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Comparison of Solution-Based versus Laser Ablation Inductively CoupledPlasma Mass Spectrometry for Analysis of Larval Fish OtolithMicroelemental Composition

机译:溶液法与激光烧蚀电感耦合等离子体质谱法比较分析幼鱼耳石中的微量元素

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Otolith microchemistry has become a widely used tool for fisheries-based research in marine systems. However, its application to systems without well- defined juvenile nursery areas in which distinct otolith elemental signatures can develop (i.e., most freshwater systems) remains limited. In large part, this deficiency is due to unsuitable protocols for reliably processing and analyzing small otoliths of larvae. Herein, we evaluate the abilities of solution-based (SO) and laser ablation (LA) inductively coupled plasma mass spectrometry (IS) to quantify the otolith elemental composition of larval yellow perch Perca flavescens captured in three distinct spawning locations in Lake Erie (USA-Canada). Analysis of otolith pairs by each technique demonstrated that both SO- and LA-I quantify the more abundant elements, such as Sr and Ba. Magnesium and zinc, analyzed by use of both SO- and LA-ICPMS, also met the criteria for inclusion in our analyses (i.e., the coefficients of variation of standards were <10.5%, and over 90% of samples were above detection limits at a single location). Upon closer inspection of the data, however, we found that estimates of Mg and Zn were only reliable for LA-ICPMS. Estimates of these two elements using SO-ICPMS were unrealistically high, probably owing to contamination during the otolith dissolution and handling phases. We also found that LA-ICPMS provided more precise estimates than did SO-ICPMS for nearly all elements explored, but LA-ICPMS was somewhat limited by high limits of detection for some elements. Despite these differences, both techniques could accurately discriminate among larvae produced in different Lake Erie spawning locations, primarily because of the significant variation in Sr among larval otoliths. Ultimately, although both methods are appropriate for analysis of otoliths from larvae, we recommend the use of LA-ICPMS in future otolith microchemical applications involving larvae.
机译:耳石微化学已成为在海洋系统中以渔业为基础的研究中广泛使用的工具。然而,其在没有可明确发育耳石元素特征的未明确界定的幼稚园区域的系统(即大多数淡水系统)中的应用仍然受到限制。在很大程度上,这种缺陷是由于不适合用于可靠地处理和分析幼体小耳石的协议所致。在这里,我们评估了基于溶液的(SO)和激光消融(LA)电感耦合等离子体质谱(IS)的能力,以量化在伊利湖(美国)三个不同产卵位置捕获的幼虫黄鲈Perca flavescens的耳石元素组成。 -加拿大)。每种技术对耳石对的分析表明,SO-和LA-1都可以量化更丰富的元素,例如Sr和Ba。通过同时使用SO-和LA-ICPMS进行分析的镁和锌也符合纳入分析的标准(即,标准品的变异系数小于10.5%,超过90%的样品在一个位置)。但是,在仔细检查数据后,我们发现Mg和Zn的估算仅对LA-ICPMS是可靠的。使用SO-ICPMS对这两个元素的估算值高得不切实际,这可能是由于耳石溶解和处理阶段的污染所致。我们还发现,对于几乎所有元素,LA-ICPMS都比SO-ICPMS提供了更精确的估计值,但是LA-ICPMS受到某些元素的高检测限的限制。尽管存在这些差异,但这两种技术都可以准确地区分在伊利湖不同产卵位置产生的幼虫,这主要是由于幼虫耳石中Sr的显着差异所致。最终,尽管这两种方法都适合分析幼虫中的耳石,但我们建议在涉及幼虫的未来耳石微化学应用中使用LA-ICPMS。

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