Petrology and Geochemistry of Mercury

Author(s):  
Shoshana Z. Weider

This is an advance summary of a forthcoming article in the Oxford Research Encyclopedia of Planetary Science. Please check back later for the full article. Although having knowledge of a terrestrial planet’s chemistry is fundamental to understanding the origin and composition of its rocks, until recently, the geochemistry of Mercury—the Solar System’s innermost planet—was largely unconstrained. Without the availability of geological specimens from Mercury, studying the planet’s surface and bulk composition relies on remote sensing techniques. Moreover, Mercury’s proximity to the Sun makes it difficult to study with Earth/space-based telescopes, or with planetary probes. Indeed, to date, only NASA’s Mariner 10 and MESSENGER missions have been sent to Mercury. The former made three “flyby” encounters of Mercury between 1974 and 1975, but did not carry any instrument to make geochemical or mineralogical measurements of the surface. Until the MESSENGER flyby and orbital campaigns (2008–2015), therefore, knowledge of Mercury’s chemical composition was severely limited and consisted of only a few facts. For example, it has long been known that Mercury has the highest uncompressed density of all the terrestrial planets (and thus a disproportionately large iron core). In addition, Earth-based spectral reflectance observations indicated a dark surface, largely devoid of iron within silicate minerals. To improve understanding of Mercury’s geochemistry, the MESSENGER payload included a suite of geochemical sensing instruments: namely the X-Ray Spectrometer, Gamma-Ray Spectrometer, and Neutron Spectrometer. Indeed, the datasets obtained from these instruments (as well as from other complementary instruments) during MESSENGER’s 3.5-year orbital mission allow a much more complete picture of Mercury’s geochemistry to be drawn, and quantitative abundance estimates for several major rock-forming elements in Mercury’s crust are now available. Overall, the MESSENGER data reveal a surface that is rich in Mg, but poor in Al and Ca, compared with typical terrestrial and lunar crustal materials. Mercury’s surface also contains high concentrations of the volatile elements Na, S, K, and Cl. Furthermore, the total surface Fe abundance is now known to be <2 wt%, and the planet’s low reflectance is thought to be primarily caused by the presence of C (in graphite) at a level of >1 wt%. Such data are key to constraining models for Mercury’s formation and early evolution. Large-scale spatial variations in the MESSENGER geochemical datasets have also led to the designation of several geochemical “terrains” across Mercury’s surface, which do not always align to otherwise mapped geological regions. Based on the MESSENGER geochemical results, several recent petrological experiments and calculations have been, and continue to be, performed to study Mercury’s surface mineralogy. The results show that there are substantial differences in the precise mineral compositions and abundances among the different terrains, but Mercury’s surface appears to be dominated by Mg-rich olivines and pyroxenes, as well as plagioclase and sulphide phases. Depending on the classification scheme used, Mercury’s ultramafic surface rocks can thus be described as similar in nature to terrestrial boninites, andesites, norites, or gabbros.

Author(s):  
Frances E. G. Butcher

This is an advance summary of a forthcoming article in the Oxford Research Encyclopedia of Planetary Science. Please check back later for the full article. Mars’ mid-latitudes (roughly 30–60° N and S) host voluminous deposits of water ice in the subsurface. At present, perennial water ice cannot exist at the surface in these regions. This is because, for a significant portion of the Martian year, surface temperatures exceed the sublimation point of water ice under Mars’ low atmospheric pressure. Therefore, any seasonal water-ice frost that accumulates in winter sublimates back into the atmosphere in spring. However, a centimeters-to-meters-thick covering of lithic material can inhibit sublimation sufficiently to allow perennial stability of ice in the subsurface. Perennial ice in Mars’ mid-latitudes exists as pore-ice and excess-ice lenses within the regolith, and as massive accumulations of buried, high-purity ice akin to debris-covered glaciers on Earth. The ice is thought to range in age from hundreds of thousands to many hundreds of millions of years old. Its emplacement and modification has been widely attributed to cyclical climate changes induced by variations in Mars’ orbital parameters (primarily its axial tilt). Water ice in Mars’ mid-latitudes is therefore of significant interest for reconstructing such climate changes. It could also provide an essential in situ supply of water for future human missions to Mars. It is possible to infer the presence of water ice in Mars’ subsurface without direct imaging of the ice itself. For example, the distribution of near-surface ice was mapped using Mars Odyssey Neutron Spectrometer detections to calculate the percentage of water-equivalent hydrogen in the upper 1 m of the regolith. Orbital images have revealed a great diversity of ice-related landforms which suggest flow, thermal cycling, sublimation, and disruption (e.g. by impact cratering) of subsurface ice. In some locations, orbital ground-penetrating radar observations have been used to confirm subsurface ice content in areas where its presence has been inferred from the geomorphology of the surface. Water ice in Mars’ mid-latitudes has also been imaged directly by landed and orbital missions. The Phoenix lander exposed water-ice lenses just centimeters beneath the surface, in trenches that it excavated at 68 °N latitude. Orbital images from the High Resolution Imaging Science Experiment (HiRISE) camera on board Mars Reconnaissance Orbiter revealed transient bright ice deposits exhumed by small, fresh impacts into mid-latitude terrains, and ~100 m-high scarps of water ice in exposures through debris-covered ice deposits. In all these cases, the exposed ice has been observed to lose mass by sublimation over time. This demonstrates the essential role of lithic cover in preserving subsurface water ice in Mars’ mid-latitudes.


Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 672
Author(s):  
Anette Regelous ◽  
Lars Scharfenberg ◽  
Helga De Wall

The origin and evolution of granites remain a matter of debate and several approaches have been made to distinguish between different granite types. Overall, granite classification schemes based on element concentrations and ratios, tectonic settings or the source rocks (I-, A-, S-type) are widely used, but so far, no systematic large-scale study on Th/U ratio variations in granites based on their source or tectonic setting has been carried out, even though these elements show very similar behavior during melting and subsequent processes. We therefore present a compiled study, demonstrating an easy approach to differentiate between S-, A- and I-type granites using Th and U concentrations and ratios measured with a portable gamma ray spectrometer. Th and U concentrations from 472 measurements in S- and I-type granites from the Variscan West-Bohemian Massif, Germany, and 78 measurements from Neoproterozoic A-type Malani granites, India, are evaluated. Our compendium shows significant differences in the average Th/U ratios of A-, I- and S-type granites and thus gives information about the source rock and can be used as an easy classification scheme. Considering all data from the studied A-, I- and S-type granites, Th/U ratios increase with rising Th concentrations. A-type granites have the highest Th/U ratios and high Th concentrations, followed by I-type granites. Th/U ratios in S- to I-type granites are lower than in A-type and I-type granites, but higher than in S-type granites. The variation of Th/U ratios in all three types of granite cannot be explained by fractional crystallization of monazite, zircon and other Th and U bearing minerals alone, but are mainly due to source heterogeneities and uranium mobilization processes.


2005 ◽  
Vol 13 ◽  
pp. 730-736 ◽  
Author(s):  
C. T. Russell

AbstractThe Dawn mission, the ninth in the series of NASA Discovery missions, is scheduled for launch in late May 2006 on a voyage to both Vesta and Ceres. The mission carries a framing camera, visible and infrared mapping spectrometer, gamma ray and neutron spectrometer, laser altimeter and magnetometer to understand and contrast these two very different bodies. Vesta apparently accreted dry, differentiated, and formed an iron core. Ceres apparently contains much water and ice and has remained relatively cool over its lifetime. The community of 1AU observers can help optimize the Dawn mission by improving the knowledge of Vesta and Ceres rotation axes, thus improving our knowledge of when regions and features will be best illuminated. The detection of any satellites would not just identify a potential hazard, and a secondary target of interest, but would also determine the mass of the primaries, enabling better mission planning. Characterization of the surface in any way, including identifying potential targets for detailed study, is also most welcome.


Author(s):  
J-F. Moyen ◽  
M. Cuney ◽  
D. Baratoux ◽  
P. Sardini ◽  
S. Carrouée

Abstract We describe the multi-scale distribution of K, Th and U in the ca. 3.1 Ga Heerenveen batholith of the Barberton Granite-Greenstone Terrain. Data were obtained with a combination of tools, including a portable gamma-ray spectrometer from the scale of the whole batholith to the scale of outcrops, and autoradiography for the thin section scale. U is concentrated preferentially in minor phases in the border shear zones of the batholith and, within these shear zones, in late pegmatites as well as fractures. The processes responsible for the concentration of U in the Heerenveen batholith is discussed in terms of magmatism, hydrothermalism (redistribution of U in fissures associated with magmato-hydrothermal fluids), and supergene alteration. The statistical properties of K, Th and U concentrations are different. K shows spatial correlation over large distance, largely mirroring mappable rock types, with increased variability at larger scales. In contrast, U is dominated by small-scale variations (“nugget effect”) and its variability is, averaged and smoothed by large-scale integration. Spatial and statistical features thus offer useful and complementary insights on petrogenetic and metallogenic processes in granitoids in addition to standard approaches (petrography, geochemistry).


2020 ◽  
Vol 216 (7) ◽  
Author(s):  
Morgan T. Burks ◽  
Owen B. Drury ◽  
John O. Goldsten ◽  
Lisle B. Hagler ◽  
Lena E. Heffern ◽  
...  

2019 ◽  
Vol 22 (5) ◽  
pp. 346-354
Author(s):  
Yan A. Ivanenkov ◽  
Renat S. Yamidanov ◽  
Ilya A. Osterman ◽  
Petr V. Sergiev ◽  
Vladimir A. Aladinskiy ◽  
...  

Aim and Objective: Antibiotic resistance is a serious constraint to the development of new effective antibacterials. Therefore, the discovery of the new antibacterials remains one of the main challenges in modern medicinal chemistry. This study was undertaken to identify novel molecules with antibacterial activity. Materials and Methods: Using our unique double-reporter system, in-house large-scale HTS campaign was conducted for the identification of antibacterial potency of small-molecule compounds. The construction allows us to visually assess the underlying mechanism of action. After the initial HTS and rescreen procedure, luciferase assay, C14-test, determination of MIC value and PrestoBlue test were carried out. Results: HTS rounds and rescreen campaign have revealed the antibacterial activity of a series of Nsubstituted triazolo-azetidines and their isosteric derivatives that has not been reported previously. Primary hit-molecule demonstrated a MIC value of 12.5 µg/mL against E. coli Δ tolC with signs of translation blockage and no SOS-response. Translation inhibition (26%, luciferase assay) was achieved at high concentrations up to 160 µg/mL, while no activity was found using C14-test. The compound did not demonstrate cytotoxicity in the PrestoBlue assay against a panel of eukaryotic cells. Within a series of direct structural analogues bearing the same or bioisosteric scaffold, compound 2 was found to have an improved antibacterial potency (MIC=6.25 µg/mL) close to Erythromycin (MIC=2.5-5 µg/mL) against the same strain. In contrast to the parent hit, this compound was more active and selective, and provided a robust IP position. Conclusion: N-substituted triazolo-azetidine scaffold may be used as a versatile starting point for the development of novel active and selective antibacterial compounds.


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