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At least 577 records · Page 32Linked to original sources

Zircon reveals protracted magma storage and recycling beneath Mount St. Helens

Current data and models for Mount St. Helens volcano (Washington, United States) suggest relatively rapid transport from magma genesis to eruption, with no evidence for protracted storage or recycling of magmas. However, we show here that complex zircon age populations extending back hundreds of thousands of years from eruption age indicate that magmas regularly stall in the crust, cool and crystallize beneath the volcano, and are then rejuvenated and incorporated by hotter, young magmas on their way to the surface. Estimated dissolution times suggest that entrained zircon generally resided in rejuvenating magmas for no more than about a century. Zircon elemental compositions reflect the increasing influence of mafic input into the system through time, recording growth from hotter, less evolved magmas tens of thousands of years prior to the appearance of mafic magmas at the surface, or changes in whole-rock geochemistry and petrology, and providing a new, time-correlated record of this evolution independent of the eruption history. Zircon data thus reveal the history of the hidden, long-lived intrusive portion of the Mount St. Helens system, where melt and crystals are stored for as long as hundreds of thousands of years and interact with fresh influxes of magmas that traverse the intrusive reservoir before erupting. ?? 2010 Geological Society of America.

Geology↗

Geophysical study of the San Juan Mountains batholith complex, southwestern Colorado

One of the largest and most pronounced gravity lows over North America is over the rugged San Juan Mountains of southwestern Colorado (USA). The mountain range is coincident with the San Juan volcanic field (SJVF), the largest erosional remnant of a widespread mid-Cenozoic volcanic field that spanned much of the southern Rocky Mountains. A buried, low-density silicic batholith complex related to the volcanic field has been the accepted interpretation of the source of the gravity low since the 1970s. However, this interpretation was based on gravity data processed with standard techniques that are problematic in the SJVF region. The combination of high-relief topography, topography with low densities, and the use of a common reduction density of 2670 kg/m 3 produces spurious large-amplitude gravity lows that may distort the geophysical signature of deeper features such as a batholith complex. We applied an unconventional processing procedure that uses geologically appropriate densities for the uppermost crust and digital topography to mostly remove the effect of the low-density units that underlie the topography associated with the SJVF. This approach resulted in a gravity map that provides an improved representation of deeper sources, including reducing the amplitude of the anomaly attributed to a batholith complex. We also reinterpreted vintage seismic refraction data that indicate the presence of low-velocity zones under the SJVF. Assuming that the source of the gravity low on the improved gravity anomaly map is the same as the source of the low seismic velocities, integrated modeling corroborates the interpretation of a batholith complex and then defines the dimensions and overall density contrast of the complex. Models show that the thickness of the batholith complex varies laterally to a significant degree, with the greatest thickness (∼20 km) under the western SJVF, and lesser thicknesses (<10 km) under the eastern SJVF. The largest group of nested calderas on the surface of the SJVF, the central caldera cluster, is not correlated with the thickest part of the batholith complex. This result is consistent with petrologic interpretations from recent studies that the batholith complex continued to be modified after cessation of volcanism and therefore is not necessarily representative of synvolcanic magma chambers. The total volume of the batholith complex is estimated to be 82,000–130,000 km 3 . The formation of such a large felsic batholith complex would inevitably involve production of a considerably greater volume of residuum, which could be present in the lower crust or uppermost mantle. The interpreted vertically averaged density contrast (–60 to –110 kg/m 3 ), density (2590–2640 kg/m 3 ), and seismic expression of the batholith complex are consistent with results of geophysical studies of other large batholiths in the western United States.

Colorado↗

Redefinition of the Petersburg batholith and implications for crustal inheritance in the Dinwiddie terrane, Virginia, USA

