Behavior of epidote at high pressure and high temperature: a powder diffraction study up to 10 GPa and 1,200 K

The thermo-elastic behavior of a natural epidote [Ca_1.925 Fe_0.745Al_2.265Ti_0.004Si_3.037O₁₂(OH)] has been investigated up to 1,200 K (at 0.0001 GPa) and 10 GPa (at 298 K) by means of in situ synchrotron powder diffraction. No phase transition has been observed within the temperature and pressure range investigated. P–V data fitted with a third-order Birch–Murnaghan equation of state (BM-EoS) give V ₀ = 458.8(1)ų, K _T0 = 111(3) GPa, and K′ = 7.6(7). The confidence ellipse from the variance–covariance matrix of K _T0 and K′ from the least-square procedure is strongly elongated with negative slope. The evolution of the “Eulerian finite strain” vs “normalized stress” yields Fe(0) = 114(1) GPa as intercept values, and the slope of the regression line gives K′ = 7.0(4). The evolution of the lattice parameters with pressure is slightly anisotropic. The elastic parameters calculated with a linearized BM-EoS are: a ₀ = 8.8877(7) Å, K _T0(a) = 117(2) GPa, and K′(a) = 3.7(4) for the a-axis; b ₀ = 5.6271(7) Å, K _T0(b) = 126(3) GPa, and K′(b) = 12(1) for the b-axis; and c ₀ = 10.1527(7) Å, K _T0(c) = 90(1) GPa, and K’(c) = 8.1(4) for the c-axis [K _T0(a):K _T0(b):K _T0(c) = 1.30:1.40:1]. The β angle decreases with pressure, β_P(°) = β_P0 −0.0286(9)P +0.00134(9)P ² (P in GPa). The evolution of axial and volume thermal expansion coefficient, α, with T was described by the polynomial function: α(T) = α₀ + α₁ T ^−1/2. The refined parameters for epidote are: α₀ = 5.1(2) × 10⁻⁵ K⁻¹ and α₁ = −5.1(6) × 10⁻⁴ K^1/2 for the unit-cell volume, α₀(a) = 1.21(7) × 10⁻⁵ K⁻¹ and α₁(a) = −1.2(2) × 10⁻⁴ K^1/2 for the a-axis, α₀(b) = 1.88(7) × 10⁻⁵ K⁻¹ and α₁(b) = −1.7(2) × 10⁻⁴ K^1/2 for the b-axis, and α₀(c) = 2.14(9) × 10⁻⁵ K⁻¹ and α₁(c) = −2.0(2) × 10⁻⁴ K^1/2 for the c-axis. The thermo-elastic anisotropy can be described, at a first approximation, by α₀(a): α₀(b): α₀(c) = 1 : 1.55 : 1.77. The β angle increases continuously with T, with β_T(°) = β_T0 + 2.5(1) × 10⁻⁴ T + 1.3(7) × 10⁻⁸ T ². A comparison between the thermo-elastic parameters of epidote and clinozoisite is carried out.     

The A and B mica layers and the crystal structure of sheet silicates

A discussion of the transition from the ideal hexagonal mica structure to the ideal ditrigonal one, leads to the conclusion that the single mica layer may have two different structures (labelled A and B). The recent literature data show that both the A and B structures have been detected in some triocahedral layer lattice silicates found in nature. An examination of the structural stability of the A and B structures suggests that the last one may not be realized by dioctahedral layer lattice silicates. The concept of two structurally different mica layers, which however have the same lattice constants, greatly improves the understanding of polymorphism and twin laws in layer lattice silicates.The structural features of the tetrahedral sheet, octahedral sheet and interlayer region are carefully examined. Thus we can reach the following conclusions: the tetrahedal sheet is not entirely free to reduce its lateral dimensions by the mechanism of tetrahedal rotation owing to the repulsion among O_bas atoms; the octahedral sheet in layer lattice silicates, may increase or reduce its lateral dimensions as compared to the lateral dimensions it has in the hydroxide minerals; the interlayer region is characterized by a regular octahedral coordination of the O_bas around the interlayer cation. On the ground of these conclusions, new structural models for some selected layer lattice silicates are proposed.Notations O_bas basal oxygen atoms of the (Al, Si)O₄ tetrahedra - O_ap apical oxygen atoms of the (Al, Si)O₄ tetrahedra - b _tetr b dimension which the tetrahedral sheet would assume if unconstrained - b _oct b dimension which the octahedral sheet has in the hydroxide minerals - b _obs observed value of b - c _oct ^* thickness of the octahedral sheet - d _o distance between an octahedral cation and an O_ap atom - d _int distance between an interlayer cation and an O_bas atom - average tetrahedral rotation from ideal hexagonal symmetry     

