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Description
As the detection of planets become commonplace around our neighboring stars, scientists can now begin exploring their possible properties and habitability. Using statistical analysis I determine a true range of elemental compositions amongst local stars and how this variation could affect possible planetary systems. Through calculating and analyzing the variation in elemental abundances of nearby stars, the actual range in stellar abundances can be determined using statistical methods. This research emphasizes the diversity of stellar elemental abundances and how that could affect the environment from which planets form. An intrinsic variation has been found to exist for almost all of the elements studied by most abundance-finding groups. Specifically, this research determines abundances for a set of 458 F, G, and K stars from spectroscopic planet hunting surveys for 27 elements, including: C, O, Na, Mg, Al, Si, S, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Mo, Ba, La, Ce, Nd, Eu, and Hf. Abundances of the elements in many known exosolar planet host stars are calculated for the purpose investigating new ways to visualize how stellar abundances could affect planetary systems, planetary formation, and mineralogy. I explore the Mg/Si and C/O ratios as well as place these abundances on ternary diagrams with Fe. Lastly, I emphasize the unusual stellar abundance of τ Ceti. τ Ceti is measured to have 5 planets of Super-Earth masses orbiting in near habitable zone distances. Spectroscopic analysis finds that the Mg/Si ratio is extremely high (~2) for this star, which could lead to alterations in planetary properties. τ Ceti's low metallicity and oxygen abundance account for a change in the location of the traditional habitable zone, which helps clarify a new definition of habitable planets.
ContributorsPagano, Michael (Author) / Young, Patrick (Thesis advisor) / Shim, Sang-Heon (Committee member) / Patience, Jennifer (Committee member) / Desch, Steven (Committee member) / Anbar, Ariel (Committee member) / Arizona State University (Publisher)
Created2014
Description
Seismic observations have revealed two large low shear velocity provinces (LLSVPs) in the lowermost mantle beneath Pacific and Africa. One hypothesis for the origin of LLSVPs is that they are caused by accumulation of subducted oceanic crust on the core-mantle boundary (CMB). Here, I perform high resolution geodynamical calculations to test this hypothesis. The result shows that it is difficult for a thin (~ 6 km) subducted oceanic crust to accumulate on the CMB, and the major part of it is viscously stirred into the surrounding mantle. Another hypothesis for the origin of LLSVPs is that they are caused by thermochemical piles of more-primitive material which is remnant of Earth's early differentiation. In such case, a significant part of the subducted oceanic crust would enter the more-primitive reservoir, while other parts are either directly entrained into mantle plumes forming on top of the more-primitive reservoir or stirred into the background mantle. As a result, mantle plumes entrain a variable combination of compositional components including more-primitive material, old oceanic crust which first enters the more-primitive reservoir and is later entrained into mantle plumes with the more-primitive material, young oceanic crust which is directly entrained into mantle plumes without contacting the more-primitive reservoir, and depleted background mantle material. The result reconciles geochemical observation of multiple compositional components and varying ages of oceanic crust in the source of ocean-island basalts. Seismic studies have detected ultra-low velocity zones (ULVZs) in some localized regions on the CMB. Here, I present 3D thermochemical calculations to show that the distribution of ULVZs provides important information about their origin. ULVZs with a distinct composition tend to be located at the edges of LLSVPs, while ULVZs solely caused by partial melting tend to be located inboard from the edges of LLSVPs. This indicates that ULVZs at the edges of LLSVPs are best explained by distinct compositional heterogeneity, while ULVZs located insider of LLSVPs are better explained by partial melting. The results provide additional constraints for the origin of ULVZs.
