Biodegradation of phthalic acid esters by acclimated activated sludge

The microbial degradation by acclimated activated sludge of three phthalates, priority pollutants listed by both the China National Environmental Monitoring Centre and the U.S. EPA, i.e., dimethyl (DMP), di-n-butyl (DBP), and di-n-octyl (DOP) phthalate was investigated. The experimental results demonstrated that DMP and DBP with the shorter alkyl-side chain phthalic acid esters (PAEs) can be rapidly degraded—nearly 90% within 3 d for DMP and 8 d for DBP. However, the degradation rate of DOP was slow. The degradation of PAEs can be described by the first-order reaction model. The first-order rate constants (k₁) of three PAEs determined in this study can correlate with the corresponding second-order hydrolysis rate constants (K_OH).     

Phthalate metabolites in urine from China, and implications for human exposures

Phthalates are esters of phthalic acid and are mainly used as plasticizers (added to plastics to increase their flexibility, transparency, durability, and longevity). Humans are exposed to phthalates through several routes. Urinary phthalate metabolites can be used as biomarkers of human exposures to phthalates. In this study, 14 phthalate metabolites were analyzed in 183 urine samples collected in 2010 from Shanghai, Guangzhou, and Qiqihaer, China. Phthalate metabolites were found in all urine samples and their total concentrations ranged from 18.6 to 3160 ng/mL (median: 331 ng/mL). Mono-n-butyl phthalate (mBP) and mono-2-isobutyl phthalate (miBP) were the major metabolites found in urine, and their respective median concentrations were 61.2 and 51.7 ng/mL; concentrations of miBP were higher than the concentrations reported for other countries, to date. Based on the urinary concentrations of phthalate metabolites, we estimated the daily intake rates in the Chinese population. The estimated daily intakes of dibutyl phthalate (DBP), diethyl phthalate (DEP), and di-(2-ethylhexyl) phthalate (DEHP) in China were 12.2, 3.8, and ~5 μg/kg bw/day, respectively. Thirty nine percent of the samples exceeded the tolerable daily intake of 10 μg/kg bw/day, proposed for DBP, by the European Food Safety Authority, but none of the estimated daily intake values exceeded the reference dose recommended by the U.S. Environmental Protection Agency.     

Comparison and analysis of different approaches for estimating the human exposure to phthalate esters

The human exposure estimates for dibutyl (DBP) and bis(2-ethylhexyl) phthalate (DEHP) made by two models EUSES and ACC-Human, and by an estimation approach which utilized measured concentrations in exposure media, were compared. The approach which utilized the latest monitoring data for important exposure media, yielded median daily intakes for adult humans for DBP and DEHP of 2.7 and 5.6 microg/kg body weight per day, respectively, which were in the same range as previous estimates based on back-calculation from urinary metabolites. EUSES estimated average daily intakes of DBP and DEHP for humans that were between 8 and 13 times lower. ACC-Human does not estimate average daily intakes, but ACC-Human-estimated human milk concentrations/fugacities were more than a thousand times lower than measured concentrations/fugacities in human milk. It was concluded that the two models underestimate human exposure to phthalate esters because they consider only a few key pathways that are known to be important for other, more persistent, hydrophobic organic compounds. Further, it was shown that there are differences between the two models on the methodology for estimating concentrations in exposure media such as vegetation, milk, beef and fish. ACC-Human uses a mechanistic approach for estimating transfer through aquatic and terrestrial food chains that are known to be important for human exposure to persistent, hydrophobic organics and can, unlike EUSES, account for food chain metabolism. It proved difficult, however, to obtain organism metabolism rates needed as model inputs to ACC-Human. If exposure estimates of phthalate esters are needed, it is recommended to use an estimation approach based on high quality monitoring data as presented here and/or back-calculate daily intake from concentrations of metabolites in human urine samples from the general population.     