A 3‐D study of mineral inclusions in chromite from ordinary chondrites using synchrotron radiation X‐ray tomographic microscopy—Method and applications

Abstract– A method is described for imaging in 3‐D the interiors of meteoritic chromite grains and their inclusions using synchrotron radiation X‐ray tomographic microscopy. In ordinary chondrites, chromite is the only common mineral that survives long‐term weathering on Earth. Information about the silicate matrix of the original meteorite, however, can be derived from mineral inclusions preserved in the protecting chromite. The inclusions are crucial in the classification of fossil meteorites as well as sediment‐dispersed chromite grains from decomposed meteorites and larger impacts, as these are used for characterizing the past influx of material to Earth, but have previously been difficult to locate. The method is non‐destructive and time efficient for locating inclusions. The method allowed quantitative and morphological studies of both host chromite grains and inclusions in three dimensions. The study of 385 chromite grains from eight chondrites (H4–6, L4–6, LL4, LL6) reveals that inclusions are abundant and equally common in all samples. Almost two‐thirds of all chromite grains contain inclusions, regardless of group and type. The study also shows that the size of the inclusions and the host chromite grains, as well as the number of inclusions, within the host chromite grains vary with petrographic type. Thus, the petrographic type of the host of a suite of chromite grains can be determined based solely on inclusion content. The study also revealed that the amount of fractures in the host chromite can be correlated to previously assigned shock stages for the various chondrites. The study has thus shown that the features and inclusions of fossil chromite grains can give similar information about a former host meteorite as do studies of an unweathered whole meteorite, meaning that this technique is essential in the studies of ancient meteorite flux to Earth.     

Emerging trends in urbanizing Palestine: neglected city-builders beyond the occupation

In this article, we draw attention to trends in land transformation in the West Bank since the Second Intifada, after which a surge of investment from Gulf countries entered Palestine, almost exclusively in the West Bank. The occupied Palestinian territories have attracted a great deal of attention from media and academics, yet the vast majority of scholarship focuses on the conflict and the variety of social, economic, and political repercussions of the on-going Israeli occupation. While the occupation has undeniably serious impacts on every aspect of life for Palestinians, the near-exclusive focus on the conflict means that significant new trends, such as urban mega-developments and emerging market-based urbanisation processes, have been largely overlooked. We outline three directions for future research: the assemblage of “neglected city-builders” shaping current urbanization processes in Palestine; the ideas, policies, and norms circulating in the West Bank; and the social, spatial, economic, and other impacts of these new urban developments.     

Granulation deformation near and in sunspot regions

High-resolution white-light pictures are analyzed to study the differences between the granular size near sunspot penumbrae and in light-bridges presenting granular structure and that of the quiet photosphere. No difference is found between the mean granular diameter in light-bridges and the quiet photosphere. The dispersion found in the results corresponding to different zones around the sunspots indicates that the size of the granulation may vary from place to place near the sunspots, its mean value not differing significantly from that of the quiet photosphere. A possible systematic bias in the selection of the granules by Macris (1979) is found.     

