Schwertmannite in wet, acid, and oxic microenvironments beneath polar and polythermal glaciers
Schwertmannite in wet, acid, and oxic microenvironments beneath polar and polythermal glaciers
Geology (Boulder) (May 2009) 37 (5): 431-434
- Admiralty Bay
- aerobic environment
- Antarctic ice sheet
- Antarctica
- Arctic region
- authigenic minerals
- crystal growth
- EDS spectra
- electron diffraction data
- experimental studies
- ferrihydrite
- glacial geology
- glaciers
- goethite
- ice sheets
- ice streams
- icebergs
- McMurdo dry valleys
- mineral-water interface
- nanoparticles
- oxidation
- oxides
- pH
- sampling
- schwertmannite
- sediments
- Southern Ocean
- spectra
- subglacial environment
- sulfates
- Svalbard
- Taylor Glacier
- Victoria Land
- Weddell Sea
- West Antarctic ice sheet
- X-ray diffraction data
- X-ray spectra
- Canada Glacier
- Monaco Glacier
Glacial and iceberg sediments contain nanoparticulates of schwertmannite, ferrihydrite, and goethite formed where pyrite was oxidized by dissolved oxygen in aqueous subglacial environments. Schwertmannite, typically found in acid mine drainage, only forms at low pH by the oxidative weathering of pyrite. Stoichiometric models show that these conditions can be created in closed-system microenvironments containing at least 10 (super -4) M dissolved oxygen, where volume ratios of water/pyrite are approximately 10 (super 5) to 10 (super 6) . Ferrihydrite is the only product at higher and lower volume ratios. In these microenvironments the oxidation of pyrite to form schwertmannite is possible in several decades. Schwertmannite and ferrihydrite are metastable in contact with water and are transformed to goethite in <100 yr unless preserved in ice. The presence of these nanoparticulates demonstrates the existence of transient, acidic, and oxic aqueous microenvironments where enhanced biochemical and/or geochemical activity occurs beneath glaciers and ice sheets.