Patricia Dove | |
---|---|
Born | Patricia Ann Martin September 12, 1958 |
Alma mater | Virginia Polytechnic Institute and State University (MS, BS) Princeton University (PhD) |
Awards | Dana Medal (2014) National Academy of Sciences (2012) F.W. Clarke Medal (1996) |
Scientific career | |
Fields | Biomineralization Weathering Mineral Surface Science Carbonate Minerals Silicas Kinetics [1] Thermodynamics |
Institutions | Virginia Tech Georgia Institute of Technology Stanford University |
Thesis | Quartz Dissolution Kinetics in Electrolyte Solutions (1991) |
Doctoral advisors | Alexandra Navrotsky, David Crerar |
Website | geos |
Patricia Martin Dove is an American geochemist. She is a university distinguished professor and the C.P. Miles Professor of Science at Virginia Tech with appointments in the department of Geosciences, department of Chemistry, and department of Materials Science and Engineering. [1] Her research focuses on the kinetics and thermodynamics of mineral reactions with aqueous solutions in biogeochemical systems. Much of her work is on crystal nucleation and growth during biomineralization and biomaterial interactions with mineralogical systems. She was elected a member of the National Academy of Sciences (NAS) in 2012 and currently serves as chair of Class I, Physical and Mathematical Sciences. [2]
Dove grew up on a working farm in Bedford County, Virginia. [3] With the encouragement of her parents, she became interested in science as a child, collecting specimens of tree leaves and Indian arrowhead artifacts in the Piedmont region of Virginia. Dove participated in the local science fairs and presented her research projects on plant growth at the Virginia Junior Academy of Science and the 1976 Westinghouse International Science and Engineering Fair, which later became the Intel International Science and Engineering Fair.
She studied soil science and plant physiology in the Department of Agronomy at Virginia Tech and earned the bachelor's degree in 1980. Under the advisement of J. Donald Rimstidt, she further earned the Master's degree in environmental geochemistry at Virginia Tech with investigations of scorodite solubility and the geochemistry of Brinton Arsenic Mine. [4] Dove completed a PhD degree in 1991 at Princeton University, where she worked with David Crerar [5] to develop the hydrothermal mixed flow reactor (MFR). [6] Using the MFR, she determined the hydrothermal dissolution kinetics of quartz in electrolyte solutions and dissolution of the isostructural sulfate minerals- celestine, anglesite and baryte. [7] Dove subsequently received a National Science Foundation Postdoctoral Fellowship (1991-1993) to work with Michael Hochella in investigations of mineral surface-water interactions at Stanford University using the newly-developed Atomic Force Microscope. [8]
Patricia Dove was born to Fuller Emerson Martin and Lou Ellen Martin, the oldest of four children. She met Joseph Dove at Virginia Tech, and they married in September 1980. They have a daughter, Meredith Dove, and a son, Emerson Dove. Patricia Dove has a life-long passion for horses and has competed in the dressage and reining disciplines.
Dove was an assistant and tenured associate professor in the School of Earth and Atmospheric Sciences at the Georgia Institute of Technology from 1993 to 2000. [8] She returned to her Alma mater, Virginia Polytechnic Institute and State University, in 2000 [8] and leads the Biogeochemistry of Earth Processes research group. In 2008, Dove was appointed the C.P. Miles Professor of Science. In 2013, she was named a university distinguished professor. [3] [9]
Dove and collaborators have made notable contributions to understanding mineral-water interactions in silica geochemistry (gca, pnas_ab) and the biomineralisation of carbonate mineral systems. She combines chemical principles with nanoanalysis and in-situ measurements of crystal nucleation, growth, and dissolution reactions.[ citation needed ]
Using in situ Atomic Force Microscopy they show how elemental impurities are incorporated into the minerals of shells to affect the chemical composition and can be used to reconstruct past environmental conditions. [10] Dove demonstrated that temperature and the magnesium carbonate availability can alter the composition and crystal form of minerals. Other work demonstrated the amino acids and peptides in macromolecules often associated with biomineralizing tissues can act as crystal growth promoters or inhibitors to regulate the rate of skeletal formation. [11]
In 2003, Dove led an international endeavor to establish current knowledge of the chemical processes that control biomineralisation and called for an interdisciplinary endeavor to advance the field using new quantitative and high-resolution experimental and theoretical methods (Napa, California). [12] Over the next decade, many biominerals and synthetic biomaterials were determined to involve small particles rather than by classical crystallization. In 2013, she organized an interdisciplinary workshop to find consensus for the basis of these observations (Berkeley, California). A multi-disciplinary consensus emerged for the concept of Crystallization by Particle Attachment (CPA) that was published in Science and rapidly showing applications to diverse fields. [13] [14] The physical-chemical model for non-classical crystallization hypothesizes how an interplay of thermodynamic and kinetic factors allow the multiple pathways to crystal formation that are observed. [15]
Dove is a charter member of the Virginia Academy of Science, Engineering, and Medicine. [16] The Virginia Academy of Science, Engineering, and Medicine (VASEM) was co-founded by Senator Mark Warner and the presidents of Virginia’s research universities in collaboration with members of the National Academy of Sciences, National Academy of Engineering, and National Academy of Medicine who live or work in the Commonwealth of Virginia. As a state academy, VASEM provides technical expertise to the Virginia government. In 2016, Dove was appointed the second president of VASEM (2016-2019).
