Contrasting trace element geochemistry in two American and French salt marshes

Abstract

Trace metals were analyzed in the bulk fine phase of two contrasting salt marsh cores on the North Atlantic east (Baie de l'Aiguillon, LaRochelle, France) and west (Lewes, DE, USA) coasts. The purpose is to gauge how the different clay mineral sources and surface sedimentary diagenetic conditions affect the respective trace element geochemistries. It has been established that there is considerably more clay mineral diagenesis at the zone of redox transition in the Delaware core than in the l'Aiguillon core. The Delaware core shows unweathered glacial sedimentary material directly deposited from the continental shelf whereas the l'Aiguillon core is formed from soil clays deposited after river and estuarine transport. Although there is strong Mn redox depletion in the Delaware salt marsh core, and enrichment in the French one at l'Aiguillon, transition elements seem to follow iron content in both cores. The trace pollutant elements Pb, Sn and Zn show pronounced depth profiles in both North Atlantic cores. The Pb, Sn and Zn appear to be carried by clay sources into the French marshes, while appearing to be largely deposited by atmospheric processes as well into the Delaware marsh. Upon deposition, the Zn appears to become decoupled from lead, which is probably more strongly fixed on clays. The Sn seems to be both air transported, and carried as well on non-clay phases contaminated by industrial organo-tins, including antifouling bottom paints. Copper while uniformly enriched in France, probably from use in regional vineyards, appears enriched only near the top at Delaware, suggesting diagenetic recycling in the more abundant peat in the surface. The Cs and Li appear to be tracers for specific soil-derived clay sources in the French core source materials. These observations suggest that clay is a very important carrier in fixing trace elements for historical records as salt marsh sediments.