Description: The Asian summer monsoon affects the lives of billions of people. With the aim of identifying geochemical tracers for the monsoon related freshwater input from the major rivers draining into the Bay of Bengal and Andaman Sea we have taken surface seawater samples from various locations up and down the Andaman Islands during 2011. Importantly, in some locations samples have been taken in March, July and November, covering most of a seasonal cycle and different monsoon phases. Samples were collected from the side of small wooden boats or while swimming and were filtered within a few hours at 0.45 or 0.22 microns using the vacuum produced by a water jet or a hand operated peristaltic pump. Filtered and unfiltered samples were acidified to 〈 pH 2 and analysed for Y and the REEs with an automated online preconcentration ICP-MS technique [1]. The local input of REEs from streams and sediment rich areas such as mangrove environments is clearly identified by middle REE enrichments in the shale normalised patterns of some samples. These middle REE bulges accompany large increases in dissolved REE concentrations at some locations, especially for the July samples obtained during the peak monsoon season with frequent storms. Y/Ho fractionation aslo occurs during the local input of dissolved REEs with affected samples having lower Y/Ho ratios. Conversly, some samples, in particular those taken after heavy rainfall in March, show strong REE scavenging accompanied by the prefferential removal of dissolved light REEs and higher Y/Ho ratios. The time series at a location away from local input sources shows remarkably similar REE patterns and concentraions in March and July. Then in October-November, following the peak in monsoon river discharge, the dissolved REE concentration increases by almost a factor of 2. The notable exception to this seasonal pattern is the Ce anomally which is around 0.3 in March and November but 0.6 in July, implying less oxidative removal of Ce(IV) during the peak summer monsoon rains. With the exception of elevated dissolved Ce concentrations, the North Pacific Deep Water normalised REE patterns are similar to those reported for offshore samples from the Bay of Bengal and Andaman Sea [2]. These seawater normalised patterns are distinctive having a middle REE enriched arc with similar light and heavy REE values suggesting the input from large rivers in the region is traceable using seawater REE chemistry. [1] Hathorne et al. (2012), Online preconcentration ICP-MS analysis of rare earth elements in seawater, Geochem. Geophys. Geosyst., 13, Q01020, doi:10.1029/2011GC003907. [2] Amakawa et al. (2000), Geochim. Cosmochim. Acta 64, 1715-1727.

Description: The Asian summer monsoon affects the lives of billions of people. With the aim of identifying geochemical tracers for the monsoon-related freshwater input from the major rivers draining into the Bay of Bengal (BoB) and the Andaman Sea (AnS), we have analyzed the yttrium and rare earth element (YREE) concentration of surface seawater samples from various locations spanning the Andaman Islands in 2011 to 2013. In some locations, samples have been taken in March, July, and November 2011, thus spanning the seasonal cycle and including different monsoon phases. Generally, the YREE patterns are similar to those reported for offshore samples from the BoB and AnS in January 1997, with seawater-normalized patterns of most samples characterized by middle REE enrichments. An enhancement of these middle REE bulges accompanies large increases in dissolved REE concentrations from streams and sediment-rich areas such as mangrove environments. Conversely, some samples, in particular those taken 1–2 days after heavy rainfall in March 2011, show pronounced REE scavenging accompanied by the preferential removal of dissolved light REEs (LREEs) and by higher Y/Ho ratios. The Nd isotope signature of the remaining dissolved REE phase of these low YREE samples is more radiogenic than local rocks and sediments. The time series at a location away from local input sources show remarkably similar REE patterns and concentrations in March and July. Then in October–November, following the peak in monsoon-induced river discharge, the dissolved REE concentrations increase by almost a factor of two, whereas Nd isotopes become less radiogenic by 1.5 εNd units. These unradiogenic values are found at the same site in the winter dry season of the following year, demonstrating the decoupling of sea surface salinity (SSS) and Nd. The large sub-annual variability of YREE concentrations and Nd isotopes encountered was likely caused by the conversion of YREE from the dissolved (probably colloidal) pool to the labile particulate fraction. The comparison of unfiltered and filtered sample concentrations reveals the existence of a large labile particulate pool in the BoB and AnS that most likely originates from the massive river sediment fluxes and is instrumental in the seasonal changes observed.