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has generic name (help)Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization.
Calcite is a carbonate mineral and the most stable polymorph of calcium carbonate (CaCO3). It is a very common mineral, particularly as a component of limestone. Calcite defines hardness 3 on the Mohs scale of mineral hardness, based on scratch hardness comparison. Large calcite crystals are used in optical equipment, and limestone composed mostly of calcite has numerous uses.
Goethite is a mineral of the diaspore group, consisting of iron(III) oxide-hydroxide, specifically the α-polymorph. It is found in soil and other low-temperature environments such as sediment. Goethite has been well known since ancient times for its use as a pigment. Evidence has been found of its use in paint pigment samples taken from the caves of Lascaux in France. It was first described in 1806 based on samples found in the Hollertszug Mine in Herdorf, Germany. The mineral was named after the German polymath and poet Johann Wolfgang von Goethe (1749–1832).
Dolomite is an anhydrous carbonate mineral composed of calcium magnesium carbonate, ideally CaMg(CO3)2. The term is also used for a sedimentary carbonate rock composed mostly of the mineral dolomite (see Dolomite (rock)). An alternative name sometimes used for the dolomitic rock type is dolostone.
Aragonite is a carbonate mineral and one of the three most common naturally occurring crystal forms of calcium carbonate, the others being calcite and vaterite. It is formed by biological and physical processes, including precipitation from marine and freshwater environments.
Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe2+Fe3+2O4. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.
Dolomite (also known as dolomite rock, dolostone or dolomitic rock) is a sedimentary carbonate rock that contains a high percentage of the mineral dolomite, CaMg(CO3)2. It occurs widely, often in association with limestone and evaporites, though it is less abundant than limestone and rare in Cenozoic rock beds (beds less than about 66 million years in age). The first geologist to distinguish dolomite from limestone was Déodat Gratet de Dolomieu; a French mineralogist and geologist whom it is named after. He recognized and described the distinct characteristics of dolomite in the late 18th century, differentiating it from limestone.
Carbonate rocks are a class of sedimentary rocks composed primarily of carbonate minerals. The two major types are limestone, which is composed of calcite or aragonite (different crystal forms of CaCO3), and dolomite rock (also known as dolostone), which is composed of mineral dolomite (CaMg(CO3)2). They are usually classified based on texture and grain size. Importantly, carbonate rocks can exist as metamorphic and igneous rocks, too. When recrystallized carbonate rocks are metamorphosed, marble is created. Rare igneous carbonate rocks even exist as intrusive carbonatites and, even rarer, there exists volcanic carbonate lava.
Biomineralization, also written biomineralisation, is the process by which living organisms produce minerals, often resulting in hardened or stiffened mineralized tissues. It is an extremely widespread phenomenon: all six taxonomic kingdoms contain members that are able to form minerals, and over 60 different minerals have been identified in organisms. Examples include silicates in algae and diatoms, carbonates in invertebrates, and calcium phosphates and carbonates in vertebrates. These minerals often form structural features such as sea shells and the bone in mammals and birds.
A calcite sea is a sea in which low-magnesium calcite is the primary inorganic marine calcium carbonate precipitate. An aragonite sea is the alternate seawater chemistry in which aragonite and high-magnesium calcite are the primary inorganic carbonate precipitates. The Early Paleozoic and the Middle to Late Mesozoic oceans were predominantly calcite seas, whereas the Middle Paleozoic through the Early Mesozoic and the Cenozoic are characterized by aragonite seas.
An aragonite sea contains aragonite and high-magnesium calcite as the primary inorganic calcium carbonate precipitates. The chemical conditions of the seawater must be notably high in magnesium content relative to calcium for an aragonite sea to form. This is in contrast to a calcite sea in which seawater low in magnesium content relative to calcium favors the formation of low-magnesium calcite as the primary inorganic marine calcium carbonate precipitate.
The molluscshell is typically a calcareous exoskeleton which encloses, supports and protects the soft parts of an animal in the phylum Mollusca, which includes snails, clams, tusk shells, and several other classes. Not all shelled molluscs live in the sea; many live on the land and in freshwater.
