Atmospheric contamination of the primary Ne and Ar signal in mid-ocean ridge basalts and its implications for ocean crust formation

Abstract Both, terrestrial and extra-terrestrial applications of noble gases have demonstrated their importance as tracers for source identification, process characterisation and mass and heat flux quantification. However, the interpretation of noble gas isotope data from terrestrial igneous rocks is often complicated by the ubiquitous presence of heavy noble gases (Ne, Ar, Kr, Xe) with an atmospheric origin. Up to now there has been no consensus on how atmospheric noble gases are entrained into igneous rocks. Suggested processes range from contamination during sample preparation to mantle recycling through subduction. Here we present Ne, Ar, Mg, K, and Cl data of fresh glasses from the Mid-Atlantic Ridge north and south of the Ascension Fracture Zone which show that incorporation of atmospheric noble gases into igneous rocks is in general a two-step process: (1) magma contamination by assimilation of altered oceanic crust results in the entrainment of noble gases from air-equilibrated seawater; (2) atmospheric noble gases are adsorbed onto grain surfaces during sample preparation. This implies, considering the ubiquitous presence of the contamination signal, that magma contamination by assimilation of a seawater-sourced component is an integral part of mid-ocean ridge basalt evolution. Combining the results obtained from noble gas and Cl/K data with estimates of crystallisation pressures for the sample suite shows that the magma contamination must have taken place at a depth between 9 and 13 km. Taking thickness estimates for the local oceanic crust into account, this implies that seawater penetration in this area reaches lower crustal levels, indicating that hydrothermal circulation might be an effective cooling mechanism even for the deep parts of the oceanic crust.