To better address how Mid-Ocean Ridge Basalt (MORB) sulfur isotope composition can be modified by assimilation and/or by immiscible sulfide fractionation, we report sulfur (S), chlorine (Cl) and copper (Cu) abundances together with multiple sulfur isotope composition for 38 fresh basaltic glasses collected on the Pacific-Antarctic ridge. All the studied glasses-with the exception of 8 off-axis samples-exhibit relatively high Cl/K, as the result of pervasive Cl-rich fluid assimilation. This sample set hence offers an opportunity to document both the upper mantle S isotope composition and the effect of hydrothermal fluids assimilation on the S isotope composition of erupted basalts along segments that are devoid of plume influence. Δ33 S and Δ 36 S yield homogenous values within error of Canyon Diablo Troilite (CDT), whereas δ 34 S are variable, ranging between-1.57±0.11‰ and +0.60±0.10‰ with a mean value of-0.64±0.40 ‰ (1σ, vs. V-CDT). The geographic distribution of δ 34 S follows a spike-like pattern, with local 34 S-enrichments by up to +1.30‰ compared to a low-δ 34 S baseline. As hydrothermal massive sulfides are characterized by relative 34 S-enrichments, such first-order variability can be accounted for by hydrothermal sulfide assimilation, a process that would occur for a subset of samples (n=10). Excluding these particular samples, the mean δ 34 S is significantly less variable, averaging at-0.89±0.11‰ (1σ, n=28), a value that we suggest to be representative of the average MORB source value for Pacific-Antarctic basalts. Weak trends between δ 34 S and 206 Pb/ 204 Pb are displayed by such uncontaminated samples suggesting the recycled oceanic crust to have a modest impact on the S budget of mantle. Their positive signs, however, suggest the depleted mantle to have a δ 34 S of-1.40±0.50 ‰. The sub-chondritic 34 S/ 32 S value that was previously observed for the South-Atlantic mantle is here extended to the Pacific-Antarctic domain. Such feature cannot originate from oceanic crust recycling and substantiates the concept of a core-mantle fractionation relict. 2 Antarctic domain. Such feature cannot originate from oceanic crust recycling and substantiates the concept of a core-mantle fractionation relict. 1. Introduction Sulfur is one of the light elements entering the core composition thereby satisfying a part of its 5-10% density deficit (Birch, 1964). More than 97% of terrestrial sulfur would reside in the Earth's core (Dreibus and Palme, 1996), providing an upper estimate of 1.7 wt% S in the core (see also McDonough, 2003). Any S isotopic fractionation between silicate and metal would lead the silicate reservoir to exhibit a 34 S/ 32 S shift with respect to chondrites. Since the landmark study of Thode et al. (1961), however, the sulfur (S) isotope composition of the Earth's mantle is thought to be homogeneous with a mean 34 S of 0.0‰, a value indistinguishable from chondrites that display an average 34 S of +0.04±0.31 ‰ (1 , n=24, Gao and Thiemens, 1993a,b, Orgueil excluded) , n=24, Gao and Thiemens, 1993a,...