The influence of resource strategies on childhood phthalate exposure—The role of REACH in a zero waste society

The present study aims to investigate how resource strategies, which intend to reduce waste and increase recycling, influence on human exposure to hazardous chemicals from material recycling. In order to examine the flows of hazardous chemicals in recycled material, a mass flow analysis of plastics and paper at European level, including the flow of phthalates, i.e. di(2-ethylhexyl) phthalate (DEHP), di-n-butyl phthalate (DBP), and benzyl-butyl phthalate (BBP), has been performed. The result for the year 2012 shows that 26% of plastic wastes and 60% of paper consumed in Europe were recycled. This corresponds to the finding that approximately 4% of DEHP and BBP and 18% of DBP annual demands in Europe as raw material re-enter the product cycle with recycled plastics and paper. To examine the potential contribution of the phthalate exposure through recycled plastics and paper, a case study assessing the childhood exposures to phthalates from foods packed in recycled paper and plastics has been performed for 2-year-old children in Denmark. The result verifies that an increase in recycled paperboard and PET bottles in food packaging material causes a significant increase in childhood exposure to DBP corresponding to an additional exposure of 0.116–0.355 μg/kg bw/day; up to 18% of the total DBP exposure in Danish 2-year-olds. While most of the DEHP exposure can be explained, more than 50% of DBP and 70% of BBP exposure sources still remain to be identified. Finally, a conceptual framework for a circular economy based on sustainable and clean resource flows is proposed in order to increase material recycling without increasing adverse health effects.     

Determination of phthalate ester plasticizers in the aquatic environment of Southwestern Nigeria

Water from the Lagos, Oyo, Osun, Ondo, and Delta states of Nigeria and the cities' water treatment plants had been analized for the presence of ubiquitous phthalate esters using liquid chromatography. Extraction with CH₂Cl₂ and liquid chromatography was used for compound separation. Several phthalate esters, dimethyl- (DMP), diethyl- (DEP), and di-n-butyl- (DBP) were found present at levels of 10 mg L⁻¹ to 1472 mg L⁻¹ in river water and 91 mg L⁻¹ to 1219 mg L⁻¹ in tap water from the cities' water treatment plants. A study of uncontaminated water was done to establish blank levels.     

Evaluation of the aerobic biodegradation of trichloroethylene via response surface methodology

Response surface methodology (RSM) was used to evaluate the effect of additives for enhancing the aerobic biodegradation of trichloroethylene (TCE). The parameters investigated include the initial TCE concentration, addition of extra bacteria, use of toluene as an inducer and hydrogen peroxide as terminal electron acceptor (TEA). Without additive, degradation efficiencies of >or=80% were obtained for TCE concentrations<700 mg/L. According to the second-order polynomial RSM and biodegradation results, the use of toluene to induce enzyme production inhibited degradation at TCE concentrations<300 mg/L. The addition of hydrogen peroxide did improve the overall degradation efficiency but decreased the degradation rate. The RSM model for toluene, extra bacteria and TEA predicted that the best approach to optimize degradation of high TCE concentrations is to ensure adequate population in conjunction with supplemental TEA.     

Thyroid hormone disrupting activities associated with phthalate esters in water sources from Yangtze River Delta

Thyroid hormone disrupting compounds in water sources is a concern. Thyroid hormone (TH) agonist and antagonist activities of water sources from the Yangtze River, Huaihe River, Taihu Lake and ground water in the Yangtze River Delta region were evaluated by use of a TH reporter gene assay based on the green monkey kidney fibroblast (CV-1). While weak TH receptor (TR) agonist potency was observed in only one of 15 water sources, antagonist potency was present in most of the water sources. TR antagonist equivalents could be explained by the presence of dibutyl phthalate (DBP), with concentrations ranging from 2.8 × 10¹ to 1.6 × 10³ μg DBP /L (ATR-EQ₅₀s). None of the ground waters exhibited TH agonist potencies while all of the samples from Taihu Lake displayed notable TR antagonist potencies. To identify the responsible thyroid active compounds, instrumental analysis was conducted to measure a list of potential thyroid-disrupting chemicals, including organochlorine (OC) pesticides and phthalate esters. Combining the results of the instrumental analysis with those of the bioassay, DBP was determined to account for 17% to 144% of ATR-EQ₅₀s in water sources. Furthermore, ATR-EQ_20–80 ranges for TR antagonist activities indicated that samples from locations WX-1 and WX-2 posed the greatest health concern and the associated uncertainty may warrant further investigation.     