ContributorsLi, Mingming (Author) / McNamara, Allen K (Thesis advisor) / Garnero, Edward J (Committee member) / Shim, Sang-Heon (Committee member) / Tyburczy, James (Committee member) / Clarke, Amanda (Committee member) / Arizona State University (Publisher)
Created2015
Description
Oxygen fugacity (ƒO2) is a thermodynamic variable used to represent the redox state of a material or a system. It is equivalent to the partial pressure of oxygen in a particular environment corrected for the non-ideal behavior of the gas. ƒO2 is often used to indicate the potential for iron to occur in a more oxidized or reduced state at a particular temperature and pressure in a natural system. Secondary ion mass spectrometry (SIMS) is a powerful analytical instrument that can be used to analyze elemental and isotopic compositional information about microscopic features within solid materials. SIMS analyses of the secondary ion energy distribution of semi-pure metals demonstrate that the energy spectrum of individual mass lines can provide information about alterations in its surface environment.
The application of high-resolution (see Appendix C) energy spectrum calibrations to natural ilmenite led to the investigation of zirconium (90Zr+) and niobium (93Nb+) as potential indicators of sample ƒO2. Energy spectrum measurements were performed on an array of ilmenite crystals from the earth’s upper mantle retrieved from kimberlites and from a reduced meteorite. In all studied materials, variability in the peak shape and width of the energy spectra has been correlated with inferred sample ƒO2. The best descriptor of this relationship is the full-width at half-maximum (FWHM; see Appendix C) of the energy spectra for each sample. It has been estimated that a 1eV change in the FWHM of 93Nb+ energy spectra is roughly equivalent to 1 log unit ƒO2. Simple estimates of precision suggest the FWHM values can be trusted to 1eV and sample ƒO2 can be predicted to ±1 log unit, assuming the temperature of formation is known.
The work of this thesis also explores the applicability of this technique beyond analysis of semi-pure metals and ilmenite crystals from kimberlites. This technique was applied to titanium oxides experimentally formed at known ƒO2 as well as an ilmenite crystal that showed compositional variations across the grain (i.e., core to rim chemical variations). Analyses of titanium oxides formed at known ƒO2 agree with the estimation that 1 eV change in the FWHM of 93Nb+ is equivalent to ~1 log unit ƒO2 (in all cases but one); this is also true for analyses of a natural ilmenite crystal with compositional variations across the grain.
The application of high-resolution (see Appendix C) energy spectrum calibrations to natural ilmenite led to the investigation of zirconium (90Zr+) and niobium (93Nb+) as potential indicators of sample ƒO2. Energy spectrum measurements were performed on an array of ilmenite crystals from the earth’s upper mantle retrieved from kimberlites and from a reduced meteorite. In all studied materials, variability in the peak shape and width of the energy spectra has been correlated with inferred sample ƒO2. The best descriptor of this relationship is the full-width at half-maximum (FWHM; see Appendix C) of the energy spectra for each sample. It has been estimated that a 1eV change in the FWHM of 93Nb+ energy spectra is roughly equivalent to 1 log unit ƒO2. Simple estimates of precision suggest the FWHM values can be trusted to 1eV and sample ƒO2 can be predicted to ±1 log unit, assuming the temperature of formation is known.
The work of this thesis also explores the applicability of this technique beyond analysis of semi-pure metals and ilmenite crystals from kimberlites. This technique was applied to titanium oxides experimentally formed at known ƒO2 as well as an ilmenite crystal that showed compositional variations across the grain (i.e., core to rim chemical variations). Analyses of titanium oxides formed at known ƒO2 agree with the estimation that 1 eV change in the FWHM of 93Nb+ is equivalent to ~1 log unit ƒO2 (in all cases but one); this is also true for analyses of a natural ilmenite crystal with compositional variations across the grain.
ContributorsDillon, Sarah Marie (Author) / Hervig, Richard L (Thesis advisor) / Shim, Sang-Heon (Committee member) / Williams, Peter (Committee member) / Arizona State University (Publisher)
Created2019
Description
Amorphous phases are detected over large regions of the Martian surface from orbit and in more localized deposits by rovers on the surface. Amorphous silicates can be primary or secondary in origin, both having formed through very different processes, so the unambiguous identification of these phases is important for understanding the geologic history of Mars. Secondary amorphous silicates are poorly understood and underrepresented in spectral libraries because they lack the long-range structural order that makes their crystalline counterparts identifiable in most analytical techniques. Fortunately, even amorphous materials have some degree of short-range order so that distinctions can be made with careful characterization.