Field relations as well as geochemical and petrologic studies of metaigneous rocks assigned to the Pennsylvanian–Permian Petersburg batholith identify at least two distinct rock types: foliated metagranitoid gneiss and massive to porphyritic granite. Foliated metagranitoid gneiss of mostly granodioritic composition is geochemically distinct from associated massive and porphyritic granitic rocks. These gneissic rocks yield radiometric ages from ca. 425 Ma to ca. 403 Ma and document that many of the rocks assigned to the late Paleozoic Petersburg batholith are 100 m.y. older than the youngest portions of the composite batholith and are part of an earlier infrastructural terrane. Two samples of massive equigranular granite southwest of Petersburg, Virginia, yield ages of ca. 321 Ma and ca. 317 Ma, which are 15–20 m.y. older than ca. 300 Ma ages for porphyritic granite, massive granite, and monzodiorite near Richmond, Virginia. Geologic mapping shows that the Early Pennsylvanian granite southwest of Petersburg is separated from Late Pennsylvanian to early Permian granite near Richmond by a map-scale septum of Silurian–Devonian foliated metagranitoid gneiss, referred to herein as the informal Pocoshock Creek gneiss. Laser ablation–inductively coupled plasma–mass spectrometry data from one sample of a quartz-muscovite felsic schist xenolith show a peak age mode of ca. 529 Ma that we interpret to be the maximum depositional age. Inherited zircons from foliated metagranitoid gneiss and massive equigranular granite range from ca. 631 Ma to ca. 376 Ma, but many are Cambrian. Neoproterozoic–Cambrian quartz-muscovite felsic schist and amphibolite, Silurian–Devonian Pocoshock Creek gneiss, and Pennsylvanian–Permian granite comprise a fault-bounded terrane referred to herein as the Dinwiddie terrane. Ages of inherited cores in zircon from igneous rocks and limited detrital zircon geochronology suggest the terrane is of peri-Gondwanan affinity. U/Pb ages of healed fractures in zircon grains from foliated metagranitoid gneiss indicate low-grade deformation of the gneiss at ca. 378–376 Ma, while ca. 320–280 Ma rims on many grains record intrusion of late Paleozoic granite. The temperature-time-deformation history of the Dinwiddie terrane is distinct from the adjacent Goochland and Roanoke Rapids terranes. Orogen-scale dextral transpression likely translated the Dinwiddie terrane southward during the Alleghanian orogeny, at which time they were intruded by Pennsylvanian to Permian granite.

Virginia↗

Monazite and xenotime petrochronologic constraints on four Proterozoic tectonic episodes and ca. 1705 Ma age of the Uncompahgre Formation, southwestern Colorado, USA

The Proterozoic tectonic evolution of the south-western USA remains incompletely understood due to limited constraints on the timing and conditions of the tectono-metamorphic phases and depositional age of metasedimentary successions. We integrated multi-scale compositional mapping, petrologic modeling, and in situ geochronology to constrain pressure-temperature-time paths from samples of Paleoproterozoic basement gneisses and overlying quartzites in southwestern Colorado, USA. Basement gneiss from the western Needle Mountains records metamorphic conditions of 600 °C at 0.75 GPa at 1764 ± 9 Ma and ~575 °C at 1741 ± 10 Ma. Gneiss sampled from drill core near Pagosa Springs, Colorado, records conditions of 700 °C at 1748 ± 9 Ma, 800 °C at 1.1 GPa at 1650 ± 40 Ma, 540 °C at 1570 ± 36 Ma, and 440 °C at 1424 ± 12 Ma. The Uncompahgre Formation was deposited at ca. 1705 Ma, as constrained by detrital monazite (1707 ± 8 Ma) and xenotime (1692 ± 40, 1725 ± 50 Ma), metamorphic xenotime (1650 ± 10 Ma), and published 40 Ar/ 39 Ar and detrital zircon data. Compositions of ca. 1705 Ma detrital monazite and xenotime are consistent with derivation from a garnet-bearing source in the Yavapai orogenic hinterland. The Vallecito Conglomerate and Uncompahgre Formation record macroscopic folding and greenschist-facies metamorphism at 1650 ± 10 Ma and temperatures of 270 °C to >570 °C at 1470–1400 Ma. Laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) zircon geochronology yielded dates of 1775 ± 18 Ma from the Twilight Gneiss and 1696 ± 7 Ma from the Bakers Bridge Granite, supporting previous isotope dilution–thermal ionization mass spectrometry (ID-TIMS) dates. The Eolus Granite yielded a date of 1463 ± 6 Ma, which is older than previous 1.44–1.43 Ga ID-TIMS dates. The newly dated granite of Cataract Gulch is 1421 ± 12 Ma. In situ analysis of detrital and metamorphic monazite and xenotime, igneous zircon, and quantitative thermobarometry, integrated with previously published constraints, indicate multiple tectonic episodes after the emplacement of 1800–1760 Ma arc-related rocks. The region experienced greenschist- to amphibolite-facies metamorphism (M1) from 1760 Ma to 1740 Ma, which was followed by the intrusion of granites at 1730–1695 Ma and deposition of the Uncompahgre Formation at ca. 1705 Ma, contemporaneous with the Yavapai orogeny. Metamorphism at 1680–1600 Ma was characterized by greenschist-facies conditions near Ouray, Colorado, and granulite-facies conditions near Pagosa Springs (M2) during the Mazatzal orogeny. From 1470 Ma to 1400 Ma, greenschist- to amphibolite-facies metamorphism (M3) and largely granitic plutonism occurred during the protracted Picuris orogeny. These results demonstrate the power of monazite and xenotime analyses to constrain depositional ages, provenance, and pressure-temperature-time ( P - T - t ) paths to resolve the compound orogenic history that is characteristic of most mountain belts.

