Middle Jurassic terrestrial environmental and floral changes linked to volcanism: Evidence from the Qinghai-Tibet Plateau, China

A 200,000-yr interval of extreme global warming marked the start of the Eocene epoch about 55 million years ago. Negative carbon- and oxygen-isotope excursions in marine and terrestrial sediments show that this event was linked to a massive and rapid (approximately 10,000 yr) input of isotopically depleted carbon. It has been suggested previously that extensive melting of gas hydrates buried in marine sediments may represent the carbon source and has caused the global climate change. Large-scale hydrate melting, however, requires a hitherto unknown triggering mechanism. Here we present evidence for the presence of thousands of hydrothermal vent complexes identified on seismic reflection profiles from the Vøring and Møre basins in the Norwegian Sea. We propose that intrusion of voluminous mantle-derived melts in carbon-rich sedimentary strata in the northeast Atlantic may have caused an explosive release of methane--transported to the ocean or atmosphere through the vent complexes--close to the Palaeocene/Eocene boundary. Similar volcanic and metamorphic processes may explain climate events associated with other large igneous provinces such as the Siberian Traps (approximately 250 million years ago) and the Karoo Igneous Province (approximately 183 million years ago).

Dissolved organic matter (DOM) interacts very strongly with mercury, affecting its speciation, solubility, mobility, and toxicity in the aquatic environment. Strong binding of mercury by DOM is attributed to coordination of mercury at reduced sulfur sites within the organic matter, which are present at concentrations much higher than mercury concentrations found in most natural waters. The ability of organic matter to enhance the dissolution and inhibit the precipitation of mercuric sulfide, a highly insoluble solid, suggests that DOM competes with sulfide for mercury binding. This is confirmed by very high conditional stability constants for mercury-organic sulfur (RSHg+) complexes (10(25)-10(32)) recently reported in literature. DOM appears to play a key role in the photochemical reduction of ionic mercury to elemental mercury and subsequent reoxidation of elemental mercury to ionic mercury, thus affecting volatilization loss and bioavailability of mercury to organisms. DOM affects the production and bioaccumulation of methylmercury, the most bioaccumulative mercury species in fish.