Two sets of laboratory experiments were used to produce and characterize amorphous weathering products under probable conditions for the Martian surface, and one global spectral analysis using thermal-infrared (TIR) data from the Thermal Emission Spectrometer (TES) instrument was used to constrain variations in amorphous silicates across the Martian surface. The first set of experiments altered crystalline and glassy basalt samples in an open system under strong (pH 1) and moderate (pH 3) acidic conditions. The second set of experiments simulated a current-day Martian weathering scenario involving transient liquid water where basalt glass weathering solutions, formed in circumneutral (pH ~5.5 and 7) conditions, were rapidly evaporated, precipitating amorphous silicates. The samples were characterized using visible and near-infrared (VNIR) spectroscopy, TIR spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD).
All experiments formed amorphous silicate phases that are new to spectral libraries. Moderately acidic alteration experiments produced no visible or spectral evidence of alteration products, whereas exposure of basalt glass to strongly acidic fluids produced silica-rich alteration layers that are spectrally consistent with VNIR and TIR spectra from the circum-polar region of Mars, indicating this region has undergone acidic weathering. Circum-netural pH basalt weathering solution precipitates are consistent with amorphous materials measured by rovers in soil and rock surface samples in Gale and Gusev Craters, suggesting transient water interactions over the last 3 billion years. Global spectral analyses determine that alteration conditions have varied across the Martian surface, and that alteration has been long lasting.
Two sets of laboratory experiments were used to produce and characterize amorphous weathering products under probable conditions for the Martian surface, and one global spectral analysis using thermal-infrared (TIR) data from the Thermal Emission Spectrometer (TES) instrument was used to constrain variations in amorphous silicates across the Martian surface. The first set of experiments altered crystalline and glassy basalt samples in an open system under strong (pH 1) and moderate (pH 3) acidic conditions. The second set of experiments simulated a current-day Martian weathering scenario involving transient liquid water where basalt glass weathering solutions, formed in circumneutral (pH ~5.5 and 7) conditions, were rapidly evaporated, precipitating amorphous silicates. The samples were characterized using visible and near-infrared (VNIR) spectroscopy, TIR spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD).
All experiments formed amorphous silicate phases that are new to spectral libraries. Moderately acidic alteration experiments produced no visible or spectral evidence of alteration products, whereas exposure of basalt glass to strongly acidic fluids produced silica-rich alteration layers that are spectrally consistent with VNIR and TIR spectra from the circum-polar region of Mars, indicating this region has undergone acidic weathering. Circum-netural pH basalt weathering solution precipitates are consistent with amorphous materials measured by rovers in soil and rock surface samples in Gale and Gusev Craters, suggesting transient water interactions over the last 3 billion years. Global spectral analyses determine that alteration conditions have varied across the Martian surface, and that alteration has been long lasting.
ContributorsSmith, Rebecca (Author) / Christensen, Philip R. (Philip Russel) (Thesis advisor) / Shock, Everett (Committee member) / Hartnett, Hilairy (Committee member) / Shim, Sang-Heon (Committee member) / Sharp, Thomas (Committee member) / Arizona State University (Publisher)
Created2016
Description
Though large amounts of nitrogen are allocated to the Earth's mantle, not much is known concerning how it is stored and transported. In this study, stishovite is proposed as a host for nitrogen within the Earth's deep interior. Stishovite was synthesized and heated under nitrogen rich conditions using diamond-anvil cell equipment and double-sided laser heating. Synthesis pressures ranged from 16 to 44 GPa and temperatures centered at ~1800 K. Experimental products were removed from diamond anvil cells and analyzed for nitrogen content via SIMS and SEM/EDX analysis. Unit cell parameters were obtained through XRD analysis. N solubility in stishovite was calculated to be up to 1.54 wt % from SIMS data through the use of an ion implant and a relative sensitivity factor. XRD data indicated a decrease in unit cell volume at higher pressures, with the c-axis length showing larger compressibility than the a-axis length. Through SEM and EDX analysis, a uniformly low level of N was observed throughout the sample indicating that N was uniformly incorporated into the crystal structure of stishovite. The data suggests that, rather than existing separately from stishovite as a silicon or carbon nitride, N has substituted into the crystal structure of stishovite. Both O and N have largely similar atomic radii, with N being slightly smaller, indicating that N can substitute for O. With the levels of N observed in the experiment, it is implicated that the mantle has an extremely large storage capacity for N. Further experimentation, with the addition of TEM analysis, should be conducted in order to determine the effects of pressure and temperature on the solubility of N in stishovite. Additionally, substitution of N as HN into stishovite should be investigated as HN accounts for the charge imbalance seen when substituting N for O.