Colorado↗

Oligocene–Miocene development and evolution of the south Dome Rock Mountains basin, lower Colorado River corridor, Arizona, USA

Sedimentary basins in the Colorado River extensional corridor record large-magnitude Basin and Range extension and younger dextral shear deformation in the evolving Pacific−North America plate boundary. The south Dome Rock Mountains basin is located in west-central Arizona (USA), where the history of basin evolution, style of deformation, and timing of the transition between extension and dextral shear are not well constrained. We integrate new geologic mapping of the south Dome Rock Mountains basin with zircon U-Pb geochronology of six marker beds to characterize the timing of basin evolution and the slip history of the south Dome Rock Mountains normal fault. Structural analysis defines structures consistent with regional extension and younger dextral shear deformation. We use sedimentological and petrological analysis to interpret the depositional environments of three basin sequences. A lower basin sequence consists of fluvial strata deposited in an internally drained intermontane basin from ca. 35 Ma to 24.4 Ma. A sequence of volcanic rocks was emplaced in the basin between 24.4 Ma and 23.3 Ma, before the onset of local extensional faulting. An upper basin sequence of coarse conglomerate and sedimentary breccia was deposited on the hanging wall of a half graben structure after 23.3 Ma and through ca. 12.8 Ma, synchronous with 3−7 km of dip slip on the west-dipping, listric south Dome Rock Mountains fault. The basin was subsequently deformed by dextral shear after 12.8 Ma and before 4.8 Ma. These results document how distributed deformation related to the evolving Pacific−North America plate boundary occurred >100 km from the primary plate boundary.

Arizona, California↗

Chemical compositions of rock types as factors in our environment

The types of rocks that form geologic units in the Earth’s crust supply most of the raw materials from which soils are formed and from which water derives its inorganic constituents. The compositions of what we eat and drink thus depend in part upon the compositions of the source rocks. Igneous rocks are formed by crystallization and solidification of a rock melt. Metamorphic rocks are formed by recrystallization of both igneous and sedimentary rocks caused by heat and pressure within the Earth’s crust. Sedimentary rocks are formed chiefly by the deposition in water of weathering and erosion products of pre-existing igneous, metamorphic, or other sedimentary rocks. The compositions of metamorphic rocks are generally similar to the compositions of the rocks that were metamorphosed, and only igneous and sedimentary rock compositions are considered here. Igneous rocks range in SiO 2 content from about 40 to nearly 80 percent, and other constituents increase in amount as SiO 2 decreases. The changes in the other constituents are not large, however, except for the quantitatively unimportant least silicic rocks; these contain conspicuously more magnesium and less aluminum than the other kinds of igneous rocks. Sedimentary rocks range in SiO 2 content from nearly zero for the carbonate rocks to almost 100 percent for quartzite and pure sandstone. Shale and clay contain intermediate amounts of SiO 2 and as much as 25 percent AI 2 O 3 , more than any of the igneous rocks. Carbonate rocks are composed mostly of calcium and magnesium carbonates. The contents of individual trace elements vary widely with rock type. Chromium, titanium, nickel, and cobalt are conspicuously concentrated in low-silica igneous rocks that are quantitatively unimportant. Arsenic, iodine, molybdenum, and selenium are conspicuously concentrated in shale and clay. In addition, most other elements occur in largest amounts in shale and clay compared to other sedimentary rocks, and in amounts nearly equal to those in igneous rocks. Soils derived from different kinds of igneous rocks do not differ from each other as much as do soils derived from different kinds of sedimentary rocks. This is partly because igneous rocks generally are more resistant to weathering than sedimentary rocks that were deposited in water. Some of the important constituents of sedimentary rocks have been precipitated from solution, which makes them more susceptible to weathering and re-solution. Similarly, sedimentary rocks have a greater effect than igneous rocks on the composition of ground water. Determination of areal variations in composition should be more detailed than normal petrologic investigations if the results are to be usable for environmental studies. Statistical principles should be used in planning the sampling, analysis, and interpretation of results.