Association between prenatal exposure to phthalates and the health of newborns

Phthalates are developmental and reproductive toxicants for the fetus in pregnant rodents, and the ability of phthalates to penetrate the placenta have been reported. The aims of this study were to evaluate the association between maternal urine excretion, the exposure of fetus to phthalates in amniotic fluid, and the health of newborns. Amniotic fluid and urine samples from pregnant women were collected to measure five phthalate monoesters using liquid chromatography/tandem mass spectrometry (LC/MS-MS) and the newborns' birth weight, gestational age, and anogenital distance (AGD) were collected. The median levels of three phthalate monoesters in urine and amniotic fluid were 78.4 and 85.2 ng/mL monobutyl phthalate (MBP); 24.9 and 22.8 ng/mL mono-(2-ethylhexyl) phthalate (MEHP); 19.8 and Not Detected monoethyl phthalate (MEP). We found a significant positive correlation only between creatinine adjusted urinary MBP and amniotic fluid MBP (R(2)=0.156, p<0.05) in all infants and, only in female infants, a significantly negative correlation between amniotic fluid MBP, AGD (R=-0.31, p<0.06), and the anogenital index adjusted by birth weight (AGI-W) (R=-0.32, p<0.05). Although the influence of prenatal di-n-butyl phthalate (DBP) exposure on the endocrinology and physiology of the fetus is still a puzzle, our data clearly show that in utero exposure to phthalates in general has anti-androgenic effects on the fetus.     

Extent of sonochemical degradation and change of toxicity of a pharmaceutical precursor (triphenylphosphine oxide) in water as a function of treatment conditions

The degradation of triphenylphosphine oxide (TPPO) in water, a toxic compound typically found in effluents from the pharmaceutical industry, by means of ultrasonic irradiation at 20 kHz has been investigated with emphasis on the effect of various parameters on conversion and acute toxicity. Experiments were carried out at liquid volumes of 50 and 80 ml, electric power outputs of 125, 187.5 and 250 W, initial TPPO concentrations of 10, 100 and 350 mg/L and temperatures of 5, 20, 35, 50 and 70 degrees C. TPPO conversion was found to increase with increasing power output and decreasing initial concentration and temperature. Measurements of dissolved total carbon showed that liquid-phase degradation by-products were more stable to ultrasonic irradiation than TPPO. Addition of t-butanol as a radical scavenger at a concentration of 1000 mg/L nearly completely suppressed TPPO degradation. Conversely, addition of radical promoters (Fe(2+) ions or H(2)O(2)) had a positive effect on degradation. Acute toxicity to marine bacteria vibrio fischeri was measured before and after ultrasonic irradiation. At the conditions employed in this study, irradiated TPPO samples were always more toxic than TPPO itself with toxicity levels being a function of treatment conditions.     

Cadmium biosorption by cells of Spirulina platensis TISTR 8217 immobilized in alginate and silica gel

The biosorption of cadmium by immobilized Spirulina platensis on alginate gel and silica gel was studied. The maximum biosorption capacities for alginate immobilized cells and silica immobilized cells were 70.92 and 36.63 mg Cd/g biomass, respectively. Temperature did not have an influence on metal sorption, whereas an initial pH solution did. Sorption occurred in a wide pH range (pH 3-8). The highest adsorption of alginate immobilized cells was at pH 6, while silica immobilized cell adsorption was not affected at pH between 4 and 7. The immobilized cells were reused in consecutive adsorption-desorption. The results showed that immobilized cells could be repeatedly used in the sorption process up to five times.     

The internal exposure of Taiwanese to phthalate--an evidence of intensive use of plastic materials

Phthalates are widely used in industry and consumer products. Di-(2-ethylhexyl) phthalate (DEHP) and di-n-butylphthalate (DBP) show the greatest potency of reproductive toxicants among phthalates. The purposes of this study are to examine the migration level of phthalate from PVC films by simulating food handling and to reveal the body burden of phthalate for Taiwanese. In order to estimate a worst-case of phthalate migration, food was covered with polyvinyl chloride (PVC) films and then microwave heated. Results show that DEHP level in food increased significantly after heating for 3 min. Under the heating condition, the calculated intake of phthalate and the percentage of the tolerable daily intake (TDI, based on body weight of 60 kg) from eating one 400-g meal were 1705.6 microg and 92.2% for DEHP. Determination of urinary metabolites from 60 subjects reveals more than 90% of samples were detectable for mono-methyl phthalate (MMP), mono-butyl phthalate (MBP) and mono-ethylhexyl phthalate (MEHP). Notably, the median value of estimated daily intake of DEHP had reached 91.6% of TDI established by the European Union Scientific Committee for Toxicity, Ecotoxicity and the Environment (CSTEE) (1998). Thirty-seven percent of the study population exceeded the TDI and 85% exceeded the reference dose (RfD) of the US EPA. We conclude that the body burden of DEHP for Taiwanese reflects the intensives use of plastic materials in the region. The regulation of PVC for food preparation is necessary.     

