Tsunami bore runup

Nearshore behaviors of tsunamis, specifically those formed as a single uniform bore, are investigated experimentally in a laboratory environment. The transition process from tsunami bore to runup is described by the momentum exchange process between the bore and the small wedge-shaped water body along the shore: the bore front itself does not reach the shoreline directly, but the large bore mass pushes the small, initially quiescent water in front of it. The fluid motions near the runup water line appear to be complex. The complex flow pattern must be caused by irregularities involved in the driving bore and turbulence advected into the runup flow. Those experimental results suggest that the tsunami actions at the shoreline involve significant mean kinetic energy together with violent turbulence. Even though the behaviors of bore motion were found to be different from those predicted by the shallow-water wave theory, the maximum runup height appears to be predictable by the theory if the value of the initial runup velocity is modified (reduced). Besides the friction effect, this reduction of the initial runup velocity must be related to the transition process as well as the highly interacting three-dimensional runup motion.     

Cr isotopes in physically separated components of the Allende CV3 and Murchison CM2 chondrites: Implications for isotopic heterogeneity in the solar nebula and parent body processes

Chromium isotopic data of physically separated components (chondrules, CAIs, variably magnetic size fractions) of the carbonaceous chondrites Allende and Murchison and bulk rock data of Allende, Ivuna, and Orgueil are reported to evaluate the origin of isotopic heterogeneity in these meteorites. Allende components show ε⁵³Cr and ε⁵⁴Cr from ?0.23 ± 0.07 to 0.37 ± 0.05 and from ?0.43 ± 0.08 to 3.7 ± 0.1, respectively. In components of Murchison, ε⁵³Cr and ε⁵⁴Cr vary from ?0.06 ± 0.08 to 0.5 ± 0.1 and from 0.7 ± 0.2 to 1.7 ± 0.1, respectively. The non‐systematic variations of ε⁵³Cr and ⁵⁵Mn/⁵²Cr in the components of Allende and Murchison were likely caused by small‐scale, alteration‐related redistribution of Mn >20 Ma after formation of the solar system. Chondrule fractions show the lowest ⁵⁵Mn/⁵²Cr and ε⁵⁴Cr values of all components, consistent with evaporation of Mn and ε⁵⁴Cr‐rich carrier phases from chondrule precursors. Components other than the chondrules show higher Mn/Cr and ε⁵⁴Cr, suggestive of chemical and isotopic complementarity between chondrules and matrix‐rich fractions. Bulk rock compositions calculated based on weighted compositions of components agree with measured Cr isotope data of bulk rocks, in spite of the Cr isotopic heterogeneity reported by the present and previous studies. This indicates that on a sampling scale comprising several hundred milligrams, these meteorites sampled isotopically and chemically homogeneous nebular reservoirs. The linear correlation of ⁵⁵Mn/⁵²Cr with ε⁵³Cr in bulk rocks likely was caused by variable fractionation of Mn/Cr, subsequent mixing of phases in nebular domains, and radiogenic ingrowth of ⁵³Cr.     

Mg-rich harzburgites from Vesta: Mantle residua or cumulates from planetary differentiation?

We describe petrographic, electron microprobe, and laser ablation ICP-MS analyses of Mg-rich harzburgite clasts in the Dominion Range 2010 howardites, and conclude that they are xenolithic samples of the vestan mantle. Key chemical and petrologic characteristics of these rocks provide tests for differentiation models. Our results indicate the mantle of Vesta formed through variable degrees of partial melting, which left behind a harzburgite and possibly dunite residuum. The Mg-rich clasts are composed of orthopyroxene and olivine, with minor clinopyroxene, FeNi metal, and distinctive pyroxene–chromite symplectites. We use mineral chemistry to demonstrate the absence of a genetic link between diogenites and the Mg-rich harzburgites. We propose a secondary origin for the formation of symplectites: interaction of silicate and metallic melts during primordial differentiation and core formation. The occurrence of FeNi metal containing ~1.5 wt% Cr within the assemblage indicates a very reducing environment during mantle differentiation (≪IW). Our study suggests that Vesta did not experience complete melting early in its history, and instead supports the formation of a shallow magma ocean.     

