979 resultados para Pantanal de Nhecolandia (MS)


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Se analiza la necesidad de conservación de los ecosistemas oceánicos mundiales, y la urgencia de crear áreas protegidas en mar abierto. Los siete mares inspiran imágenes de vastedad, de grandiosa expansión, de variedad y tolerancia casi infinitas. Siempre en el marco de la metáfora, este trabajo se aparta de la visión de los siete mares para apoyar a la de 'un solo océano'. En lenguaje más formal, el objetivo es promover el pensamiento ecosistémico integrado, difundir el mensaje de que el océano es uno, agotable, e incapaz de resisitir el abuso ambiental sostenido. El artículo incluye definiciones, información sobre el primer Ärea Marina Protegida (AMP) en Mar abierto en el Atlántico sudoccidental, Naumuncurá, Banco Burdwood y finaliza con otras lecturas sugeridas.

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An experiment was undertaken in order to determine an adequate anaesthetic and optimum concentrations for use in the handling of fingerling milkfish (Chanos chanos). The compounds 2-phenoxy ethanol and MS-222 were investigated. Results show the latter to be adequate with optimum concentrations between 100 and 200 ppm.

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利用水蒸气蒸馏法从湖北栀子花鲜花中提取栀子花挥发油。通过 DB 5弹性石英毛细管柱 GC MS分析所得栀子花挥发油 ,共鉴定了 4 0个化合物并测定了其相对含量。湖北栀子花挥发油的主要成分为芳樟醇 ( 1 7 92 %)、茉莉内酯 ( 9 1 1 %)和惕各酸顺 3 己烯酯( 6 5 4 %)

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应用GC/MS联用技术,对除臭大蒜口服液进行了检测,定性鉴定了25种含硫有机化合物。二烯丙基硫醚、甲基烯丙基三硫醚、3-乙烯基-1,2-二硫杂-5-环己烯、2-乙烯基-1,3-二硫杂-5-环己烯和二烯丙基三硫醚是主要组分;二烯丙基四硫醚、烯丙基四硫化氢、2-和3-(2’,3’-二硫杂-5’-己烯基)-3,4-二氢-2H-噻喃、2-(2’-[3’,4’-二氢-2H噻喃基])-1,3-二硫杂-5-环己烯和3-(2’-[3’,4’-二氢-2H-噻喃基])-1,2-二硫杂-5-环己烯是次要组分。最后4种次要组分在

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东湖沉积物阴干后用二氯甲烷溶剂萃取,用DB-5弹性石英毛细管柱GC/MS分离鉴定,并结合m/z149质量色谱图,确证东湖沉积物中含有9种邻苯二甲酸酯类化合物,它们是邻苯二甲酸二乙酯、二异丁酯、二正丁酯、二己酯、己基辛基酯、二-(2-乙基己基)酯、二辛酯、己基癸基酯和辛基癸基酯,其特征离子及峰度见表1。

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本文采用XAD-2和XAD-8(1:1)混合树脂现场富集采样,循环提取器提取,毛细管GC/MS定性的方法,通过对冬夏两季的采样分析,初步分析了某地自来(饮用)水中非挥发性有机氯化产物。从夏天自来水中检测出了28种有机氯化合物。从冬天自来水中只检出了1种有机氯化合物。

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<正> 1 简介与实验大蒜(Allium sativun L.)系石蒜科葱属植物,世界各地均有栽培,大蒜作为民间药物广泛应用于世界各地。我国用大蒜作为药物有悠久的历史,大蒜在临床上的重要作用引起了广大化学家的重视,对大蒜的分析国内外均有报道。Stoll 等人认为大蒜的主要成分是大蒜辣素(Allicm),其结构式为 CH_2=

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白暨豚是一种珍稀水生动物.本文报道了运用 Dexsil-300GC 毛细管柱色质联用仪,对白(?)豚油中脂肪酸进行了分析鉴定,并检测到了22种脂肪酸,其中主要脂肪酸是十四碳烯酸、十六碳烯酸和十八碳烯酸.

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A rapid and sensitive method was developed and validated for the determination of MCYST (microcystin)-RR, -LR, and [Dha(7)] MCYST-LR in rat plasma by liquid chromatography-tandem mass spectrometry. The analytes were extracted from rat plasma by protein precipitation, followed by solid-phase extraction. Liquid chromatography with electrospray ionization mass spectrometry, operating in selected reaction monitoring (SRM) mode, was used to quantify MCYST-RR, -LR, and [Dha(7)] MCYST-LR in rat plasma. The recoveries for each analyte in rat plasma ranged from 70.8 to 88.7%. The calibration curve was linear within the range from 0.005 to 1.25 mu g mL(-1). The limit of detection were 1.4, 1.0, 0.6 ng mL(-1) for MCYST-RR, -LR, and [Dha(7)] MCYST-LR. The overall precision was determined on three different days. The values for within- and between-day precision in rat plasma were within 15%. This method was applied to the identification and quantification of microcystins in rat plasma with acute exposure of microcystins via intravenous injection.

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The antibacterial drug furazolidone belonging to the group of nitrofuran antibacterial agents has been widely used as an antibacterial and antiprotozoal feed additive for poultry, cattle, and farmed fish in China. During application a large proportion of the administered drug may reach the environment directly or via feces. Although the use of furazolidone is prohibited in numerous countries, there are indications of its illegal use. It is known that furazolidone can be rapidly metabolized to 3-amino-2-oxazolidinone (AOZ) in the body of the target organism. In this study, a total of 21 fish feed samples, including 17 commercial fish feeds from local markets in China (representing 15 different formulations) and 4 fish feeds obtained from Germany and Turkey, respectively, are analyzed to determine whether the drug is still illegally used or commercially available feeds are contaminated by this drug. High-performance liquid chromatography (HPLC) and liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) methods have been implemented to determine furazolidone and its metabolite AOZ in fish feeds containing animal protein, respectively. An efficient and convenient cleanup method for the determination of furazolidone in fish feeds is developed, and a simple cleanup method for the determination of AOZ is used. Method recoveries for samples used were determined as 87.7-98.3% for furazolidone at two spike levels of 2.0 and 5.0 ng g(-1) and as 95.6-102.8% for AOZ at spike levels of 0.4 and 0.8 ng g(-1). Limits of detections were 0.4 ng g(-1) for furazolidone and 0.05 ng g(-1) for AOZ. The established methods are therefore suitable for the determination of furazolidone and its metabolite AOZ in fish feeds at trace contamination levels. Using the established methods, all fish feed samples have been proved to be furazolidone negative; however, AOZ is tested in 16 of 17 fish feeds obtained from local markets in the Hubei province of China, with a positive rate as high as 94.1%.

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A monolithically integrated optoelectronic receiver was realized utilizing a deep sub-micron MS/RF CMOS process. Novel photo-diode with STI and highspeed receiver circuit were designed. This OEIC takes advantage of several new features to improve the performance.

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