Greenop, Rosanna; Hain, Mathis P; Sosdian, Sindia M; Oliver, Kevin I C; Goodwin, Philip; Chalk, Thomas B; Lear, Caroline H; Wilson, Paul A; Foster, Gavin L (2017): Planktic and benthic boron and carbon isotopes from ODP sites 121-758, 165-999, 154-926 and 122-761 [dataset publication series]. PANGAEA, https://doi.org/10.1594/PANGAEA.871900,

---

Supplement to: Greenop, R et al. (2017): A record of Neogene seawate d11B reconstructed from paired d11B analyses on benthic and planktic foraminifera. Climate of the Past, 13(2), 149-170, https://doi.org/10.5194/cp-13-149-2017

The boron isotope composition (d11B) of planktic foraminiferal calcite, which reflects seawater pH, is a well-established proxy for reconstructing palaeo-atmospheric CO2 and seawater carbonate chemistry. However, to translate d11B measurements determined in calcareous fossils into pH we need to know the boron isotope composition of the parent seawater (d11Bsw). While a number of d11Bsw reconstructions exist, the discrepancies between them reveals uncertainties and deficiencies that need to be addressed. Here we present a new d11Bsw record based on the d11B difference between planktic and benthic foraminifera and an estimate of the pH gradient between surface and deep water. We then calculate d11Bsw two different ways. One variant of our method assumes that the pH gradient between surface and deep has remained the same as today over the past 23 Ma; the other uses the d13C gradient between surface and deep to represent change in the pH gradient through time. The results of these two methods of calculating d11Bsw are broadly consistency with each other, however, based on extensive carbon cycle modelling using CYCLOPS and GENIE we favour the d13C gradient method. In our favoured d11Bsw reconstruction, d11Bsw is around 2 per mil lower than today at ~37.5 per mil during the early and middle Miocene and increases to the modern value (39.61 per mil) by ~5 Ma. A similar pattern of change is evident in the seawater composition of three other stable isotope systems, Mg, Li and Ca. Concurrent shifts in the seawater isotopic composition of all four of these elements during the late Miocene, suggest a common forcing mechanism. We hypothesise the most likely cause of these shifts is a change in the isotopic composition of the riverine input, potentially driven by an increase in secondary mineral formation since ~15 Ma.