Exposure assessment issues in epidemiology studies of phthalates

PurposeThe purpose of this paper is to review exposure assessment issues that need to be addressed in designing and interpreting epidemiology studies of phthalates, a class of chemicals commonly used in consumer and personal care products. Specific issues include population trends in exposure, temporal reliability of a urinary metabolite measurement, and how well a single urine sample may represent longer-term exposure. The focus of this review is on seven specific phthalates: diethyl phthalate (DEP); di-n-butyl phthalate (DBP); diisobutyl phthalate (DiBP); butyl benzyl phthalate (BBzP); di(2-ethylhexyl) phthalate (DEHP); diisononyl phthalate (DiNP); and diisodecyl phthalate (DiDP).MethodsComprehensive literature search using multiple search strategies.ResultsSince 2001, declines in population exposure to DEP, BBzP, DBP, and DEHP have been reported in the United States and Germany, but DEHP exposure has increased in China. Although the half-lives of various phthalate metabolites are relatively short (3 to 18 h), the intraclass correlation coefficients (ICCs) for phthalate metabolites, based on spot and first morning urine samples collected over a week to several months, range from weak to moderate, with a tendency toward higher ICCs (greater temporal stability) for metabolites of the shorter-chained (DEP, DBP, DiBP and BBzP, ICCs generally 0.3 to 0.6) compared with those of the longer-chained (DEHP, DiNP, DiDP, ICCs generally 0.1 to 0.3) phthalates. Additional research on optimal approaches to addressing the issue of urine dilution in studies of associations between biomarkers and different type of health effects is needed.ConclusionsIn conclusion, the measurement of urinary metabolite concentrations in urine could serve as a valuable approach to estimating exposure to phthalates in environmental epidemiology studies. Careful consideration of the strengths and limitations of this approach when interpreting study results is required.     

构建湿地去除酞酸酯的基质微生物和酶机制研究

随着塑料制品的广泛使用，酞酸酯的污染越来越引起人们的广泛关注。目前，DBP(邻苯二甲酸二丁酯)和DEHP(邻苯二甲酸二异辛酯)已成为全球最普遍的污染物之一。报告了复合垂直流构建湿地对含酞酸酯(DBP等)的污水污染的去除效果，以及湿地去除酞酸酯的基质微生物和酶方面的净化机理。具体结果如下：复合垂直流构建湿地对酞酸酯污染具有较好的净化效果，去除率高达99．9％以上；构建湿地对酞酸酯的净化主要发生在氧气含量相对较多的下行流池，上行流他的净化作用相对较差；同时分层实验还发现，构建湿地的净化作用主要集中在湿地上层基质中。通过研究，为进一步研究利用构建湿地处理酞酸酯污染提供了有益的参考。     

丰水期鄱阳湖氮磷含量变化及来源分析

通过系统测定丰水期鄱阳湖湖水、主要支流水、长江水及部分农田水、地下水及城市污水的氮磷含量,对其氮磷含量变化及来源进行了分析,结果表明,鄱阳湖水体中主要的氮素形式是硝酸盐氮（090 mg/L）,赣江是其主要贡献者。鄱阳湖五大支流氮磷含量存在着较大的差异,赣江NO-3 N含量明显高于鄱阳湖其它主干流,而NH+4 N和TN含量以饶河的最高,TP以信江的最高。农田水、城市废水以及地下水含有较高的氮磷含量,是鄱阳湖及其五大支流氮磷的主要来源。农田水TN和TP含量最高,分别为1347、2863 mg/L。高含量的NO-3 N（735 mg/L）和NH+4 N（548 mg/L）分别出现在地下水和城市污水中。鄱阳湖水体氮负荷较大,N/P比值远大于7〖DK〗∶1。受滞留区及赣江和修水补给的影响,鄱阳湖主河道氮含量变化从上游至下游呈总体上升趋势。鄱阳湖湖体氮含量以下游最高,滞留区次之,上游主河道最低,TP含量呈相反的趋势变化。底层沉积有机物的降解和扰动导致鄱阳湖水体底层NO-3 N、NH+4 N、TN、TP的含量高于表层。     

Effect of bisphenol A with or without enzyme treatment on the proliferation and viability of MCF-7 cells

Recently, aqueous solutions polluted by BPA have been bioremediated by us using laccase immobilized on hydrophobic membranes in non-isothermal bioreactors. BPA degradation was checked using analytical methods. To assess in vitro the occurred bioremediation, the proliferation and viability indexes of MCF-7 cells incubated in the presence of aqueous solutions of BPA, or of enzyme-treated BPA solutions, have been measured as a function of the initial BPA concentration. The results demonstrated that: i) at each initial BPA concentration used, both the proliferation and viability indexes are a function of the duration of enzyme treatment; ii) proliferation and viability are uncoupled biological processes with respect to BPA enzyme treatment. Non-isothermal bioreactors are a useful tool for the bioremediation of aqueous solutions polluted by BPA, which is an example of an endocrine disruptor that belongs to the alkyl phenol family.     

