Composition and Pressure Effects on Partitioning of Ferrous Iron in Iron-Rich Lower Mantle Heterogeneities

Both seismic observations of dense low shear velocity regions and models of magma ocean crystallization and mantle dynamics support enrichment of iron in Earth’s lowermost mantle. Physical properties of iron-rich lower mantle heterogeneities in the modern Earth depend on distribution of iron between coexisting lower mantle phases (Mg,Fe)O magnesiowüstite, (Mg,Fe)SiO3 bridgmanite, and (Mg,Fe)SiO3 post-perovskite. The partitioning of iron between these phases was investigated in synthetic ferrous-iron-rich olivine compositions (Mg0.55Fe0.45)2SiO4 and (Mg0.28Fe0.72)2SiO4 at lower mantle conditions ranging from 33–128 GPa and 1900–3000 K in the laser-heated diamond anvil cell. The resulting phase assemblages were characterized by a combination of in situ X-ray diffraction and ex situ transmission electron microscopy. The exchange coefficient between bridgmanite and magnesiowüstite decreases with pressure and bulk Fe# and increases with temperature. Thermodynamic modeling determines that incorporation and partitioning of iron in bridgmanite are explained well by excess volume associated with Mg-Fe exchange. Partitioning results are used to model compositions and densities of mantle phase assemblages as a function of pressure, FeO-content and SiO2-content. Unlike average mantle compositions, iron-rich compositions in the mantle exhibit negative dependence of density on SiO2-content at all mantle depths, an important finding for interpretation of deep lower mantle structures.

From 2D to 3D Characterization of Materials Subjected to Extreme Pressure and Temperature Conditions

Farhang Nabiei

Planetesimal were the first planetary objects to form in the solar system, which later grew to make the proto-planets. Most of these bodies were differentiated as a result of internal heating. Several differentiated bodies have, then, been accreted following the giant impacts to create the terrestrial planets. As a result of these impacts, the newly formed Earth was molten and completely differentiated. Subsequent crystallization has given rise to Earth's current structure. In order to bring new constraints on the differentiation and melting relationship in the planets we have studied natural and synthetic samples corresponding to different stages of planetary evolution through state of the art electron microscopy techniques. We have, first, looked at carbonaceous materials in a ureilite meteorite (Almahata Sitta MS-170). Thin sections from ureilite diamonds were prepared with the focused ion beam (FIB) are observed by transmission electron microscopy and spectroscopy. The morphology of graphite bands in diamonds indicated that they result from the diamond to graphite transformation during a shock event. Moreover, the diamonds in this meteorite with crystallite sizes as large as ~20 ÎŒm can only form under static high-pressure condition of planetary interiors. We have, also, found three types of diamond inclusions in our samples. The majority of these inclusions are euhedral Fe-S inclusions. However, each of these inclusions has three phases, namely: kamacite (Fe, Ni), troilite (FeS), and schreibersite ((Fe, Ni)3 P). The chemical analysis of the intact inclusions shows them to be a stoichiometric phase, (Fe, Ni)3(S, P), that can only form above 21 GPa. The ureilite parent body (UPB) should have had the size about that of Mars to exert necessary pressure to grow the diamond inclusions in the core-mantle boundary. The other two types of inclusions are the Al- and Mg- free chromite, Cr2FeO4, and Ca-Fe phosphates that were previously observed only in iron meteorites. Our results suggest that the diamonds and their inclusions were formed from an S-rich metallic liquid. In the second part of the thesis, we have studied melting and fractional crystallization of the lower mantle using a laser-heated diamond anvil cell (LH-DAC). San Carlos olivine is used as a proxy to the mantle composition. The recovered samples are first analyzed with the 3D chemical tomography using a dual beam FIB instrument. The molten region in all the samples at pressure range from 30 to 71 GPa have at least three distinct zones: a ferropericlase shell (Fp), an intermediate bridgmanite (Brg) region and the Fe-rich melt core. Thin sections from the center of the same samples are analyzed with TEM and energy-dispersive x-ray (EDX) spectroscopy. The results from the samples heated at 45 GPa for 1, 3, and 6 minutes demonstrated that the temperature gradient in the heated zone shrinks through the time and, thus, the crystallization continues toward the center of the heating. Consequently, the melt becomes richer in iron. The melt core also gets more iron-rich with increasing pressure. In fact, in ~70 GPa we observe an Fe-O core with small Si and Mg concentration. This implies that the melt at the bottom of the mantle could become denser than the solid phases and sink down. The presence of the iron-rich melt or the oxides crystallizing from such a melt can explain the ultra-low velocity zones (ULVZs) found in the seismic surveys of the core-mantle boundary.