ContributorsNoble, Shaela Marie (Author) / Shim, Sang-Heon (Thesis director) / Hervig, Richard (Committee member) / School of Life Sciences (Contributor) / School of Molecular Sciences (Contributor) / Barrett, The Honors College (Contributor) / School of Earth and Space Exploration (Contributor)
Created2016-05
Description
Chemical composition affects virtually all aspects of astrobiology, from stellar astrophysics to molecular biology. We present a synopsis of the research results presented at the “Stellar Stoichiometry” Workshop Without Walls hosted at Arizona State University April 11–12, 2013, under the auspices of the NASA Astrobiology Institute. The results focus on the measurement of chemical abundances and the effects of composition on processes from stellar to planetary scales. Of particular interest were the scientific connections between processes in these normally disparate fields. Measuring the abundances of elements in stars and giant and terrestrial planets poses substantial difficulties in technique and interpretation. One of the motivations for this conference was the fact that determinations of the abundance of a given element in a single star by different groups can differ by more than their quoted errors.
The problems affecting the reliability of abundance estimations and their inherent limitations are discussed. When these problems are taken into consideration, self-consistent surveys of stellar abundances show that there is still substantial variation (factors of ∼2) in the ratios of common elements (e.g., C, O, Na, Al, Mg, Si, Ca) important in rock-forming minerals, atmospheres, and biology. We consider how abundance variations arise through injection of supernova nucleosynthesis products into star-forming material and through photoevaporation of protoplanetary disks. The effects of composition on stellar evolution are substantial, and coupled with planetary atmosphere models can result in predicted habitable zone extents that vary by many tens of percent. Variations in the bulk composition of planets can affect rates of radiogenic heating and substantially change the mineralogy of planetary interiors, affecting properties such as convection and energy transport.
ContributorsYoung, Patrick (Author) / Desch, Steven (Author) / Anbar, Ariel (Author) / Barnes, Rory (Author) / Hinkel, Natalie R. (Author) / Kopparapu, Ravikumar (Author) / Madhusudhan, Nikku (Author) / Monga, Nikhil (Author) / Pagano, Michael (Author) / Riner, Miriam A. (Author) / Scannapieco, Evan (Author) / Shim, Sang-Heon (Author) / Truitt, Amanda (Author) / College of Liberal Arts and Sciences (Contributor)
Created2014-07-01
Description
The presence of ices (H2O and CO2) and liquid water is key to the evolution ofmartian geology, with implications for the potential for past or extant life, and the future
of robotic and human exploration on Mars.
In this dissertation, I present the first direct evidence that the smooth deposits
covering mid-latitude, martian pole-facing slopes are composed of shallow dusty H2O ice
covered by desiccated material. To analyze this H2O ice, I developed the first validated
radiative transfer model for dusty martian snow and glacier ice. I found that these ice
exposures have < 1% dust in them, and discovered the lowest latitude detection of H2O
ice on Mars, at 32.9°S. After observing the ice disappear, and new gully channels form, I
proposed a model for gully formation. In this model, dusty ice gets exposed by slumping,
leading to melting in the subsurface and channels eroding within the ice and the wall rock
beneath. Access to liquid water within this ice could provide potential abodes for any
extant life.