Book chapter↗

Early Paleozoic development of the Maine-Quebec boundary Mountains region

Pre-Silurian bedrock units played key roles in the early Paleozoic history of the Maine-Quebec Appalachians. These units represent peri-Laurentian material whose collision with the craton deformed the Neoproteozoic passive margin and initiated the Appalachian mountain-building cycle. We present new field, petrological, geochronological, and geochemical data to support the following interpretations related to these units. (1) The Boil Mountain Complex and Jim Pond Formation do not represent part of a coherent ophiolite. (2) Gabbro and tonalite of the Boil Mountain Complex intruded the Chain Lakes massif at ca. 477 Ma. (3) The Skinner pluton, an arc-related granodiorite, intruded the Chain Lakes massif at ca. 472 Ma. (4) The Attean pluton, with a reconfirmed age of ca. 443 Ma, is unrelated to Early Ordovician orogenesis. (5) The most likely timing for the juxtaposition of the Jim Pond Formation and the Boil Mountain Complex was during regional Devonian deformation. These interpretations suggest that the Boundary Mountains were once part of a series of arcs extending at least from central New England through Newfoundland. ?? 2006 NRC Canada.

Canadian Journal of Earth Sciences↗

Chapter 1: Previous research

Santorini has fascinated and stimulated explorers and scholars since ancient times. Jason and the Argonauts were apparently visitors to the islands and described a giant called Talos. Molten metal flowed from his feet and he threw stones at them. The island is perhaps best known for the paroxysmal eruption that took place in the Late Bronze Age at the height of the Minoan civilization that dominated Crete and the Aegean region. The legend of Atlantis, in which a whole city sank beneath the sea in a single day and night, is plausibly based on the effects of this eruption on the Minoan Civilization. The geographer Strabo described the eruption of 197 bc in the following way: ... for midway between Thera and Therasia fires broke forth from the sea and continued for four days, so that the whole sea boiled and blazed, and the fires cast up an island which was gradually elevated as though by levers and consisted of burning masses... This introduction gives a brief synopsis of research on the volcano since this dramatic chronicle was written. Research on Santorini has contributed substantial advances not only in the understanding of Santorini itself but to general principles in volcanology and petrology. three centres for lava eruptions on Therasia and northern Thera: the Peristeria, Simandiri and Skaros-Therasia Volcanoes.

Santorini↗

Seismic evidence for a mantle source for mid-Proterozoic anorthosites and implications for models of crustal growth

Voluminous anorthosite intrusions are common in mid-Proterozoic crust. Historically, two end-member models have been proposed for the origin of these anorthosites. In the first model anorthosites derive from fractionation of a mantle source leaving a residue of metagabbro in the lower crust; in the second model anorthosites are the product of partial melting of the lower crust with residual pyroxene and high-grade minerals (i.e. a pyroxenitic and/or metapelitic lower crust). Although a general consensus has developed that the first model provides the best fit to petrological and geochemical constraints, the sparse evidence for mafic and ultramafic counterparts to the anorthosites leaves the issue still unresolved. We use the absolute P-wave velocity and the ratio between P- and S-wave velocities ( V P / V S ) to infer the composition of the lower crust beneath the Marcy Anorthosite (New York State, USA). Seismic refraction data reveal a lower crust 20 km thick, where V P and V P /V S range from top to bottom between 7.0 km s −1 and 7.2 ± 0.1 and 1.84 km s −1 and 1.81 ± 0.02, respectively. Laboratory measurements on rock samples indicate that these seismic properties are typical of plagioclase-rich rocks. Magmatic underplating of basaltic melts is a mechanism to form plagioclase-rich bulk composition for the Grenville crust. At the bottom of the lower crust, increase of P-wave velocity, slight decrease of V P / V S ratios and the presence of a low-reflective seismic Moho are additional observations supporting crustmantle interactions related to magmatic underplating. High P-wave velocity (8.6 km s −1 ) in the upper mantle may indicate that the ultramafic portion (e.g. pyroxenites) of the underplated magma has become eclogite. High average P-wave velocity (6.7 km s −1 ) and V P / V S (1.81), and the exceptional abundance of anorthosites-norites-troctolites among the rocks exposed at the surface, indicate that the Grenville Proterozoic crust may have a unique plagioclase-rich bulk composition. We suggest magmatic underplating, occurring either over a wide time span or with separate syn- and post-collisional magmatic pulses, as being a major crust-forming mechanism operating in mid-Proterozoic time.

Geological Society Special Publication↗

Upper Cretaceous Shannon Sandstone reservoirs, Powder River Basin, Wyoming: Evidence for organic acid diagenesis?

