333 research outputs found

    Atomic spectrometry updates. Review of advances in elemental speciation

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    This is the sixth Atomic Spectrometry Update (ASU) to focus specifically on advances in elemental speciation and covers a period of approximately 12 months from December 2012. This review deals with all aspects of the analytical speciation methods developed for: the determination of oxidation states; organometallic compounds; coordination compounds; metal and heteroatom- containing biomolecules, including metalloproteins, proteins, peptides and amino acids; and the use of metal-tagging to facilitate detection via atomic spectrometry. The review does not specifically deal with fractionation, sometimes termed operationally defined speciation. As with all ASU reviews 1-5 the coverage of the topic is confined to those methods that incorporate atomic spectrometry as the measurement technique. However, molecular MS techniques are covered where the use is in parallel or series with atomic spectrometry. As with previous years As and Se speciation continues to dominate current literature. However, research is moving further towards understanding the toxicological and beneficial mechanisms of these two elements. There is also in increase in macromolecular analysis, with a decrease in detection limits for some methodologies, which increases the potential clinical use of the techniques employed. The use of both atomic and molecular spectrometry is well developed in these fields, highlighting the interdisciplinary nature of today's research environment. The trend towards lower cost more rapid analytical methods, often involving non-chromatographic speciation, also continues apace. This journal is © 2014 the Partner Organisations

    Atomic spectrometry update: Review of advances in elemental speciation

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    This is the 12th Atomic Spectrometry Update (ASU) to focus on advances in elemental speciation and covers a period of approximately 12 months from December 2018. This ASU review deals with all aspects of the analytical atomic spectrometry speciation methods developed for: the determination of oxidation states; organometallic compounds; coordination compounds; metal and heteroatom-containing biomolecules, including metalloproteins, proteins, peptides and amino acids; and the use of metal-tagging to facilitate detection via atomic spectrometry. As with all ASU reviews the focus of the research reviewed includes those methods that incorporate atomic spectrometry as the measurement technique. However, because speciation analysis is inherently focused on the relationship between the metal(loid) atom and the organic moiety it is bound to, or incorporated within, atomic spectrometry alone cannot be the sole analytical approach of interest. For this reason molecular detection techniques are also included where they have provided a complementary approach to speciation analysis. This year the number of publications concerning As speciation has fallen by about half, as have studies on Se speciation. Growth areas continue to be Hg and ‘biomolecules’, with the number of reports concerning halogen and sulfur speciation also rising. The number of elements covered this year is again over 20, showing the breadth of the elemental speciation field

    Behavioral implications of shortlisting procedures

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    We consider two-stage “shortlisting procedures” in which the menu of alternatives is first pruned by some process or criterion and then a binary relation is maximized. Given a particular first-stage process, our main result supplies a necessary and sufficient condition for choice data to be consistent with a procedure in the designated class. This result applies to any class of procedures with a certain lattice structure, including the cases of “consideration filters,” “satisficing with salience effects,” and “rational shortlist methods.” The theory avoids background assumptions made for mathematical convenience; in this and other respects following Richter’s classical analysis of preference-maximizing choice in the absence of shortlisting
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