OS43A-2006
The distribution of trace elements in a range of deep-sea sulphide ore deposits and their impact on seafloor mining 

Thursday, 17 December 2015
Poster Hall (Moscone South)
Emily K Fallon1,2, Thomas B Scott2 and Richard A. Brooker3, (1)University of Bristol, Earth Sciences, Bristol, United Kingdom, (2)University of Bristol, Interface Analysis Centre, School of Physics, Bristol, United Kingdom, (3)University of Bristol, Bristol, United Kingdom
Abstract:
Acid rock drainage is a natural weathering process that is often exacerbated by mining activities, common in onshore sulphide ore deposits, that can lead to considerable environmental impact. A similar 'weathering process' occurs at seafloor massive sulphide (SMS) ore deposits. In contrast to the onshore situation, the expected consequence in the marine environment is often considered to be oxide formation, negligible metal release and minimal net acid generation due to the high buffering capacity of seawater and low solubility of iron at near neutral pH. However, no dissolution studies exist that emulate the true composition of sulphide ore deposits that either sit passively on the seafloor or are actively mined in this colder, more saline, and alkaline environment. In particular, these deposits will include a variety of minerals, and it is the interaction of these minerals and inclusions in regards to galvanic cells that can subsequently increase the dissolution of metals into the water column. Any heavy metal release that is not balanced by subsequent oxidation and precipitation, has the potential to produce toxicity for benthic ecosystems, bioaccumulation and dispersal through currents.

The present work has sought to provide a pilot investigation on the deep sea weathering of sulphide minerals, by identifying the mineral phases, trace elements and potential galvanic couples that may arise in sulphide mineral samples collected from various tectonic settings. Samples have been analysed using EMPA and LA-ICPMS in order to identify the range of trace elements and toxins that may be contributed to the water column, especially heavy metals and environmental toxins (e.g. Fe, Cu, Zn, Pb, Co, Ni, Cd, As, Sb, Sn, Hg). Our observations raise important questions about which ore deposits could have more or less environmental impact during any mining activity.

These observations will be used to design oxidative dissolution experiments at deep-sea conditions utilising the natural sulphide ore deposits characterised here. As well as elucidation of the natural weathering process and the economic value of residual deposits, the nature of oxides formed in these experiments may be developed as a tool for detection of deposits associated with inactive vents.