Next, I developed novel methodology to search for CO2 frosts within the entire
Thermal Emission Imaging System (THEMIS) infrared dataset and found that about half
of all gullies overlap with CO2 frost detections. I also used the Thermal Emission
Spectrometer (TES) water vapor retrievals to assess the formation and distribution of
H2O frosts on Mars.
Additionally, I used radar data from the Mars Advanced Radar for Subsurface and
Ionospheric Sounding (MARSIS) instrument to investigate Mars’ ice-rich South Polar Layered Deposits (SPLD). I discovered radar signals similar to those proposed to be
caused by a subglacial lake throughout the martian SPLD.
Finally, I mapped martian polygonal ridge networks thought to represent
fossilized remnants of ancient groundwater near the Perseverance rover landing site with
the help of citizen scientists across a fifth of Mars’ total surface area and analyzed their
thermophysical properties.
All these studies highlight the key role that ices and liquid water have played in
shaping Mars’ landscape through time, and provide an intriguing path forward in martian
exploration and the search for alien life.
ContributorsKhuller, Aditya Rai (Author) / Christensen, Philip R (Thesis advisor) / Ruff, Steven W (Committee member) / Whipple, Kelin X (Committee member) / Sharp, Thomas G (Committee member) / Shim, Sang-Heon (Committee member) / Arizona State University (Publisher)
Created2023
Description
Subsolidus convection in the mantle of Earth is the driving mechanism behind plate tectonics and provides a central framework linking geophysical, geochemical, petrological, hydrological, and biological processes within the system. Seismic observations have revealed mantle heterogeneities in wide-ranging scales from less than tens of to thousands of kilometers. Understanding the origins and dynamics of these anomalies is critical to advance our knowledge on how mantle convection operates and coevolves with the surface system. This dissertation attempts to constrain the past, present and future of mantle dynamics with lines of evidence from seismology, geodynamics, petrology, geochemistry, and astrophysics. Above Earth’s core, two continent-sized large low shear velocity provinces (LLSVPs) beneath Africa and the Pacific Ocean were seismically detected decades ago. Yet their origin, composition, detailed morphology and influence over mantle convection remain elusive. First, I propose the two LLSVPs may represent the mantle remnants of the Moon-forming impactor Theia. I show that the mantle of Theia is intrinsically denser than Earth’s mantle and would have sunk and accumulated into LLSVP-like structures in the deepest mantle after 4.5 billion years. Second, I examined the maximum height of the two LLSVPs and determined that the African LLSVP is ~1,000 km higher than the Pacific counterpart. Using geodynamic simulations, I find the height of a stable LLSVP is mainly controlled by its density and the ambient mantle viscosity. With ~1,000 numerical experiments, I conclude that the origin of the great height difference between the LLSVPs is that the African LLSVP is less dense, and thus less stable than the Pacific LLSVP. Next, I numerically identified another dynamic scenario accounting for the vastly different height of the two LLSVPs, which is caused by catastrophic sinking of accumulated subducted slabs at the 660-km boundary. Last, targeting one ancient carbonatite above the African LLSVP, I show that lithium isotopes in humite measured by nanoscale secondary ion mass spectrometry was able to uncover the signature of a subducted oceanic crust in its magma source, which may return from the interior to the surface by mantle plumes.
