The effects of core formation on the Pb- and Tl- isotopic composition of the silicate Earth Bernard J. Wood a, , Sune G. Nielsen b , Mark Rehkämper c , Alex N. Halliday b a GEMOC, Department of Earth and Planetary Sciences, Macquarie University, NSW 2109, Australia b Department of Earth Sciences, University of Oxford, Parks Road, Oxford OX1 3PR, UK c Impacts and Astromaterial Research Centre (IARC), Department of Earth Science and Engineering, Imperial College, London SW7 2AZ, UK Received 21 June 2007; received in revised form 9 January 2008; accepted 20 January 2008 Editor: G.D. Price Available online 6 February 2008 Abstract We have performed metal-silicate partitioning experiments at 2 GPa and 16502180 °C to investigate the behaviour of Pb and Tl during terrestrial core formation. The aim was to test the hypothesis that metal core formation followed by late sulphide addition to the core resulted in the concentrations and isotopic compositions of Pb and Tl in the silicate Earth. We investigated D Pb met/sil and D TL met/sil as functions of the sulphur content of the metal and measured the equilibrium Tl isotope fractionation between the coexisting phases. Lead is moderately siderophile under the likely conditions (initially reducing [Wade, J., Wood, B.J., Core formation and the oxidation state of the Earth, Earth Planet. Sci. Lett. 236(2005) 7895.]) of core segregation on Earth so that the μ( 238 U/ 204 Pb) of the bulk silicate Earth should have increased by a factor of 6.5 (D Pb 13) as the core separated. In the case of Tl, core segregation should have reduced the Tl concentration of the BSE by about 50%. Neither the Pb nor Tl isotopic compositions of the bulk silicate Earth can, however, be completely explained by S-free iron core formation. Thallium isotopes were found not to be significantly fractionated by metal or sulphide separation from silicate. Addition of sulphur to the metal greatly increases metal-silicate partition coefficients for both Pb and Tl. D Pb met/sil increases by a factor of 15 and D TL met/sil by a factor of 45 as S increases from 0 to 35% in the metal phase. This means that extraction of sulphide from a molten mantle would result in D Pb sulph/sil of 40 and D TL sulph/sil of 60. We used the latter results to calculate the effects of late sulphide extraction on the Pb and Tl isotopic compositions of the silicate Earth. For a bulk Earth with μ of 0.7 addition of 1.6% sulphide to the core 100140 Myr after the beginning of the solar system is sufficient to displace the Pb-isotopic composition of the silicate Earth into the region indicated by estimates in the literature. The Tl concentration and ɛ 205 Tl of bulk silicate Earth are also consistent with this extent of sulphide addition. Raising μ of the Earth reduces the amount of sulphide addition to the core needed to satisfy the Pb and Tl isotopic constraints but for values of μ above 0.9 (b 0.65% sulphide) the sulphide has insufficient effect. Separation of sulphide from a mixture of silicate crystals and melt would, however, because of the incompatible nature of Pb and Tl amplify the sulphide effect. We show that, for initial μ of 0.7, as little as 0.1% sulphide extraction (at 150200 Myr) from a mixture of 91% crystals and 9% melt would be sufficient to displace the isotopic compositions of Pb and Tl of the BSE to the required values. Late volatile loss of Pb and Tl is, therefore, not required by the partitioning and currently available isotopic data. © 2008 Elsevier B.V. All rights reserved. Keywords: core formation; lead isotopes; thallium isotopes 1. Introduction The earliest history of the Earth was attended by accretion of planetesimals, core formation and late bombardment including the putative moon-forming giant impact (Halliday, 2004). The nature and timing of these accretionary processes are addressed using a range of chronometers whose parent and daughter isotopes have different chemical properties. The short-lived isotope 182 Hf (t 1/2 =9 Myr) which was present at the start of the solar system (Lee and Halliday, 1995) for example, provides a means of estimating the timescales of accretion and core Available online at www.sciencedirect.com Earth and Planetary Science Letters 269 (2008) 325 335 www.elsevier.com/locate/epsl Corresponding author. Fax: +61 2 98506904. E-mail address: bwood@els.mq.edu.au (B.J. Wood). 0012-821X/$ - see front matter © 2008 Elsevier B.V. All rights reserved. doi:10.1016/j.epsl.2008.01.027