The magnesium (Mg) isotopic compositions of 40 seawater samples from the Gulf of Mexico and of one seawater sample from the southwest Hawaii area were determined by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) to investigate the homogeneity of Mg isotopes in seawater. The results indicate that the Mg isotopic composition of seawater from the Gulf of Mexico is homogeneous, both vertically and horizontally, with average values for d 25 Mg = À0.43 AE 0.06 (2SD, n = 90). The magnesium isotopic composition of seawater is principally controlled by river water input, carbonate precipitation and oceanic hydrothermal interactions. The homogeneous Mg isotopic composition of seawater indicates a steady-state budget in terms of Mg isotopes in oceans, consistent with a long Mg residence time (~13 Ma). Considering that seawater is homogeneous, readily available in large amounts, can be easily accessed and processed for isotopic analysis, and has an isotopic composition near the middle of the natural range of variation, it is an excellent geostandard for accuracy assessment to rule out analytical artifacts during high-precision Mg isotopic analysis.

Abstract. The stable isotopic composition of water vapour provides information about moisture sources and processes difficult to obtain with traditional measurement techniques. Recently, it has been proposed that the D-excess of water vapour (dv  =  δ2H − 8  ×  δ18O) can provide a diagnostic tracer of continental moisture recycling. However, D-excess exhibits a diurnal cycle that has been observed across a variety of ecosystems and may be influenced by a range of processes beyond regional-scale moisture recycling, including local evaporation (ET) fluxes. There is a lack of measurements of D-excess in evaporation (ET) fluxes, which has made it difficult to assess how ET fluxes modify the D-excess in water vapour (dv). With this in mind, we employed a chamber-based approach to directly measure D-excess in ET (dET) fluxes. We show that ET fluxes imposed a negative forcing on the ambient vapour and could not explain the higher daytime dv values. The low dET observed here was sourced from a soil water pool that had undergone an extended drying period, leading to low D-excess in the soil moisture pool. A strong correlation between daytime dv and locally measured relative humidity was consistent with an oceanic moisture source, suggesting that remote hydrological processes were the major contributor to daytime dv variability. During the early evening, ET fluxes into a shallow nocturnal inversion layer caused a lowering of dv values near the surface. In addition, transient mixing of vapour with a higher D-excess from above the nocturnal inversion modified these values, causing large variability during the night. These results indicate d

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