Comparison of the petrology of shallow and deep oil reservoirs in the Upper Cretaceous Shannon Sandstone Beds of the Steele Member of the Cody Shale strongly suggests that organic acids have had a more significant impact on the diagenetic alteration of aluminosilicate grains and carbonate cements in the deep reservoirs than in the shallow reservoirs. Vitrinite reflectance and Rock-Eval measurements, as well as the time-temperature index and kinetic modeling, indicate that deep reservoirs have been subjected to maximum temperatures of approximately 110-120 degrees C, whereas shallow reservoirs have reached only 75 degrees C. Only the deep reservoirs, therefore, have reached higher temperatures and have been (and some still are) within the zone (80-120 degrees C) of maximum organic acid production. Burial history reconstruction and paragenetic relations show that oil migration into Shannon reservoirs occurred in the middle to late Tertiary. In shallow reservoirs, detrital grains exhibit minor dissolution, sparse and small overgrowths, and secondary porosity created by dissolution of early calcite cement. However, deeper sandstones are characterized by extensive dissolution of detrital K-feldspar and detrital glauconite grains, and precipitation of abundant, large quartz and feldspar overgrowths. Quartz overgrowths commonly have crystallographically controlled etch pits. Throughout the Shannon and Steele, dissolution of glauconite and degradation of kerogen were probably aided by clay mineral/organic catalysis, which caused simultaneous reduction of iron and oxidation of kerogen. This process resulted in release of ferrous iron and organic acids and was promoted in the deep reservoirs by higher formation temperatures acco nting for more extensive dissolution of aluminosilicate grains. At the temperatures of deep Shannon reservoirs, alkalinity was buffered by organic acid anions so that iron released from glauconite precipitated as chlorite and abundant, multistage ferroan carbonate overgrowths. Carbonic acid produced from the dissolution of early calcite cement, decarboxylation of organic matter, and influx of meteoric water after Laramide uplift produced additional dissolution of cements and grains. Dissolution by organic acids and complexing by organic acid anions, however, best explain the intensity of diagenesis and absence of dissolution products in secondary pores and on etched surfaces of framework grains in deep reservoirs.

Wyoming↗

Pulsed Mesozoic deformation in the Cordilleran hinterland and evolution of the Nevadaplano: Insights from the Pequop Mountains, NE Nevada

Mesozoic crustal shortening in the North American Cordillera’s hinterland was related to the construction of the Nevadaplano orogenic plateau. Petrologic and geochemical proxies in Cordilleran core complexes suggest substantial Late Cretaceous crustal thickening during plateau construction. In eastern Nevada, geobarometry from the Snake Range and Ruby Mountains-East Humboldt Range-Wood Hills-Pequop Mountains (REWP) core complexes suggests that the ~10–12 km thick Neoproterozoic-Triassic passive-margin sequence was buried to great depths (>30 km) during Mesozoic shortening and was later exhumed to the surface via high-magnitude Cenozoic extension. Deep regional burial is commonly reconciled with structural models involving cryptic thrust sheets, such as the hypothesized Windermere thrust in the REWP. We test the viability of deep thrust burial by examining the least-deformed part of the REWP in the Pequop Mountains. Observations include a compilation of new and published peak temperature estimates ( ⁠ n = 60 "> n = 60 n=60 ⁠ ) spanning the Neoproterozoic-Triassic strata, documentation of critical field relationships that constrain deformation style and timing, and new 40 Ar/ 39 Ar ages. This evidence refutes models of deep regional thrust burial, including (1) recognition that most contractional structures in the Pequop Mountains formed in the Jurassic, not Cretaceous, and (2) peak temperature constraints and field relationships are inconsistent with deep burial. Jurassic deformation recorded here correlates with coeval structures spanning western Nevada to central Utah, which highlights that Middle-Late Jurassic shortening was significant in the Cordilleran hinterland. These observations challenge commonly held views for the Mesozoic-early Cenozoic evolution of the REWP and Cordilleran hinterland, including the timing of contractional strain, temporal evolution of plateau growth, and initial conditions for high-magnitude Cenozoic extension. The long-standing differences between peak-pressure estimates and field relationships in Nevadan core complexes may reflect tectonic overpressure.

Nevada↗

Book Review: Potassic igneous rocks and associated gold-copper mineralization, Fourth edition (D. Muller and D.I. Groves)

The fourth edition of this comprehensive textbook, which succeeds those published in 1995, 1997, and 2000, very nicely summarizes the geochemical and petrological characteristics of potassic igneous rock complexes and the different tectonic settings in which they occur. The authors provide an overview and a classification of these rocks and they outline the geochemical differences between barren and mineralized potassic igneous complexes. Owing to the common association of potassic igneous rocks with many gold- and copper-rich ore deposits, this book will be of interest not only to research scientists but also to those exploring for major deposits in young and ancient terranes. In fact, there was a clear attempt by the authors to provide a good mix of theoretical discussions based on experimental work, with case studies that illustrate field and applied research. Review info: Potassic Igneous Rocks and Associated Gold-Copper Mineralization , Fourth Edition. By Daniel M&uuml;ller, David I. Groves. 2016. ISBN 978-3-319-23051-1. 311 p.