Orbital and thermal evolutions of four potential targets for a sample return space mission to a primitive near-Earth asteroid

In this paper, we present our study of the orbital and thermal evolutions, due to solar radiative heating, of four near-Earth asteroids (NEAs) considered as potential target candidates for sample return space missions to primitive asteroids. We used a dynamical model of the NEA population to estimate the most likely source region and orbital history of these objects. Then, for each asteroid, we integrated numerically over their entire lifetime a set of 14 initially indistinguishable orbit (clones), obtained by small variations of the nominal initial conditions. Using a thermal model, we then computed surface and sub-surface temperatures of these bodies during their dynamical history. Our aim is to determine whether these bodies are likely to have experienced high temperature level, and whether great temperature changes can be expected due to the orbital changes as well as their maximum and minimum values. Such information is important in the framework of sample return space missions whose goal is to bring back pristine materials. The knowledge of the temperature range of materials at different depth over the orbital evolution of potential targets can help defining sampling strategies that ensure the likelihood that unaltered material will be brought back. Our results suggest that for all the considered potential targets, the surface has experienced for some time temperatures greater than 400 K and at most 500 K with 50% probability. This probability drops rapidly with increasing temperature. Sub-surface materials at a depth of only 3 cm are much more protected from high temperature and generally do not reach temperatures exceeding 450 K (with 50% probability). They should thus be unaltered at this depth at least from a Sun-driven heating point of view. On the other hand, surface material for some of the considered objects can have a range of temperature which can make them less reliable as pristine materials. However, it is assumed here that the same material is constantly exposed to solar heat, while regolith turnover may occur. The latter can be caused by different processes such as seismic shaking and/or impact cratering. This would reduce the total time that materials are exposed to a certain temperature. Thus, it is very likely that a sample collected from any of the four considered targets, or any primitive NEA with similar dynamical properties, will have components that will be thermally unaltered as long as some of it comes from only 3 to 5 cm depth. Such a depth is not considered difficult to reach with some of the current designs of sampling devices.     

Experimental Validation of Modified Barton’s Model for Rock Fractures

Among the constitutive models for rock fractures developed over the years, Barton’s empirical model has been widely used. Although Barton’s failure criterion predicts peak shear strength of rock fractures with acceptable precision, it has some limitations in estimating the peak shear displacement, post-peak shear strength, dilation, and surface degradation. The first author modified Barton’s original model in order to address these limitations. In this study, the modified Barton’s model (the peak shear displacement, the shear stress–displacement curve, and the dilation displacement) is validated by conducting a series of direct shear tests.     

Sardignaite, a new mineral, the second known bismuth molybdate: description and crystal structure

The new mineral sardignaite, a bismuth molybdate with formula BiMo₂O₇(OH)·2H₂O, occurs in quartz veins within a granitic rock at Su Senargiu, near Sarroch, Sardegna, Italy. The name is after the locality. Sardignaite occurs a thin prismatic crystals up to 1 mm in length, with pale yellow color and a white streak. It is transparent with adamantine lustre, non fluorescent, and brittle with a conchoidal fracture. It is associated with bismuthinite, bismoclite, molybdenite, ferrimolybdite, koechlinite, wulfenite, and the new mineral IMA 2009–022. Mohs hardness is ca. 3. D _calc is 4.82 g/cm³. The mineral is monoclinic, space group P2₁/m, with a 5.7797(7), b 11.567(1), c 6.3344(8) Å, β 113.360(9)°, V 388.8(1) ų. The strongest lines in the powder X-ray diffraction pattern are d(I)(hkl): 3.206(100)(031), 5.03(80)(?101), 1.992(45)(221), 3.120(32)(130). The crystal structure of sardignaite was solved to R(F) 0.056 using single-crystal X-ray diffraction data, and is characterized by edge-sharing dimers of [MoO₅(H₂O)] octahedra, linked to each other through corner-sharing to give rise to corrugated columns running along b. Such columns are held together by Bi³⁺ cations, eight-fold coordinated by 7 O + 1 (OH). Both the mineral and its name were approved by the IMA-CNMNC.