XX. General Assembly of the International Union of Geodesy and Geophysics in Vienna,Austria, 11–24 August 1991

Report

XX. General Assembly of the International Union of Geodesy and Geophysics in Vienna, Austria, 11–24 August 1991     

Manganese deposits: Communication 2. Major epochs and phases of manganese accumulation in the Earth’s history

Accumulation of manganiferous rocks in the history of the Earth’s lithosphere evolution began not later than the end of the Middle Archean. Primary manganese sediments were accumulated at that time in shallow-water sedimentation basins with the active participation of organic matter. The concentration of Mn in the primary sediments usually did not reach economic values. The formation of genuine manganese ores is related to later processes of the transformation of primary ores—diagenesis, catagenesis, metamorphism, and retrograde diagenesis. Types of basins of manganese ore sedimentation and character of processes of the formation of manganese sediments during the Earth’s shell evolution changed appreciably and correlated with the general evolution of paleocontinents. Major periods, epochs, and phases of manganese ore genesis are defined. At the early stages of lithosphere formation (Archean-Proterozoic), manganese was deposited in basins commonly confined to the central part of Western Gondwana and western part of Eastern Gondwana, as well as the western part of the Ur paleocontinent. Basins of manganese ore sedimentation were characterized by the ferruginous-siliceous, carbonaceous-clayey, and carbonaceous-carbonate-clayey composition. The Early-Middle Paleozoic epoch of manganiferous sediment accumulation was characterized by the presence of several small sedimentation basins with active manifestation of volcanic and hydrothermal activity. Since the formation of Pangea in the Late Paleozoic until its breakup, accumulation of Mn was closely associated with processes of diagenesis and active participation of the oxidized organic matter.     

Crystal chemistry, thermal expansion, and Raman spectra of hydroxyl-clinohumite: implications for water in Earth’s interior

Two samples of hydroxyl-clinohumite, sample SZ0407B with approximate composition Mg_8.674(14)Fe_0.374(4)(Si_0.99(1)O₄)₄(OH)₂ and sample SZ0411B with composition Mg₉(SiO₄)₄(OH)₂, were synthesized at 12 GPa and 1,250 °C coexisting with olivine. Unit-cell parameters determined by single-crystal X-ray diffraction are given as follows: a = 4.7525(4) Å, b = 10.2935(12) Å, c = 13.7077(10) Å, α = 100.645(9)°, V = 659.04(9) Å³ for SZ0407B, and a = 4.7518(6) Å, b = 10.2861(12) Å, c = 13.7008(9) Å, α = 100.638(9)°, V = 658.15(9) Å³ for SZ0411B. Single-crystal X-ray intensity data were collected for crystal structure refinements of both samples. Relative to the pure-Mg sample, Fe decreases M3–OH bond lengths by ~0.010(3) Å, consistent with some ferric iron ordering into M3. Raman spectroscopy shows two strong bands in the lattice-mode region at 650 and 690 cm^?1 in the Fe-bearing sample, which are not observed in the pure-Mg sample. Spectra in the H₂O region show at least five bands, which are deconvolved into seven distinct O–H-stretching modes. Thermal expansion measurements were carried out for both samples from 153 to 787 K by single-crystal X-ray diffraction. The average a-, b-, c-axial and volumetric thermal expansion coefficients (10^?6 K^?1) are 10.5(1), 12.3(2), 12.5(2) and 34.9(5) for SZ0407B, respectively, and 11.1(1), 12.6(3), 13.7(3), 36.8(6) for SZ0411B, respectively. After heating, the unit-cell parameters were refined again for each sample at ambient condition, and no significant changes were observed, indicating no significant oxidation or dehydration during the experiment. For the DHMS phases along the brucite–forsterite join, linear regression gives a systematic linear decrease in expansivity with increasing density. Further, substitution of ferrous iron into these structures decreases thermal expansivity, making the Fe-bearing varieties slightly stiffer.     

The XVI International Meeting on Placer Geology and Weathering-Crust Deposits (PWC-2021): “Placers and Weathering-Crust Deposits of the 21st Century: Problems,Issues, Solutions”

Geology of Ore Deposits -     

Structure and evolution of the Earth’s crust in the region of junction of the Central Asian Fold Belt and the Siberian Platform: Skovorodino–Tommot profile

An integrated geological and geophysical study was performed to investigate the region of junction of the eastern part of the Central Asian Fold Belt and the Siberian Platform in the Skovorodino–Tommot 3-DV reference profile line (52°–60° N, 122°–129° E), where the belt is separated from the Aldan–Stanovoi Shield of the Platform by a series of deep faults. The main results are as follows: Seismic, density, and geoelectric characteristics of rocks were obtained and used to determine (refine) the intracrustal boundaries of tectonic structures; large-block structure of the Earth’s crust, caused by mantle faults, and the difference between the layered structure of the crust for the shield and fold regions were established; and available paleomagnetic data were used to perform palinspastic reconstructions for 180 and 140 million years, the most productive metallogenic epoch in the region, coeval with collision processes at the closure of the Mongol-Okhotsk paleobasin.     

Phase states of hydrous–hydrocarbon fluids at elevated and high temperatures and pressures: Study of the forms and maximal depths of oil occurrence in the Earth’s interior

Based on synthetic fluid inclusions in quartz grown at 240–490°C and 7–150 MPa in aqueous–oil solutions, the behavior, composition, and phase states of liquid, gaseous, and solid hydrocarbons (HC) were studied. Investigations were performed using common and fluorescent microscopy, microthermometry, local common and high-temperature IR Fourier spectroscopy, Raman spectroscopy, chromatography, and X-ray and microprobe analysis. The data obtained allowed us to understand the influence of thermobaric conditions and volume proportions of the oil, aqueous, and gaseous phases on the composition, phase state, and behavior of hydrous–hydrocarbon fluids and estimate the forms and probable maximal depths of the origin of oil in the Earth’s interior.     