Economic Geology↗

Outlook for further ore discoveries in the Little Hatchet Mountains, New Mexico

The Little Hatchet Mountains contain two mining districts, the Eureka silver-lead-zinc district and the Sylvanite gold district, the deposits of each being associated with a mass of monzonite that intrudes Lower Cretaceous sediments. The same formations crop out in both districts, having been duplicated by a large post-ore fault, and the two monzonite masses and their accompanying mineralized zones lie at essentially the same stratigraphic position in the two fault blocks. The deposits of the Eureka district are mesothermal whereas those of the Sylvanite district are hypothermal, but the two groups are mineralogically similar in many respects.As the two monzonite exposures are several miles apart, the natural inference is that there are two separate intrusions. Contrary to this inference, the evidence of structure, mineralogy, and petrology indicates that the two monzonite masses are faulted parts of the same body and that the mineralized areas of the Eureka and Sylvanite districts were originally continuous and zonally related, the original igneous mass having been a flat-lying sill-like streamer, 7 miles or more long, that was bordered by a contact-metamorphic halo and that formed the core of a zone of mineralization.The economic implications of this interpretation are three-fold: (1) the mineralized zone is limited in thickness and is restricted, like a bedded deposit, to a particular sedimentary horizon; (2) the area between the Eureka and Sylvanite districts, hitherto considered barren, should contain mineralized ground at variable depths below the surface; and (3) the deposits change along the trend of the zone from the gold deposits of the one district to the silver-bearing base-metal deposits of the other. In structure and size the deposits in the hidden parts of the mineralized zone probably are similar to those already known. Under the alternative interpretation that the two districts are separate centers of activity, the outlook for future successful prospecting depends upon the depths at which the underlying Paleozoic limestones lie and the possibility of large deposits having been formed in them.

New Mexico↗

Comparison of platinum, palladium, and rhodium distributions in some layered intrusions with special reference to the late differentiates (upper zone) of the Bushveld Complex, South Africa

The Stillwater, Fiskenaesset, and Bushveld Complexes are all composed of layered ultramafic and mafic rocks in which the cumulus phases generally appear in a regular order, which have similar petrologic and chemical characteristics, which are all Precambrian in age, and which contain platinum-group elements that vary widely in their abundances and relative proportions. Two of the complexes, the Stillwater and Bushveld, contain platinum-group element enriched horizons not yet found in the Fiskenaesset. The ratio of Pt/(Pt + Pd) in rocks from the Stillwater tends to increase from the basal zone to the middle of the ultramafic zone, decreases to the beginning of the banded zone, and then increases again through the banded zone; many fluctuations, however, are superimposed upon this generalized trend. The trends of Pt/(Pt + Pd) ratios appear to show a positive correlation with the Mg/(Mg + Fe (super +2) ) ratio in olivine. In the Fiskenaesset Complex, the Pt/(Pt + Pd) ratio increases rapidly from 0.3 to 0.7 from the lower gabbro and ultramafic units through the leucogabbro units, then increases slowly through the anorthosite and upper gabbro unit. Superimposed on this generalized trend are increasing and decreasing patterns within each unit.Analyses of platinum, palladium, and rhodium for 69 rocks from the main and upper zones of the eastern Bushveld from the Roossenekal area show generally low concentrations of less than 1 ppb Pt; 0.1 ppb Pd; and 0.1 ppb Rh, but larger amounts occur in some magnetite layers and sulfide-bearing zones. Within the main zone up to the pyroxenite marker, from the pyroxenite marker to below lower magnetite layer 2, and in the upper zone, the Pt/(Pt + Pd) ratio decreases with stratigraphic position, although with minor fluctuations in these intervals. The concentration levels of the platinum-group metals appear to be directly related to the amount of sulfide material present and the proportion of intercumulus material. Variations in Pt/(Pt + Pd) ratios in the Bushveld and Fiskenaesset Complexes are presumably related to changes in major mineral compositions as they are in the Stillwater Complex.

Economic Geology↗

Uranium mineralization in the Smith Lake district of the Grants uranium region, New Mexico.

