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C Kosore L Ojwang J Maghanga J Kamau A Kimeli J Omukoto 《African Journal of Marine Science》2018,40(3):225-234
Microplastics can be ingested by marine organisms and may lead to negative impacts at the base of marine food chains. This study investigated the occurrence and composition of microplastics in the sea-surface water and sought evidence of ingestion by zooplankton. Surface seawater was collected using a stainless-steel bucket and sieved directly through a stainless-steel sieve (250-µm mesh), while a 500-μm mesh net was towed horizontally to collect zooplankton, at 11 georeferenced stations off the Kenyan coast in February 2017, on board the national research vessel RV Mtafiti. Microplastic particles were sorted and characterised using an Optika dissecting microscope. Polymer types were identified using an ALPHA Platinum attenuated total reflection—Fourier-transform infrared (ATR-FTIR) spectrometer. A total of 149 microplastic particles, with an average abundance of 110 particles m–3, were found in the surface seawater. A total of 129 particles were found ingested by zooplankton groups, where Chaetognatha, Copepoda, Amphipoda and fish larvae ingested 0.46, 0.33, 0.22 and 0.16 particles ind.–1, respectively. Filaments dominated both the surface-water microplastics and the ingested microplastics, contributing 76% and 97% to those compositions, respectively. White particles were prevalent in the water (51%), whereas black was the colour found most commonly (42%) across the zooplankton groups. The sizes of particles that were in the water were in the range of 0.25–2.4 mm, and those ingested ranged between 0.01 and 1.6 mm. Polypropylene was predominant in the surface water, whereas low-density polyethylene was the most-ingested polymer type. The results provide the first documented evidence of the occurrence, composition and ingestion of microplastics by zooplankton in Kenya's marine environment, indicating that microplastics have the potential to enter pelagic food webs and cause pollution in the study area. 相似文献
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高聚物萃取光度法测定钯 总被引:10,自引:0,他引:10
研究了在聚乙二醇 -硫酸铵 -亚硝基R盐体系中萃取光度法测定钯。在 pH 1 .3的NaAc-HCl缓冲溶液中 ,钯与亚硝基R盐形成橙色配合物 ,被萃取到高聚物相 ,其配合物的最大吸收波长位于 50 0nm处 ,摩尔吸光系数为 1 .58× 1 0 4L·mol- 1.cm- 1,Pd(Ⅱ )与亚硝基R盐的配位比为 1∶3,Pd(Ⅱ )的质量浓度在 0~ 2 .2mg/L内符合比尔定律。方法用于碳 -钯催化剂中钯的测定 ,6次测定的RSD为 2 .7%。 相似文献
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微塑料因粒径小、比表面积大,可作为重金属、有机污染物以及病原微生物的载体。已有研究表明,微塑料表面附着的微生物主要以生物膜的形式存在。本研究以山东省海岸带环境中常见的两类软质塑料——发泡类聚苯乙烯(expanded polystyrene,EPS)和聚乙烯薄膜(polyethylene films,PE)为研究对象,比较了MP FastDNA®和MOBIO PowerSoil®两种DNA提取试剂盒对微塑料表面生物膜DNA的提取效果,探讨了不同的微塑料粒径和数量对DNA提取效果的影响。结果表明,MP FastDNA®试剂盒对两种软质微塑料表面生物膜DNA的提取浓度显著低于MOBIO PowerSoil®试剂盒(1.0~12.5倍)。采用MP FastDNA®试剂盒提取的PE表面DNA的浓度约为EPS的1.3~4.4倍。当微塑料数量不大于20片时,小粒径(1~3 mm)的EPS表面生物膜DNA浓度显著高于大粒径(3~5 mm) EPS,而对于PE薄膜则相反。对于两种粒径的EPS,微塑料表面DNA浓度均随着微塑料数量的增加而显著增加,但对于小粒径(1~3 mm)的PE薄膜,DNA浓度随微塑料数量的增加呈先增后减的趋势;而大粒径(3~5 mm)的PE薄膜表面DNA浓度随微塑料数量的增加而降低。微塑料的粒径和数量对其表面DNA提取效果影响的差异与微塑料的类型及其理化性质有关。本研究可为海洋与海岸环境中微塑料表面微生物群落组成与多样性研究提供方法支撑。 相似文献
