posted on 2017-01-11, 04:58authored byMathias Egglseder
Banded iron
formations (BIFs) are extraordinary rocks because they provide important
information about the Precambrian atmosphere and hydrosphere, the global rise
of oxygen, and they host the world’s major iron ore deposits. The unique
texture and petrology of BIF, which mainly comprise alternating layers of iron
oxides and chert remain poorly understood. Although the mineral assemblage is
of diagenetic or metamorphic origin, BIF textures are interpreted as
sedimentary structures because no comprehensive study has addressed the
processes that control their compaction, diagenesis and later orogenic
overprints. Iron ore genesis models face similar challenges to explain the
replacement and removal of chert bands by poorly understood fluids, which
dissolve around 50% of the rock volume to form giant residual,
structurally-controlled iron ore deposits.
The aim of this thesis is to determine the coupled nm- to
km-scale processes that controlled the deformation of BIF of the Hamersley
Province (Western Australia), and to evaluate the significance of these
processes for the evolution of BIF textures and iron ore genesis. A
multidisciplinary approach was adopted to characterise BIF and iron ore
mineralisation that combines classical geological disciplines (e.g., field
geology, petrography, structural geology, economic geology) with
state-of-the-art microscopy (SEM: scanning electron microscopy; 3D XRT: 3D
X-ray tomography) and 3D geological modelling.
Deformation and its effects played a fundamental role in the
evolution of BIF and in the formation of iron ore deposits. Chert, composed of
microcrystalline quartz, contains abundant iron oxide nanocrystals, which
explains the red, brown or yellow colours of chert bands. Deformation-induced
dissolution–precipitation creep led to the dissolution of quartz during burial
and subsequent reprecipitation as secondary quartz layers with strong
crystallographic preferred orientations. During this process the iron oxide
nanoparticles encapsulated within chert accumulate residually and finally
transform to iron oxide bands. Instead of recrystallising via a
dissolution/precipitation stage, the iron nanoparticles mainly build individual
iron oxide crystals through the oriented attachment of nanoparticles. This
solid-state mechanism is known as non-classical crystallisation and is
well-known in material science, environmental science, crystal chemistry and
nanotechnology but it has not yet been applied to BIF. Later large-scale
orogenic events led to a reactivation of dissolution–precipitation creep,
leading to the dissolution of quartz, liberation of nanoparticles and proximal
deposition and transformation to secondary iron oxides. Instead of replacing chert
bands, the chemistry of the associated fluids control the amount of quartz
dissolution, nanoparticle transport and their transformation to form either
hematite or goethite ore deposits.
This multiscale and multidisciplinary study provides new
insights into all aspects of BIF and iron ore research. It shows that the iron
oxide layers in BIF formed from nano-sized iron oxide particles, liberated from
dissolved chert layers during deformation. The same physico-chemical processes
were later reactivated and led to the formation of giant iron ore deposits.