Geochemistry of 4 Vesta based on HED meteorites: Prospective study for interpretation of gamma ray and neutron spectra for the Dawn mission

Abstract— Asteroid 4 Vesta, believed to be the parent body of the howardite, eucrite, and diogenite (HED) meteorites, will be investigated by the Dawn orbiting spacecraft. Dawn carries a gamma ray and neutron detector (GRaND) that will measure and map some major‐ and trace‐element abundances. Drawing on HED geochemistry, we propose a mixing model that uses element ratios appropriate for the interpretation of GRaND data. Because the spatial resolution of GRaND is relatively coarse, the analyzed chemical compositions on the surface of Vesta will likely reflect mixing of three endmember components: diogenite, cumulate eucrite, and basaltic eucrite. Reliability of the mixing model is statistically investigated based on published whole‐rock data for HED meteorites. We demonstrate that the mixing model can accurately estimate the abundances of all the GRaND‐analyzed major elements, as well as of minor elements (Na, Cr, and Mn) not analyzed by this instrument. We also show how a similar mixing model can determine the modal abundance of olivine, and we compare estimated and normative olivine data for olivine‐bearing diogenites. By linking the compositions of well‐analyzed HED meteorites with elemental mapping data from GRaND, this study may help constrain the geological context for HED meteorites and provide new insight into the magmatic evolution of Vesta.     

Ordinary (mesostasis) and not‐so‐ordinary (symplectites) late‐stage assemblages in howardites

Abstract– Two categories of symplectites have been observed in howardites: three‐phase, composed of vermicular intergrowths of ferroan augite, fayalitic olivine, and silica, and two‐phase, composed of vermicular intergrowths of orthopyroxene and troilite. Three‐phase symplectites have been previously shown to represent the breakdown products of metastable pyroxene. In howardites, they appear to be genetically related to gabbroic eucrites. In some cases and under yet‐to‐be specified conditions, ferroan clinopyroxene in gabbroic eucrites may undergo only localized decomposition resulting in oriented exsolution‐like features. Breakdown phases in those cases are fayalitic olivine, silica, and—depending on the MgO content of the system—orthopyroxene. As opposed to three‐phase symplectites, two‐phase symplectites are most likely of diogenitic origin. They probably formed via impact‐induced localized melting of diogenitic orthopyroxene in the presence of troilite (grain boundary melting). Three‐phase symplectites in howardites occasionally contain accessory amounts of ilmenite, troilite, and/or kamacite and are exclusively associated with medium‐grained FeO‐rich pyroxene, silica, and plagioclase. All minerals involved are late‐stage crystallites or mesostasis phases. In general, highly evolved eucritic lithologies constitute only a minor fraction of howardites. However, considering that three‐phase symplectites are generated in a low‐pressure, i.e., near‐surface, environment, FeO‐ and CaO‐rich eucritic rocks may be exposed locally on Vesta’s surface. This, in turn, is highly relevant to the ongoing DAWN mission.     

Shock features in iron-nickel metal and troilite of L-group ordinary chondrites

Abstract— Shock metamorphic features in opaque minerals (FeNi metal and troilite) of 22 L chondrites have been studied petrographically and geochemically in an attempt to establish a connection between the present silicate-based shock classification scheme (Stöffler et al., 1991) and the peak-shock and postshock thermal history recorded in these minerals. Unshocked to weakly shocked (S1–S3) L chondrites contain FeNi metal and troilite that display textures related to normal, slow cooling. They may also contain rare disequilibrium shock features, which suggest localized departures from equilibrium shock conditions. Above shock stage S3, selected melting of FeNi metal and troilite produces melt droplets whose composition and abundance correspond to the maximum equilibrium shock state achieved by the sample. At these higher shock levels, the abundance of other shock-induced features, such as polycrystalline kamacite, sheared and fizzed troilite, coarse-grained pearlitic plessite, polycrystalline troilite, and polymineralic melt veins serve as textural criteria that can be used to establish peak-shock conditions. Minimum postshock temperatures obtained from analyses of plessite components show a systematic increase in temperature with an increase in shock stage, thereby providing additional information about the postshock thermal histories of L chondrites. At the highest shock levels recorded in L chondrites (S6 and above), melting and chemical homogenization of FeNi metal produces flattened Ni profiles that may partially to completely obscure any evidence for an earlier, slow-cooling history. All of these features serve as aids for shock classifying L chondrites as well as for quantifying minimum peak temperatures that resulted during shock metamorphism.     

Sulfur cycling in a stratified euxinic lake with moderately high sulfate: Constraints from quadruple S isotopes