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电力设备运行中的温升现象严重影响绝缘的使用寿命,因此高温下的空间电荷测量引起了许多学者的关注.但温度升高时,聚合物材料的声阻抗、Young模量、密度、声波在其中传播的速度、衰减特性均发生变化,因此无法准确测量出介质中的空间电荷特性.而对于温度梯度场下的绝缘介质(如电缆发热场)的空间电荷测量,温度的梯度分布对介质的声阻抗、弹性模量、密度、声速及声波衰减的影响将更为复杂.本文基于电声脉冲测量方法中声波的传播特性和温度对聚乙烯材料特性的影响,分析了温度梯度场对空间电荷测量结果的影响并进行了波形恢复. 相似文献
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X射线荧光光谱(XRF)分析方法中,采用粉末压片制样存在粒度效应和矿物效应等问题,但当样品在一定的粒度、压制压力及压制时间条件下,矿物效应和粒度效应仅仅对钠、钙等轻元素的测试有影响,而对钼、铜、铅等元素的测试并无影响。基于此本文建立了粉末压片制样波长色散XRF直接测定钼矿石中Mo、W、Cu、Pb、Zn、F、S、As、Bi等9种元素的方法。采用价格低廉的低压聚乙烯粉作衬垫镶边材料,样品在35 t的压力下压制30 s,制备的样片坚固光滑、吸潮性小,长期保存不发生形变,消除了粒度效应。选用自制的钼含量呈梯度变化的钼矿石样品及钼矿石、钨矿石、铜矿石、铅矿石、铋矿石、锌矿石等国家标准物质作为校准样品建立标准曲线,降低了矿物效应,采用经验系数法消除谱线重叠和基体干扰。本方相对标准偏差小于2.1%,各元素的测定结果与电感耦合等离子发射光谱法等其他方法测量值吻合。与已报道的玻璃熔融和粉末压片制样方法相比较,检出限较低,如钼的检出限为3.67 μg/g,比玻璃熔融法的检出限(450 μg/g或24 μg/g)要低得多;砷的检出限为1.13 μg/g,低于其他粉末压片法的检出限(7.8 μg/g)。本方法提出了克服粒度效应及光谱诸干扰因素影响的详细解决方案,有利于XRF法应用于定量分析基体组成复杂的钼矿石。 相似文献
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为了研究高密度聚乙烯(HDPE)和聚对苯二甲酸乙二醇酯(PET)两种土工格栅在返包式加筋路堤中的加筋效果,基于HDPE和PET的拉伸试验结果,采用FLAC3D有限差分程序并结合现场监测数据对比,分析了加筋路堤中两种土工格栅的受力变形规律。结果表明,土工格栅特性对返包式加筋路堤变形具有明显影响,影响程度与其上部土压力大小密切相关;在加筋土路堤的中下部,土压力较大,HDPE格栅前1/3段和后1/3段的应变存在较大差别,PET格栅的应变沿长度分布相对均匀;随着上部土压力的减小,格栅材料特性的影响减弱,两种格栅的应变曲线趋于接近;PET格栅对加筋路堤水平变形的控制作用更为明显;HDPE格栅加筋路堤的垂直和水平土压力值及其分布与PET加筋路堤差别很小。 相似文献
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Glycerol-3-phosphate acyltransferase(GPAT) is considered as the rate-limiting enzyme of glycerolipid synthesis pathway and the core element in lysophosphatidic acid(LPA) synthesis. For understanding its catalytic mechanism, the structural biology study is expected, but is always hindered by obtaining crystals for X-ray diffraction analysis. In this study, a progressive strategy to optimize the crystal of microalgae plastidial GPAT was presented. After the expression and purification of GPAT, the crystals were screened by hanging-drop and only clusters were obtained. The crystals were optimized by adjusting temperature, pH, protein concentration, or precipitant, but little improvement. To improve the interaction between protein and precipitant, the isopropanol was applied as co-precipitant. The qualified crystals formed. It's suggested that isopropanol is critical to affect protein crystallization by altering polyethylene glycol(PEG)-water-protein interaction when PEG serves as precipitant. The resulting crystal diffracted to a resolution of 2.75 ? and belonged to space group P1, with unit-cell parameters a = 50.79, b = 80.09, c = 88.21 ?, and α = 62.85, β = 73.04, γ = 80.53?. This work introduced a new strategy to optimize the crystal of the heterogeneous catalysis enzymes like GPAT and provided the fundamental structural information for the oriented synthesis of marine microalgae glycerolipid. 相似文献