Patrick Cordier | |
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Born | |
Alma mater | University of Lille I |
Awards | - Fellow of the American Geophysical Union (2019) - Fellow of the Mineralogical Society of America (1996) - Dana Medal of the Mineralogical Society of America (2016) - Grand Prix Frédéric Kuhlmann of the Société des Sciences, de l’Agriculture et des Arts de Lille. |
Scientific career | |
Fields | Mineralogy, plasticity, Earth sciences |
Institutions | University of Lille I |
Patrick Cordier (born February 1, 1961) is a mineralogist who uses experimental and numerical approaches to study the plasticity of geological materials. He has authored or co-authored over 200 articles in international scientific journals. He received the Dana Medal from the Mineralogical Society of America in 2016, [1] and is currently a chief editor of the European Journal of Mineralogy . [2] and a member of Institut Universitaire de France . [3]
Cordier obtained a master's degree in materials science in 1985 from the School of Engineers of Lille (EUDIL), [4] and a DEA from the University of Lille 1 [5] in materials science. He completed a doctoral thesis on the plasticity of quartz, directed by Professor Jean-Claude Doukhan, at the University of Lille 1 [5] in 1989.
In 1989, Cordier worked as post-doctoral scientist with Professor Arthur Heuer (Department of Materials Science and Engineering, Case School of Engineering, Cleveland, USA). [6] The same year, he joined the University of Lille 1 as an assistant professor. [5] He passed his habilitation to lead scientific research in 1995 at Lille, and became an associate professor of physics in 1996. At the 'Unité Materiaux Transformations' research institute of the University of Lille, he led the research group for Mineral Physics from 1999 to 2017, and the research group for Plasticity from 2017 to 2020. [7]
Cordier is a specialist in transmission electron microscopy and has devoted himself particularly to the study of crystal defects such as dislocations and the plasticity of minerals. In particular, he studies the plasticity of the high-pressure mineral phases of the Earth's mantle. With Philippe Carrez, he is currently developing an approach to this problem based on multi-scale numerical modelling.
He has regularly visited at the Bayerisches Geoinstitut [8] (Bayreuth, Germany) at the University of Bayreuth since 1998 to carry out deformation experiments at very high pressures and is presently a visiting professor at the Institute of Mechanics, Materials and Civil Engineering of the Université Catholique de Louvain, Belgium.
Cordier has received French recognition for distinguished service in education (Ordre des Palmes Académiques, Chevalier in 2008; Officier in 2013), and the Grand Prix Frédéric Kuhlmann of the Société des Sciences, de l’Agriculture et des Arts de Lille (SSAAL) in 2015. [9] [ circular reference ]
He has also been a fellow of the Mineralogical Society of America since 2008 and received the Dana Medal from them in 2016. [1]
In 2019, he became the first French fellow of the American Geophysical Union in the focus group 'Mineral and Rock Physics'. [10] The same year he was elected at Institut Universitaire de France as a senior member.
He is the current president (2018–2020) of the International Mineralogical Association (IMA). [11] He has also served as the first vice-president (2016–2018) of the IMA, [11] and the vice-president (2004–2007) and president (2008–2009) of the French Mineralogical Society (Société Française de Minéralogie et Cristallographie). [12]
He has twice received ERC-Adv grants, for the projects RheoMan (2011–2017) [13] and TimeMan (2018–2022). [14]
In 2022, he was elected a member of the Academia Europaea. [15]
The mineral olivine is a magnesium iron silicate with the chemical formula (Mg,Fe)2SiO4. It is a type of nesosilicate or orthosilicate. The primary component of the Earth's upper mantle, it is a common mineral in Earth's subsurface, but weathers quickly on the surface. Olivine has many uses, such as the gemstone peridot, as well as industrial applications like metalworking processes.
A perovskite is any material of formula ABX3 with a crystal structure similar to that of the mineral perovskite, which consists of calcium titanium oxide (CaTiO3). The mineral was first discovered in the Ural mountains of Russia by Gustav Rose in 1839 and named after Russian mineralogist L. A. Perovski (1792–1856). 'A' and 'B' are two positively charged ions (i.e. cations), often of very different sizes, and X is a negatively charged ion (an anion, frequently oxide) that bonds to both cations. The 'A' atoms are generally larger than the 'B' atoms. The ideal cubic structure has the B cation in 6-fold coordination, surrounded by an octahedron of anions, and the A cation in 12-fold cuboctahedral coordination. Additional perovskite forms may exist where both/either the A and B sites have a configuration of A1x-1A2x and/or B1y-1B2y and the X may deviate from the ideal coordination configuration as ions within the A and B sites undergo changes in their oxidation states.
