B. However, the persistence of the toxin was significantly influenced by the presence of the dyes. The toxin persisted in foliage only for 7 d post‐spray When the EAR dye was added to Foray 48B, compared to 10 d when no dye was added. The average half‐life (DT₅₀) of disappearance was 17.4 h for Foray 48B with EAR, and 20.9 h when no dye was present. In contrast, the situation was reversed in Foray 76B, since the duration of persistence was 10 d when EAR was added to Foray 76B, compared to 7 d when no dye was added. The average DT₅₀ was 27.9 h for Foray 76B with EAR, and 22.2 h without the dye. Persistence was the longest (14 d) when the AB‐48 dye was added to Foray 76B, and the DT₅₀ was 44.9 h.