Triclosan in wastewaters and biosolids from Australian wastewater treatment plants

Triclosan (TCS) is an antimicrobial agent widely used in many personal care products. This study investigated the occurrence of TCS in effluents, biosolids and surface waters, and its fate in wastewater treatment plants (WWTPs). The aqueous concentrations of TCS in nineteen effluents from Australian WWTPs ranged from 23 ng/L to 434 ng/L with a median concentration of 108 ng/L, while its concentrations in nineteen biosolids ranged from 0.09 mg/kg to 16.79 mg/kg on dry weight basis with a median concentration of 2.32 mg/kg. The removal rates for TCS in five selected WWTPs were found to range between 72% and 93%. Biological degradation was believed to be the predominant removal mechanism for TCS in the WWTPs. However, adsorption onto sludge also played a significant role in the removal of TCS in the WWTPs. TCS at concentrations up to 75 ng/L was detected in surface waters (outfall, upstream, and downstream) from five rivers receiving effluent discharge from WWTPs. Preliminary risk assessment based on the worst-case scenario showed that the TCS concentrations in surface waters might lead to risks to aquatic organisms such as algae. Based on the TCS levels in the biosolids, application of biosolids on agricultural land may also cause adverse effects in the soil environment.     

Phthalates in German daycare centers: Occurrence in air and dust and the excretion of their metabolites by children (LUPE 3)

Phthalates have been used for decades in large quantities, leading to the ubiquitous exposure of the population.In an investigation of 63 German daycare centers, indoor air and dust samples were analyzed for the presence of 10 phthalate diesters. Moreover, 10 primary and secondary phthalate metabolites were quantified in urine samples from 663 children attending these facilities. In addition, the urine specimens of 150 children were collected after the weekend and before they went to daycare centers.Di-isobutyl phthalate (DiBP), dibutyl phthalate (DnBP), and di-2-ethylhexyl phthalate (DEHP) were found in the indoor air, with median values of 468, 227, and 194 ng/m³, respectively. In the dust, median values of 888 mg/kg for DEHP and 302 mg/kg for di-isononyl phthalate (DiNP) were observed. DnBP and DiBP were together responsible for 55% of the total phthalate concentration in the indoor air, whereas DEHP and DiNP were responsible for 70% and 24% of the total phthalate concentration in the dust.Median concentrations in the urine specimens were 44.7 μg/l for the DiBP monoester, 32.4 μg/l for the DnBP monoester, and 16.5 μg/l and 17.9 μg/l for the two secondary DEHP metabolites. For some phthalates, we observed significant correlations between their concentrations in the indoor air and dust and their corresponding metabolites in the urine specimens using bivariate analyses. In multivariate analyses, the concentrations in dust were not associated with urinary metabolite excretion after controlling for the concentrations in the indoor air.The total daily “high” intake levels based on the 95th percentiles calculated from the biomonitoring data were 14.1 μg/kg b.w. for DiNP and 11.9 μg/kg b.w. for DEHP. Compared with tolerable daily intake (TDI) values, our “high” intake was 62% of the TDI value for DiBP, 49% for DnBP, 24% for DEHP, and 9% for DiNP. For DiBP, the total daily intake exceeded the TDI value for 2.4% of the individuals. Using a cumulative risk-assessment approach for the sum of DEHP, DnBP, and DiBP, 20% of the children had concentrations exceeding the hazard index of one. Therefore, a further reduction of the phthalate exposure of children is needed.     