EPFL2017

Chemical Characterisation of Deep Earth Reservoirs

Hélène Marie Piet

Seismic imaging of the internal Earth has emphasized the inhomogeneity of its mantle. This interface layer of nearly 3000 km surrounding the central metallic core conducts heat released from the latter, which played a significant role in shaping the actual mantle as it currently is. The present state of the deep Earth (mainly the lower mantle and the core) is also a consequence of the physical properties of the material composing them. Large-low shear velocity provinces atop the core-mantle boundary, for example, are composed of a denser material than their surrounding environment but their origin, formation and survival over billions of years to mantle convection, is still largely debated. Here we use chemical partitioning to characterise the current composition of those deep Earth reservoirs and better understand the processes leading to their formation. In the first part, experiments were conducted in the laser-heated diamond anvil cell and the latest advances in microanalysis were used to refine iron partitioning between minerals of the lower mantle. We reconcile long-standing discrepancies in previous partitioning data and show that significant variations of silicate iron content are associated to changing ferric iron incorporation. We also note that such chemical variations might significantly affect the physical properties of the silicate, which might in turn provoke mantle rheology variations. Our results and observations thus provide a mineral physics based argument for the stabilization of deep Earth reservoirs and especially large structures like large low-shear-velocity provinces (LLSVPs). In the second and numerical part of the thesis, previous results on siderophile (iron-loving) element partitioning between metal and silicate were used to constrain some aspects of core formation. We constrain the chemical and physical state of the magma ocean during core formation explaining both the siderophile composition of the mantle and the light element composition of the core. We simulate the Moon-Forming Giant Impact in the last steps of Earth accretion, where we constrain the size of the impactor to be smaller than 15% of Earth's total mass, a roughly Mars-sized object, and further show that melting of the large fractions of the mantle upon impact by the giant impactor is consistent with siderophile composition of the bulk silicate Earth, which can have great implications for the geodynamical evolution of the mantle. In conclusions, given the fact that the mantle may have been almost fully molten, further crystallization may have isolated a layer of liquid primitive material at the base of the mantle possibly explaining the seismic signature of the LLSVPs associated with a strong thermochemical contrast with the surrounding mantle. The layered composition in iron of the actual mantle also provides a chemical argument for a viscously layered mantle, which could have helped sustain LLSVPs for billions of years from efficient convection.

EPFL2016

Core formation and core composition from coupled geochemical and geophysical constraints

James Badro, Hélène Marie Piet

The formation of Earth's core left behind geophysical and geochemical signatures in both the core and mantle that remain to this day. Seismology requires that the core be lighter than pure iron and therefore must contain light elements, and the geochemistry of mantle-derived rocks reveals extensive siderophile element depletion and fractionation. Both features are inherited from metal-silicate differentiation in primitive Earth and depend upon the nature of physio-chemical conditions that prevailed during core formation. To date, core formation models have only attempted to address the evolution of core and mantle compositional signatures separately, rather than seeking a joint solution. Here we combine experimental petrology, geochemistry, mineral physics and seismology to constrain a range of core formation conditions that satisfy both constraints. We find that core formation occurred in a hot (liquidus) yet moderately deep magma ocean not exceeding 1,800 km depth, under redox conditions more oxidized than present-day Earth. This new scenario, at odds with the current belief that core formation occurred under reducing conditions, proposes that Earth's magma ocean started oxidized and has become reduced through time, by oxygen incorporation into the core. This core formation model produces a core that contains 2.7-5% oxygen along with 2-3.6% silicon, with densities and velocities in accord with radial seismic models, and leaves behind a silicate mantle that matches the observed mantle abundances of nickel, cobalt, chromium, and vanadium.