Periclase is a magnesium mineral that occurs naturally in contact metamorphic rocks and is a major component of most basic refractory bricks. It is a cubic form of magnesium oxide (MgO). In nature it usually forms a solid solution with wüstite (FeO) and is then referred to as ferropericlase or magnesiowüstite.
Forsterite (Mg2SiO4; commonly abbreviated as Fo; also known as white olivine) is the magnesium-rich end-member of the olivine solid solution series. It is isomorphous with the iron-rich end-member, fayalite. Forsterite crystallizes in the orthorhombic system (space group Pbnm) with cell parameters a 4.75 Å (0.475 nm), b 10.20 Å (1.020 nm) and c 5.98 Å (0.598 nm).
Earth's mantle is a layer of silicate rock between the crust and the outer core. It has a mass of 4.01×1024 kg (8.84×1024 lb) and makes up 67% of the mass of Earth. It has a thickness of 2,900 kilometers (1,800 mi) making up about 46% of Earth's radius and 84% of Earth's volume. It is predominantly solid but, on geologic time scales, it behaves as a viscous fluid, sometimes described as having the consistency of caramel. Partial melting of the mantle at mid-ocean ridges produces oceanic crust, and partial melting of the mantle at subduction zones produces continental crust.
Post-perovskite (pPv) is a high-pressure phase of magnesium silicate (MgSiO3). It is composed of the prime oxide constituents of the Earth's rocky mantle (MgO and SiO2), and its pressure and temperature for stability imply that it is likely to occur in portions of the lowermost few hundred km of Earth's mantle.
Melilite refers to a mineral of the melilite group. Minerals of the group are solid solutions of several endmembers, the most important of which are gehlenite and åkermanite. A generalized formula for common melilite is (Ca,Na)2(Al,Mg,Fe2+)[(Al,Si)SiO7]. Discovered in 1793 near Rome, it has a yellowish, greenish-brown color. The name derives from the Greek words meli (μέλι) "honey" and lithos (λίθους) "stone".The name refers to a group of minerals (melilite group) with chemically similar composition, nearly always minerals in åkermanite-gehlenite series.
Raymond Jeanloz is a professor of Earth and planetary science (EPS) and Astronomy at the University of California, Berkeley. Educated at the California Institute of Technology, Amherst College and at Deep Springs College, his research contributions have been fundamental to understanding of the composition of the Earth and the behavior of materials under high temperatures and pressures. Jeanloz has created tools and experiments that enable him to recreate and study deep interior conditions in a laboratory setting, He is working with colleagues to investigate the conditions inside supergiant exoplanets.
Ringwoodite is a high-pressure phase of Mg2SiO4 (magnesium silicate) formed at high temperatures and pressures of the Earth's mantle between 525 and 660 km (326 and 410 mi) depth. It may also contain iron and hydrogen. It is polymorphous with the olivine phase forsterite (a magnesium iron silicate).
Majorite is a mineral found in the mantle of the Earth. Its chemical formula is Mg3(MgSi)(SiO4)3. It is a type of garnet, distinguished from other garnets in having silicon in octahedral as well as tetrahedral coordination. Majorite was first described in 1970 from the Coorara Meteorite of Western Australia and has been reported from various other meteorites in which majorite is thought to result from an extraterrestrial high pressure shock event. Mantle-derived xenoliths containing majorite have been reported from potassic ultramafic magmas on Malaita Island on the Ontong Java Plateau in the southwest Pacific Ocean.
Pyrolite is a term used to characterize a model composition of the Earth's mantle. This model is based on that a pyrolite source can produce mid-ocean ridge basalts (MORB) by partial melting. It was first proposed by Ted Ringwood (1962) as being 1 part basalt and 4 parts harzburgite, but later was revised to being 1 part tholeiitic basalt and 3 parts dunite. The term is derived from the mineral names PYR-oxene and OL-ivine. However, whether pyrolite is entirely representative of the Earth's mantle remains debated.
