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The Sheahan Diamond Literature Reference Compilation - Technical, Media and Corporate Articles based on Major Region - Mountains
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Region Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In addition most references have been tagged with one or more region words. In an effort to make it easier for users to track down articles related to a specific region, KRO has extracted these region words and developed a list of major region words presented in the Major Region Index to which individual region words used in the article reference have been assigned. Each individual Region Report contains in chronological order all the references with a region word associated with the Major Region word. Depending on the total for each reference type - technical, media and corporate - the references will be either in their own technical, media or corporate Region Report, or combined in a single report. Where there is a significant number of technical references there will be a technical report dedicated to the technical articles while the media and corporate references are combined in a separate region report. References that were added in the most recent monthly update are highlighted in yellow within the Region Report. The Major Region words have been defined by a scale system of "general", "continent", "country", "state or province" and "regional". Major Region words at the smaller scales have been created only when there are enough references to make isolating them worthwhile. References not tagged with a Region are excluded, and articles with a region word not matched with a Major Region show up in the "Unknown" report.
Kimberlite - diamondiferous
Lamproite - diamondiferous
Lamprophyre - diamondiferous
Other - diamondiferous
Kimberlite - non diamondiferous
Lamproite - non diamondiferous
Lamprophyre - non diamondiferous
Other - non diamondiferous
Kimberlite - unknown
Lamproite - unknown
Lamprophyre - unknown
Other - unknown
Future Mine
Current Mine
Former Mine
Click on icon for details about each occurrence. Works best with Google Chrome.
CITATION: Faure, S, 2010, World Kimberlites CONSOREM Database (Version 3), Consortium de Recherche en Exploration Minérale CONSOREM, Université du Québec ŕ Montréal, Numerical Database on consorem.ca. NOTE: This publicly available database results of a compilation of other public databases, scientific and governmental publications and maps, and various data from exploration companies reports or Web sites, If you notice errors, have additional kimberlite localizations that should be included in this database, or have any comments and suggestions, please contact the author specifying the ID of the kimberlite: [email protected]
The Browns Peak Formation and its Relationship to the Late Tertiary Geologic History of the Elkhead Region, Northwestern Colorado and South Central Wyoming.
Ph.d. Thesis, University California At Berkeley, 175P.
Petrology of Alkaline Rocks in the Carbonatite Complex at Iron Hill, Powderhorn District, Gunnison County, Colorado - New Geochemical and isotopic Data.
Geological Society of America (GSA), Vol. 17, No. 3, FEBRUARY P. 149. (abstract.).
Complex Zoning of Clinopyroxene in Shonkinites from Mafic Phonolites, Highwood Mountains, Montana: Evidence for Periodic Mixing with a K Rich Bananitic Magma.
Geological Society of America (GSA), Vol. 17, No. 3, P. 187. (abstract.).
A tale of two continents: some tectonic contrasts between the Central Andes and the North America Cordillera as illustrated by their paleomagneticsignatures
Upper mantle temperature determined from combining mineral composition, electrical conductivity laboratory studies and magnetotelluric field observations:
Earth and Planetary Science Letters, Vol. 236, 1-2, pp. 258-268.
Canada, British Columbia, Alberta, Yukon, Cordillera
Physics and Chemistry of Minerals, dor.org/10.1007/ d00269-018-0987-5 13p.
Russia, Kazakhstan, Alps
coesite, UHP
Abstract: The high-pressure silica polymorphs coesite and stishovite were synthesized under water-saturated conditions from a natural granitic composition doped with Li and B. Experiments were performed in a Multi-Anvil apparatus between 4 and 9.1 GPa and 900 and 950 °C, based on the conditions of a subducting continental crust as realistic for the ultrahigh-pressure metamorphic units Dora Maira and Kochetav massifs. Run products consisted of coesite/stishovite?+?kyanite?±?phengite?±?omphacite, and quench material. The synthesized silica polymorphs were successively analyzed by infrared spectroscopy, electron microprobe, and Secondary-Ion Mass Spectrometry (SIMS). No hydrous defects were observed in coesite synthesized at 4 GPa and 900 °C, whereas coesite grown at higher pressures revealed a triplet of infrared absorptions bands at 3575, 3523, and 3459 cm??1, two minor bands at 3535 and 3502 cm??1, and a small band at 3300 cm??1 that was only visible at 7.7 GPa. The total amount of Al was charge-balanced by H and the other monovalent cations. However, the band triplet could not be associated with AlOH defects, while the band doublet was inferred to BOH defects and the small band probably corresponded to interstitial H. Stishovite displayed one dominant band at 3116 cm??1 with a shoulder at 3170 cm??1, and a minor band at 2665 cm??1, probably all associated with AlOH defects. BOH defects were not observed in stishovite, and LiOH defects were neither observed in coesite nor stishovite, probably because of preferentially partition of Li in other phases such as omphacite. The total amount of defect protons increased with pressure and with metal impurity concentrations. The general increase in OH defects in silica polymorphs with increasing pressure (this study) contrasted the negative pressure trend of OH in quartz observed previously from the same starting material, and revealed an incorporation minimum of OH in silica polymorphs around the quartz/coesite phase transition.