The Mariano Lake and Ruby 1 uranium orebodies, which together comprise much of the uranium ore in the Smith Lake district of the Grants uranium region, New Mexico, occur in sandstones in the lower part of the Brushy Basin Member of the Upper Jurassic Morrison Formation. The orebodies, which are offset by faults of Laramide age, are enriched in an amorphous organic material that was introduced into the host sandstone after deposition. The enrichment by this organic material, in ore, is an important characteristic of the primary uranium deposits in the Grants uranium region. However, the close proximity of the chemically reduced ore zones to oxidized rock is suggestive that the deposits represent accumulations of uranium redistributed by reduction-oxidation processes from preexisting primary deposits.Within the ores, whole-rock abundances of organic carbon correlate positively with uranium contents. This correlation is consistent with petrologic evidence which indicates that uranium is everywhere intimately admixed with the amorphous organic material. Ore zones are also enriched in vanadium (as ore-stage vanadiferous chlorite) and sulfur (as ore-stage iron disulfide minerals with delta 34 S values ranging from -29 to -42ppm).Petrographic observations demonstrate that Smith Lake uranium mineralization occurred early (before major burial compaction) in the paragenetic sequence of host-rock diagenetic alterations but was preceded by precipitation of authigenic iron disulfides (delta 34 S values ranging from -11 to -38ppm), mixed-layered smectite-illite clays, and potassium feldspars.Additional preore alterations included dissolution of detrital sanidine and plagioclase and the leaching of iron from detrital iron-titanium oxide grains. Following mineralization, varying amounts of authigenic calcite and barite formed, both of which were partly replaced by kaolinitc. Oxidation of some previously formed iron disulfide minerals occurred late in the paragenetic sequence, as did localized precipitation of native selenium, pyrite, and very minor amounts of uranium minerals.The positive correlation between contents of uranium and organic carbon and the admixture of uranium with the amorphous organic material indicates that the Mariano Lake and Ruby 1 deposits are primary-type uranium orebodies. The offset of orebodies by Laramide faults and radiometric age determinations of the ores are also consistent with a primary origin for the deposits. Late Tertiary oxygenated ground waters locally modified original chemical and mineralogical characteristics of the ores in part by leaching some uranium. Secondary uranium minerals precipitated from the partly leached primary ores are sparse in the mine area; such recycled uranium appears to represent an insignificant proportion of the total uranium in the Smith Lake district.

Economic Geology↗

Lead isotope compositions of Late Cretaceous and early Tertiary igneous rocks and sulfide minerals in Arizona: Implications for the sources of plutons and metals in porphyry copper deposits

Porphyry copper deposits in Arizona are genetically associated with Late Cretaceous and early Tertiary igneous complexes that consist of older intermediate volcanic rocks and younger intermediate to felsic intrusions. The igneous complexes and their associated porphyry copper deposits were emplaced into an Early Proterozoic basement characterized by different rocks, geologic histories, and isotopic compositions. Lead isotope compositions of the Proterozoic basement rocks define, from northwest to southeast, the Mojave, central Arizona, and southeastern Arizona provinces. Porphyry copper deposits are present in each Pb isotope province. Lead isotope compositions of Late Cretaceous and early Tertiary plutons, together with those of sulfide minerals in porphyry copper deposits and of Proterozoic country rocks, place important constraints on genesis of the magmatic suites and the porphyry copper deposits themselves. The range of age-corrected Pb isotope compositions of plutons in 12 Late Cretaceous and early Tertiary igneous complexes is 206 Pb/ 204 Pb = 17.34 to 22.66, 207 Pb/ 204 Pb = 15.43 to 15.96, and 208 Pb/ 204 Pb = 37.19 to 40.33. These Pb isotope compositions and calculated model Th/U are similar to those of the Proterozoic rocks in which the plutons were emplaced, thereby indicating that Pb in the younger rocks and ore deposits was inherited from the basement rocks and their sources. No Pb isotope differences distinguish Late Cretaceous and early Tertiary igneous complexes that contain large economic porphyry copper deposits from less rich or smaller deposits that have not been considered economic for mining. Lead isotope compositions of Late Cretaceous and early Tertiary plutons and sulfide minerals from 30 metallic mineral districts, furthermore, require that the southeastern Arizona Pb province be divided into two subprovinces. The northern subprovince has generally lower 206 Pb/ 204 Pb and higher model Th/U, and the southern subprovince has higher 206 Pb/ 204 Pb and lower model Th/U. These Pb isotope differences are inferred to result from differences in their respective post-1.7 Ga magmatic histories. Throughout Arizona, Pb isotope compositions of Late Cretaceous and early Tertiary plutons and associated sulfide minerals are distinct from those of Jurassic plutons and also middle Tertiary igneous rocks and sulfide minerals. These differences most likely reflect changes in tectonic setting and magmatic sources. Within Late Cretaceous and early Tertiary igneous complexes that host economic porphyry copper deposits, there is commonly a decrease in Pb isotope composition from older to younger plutons. This decrease in Pb isotope values with time suggests an increasing involvement of crust with lower U/Pb than average crust in the source(s) of Late Cretaceous and early Tertiary magmas. Lead isotope compositions of the youngest porphyries in the igneous complexes are similar to those in most sulfide minerals within the associated porphyry copper deposit. This Pb isotope similarity argues for a genetic link between them. However, not all Pb in the sulfide minerals in porphyry copper deposits is magmatically derived. Some sulfide minerals, particularly those that are late stage, or distal to the main orebody, or in Proterozoic or Paleozoic rocks, have elevated Pb isotope compositions displaced toward the gross average Pb isotope composition of the local country rocks. The more radiogenic isotopic compositions argue for a contribution of Pb from those rocks at the site of ore deposition. Combining the Pb isotope data with available geochemical, isotopic, and petrologic data suggests derivation of the young porphyry copper-related plutons, most of their Pb, and other metals from a hybridized lower continental crustal source. Because of the likely involvement of subduction-related mantle-derived basaltic magma in the hybridized lower crustal source, an indiscernible mantle contribution is probable in the porphyry magmas. Clearly, in addition, Pb was contributed from the local country rocks. This is most evident in sulfide minerals in veins that are late stage, hosted in Proterozoic gneiss, and/or peripheral to the porphyry copper deposit.

