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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Romain Brossier</dc:contributor>
  <dc:contributor>Sarah E. Janssen</dc:contributor>
  <dc:contributor>Tylor Rosera</dc:contributor>
  <dc:contributor>David P. Krabbenhoft</dc:contributor>
  <dc:contributor>Yves Cherel</dc:contributor>
  <dc:contributor>Paco Bustamante</dc:contributor>
  <dc:contributor>Brett Poulin</dc:contributor>
  <dc:creator>Alain Manceau</dc:creator>
  <dc:date>2021</dc:date>
  <dc:description>&lt;div class="container container_scaled-down"&gt;&lt;div class="row"&gt;&lt;div class="col-xs-12"&gt;&lt;div id="abstractBox" class="article_abstract-content hlFld-Abstract"&gt;&lt;p class="articleBody_abstractText"&gt;A prerequisite for environmental and toxicological applications of mercury (Hg) stable isotopes in wildlife and humans is quantifying the isotopic fractionation of biological reactions. Here, we measured stable Hg isotope values of relevant tissues of giant petrels (&lt;i&gt;Macronectes&lt;/i&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;spp.). Isotopic data were interpreted with published HR-XANES spectroscopic data that document a stepwise transformation of methylmercury (MeHg) to Hg-tetraselenolate (Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;) and mercury selenide (HgSe) (Sec = selenocysteine). By mathematical inversion of isotopic and spectroscopic data, identical δ&lt;sup&gt;202&lt;/sup&gt;Hg values for MeHg (2.69 ± 0.04‰), Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;(−1.37 ± 0.06‰), and HgSe (0.18 ± 0.02‰) were determined in 23 tissues of eight birds from the Kerguelen Islands and Adélie Land (Antarctica). Isotopic differences in δ&lt;sup&gt;202&lt;/sup&gt;Hg between MeHg and Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;(−4.1 ± 0.1‰) reflect mass-dependent fractionation from a kinetic isotope effect due to the MeHg → Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;demethylation reaction. Surprisingly, Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;and HgSe differed isotopically in δ&lt;sup&gt;202&lt;/sup&gt;Hg (+1.6 ± 0.1‰) and mass-independent anomalies (i.e., changes in Δ&lt;sup&gt;199&lt;/sup&gt;Hg of ≤0.3‰), consistent with equilibrium isotope effects of mass-dependent and nuclear volume fractionation from Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;→ HgSe biomineralization. The invariance of species-specific δ&lt;sup&gt;202&lt;/sup&gt;Hg values across tissues and individual birds reflects the kinetic lability of Hg-ligand bonds and tissue-specific redistribution of MeHg and inorganic Hg, likely as Hg(Sec)&lt;sub&gt;4&lt;/sub&gt;. These observations provide fundamental information necessary to improve the interpretation of stable Hg isotope data and provoke a revisitation of processes governing isotopic fractionation in biota and toxicological risk assessment in wildlife.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1021/acs.est.1c04388</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>American Chemical Society</dc:publisher>
  <dc:title>Mercury isotope fractionation by internal demethylation and biomineralization reactions in seabirds: Implications for environmental mercury science</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>