Physics and Chemistry of Minerals, Vol. 46, pp. 77-89.
Russia, Europe, Alps
UHP
Abstract: The high-pressure silica polymorphs coesite and stishovite were synthesized under water-saturated conditions from a natural granitic composition doped with Li and B. Experiments were performed in a Multi-Anvil apparatus between 4 and 9.1 GPa and 900 and 950 °C, based on the conditions of a subducting continental crust as realistic for the ultrahigh-pressure metamorphic units Dora Maira and Kochetav massifs. Run products consisted of coesite/stishovite?+?kyanite?±?phengite?±?omphacite, and quench material. The synthesized silica polymorphs were successively analyzed by infrared spectroscopy, electron microprobe, and Secondary-Ion Mass Spectrometry (SIMS). No hydrous defects were observed in coesite synthesized at 4 GPa and 900 °C, whereas coesite grown at higher pressures revealed a triplet of infrared absorptions bands at 3575, 3523, and 3459 cm??1, two minor bands at 3535 and 3502 cm??1, and a small band at 3300 cm??1 that was only visible at 7.7 GPa. The total amount of Al was charge-balanced by H and the other monovalent cations. However, the band triplet could not be associated with AlOH defects, while the band doublet was inferred to BOH defects and the small band probably corresponded to interstitial H. Stishovite displayed one dominant band at 3116 cm??1 with a shoulder at 3170 cm??1, and a minor band at 2665 cm??1, probably all associated with AlOH defects. BOH defects were not observed in stishovite, and LiOH defects were neither observed in coesite nor stishovite, probably because of preferentially partition of Li in other phases such as omphacite. The total amount of defect protons increased with pressure and with metal impurity concentrations. The general increase in OH defects in silica polymorphs with increasing pressure (this study) contrasted the negative pressure trend of OH in quartz observed previously from the same starting material, and revealed an incorporation minimum of OH in silica polymorphs around the quartz/coesite phase transition.
Geophysical Research Abstracts EGRU2019-3091, Vol. 21, 3091, 1p.
Europe, Alps
garnet
Abstract: Garnet is the paradigmatic cubic mineral of metamorphic and igneous rocks, and is generally regarded as optically isotropic. Nonetheless, evident birefringence is observed, particularly in the rare CaFe 3+ hydrogarnets, which is attributed to the coexistence of two or more cubic phases. A weak birefringence, with rare examples of optical sector zoning, has also been documented in much more common Fe 2+-Mg-Mn garnets, but an adequate explanation for its cause is, so far, lacking. Here we show that optically anisotropic garnets are much more widespread than previously thought, both in blueschists and blueschist-facies rocks, as well as in lower greenschist-facies phyllites, but they are frequently overlooked when working with conventional, 30-µm-thick thin sections. Utilizing a multi-technique approach including optical microstructural analysis, BSEM, EMPA, EBSD, FTIR, TEM, EDT and single-crystal XRD, we demonstrate here that the birefringence in these garnets is related to their tetragonal symmetry, that it is not due to strain, and that crystals are twinned according to a merohedral law. We also show that the birefringent garnets from blueschists and phyllites are anhydrous, lacking any hydrogarnet component, and have compositions dominated by almandine (58-79%) and grossular (19-30%) with variable spessartine (0-21%) and very low pyrope (1-7%). Considering the widespread occurrence of optically anisotropic OH-free garnets in blueschists and phyllites, their common low-grade metamorphic origin, and the occurrence of optically isotropic garnets with similar Ca-rich almandine composition in higher-grade rocks, we conclude that garnet does not grow with cubic symmetry in low-temperature rocks (< 400 • C). The tetragonal structure appears to be typical of Fe-Ca-rich compositions, with very low Mg contents. Cubic but optically sector-zoned garnet in a lower amphibolite-facies metapelite from the eastern Alps suggests that preservation of tetragonal garnet is favored in rocks which did not progress to T> ?500 • C, where transition to the cubic form, accompanied by change of stable chemical composition, would take place. Our data show that the crystal-chemistry of garnet, its thermodynamics and, in turn, its use in unravelling petrogenetic processes in cold metamorphic environments need to be reassessed.