We present a 3-year study of concentrations and sulfur isotope values (δ³⁴S, Δ³³S, and Δ³⁶S) of sulfur compounds in the water column of Fayetteville Green Lake (NY, USA), a stratified (meromictic) euxinic lake with moderately high sulfate concentrations (12-16 mM). We utilize our results along with numerical models (including transport within the lake) to identify and quantify the major biological and abiotic processes contributing to sulfur cycling in the system. The isotope values of sulfide and zero-valent sulfur across the redox-interface (chemocline) change seasonally in response to changes in sulfide oxidation processes. In the fall, sulfide oxidation occurs primarily via abiotic reaction with oxygen, as reflected by an increase in sulfide δ³⁴S at the redox interface. Interestingly, S isotope values for zero-valent sulfur sampled at this time still reflect production and recycling by phototrophic S-oxidation. In the spring, sulfide S isotope values suggest an increased input from phototrophic oxidation, consistent with a more pronounced phototroph population at the chemocline. This trend is associated with smaller fractionations between sulfide and zero-valent sulfur, suggesting a metabolic rate control on fractionation similar to that for sulfate reduction. Comparison of our data with previous studies indicates that the S isotope values of sulfate and sulfide in the deep waters are remarkably stable over long periods of time, with consistently large fractionations of up to 58‰ in δ³⁴S. Models of the δ³⁴S and Δ³³S trends in the deep waters (considering mass transport via diffusion and advection along with biological processes) require that these fractionations are a consequence of sulfur compound disproportionation at and below the redox interface in addition to large fractionations during sulfate reduction. The large fractionations during sulfate reduction appear to be a consequence of the high sulfate concentrations and the distribution of organic matter in the water column. The occurrence of disproportionation in the lake is supported by profiles of intermediate sulfur compounds and by lake microbiology, but is not evident from the δ³⁴S trends alone. These results illustrate the utility of including minor S isotopes in sulfur isotope studies to unravel complex sulfur cycling in natural systems.     

Pyroxene thermobarometry in LL-group chondrites and implications for parent body metamorphism

Abstract— Geothermometry based on the compositions of clinopyroxenes in type 6 and 7 LL chondrites gives coherent results, but the estimated temperatures from coexisting orthopyroxenes are consistently lower than for clinopyroxenes. Orthopyroxene thermometry is suspect because of compositional effects of polymorphic inversions and/or unknown kinetic factors. Lack of clinopyroxene equilibration precludes accurate estimation of peak metamorphic temperatures for type 4 and 5 chondrites. There is no apparent correlation between Al content (a pressure-dependent variable) and equilibration temperature in chondritic pyroxenes. This finding, which is at variance with a previously published conclusion that temperature and pressure are correlated in metamorphosed chondrites, may have important implications for asteroid thermal models.     

Metamorphism in the Martian crust

Compositions of basaltic and ultramafic rocks analyzed by Mars rovers and occurring as Martian meteorites allow predictions of metamorphic mineral assemblages that would form under various thermophysical conditions. Key minerals identified by remote sensing roughly constrain temperatures and pressures in the Martian crust. We use a traditional metamorphic approach (phase diagrams) to assess low‐grade/hydrothermal equilibrium assemblages. Basaltic rocks should produce chlorite + actinolite + albite + silica, accompanied by laumontite, pumpellyite, prehnite, or serpentine/talc. Only prehnite‐bearing assemblages have been spectrally identified on Mars, although laumontite and pumpellyite have spectra similar to other uncharacterized zeolites and phyllosilicates. Ultramafic rocks are predicted to produce serpentine, talc, and magnesite, all of which have been detected spectrally on Mars. Mineral assemblages in both basaltic and ultramafic rocks constrain fluid compositions to be H₂O‐rich and CO₂‐poor. We confirm the hypothesis that low‐grade/hydrothermal metamorphism affected the Noachian crust on Mars, which has been excavated in large craters. We estimate the geothermal gradient (>20 °C km^?1) required to produce the observed assemblages. This gradient is higher than that estimated from radiogenic heat‐producing elements in the crust, suggesting extra heating by regional hydrothermal activity.     

The water content and parental magma of the second chassignite NWA 2737: Clues from trapped melt inclusions in olivine

NWA 2737, the second known chassignite, mainly consists of cumulate olivine crystals of homogeneous composition (Fo = 78.7 ± 0.9). These brown colored olivine grains exhibit two sets of perpendicular planar defects due to shock. Two forms of trapped liquids, interstitial melts and magmatic inclusions, have been examined. Mineral assemblages within the olivine‐hosted magmatic inclusions include low‐Ca pyroxene, augite, kaersutite, fluorapatite, biotite, chromite, sulfide, and feldspathic glass. The reconstructed parental magma composition (A^#) of the NWA 2737 is basaltic and resembles both the experimentally constrained parental melt composition of chassiginites and the Gusev basalt Humphrey, albeit with lower Al contents. A^# also broadly resembles the average of shergottite parent magmas or LAR 06319. However, we suggest that the mantle source for the chassignite parental magmas was distinct from that of the shergottite meteorites, particularly in CaO/Al₂O₃ ratio. In addition, based on the analysis of the volatile contents of kaersutite, we derived a water content of 0.48–0.67 wt% for the parental melt. Finally, our MELTS calculations suggest that moderate pressure (approximately 6.8 kb) came closest to reproducing the crystallized melt‐inclusion assemblages.