Geographies of identity theft in the U.S.: understanding spatial and demographic patterns, 2002–2006

Identity theft is among the fastest growing white-collar crimes in the United States, although official recognition of it as a criminal act is a relatively recent development. Utilizing theoretical framework established in crime geography, GIS mapping and spatial statistics are employed to conduct a spatial analysis of identity theft in the U.S. from 2002 to 2006. Distinct regional variations, such as high rates in the western and southwestern states, and low rates in New England and the central plains states, are identified for identity theft. Significant spatial patterns of identity theft victims alongside social demographic variables are also revealed in order to better understand the regional patterns that may suggest underlying social causes contributing to identity theft. Potential social variables, such as race/ethnicity and urban–rural populations, are shown to have similar patterns that may be directly associated with U.S. identity theft victims.     

Influence of hydrogen on Fe–Mg interdiffusion in (Mg,Fe)O and implications for Earth’s lower mantle

Interdiffusion of Fe and Mg in (Mg,Fe)O has been investigated experimentally under hydrous conditions. Single crystals of MgO in contact with (Mg_0.73Fe_0.27)O were annealed hydrothermally at 300 MPa between 1,000 and 1,250°C and using a Ni–NiO buffer. After electron microprobe analyses, the dependence of the interdiffusivity on Fe concentration was determined using a Boltzmann–Matano analysis. For a water fugacity of ∼300 MPa, the Fe–Mg interdiffusion coefficient in Fe _x Mg_1−x O with 0.01 ≤ x ≤ 0.25 can be described by with and C = −80 ± 10 kJ mol⁻¹. For x = 0.1 and at 1,000°C, Fe–Mg interdiffusion is a factor of ∼4 faster under hydrous than under anhydrous conditions. This enhanced rate of interdiffusion is attributed to an increased concentration of metal vacancies resulting from the incorporation of hydrogen. Such water-induced enhancement of kinetics may have important implications for the rheological properties of the lower mantle.

Thermodynamics of arsenates, selenites, and sulfates in the oxidation zone of sulfide ores: VI. Solubility of synthetic analogs of ahlfeldite and cobaltomenite at 25°C

The understanding of the mechanisms of the selenium behavior under near-surface conditions is an urgent problem of modern mineralogy and geochemistry, and is very important for solving environmental problems. The objective of this study is to synthesize analogs of ahlfeldite and cobaltomenite and to estimate their solubility in water. These analogs have been synthesized by mixing aqueous solutions of cobalt and nickel nitrates, respectively, and sodium selenite acidified with a solution of nitric acid. The obtained samples have been identified by X-ray diffraction and IR spectroscopy. The solubility has been determined by the isothermal saturation method in ampoules at 25°C, while the solubility products have been calculated using the Geochemist’s Workbench (GMB 7.0) software package. The solubility products of ahlfeldite and cobaltomenite are 10^?9.20 and 10^?9.44, respectively. The Eh-pH diagrams were calculated and plotted with the GMB 7.0 software package. The Eh-pH diagrams of the Ni-Se-H₂O and Co-Se-H₂O systems have been calculated for the average contents of these elements in underground water and their contents in acidic water of the oxidation zone of sulfide deposits. The formation of ahlfeldite and cobaltomenite under near-surface conditions is discussed.     

Quartzite–Schist Sequences of the Aktau–Mointy Massif (Central Kazakhstan): Structural Position,Provenance, and Formation Stages of the Earth Crust in the Precambrian

Geotectonics - Detrital zircons from quartzite–schist sequences of the Aktau–Mointy Massif (Central Kazakhstan), which occur in various structural positions relative to the Early...     

Thermodynamics of arsenates, selenites, and sulfates in the oxidation zone of sulfide Ores: Part VII. Solubility of synthetic analogs of erythrite and annabergite at 25°C

Understanding the mechanisms of arsenic’s behavior under near-surface conditions is one of the actual problems of contemporary mineralogy and geochemistry and is important for solving environmental problems. The aim of this study is to synthesize analogs of erythrite and annabergite and to investigate their solubility in water. These phases have been synthesized by the boiling-dry of aqueous solutions of cobalt and nickel nitrates mixed with sodium hydroarsenate alkalized with NaOH. The samples obtained have been identified with electron microprobe, X-ray diffraction, and IR spectroscopy. Solubility has been determined by the isothermal saturation method in ampoules at 25°C. The solubility has been calculated using the Geochemist’s Workbench (GMB 7.0) software package. The measured solubilities of erythrite and annabergite are 10^?35.76 and 10^?36.43, respectively. Eh-pH diagrams were calculated and plotted using the GMB 7.0 software package. The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 552 particles in solution, 624 solid phases, and 10 gases. The Eh-pH diagrams of the Ni-As-H₂O and Co-As-H₂O systems were plotted for the average contents of these elements in the acidic waters in the oxidation zones of sulfide deposits. The formation of erythrite and annabergite under near-surface conditions is discussed.     

Training Programme on Major Tectonics and Lithounits in the Indus and Shyok Suture Zones of Ladakh Himalaya — M. Ram Mohan, (NGRI-CSIR,Hyderabad. Email: rammohan@ngri.res.in) and Sita Bora (Kumaun University,Nainital; Email: sitabora@yahoo.com)

News and Notes

Training Programme on Major Tectonics and Lithounits in the Indus and Shyok Suture Zones of Ladakh Himalaya — M. Ram Mohan, (NGRI-CSIR, Hyderabad. Email: rammohan@ngri.res.in) and Sita Bora (Kumaun University, Nainital; Email: sitabora@yahoo.com)