www.minsoccam.org/ MSA/Centennial/ MSA_Centennial _Symposium.html The next 100 years of mineral science, June 20-21, p. 19. Abstract
Europe, Alps
petrology
Abstract: Estimates of the bulk chemical composition of Earth continental crust are highly variable and range from 55-65 wt% SiO2 (Rudnick & Gao 2003). In particular, no consensus exists about the composition of the lower crust. While it is appropriate in some places to distinguish an upper, middle and lower crust, more recent studies advocate that in some places middle and lower crust cannot readily be distinguished based on seismic wave speeds, geochemical compositions and heat flow constraints (Hacker et al. 2015). Analysis of global or regional datasets, however, cannot readily disentangle the relevant processes that control the composition of the crust and, in particular, the lower crust. Crucial for this issue are changes in composition over time. Thus, studying one of best known crustal sections – the Ivrea zone in the Alps – provides new insights as it is unique by exposing an almost complete section of crustal rocks of about 30-35 km, approaching close to the crust-mantle transition. The Ivrea zone represents a Paleozoic continental crust section that is affected by Permian transcrustal magmatism on all crustal levels, allowing for evaluation of the temporal evolution of continental crust. An evaluation of major element chemical trajectories of pre-Permian Ivrea crust and the Permian magmatic addition indicates that the metasedimentary crust is dominated by crustal reworking (mechanical mixing trends), while the magmatic addition closely follows phase equilibria controlled by major element geochemical trends and can be considered as net crustal growth. Recent equilibrium and fractional crystallization experiments designed to understand fractionation processes in the lower crust simulated the liquid (LLD) and cumulate lines of descent (CLD) of primary mantle derived magmas (Müntener & Ulmer 2018). An evaluation of the major element composition indicates that the CLD of hydrous systems is fundamentally different from dry systems. Cumulates derived from hydrous experiments display elevated Al2O3 and CaO contents at low SiO2, producing voluminous andesitic to rhyolitic liquids, which closely overlap with compositions of natural systems, while dry systems follow different fractionation paths. Melting experiments on amphibolite or remelting of basaltic to andesitic cumulates equally produce granitic – rhyolitic liquids of similar composition yet their restites do not present the same variability of the CLD of fractional crystallization experiments. Despite widespread evidence for partial melting and assimilation processes during Permian transcrustal magmatic activity, CLDs from experimental studies on lower crustal differentiation in H2O-bearing systems are comparable to the magmatic evolution in the Ivrea zone and other crustal sections. Dry crystallization and moderate amounts of assimilation may provide similar results. This indicates that global datasets from metamorphic terrains at moderate to high pressure can be evaluated for their igneous versus metasedimentary contribution to the bulk continental lower crust.
Earth and Planetary Science Letters, Vol. 543, 116328 14p. Pdf
Europe, Switzerland, Alps
boron diamonds
Abstract: Understanding the volatile cycles at convergent margins is fundamental to unravel the Earth's evolution from primordial time to present. The assessment of fluid-mobile and incompatible element uptake in serpentinites via interaction with seawater and subduction-zone fluids is central to evaluate the global cycling of the above elements in the Earth's mantle. Here, we focus on the carbon (C), nitrogen (N) and C isotope compositions of chlorite harzburgites and garnet peridotites deriving from subduction-zone dehydration of former oceanic dehydration of serpentinite - i.e., metaperidotites (Cima di Gagnone, Swiss Central Alps) with the aim of evaluating the contribution of these rocks to the global C-N cycling. These ultramafic rocks, enclosed as lenses in a metasedimentary mélange, represent the destabilization of antigorite and chlorite at high-pressure/temperature (P/T) along a slab-mantle interface. Chlorite- and garnet-bearing rocks have similar ranges in C concentration ([C] = 210 - 2465 ppm and 304 - 659 ppm, respectively), with one magnesite-bearing chlorite harzburgite hosting 11000 ppm C. The average N concentrations ([N]) of the garnet peridotites (54 ± 15 ppm, one standard deviation indicated) are higher than those of the chlorite harzburgites (29 ± 6 ppm). The C of total C (TC) and total organic C (TOC) values of the Gagnone metaperidotites range from -12.2 to -17.8‰ and from -27.8 to -26.8‰, respectively, excluding the magnesite-bearing chlorite harzburgites with higher values of -7.2‰ (TC) and -21.2‰ (TOC). The [C] of these rocks are comparable to those of serpentinites form modern and ancient oceanic environments and with [C] of high-P serpentinites. However, the lack of preserved serpentinite precursors makes it difficult to determine whether release of H2O during high-P breakdown of antigorite and chlorite is coupled with significant C release to fluids. The C values appear to reflect mixing between seawater-derived carbonate and a reduced C source and a contribution from the host metasedimentary rocks ([C] = 301 ppm; [N] = 33 ppm; TC C = -24.4‰; TOC C = -27.0‰) cannot be completely excluded. The C-O isotope composition of the carbonate in magnesite-bearing chlorite harzburgites is compatible with progressive devolatilization at oxidized conditions, whereas the signatures of the majority of the other Gagnone samples appear to reflect different degree of interaction with sedimentary fluids. The [N] of the Gagnone metaperidotites are higher than those of oceanic and subducted serpentinites and show a range similar to that of high-P antigorite-serpentinites from mantle wedges. This enrichment is compatible with fluid-mediated chemical exchange with the surrounding metasedimentary rocks leading to strong modification of the Gagnone metaperidotites' geochemistry during prograde subduction along the slab-mantle interface. Comparing the C data reported in this study with published C values for diamonds, we suggest that the volatile recycling via Gagnone-like metaperidotites in subduction zones could contribute to deep-Earth diamond genesis and in particular to the formation of blue boron (B)-bearing diamonds. Our results highlight that the subduction of secondary peridotites evolved along the slab-mantle interface is a viable mechanism to inject volatiles into the deep mantle, particularly in hotter geothermal regimes such as the ones active during the early Earth's history.