Amorphous calcium carbonate (ACC) is the amorphous and least stable polymorph of calcium carbonate. ACC is extremely unstable under normal conditions and is found naturally in taxa as wide-ranging as sea urchins, corals, mollusks, and foraminifera. It is usually found as a monohydrate, holding the chemical formula CaCO3·H2O; however, it can also exist in a dehydrated state, CaCO3. ACC has been known to science for over 100 years when a non-diffraction pattern of calcium carbonate was discovered by Sturcke Herman, exhibiting its poorly-ordered nature.
Titanium in zircon geothermometry is a form of a geothermometry technique by which the crystallization temperature of a zircon crystal can be estimated by the amount of titanium atoms which can only be found in the crystal lattice. In zircon crystals, titanium is commonly incorporated, replacing similarly charged zirconium and silicon atoms. This process is relatively unaffected by pressure and highly temperature dependent, with the amount of titanium incorporated rising exponentially with temperature, making this an accurate geothermometry method. This measurement of titanium in zircons can be used to estimate the cooling temperatures of the crystal and infer conditions during which it crystallized. Compositional changes in the crystals growth rings can be used to estimate the thermodynamic history of the entire crystal. This method is useful as it can be combined with radiometric dating techniques that are commonly used with zircon crystals, to correlate quantitative temperature measurements with specific absolute ages. This technique can be used to estimate early Earth conditions, determine metamorphic facies, or to determine the source of detrital zircons, among other uses.
Pupa Gilbert is an American biophysicist and geobiologist. She has been pioneering synchrotron spectromicroscopy methods since 1989, and she continues to use and develop them today. Since 2004 she has focused on biomineralization in sea urchins, mollusk shells, and tunicates. She and her group are frequent users of the Berkeley-Advanced Light Source.
Jiwchar Ganor is a professor in the Department of Geological and Environmental Sciences at Ben-Gurion University of the Negev, and currently serves as Dean of the Faculty of Natural Sciences.
Michael F. Hochella, Jr. is an American geoscientist and currently a university distinguished professor (Emeritus) at Virginia Tech and a laboratory fellow at Pacific Northwest National Laboratory. He is a Fellow of the American Association for the Advancement of Science, Royal Society of Chemistry, Geochemical Society, European Association of Geochemistry, Mineralogical Society of America, International Association of GeoChemistry, Geological Society of America and American Geophysical Union. His interests are nanogeoscience, minerals, biogeochemistry and geochemistry. Currently among greater than 22,500 citations, his highest cited first-author paper is Nanominerals, mineral nanoparticles, and earth systems at over 940 citations, and published in the journal Science in 2008, and his highest cited co-authored paper is Nanotechnology in the real world: Redeveloping the nanomaterial consumer products inventory at over 1,995 citations, and published in the Beilstein Journal of Nanotechnology in 2015, according to Google Scholar. He is a former President of both the Geochemical Society and the Mineralogical Society of America. He is also the Founder and former Director of NanoEarth, a node of the National Nanotechnology Coordinated Infrastructure (NNCI), an NSF-funded network of 16 centers spread throughout the United States serving as user facilities for cutting edge nanotechnology research. NanoEarth is part of Virginia Tech's Institute for Critical Technology and Applied Science (ICTAS), and headquartered in Blacksburg, Virginia. Hochella has won many honors, medals, and awards for both research and teaching, including the Dana Medal of the Mineralogical Society of America, the Clair C. Patterson Medal of the Geochemical Society, the Geochemistry Division Medal of the American Chemical Society, and the Virginia Outstanding Faculty Award, the highest honor for faculty in the Commonwealth of Virginia.
Lia Addadi is a professor of structural biology at the Weizmann Institute of Science. She works on crystallisation in biology, including biomineralization, interactions with cells and crystallisation in cell membranes. She was elected a member of the National Academy of Sciences (NAS) in 2017 for “distinguished and continuing achievements in original research”, and the American Philosophical Society (2020).
Wendy Li-Wen Mao is an American geologist who is a professor at SLAC National Accelerator Laboratory. Her research considers the mineral physics of planetary interiors, new materials under extreme environments and novel characterisation techniques. In 2021 she was elected Fellow of the European Association of Geochemistry.
Silicon isotope biogeochemistry is the study of environmental processes using the relative abundance of Si isotopes. As the relative abundance of Si stable isotopes varies among different natural materials, the differences in abundance can be used to trace the source of Si, and to study biological, geological, and chemical processes. The study of stable isotope biogeochemistry of Si aims to quantify the different Si fluxes in the global biogeochemical silicon cycle, to understand the role of biogenic silica within the global Si cycle, and to investigate the applications and limitations of the sedimentary Si record as an environmental and palaeoceanographic proxy.