滇池外海规模化控养水葫芦局部死亡原因分析

为了找出外海规模化控养水葫芦(E.crassipes)局部死亡的原因,于2013年8月对控养水域水葫芦空白对照区、健壮区、轻度枯死区以及重度枯死区的水质理化性质、蓝藻生物量及水生植物病理学等方面进行了比较研究。结果表明:轻度和重度枯死区蓝藻生物量高达(4.21±0.49)×109 cells/L和(757.00±19.00)×109 cells/L,均显著高于空白区和健壮区(0.14±0.09)×109 cells/L和(1.46±0.11)×109 cells/L(P0.05);NH+4-N浓度为11.44±0.02mg/L和369.87±15.37mg/L,均显著高于空白区和健壮区0.32±0.01mg/L和0.34±0.01mg/L(P0.05);轻度和重度枯死区溶氧仅1.40±0.13mg/L和0.30±0.04mg/L显著低于空白区和健壮区的7.70±0.83mg/L和6.80±0.97mg/L(P0.05);枯死区水体氧化还原电位(Eh)较低,重度死亡区水体Eh为-279.70±29.70mv显著低于其他3处水域。并且,通过对枯死水葫芦常规病理学检测,并未发现病变迹象。由此推断:水葫芦死亡原因可能主要由下风向种养区蓝藻过量堆积死亡,致使水质恶化,水体严重缺氧,进而引起水体NH+4-N浓度过高,最终导致水葫芦死亡。这为今后种养水葫芦进行水体生态修复理论研究与实践运用提供借鉴和参考,也为利用水葫芦作为蓝藻拦截带,在水葫芦影响下的湖泊营养物质迁移与氮、磷、碳循环动力学提出了新的研究内容。     

太湖主体湖区对梅梁湾藻类影响定量化研究

针对太湖梅梁湾独特的地理位置和富营养化严重的问题,利用太湖水量水质模型和梅梁湾藻类生长模型,在对模型进行了率定、验证的基础下,模拟了在东南风和西北风两种常见风向的条件下,太湖主体湖区对梅梁湾内营养盐浓度和藻类浓度的影响情况,并将其影响定量化。本次模拟较好地反映了太湖主体湖区在两种常见风场的条件下对梅梁湾内水质影响情况。模拟得到以下结果：在不考虑风场和流场的情况下,梅梁湾内部2001年8月藻类平均浓度为43.18 mg/m³,总氮浓度为2.48 mg/L,总磷浓度为0.248 mg/L,只考虑东南风引起流场的情况下,藻类浓度为41.92 mg/m3,总氮浓度为2.07 mg/L,总磷浓度为0.231 mg/L;考虑东南风风场和流场两个因素的情况下,藻类浓度为53.86 mg/m3,总氮浓度为2.06 mg/L,总磷浓度为0.229 mg/L;同期,只考虑西北风风场的情况下,藻类浓度为42.55 mg/m³,总氮浓度为2.19 mg/L,总磷浓度为0.232 mg/L;考虑西北风风场和流场两个因素的情况下,藻类浓度为50.71 mg/m³,总氮浓度为2.17 mg/L,总磷浓度为0.233 mg/L。结果表明,梅梁湾内部的氮、磷等营养盐浓度受到由太湖主体湖区的风场变化引起的湖流扰动的一定影响;太湖主体湖区对梅梁湾内部藻类浓度的影响主要是由藻类漂移引起的,由营养盐浓度改变而引起的藻类浓度变化非常小。     

博落回植物与肥料复合的杀螺效应及对水稻生长影响

探索一种杀螺施肥双效作用的新型杀螺剂。将博落回植物粉末分别与氮、磷、钾肥复合制成植物3种单肥复合杀螺剂(简称MPF),与3种肥料混合配成植物混合肥复合杀螺剂(简称MCF)。采用浸杀法进行杀螺试验, 同时检验该复合杀螺剂对水稻萌发及生长的影响。结果显示,3种MPF(博落回植物分别与氮、磷、钾肥复合杀螺剂)处理钉螺,48 h钉螺死亡率分别为100%、533%、667%;作用于水稻,能明显促进种子萌发和幼苗生长,如3种MPF使水稻种子萌发率分别为100%、80%和53%,分别比对照（40%）提高了60%、40%和13%;水稻幼苗分别增长了1268%、707%和605%。MCF随处理浓度增加及处理时间延长,钉螺死亡率上升,较低浓度（200 mg/L）处理48 h 和72 h,钉螺死亡率分别为733%和867%;较高浓度（400 mg/L）复合处理48 h和72 h,钉螺死亡率分别为833%、100%。然而,低浓度（200 mg/L）MCF对水稻萌发和生长有促进作用,如水稻幼苗比对照增长了876%,但高浓度（400 mg/L）则有一定抑制作用。因此,MPF对钉螺具有较好的杀螺活性,同时能促进水稻萌发和生长,其中植物氮肥复合杀螺剂效果最佳;MCF对钉螺均有杀螺活性,但低浓度对水稻有促进作用,而高浓度则有抑制作用