ContributorsYuan, Qian (Author) / Li, Mingming (Thesis advisor) / Garnero, Edward (Committee member) / Shim, Sang-Heon (Committee member) / Hervig, Richard (Committee member) / Bose, Maitrayee (Committee member) / Arizona State University (Publisher)
Created2022
Description
The transport of hydrogen to the Earth’s deep interior remains uncertain. The upper mantle minerals have very low hydrogen solubilities (hundreds of ppm). The hydrogen storage capability in the transition zone minerals (2 wt%) is high compared to those of the upper mantle. The hydrogen storage in the lower mantle is not well known. The main minerals in the lower mantle bridgmanite and ferropericlase have very low hydrogen storage capacities (less than 20 ppm). In order to further understand the hydrogen storage in the lower mantle, a series of experiments had been conducted to simulate the environment similar to the Earth’s mantle. The experiments with hydrous Mg2SiO4 ringwoodite (Rw) show that it converts to crystalline dense hydrous silica, stishovite (Stv) or CaCl2-type SiO2(mStv), containing ∼1 wt% H2O together with bridgmanite (Brd) and MgO at the pressure-temperature conditions expected for lower mantle depths between approximately 660 to 1600 km. Brd would break down partially to dense hydrous silica (6–25 mol%) and(Mg,Fe)O in mid-mantle regions with 0.05–0.27 wt% H2O. The hydrous stishovite has a CaCl2 structure, which is common among hydrous minerals in the lower mantle. Based on this observation, I hypothesize the existence of hydrous phases in the lower mantle. The experiments found a new hexagonal iron hydroxide (η-Fe12O18+x/2Hx) between the stability fields of the epsilon and pyrite-type FeOOH at 60–80 GPa and high temperature. The new phase contains less H2O, limiting the H2O transport from the shallow to the deep mantle in the Fe–O–H system. Possible hydrogen storage in Ca-perovskite was studied. CaPv could contain 0.5–1 wt% water and the water in CaPv could distort the crystal structure of CaPv from cubic to tetragonal structure. In conclusion, hydrogen can be stored in hydrous stishovite in the shallower depth of the lower mantle. At greater depth, the new η phase and pyrite-type phase would take over the hydrogen storage. The role of CaPv in deep water storage needs to be considered in future studies.
ContributorsChen, Huawei (Author) / Shim, Sang-Heon (Thesis advisor) / Garnero, Edward (Committee member) / Bose, Maitrayee (Committee member) / Li, Mingming (Committee member) / Leinenweber, Kurt (Committee member) / Arizona State University (Publisher)
Created2019
Description
The interior of Earth is stratified due to gravity. Therefore, the lateral heterogeneities observed as seismic anomalies by seismologists are extremely interesting: they hold the key to understand the composition, thermal status and evolution of the Earth. This work investigates seismic anomalies inside Earth’s lowermost mantle and focuses on patch-like ultra-low velocity zones (ULVZs) found on Earth’s core-mantle boundary (CMB). Firstly, all previous ULVZ studies are compiled and ULVZ locations on the CMB are digitized. The result is a database, which is publicly available online. A key finding is that there is not a simple mapping between the locations of the observed ULVZs and the large low velocities provinces (LLVPs). Instead, ULVZs are more likely to occur near LLVP boundaries. This spatial correlation study supports a compositionally distinct origin for at least some ULVZs. Next, the seismic structure of the basal mantle beneath the Central America is investigated. This region hosts present and past subducted slabs, which could have brought compositionally distinct oceanic basalt all the way down to the CMB. The waveform distortions of a core-reflected seismic phase and a forward modeling method are used to constrain the causes of the CMB structures. In addition to ULVZ structures, isolated patches of thin zones with shear velocity increased by over 10% relative to background mantle are found for the first time. Ultra-high velocity zones (UHVZs) are interspersed with ULVZs and could be caused by subducted mid-ocean ridge basalt (MORB) that undergoes partial melting and melt segregation. Fe-rich partial melt of MORB can form ULVZs, and silica polymorphs (SiO2) and calcium-perovskite (CaPv) rich solid residue can explain the UHVZs. Finally, large-scale heterogeneities in the lowermost mantle are investigated using S waveform broadening observations. Several basal layer models are case-studied via synthetic calculations. S wave arrivals received at a distance larger than 80˚ in a global dataset from large earthquakes between the years 1994 and 2017 are examined and S waveform broadenings are documented. This approach exploits large distance data for the first time, and therefore is complementary to previous studies in terms of sampling locations. One possible explanation of S waveform broadening is velocity discontinuity inside the D″ layer due to the temperature controlled Bm-pPv phase transition.
ContributorsYu, Shule (Author) / Garnero, Edward J (Thesis advisor) / Li, Mingming (Committee member) / Shim, Sang-Heon (Committee member) / Tyburczy, James A. (Committee member) / Till, Christy B. (Committee member) / Arizona State University (Publisher)
Created2020