Theoretical and experimental investigation of nickel isotopic fractionation in species relevant to modern and ancient oceans

Abstract

Nickel plays a central role as an enzyme co-factor in the metabolism of methanogenic Archaea. Methanogens can fractionate Ni isotopes during assimilation, opening the possibility of using the stable isotopic composition of Ni as a biomarker. However, other sources of Ni isotopic variations need to be evaluated before one can establish Ni isotopes as an unambiguous tracer of methanogenesis in the rock record. Equilibrium exchange of Ni between the different species present in the ocean is a potential source of isotopic fractionation. Through controlled laboratory experiments and theoretical calculations, we quantify equilibrium Ni isotope fractionation between different species relevant to the modern and ancient ocean: Ni(H<inf>2</inf>O)<inf>6</inf> ²⁺, Ni(H<inf>2</inf>O)<inf>18</inf> ²⁺, NiOH(H<inf>2</inf>O)<inf>5</inf> ⁺, Ni(OH)<inf>2</inf>(H<inf>2</inf>O)<inf>4</inf>, NiCl(H<inf>2</inf>O)<inf>5</inf> ⁺, cis-NiCl<inf>2</inf>(H<inf>2</inf>O)<inf>4</inf>, trans-NiCl<inf>2</inf>(H<inf>2</inf>O)<inf>4</inf>, NiHS(H<inf>2</inf>O)<inf>5</inf> ⁺, Ni(HS)<inf>2</inf>(H<inf>2</inf>O)<inf>4</inf>, NiSO<inf>4</inf>(H<inf>2</inf>O)<inf>4</inf>, NiHCO<inf>3</inf>(H<inf>2</inf>O)<inf>4</inf> ⁺, NiCO<inf>3</inf>(H<inf>2</inf>O)<inf>4</inf>, and organic ligands (crown ether and oxalic acid). The magnitude of ligand-controlled Ni isotopic fractionation, approximately 1.25‰/amu (2.5‰ for the ⁶⁰Ni/⁵⁸Ni ratio), is similar to that previously measured in cultures of methanogenic Archaea. © 2010 Elsevier Ltd.