Ferropericlase or magnesiowüstite is a magnesium/iron oxide with the chemical formula (Mg,Fe)O that is interpreted to be one of the main constituents of the Earth's lower mantle together with the silicate perovskite, a magnesium/iron silicate with a perovskite structure. Ferropericlase has been found as inclusions in a few natural diamonds. An unusually high iron content in one suite of diamonds has been associated with an origin from the lowermost mantle. Discrete ultralow-velocity zones in the deepest parts of the mantle, near the Earth's core, are thought to be blobs of ferropericlase, as seismic waves are significantly slowed as they pass through them, and ferropericlase is known to have this effect at the high pressures and temperatures found deep within the Earth's mantle. In May 2018, ferropericlase was shown to be anisotropic in specific ways in the high pressures of the lower mantle, and these anisotropies may help seismologists and geologists to confirm whether those ultra-low velocity zones are indeed ferropericlase, by passing seismic waves through them from various different directions and observing the exact amount of change in the velocity of those waves.
Akimotoite is a rare silicate mineral in the ilmenite group of minerals, with the chemical formula (Mg,Fe)SiO3. It is polymorphous with pyroxene and with bridgmanite, a natural silicate perovskite that is the most abundant mineral in Earth's silicate mantle. Akimotoite has a vitreous luster, is colorless, and has a white or colorless streak. It crystallizes in the trigonal crystal system in space group R3. It is the silicon analogue of geikielite (MgTiO3).
Tenham meteorites are the fragments of a larger meteorite that fell in 1879 in a remote area of Australia near the Tenham station, South Gregory, in western Queensland. Although the fall was seen by a number of people, its exact date has not been established. Bright meteors were seen to be moving roughly from west to east. Stones were subsequently recovered from over a large area, about 20 kilometres (12 mi) long by 5 kilometres (3.1 mi) wide.
In chemistry, germanate is a compound containing an oxyanion of germanium. In the naming of inorganic compounds it is a suffix that indicates a polyatomic anion with a central germanium atom, for example potassium hexafluorogermanate, K2GeF6.
Geikielite is a magnesium titanium oxide mineral with formula: MgTiO3. It is a member of the ilmenite group. It crystallizes in the trigonal system forming typically opaque, black to reddish black crystals.
Silicate perovskite is either (Mg,Fe)SiO3 or CaSiO3 when arranged in a perovskite structure. Silicate perovskites are not stable at Earth's surface, and mainly exist in the lower part of Earth's mantle, between about 670 and 2,700 km depth. They are thought to form the main mineral phases of the lower mantle, together with ferropericlase.
Mantle oxidation state (redox state) applies the concept of oxidation state in chemistry to the study of the Earth's mantle. The chemical concept of oxidation state mainly refers to the valence state of one element, while mantle oxidation state provides the degree of decreasing of increasing valence states of all polyvalent elements in mantle materials confined in a closed system. The mantle oxidation state is controlled by oxygen fugacity and can be benchmarked by specific groups of redox buffers.
The lower mantle, historically also known as the mesosphere, represents approximately 56% of Earth's total volume, and is the region from 660 to 2900 km below Earth's surface; between the transition zone and the outer core. The preliminary reference Earth model (PREM) separates the lower mantle into three sections, the uppermost (660–770 km), mid-lower mantle (770–2700 km), and the D layer (2700–2900 km). Pressure and temperature in the lower mantle range from 24–127 GPa and 1900–2600 K. It has been proposed that the composition of the lower mantle is pyrolitic, containing three major phases of bridgmanite, ferropericlase, and calcium-silicate perovskite. The high pressure in the lower mantle has been shown to induce a spin transition of iron-bearing bridgmanite and ferropericlase, which may affect both mantle plume dynamics and lower mantle chemistry.
Davemaoite is a high-pressure calcium silicate perovskite (CaSiO3) mineral with a distinctive cubic crystal structure. It is named after geophysicist Ho-kwang (Dave) Mao, who pioneered in many discoveries in high-pressure geochemistry and geophysics.
Patrick Cordier publications indexed by Google Scholar