Economic Geology↗

Lead in the Getchell-Turquoise ridge Carlin-type gold deposits from the perspective of potential igneous and sedimentary rock sources in Northern Nevada: Implications for fluid and metal sources

Lead isotope compositions of bulk mineral samples (fluorite, orpiment, and realgar) determined using conventional techniques and of ore-stage arsenian pyrite using the Sensitive High Resolution Ion-Microprobe (SHRIMP) in the Getchell and Turquoise Ridge Carlin - type gold deposits (Osgood Mountains) require contribution from two different Pb sources . One Pb source dominates the ore stage. It has a limited Pb isotope range characterized by 208 Pb/ 206 Pb values of 2.000 to 2.005 and 207 Pb/ 206 Pb values of 0.8031 to 0.8075, as recorded by 10-μm-diameter spot SHRIMP analyses of ore-stage arsenian pyrite. These values approximately correspond to 206 Pb/ 204 Pb of 19.3 to 19.6, 207 Pb/ 204 Pb of 15.65 to 15.75, and 208 Pb/ 204 Pb of 39.2 to 39.5. This Pb source is isotopically similar to that in average Neoproterozoic and Cambrian elastic rocks but not to any potential magmatic sources . Whether those clastic rocks provided Pb to the ore fluid cannot be unequivocally proven because their Pb isotope compositions over the same range as in ore-stage arsenian pyrite are similar to those of Ordovician to Devonian siliciclastic and calcareous rocks. The Pb source in the calcareous rocks most likely is largely detrital minerals, since that detritus was derived from the same sources as the detritus in the Neoproterozoic and Cambrian clastic rocks. The second Pb source is characterized by a large range of 206 Pb/ 204 Pb values (18-34) with a limited range of 208 Pb/ 204 Pb values (38.1-39.5), indicating low but variable Th/U and high and variable U/Pb values. The second Pb source dominates late and postore-stage minerals but is also found in preore sulfide minerals. These Pb isotope characteristics typify Ordovician to Devonian siliciclastic and calcareous rocks around the Carlin trend in northeast Nevada . Petrologically similar rocks host the Getchell and Turquoise Ridge deposits . Lead from the second source was either contributed from the host sedimentary rock sequences or brought into the hydrothermal system by oxidized ground water as the system collapsed. Late ore- and postore-stage sulfide minerals (pyrite, orpiment, and stibnite) from the Betze-Post and Meikle deposits in the Carlin trend and from the Jerritt Canyon mining district have Pb isotope characteristics similar to those determined in Getchell and Turquoise Ridge . This observation suggests that the Pb isotope compositions of their ore fluids may be similar to those at Getchell and Turquoise Ridge . Two models can explain the Pb isotope compositions of the ore-stage arsenian pyrite versus the late ore or postore sulfide minerals. In either model, Pb from the Ordovician to Devonian siliciclastic and calcareous rock source enters the hydrothermal system late in the ore stage but not to any extent during the main stage of ore deposition. In one model, ore-stage Pb was derived from a source with Pb isotope compositions similar to those of the Neoproterozoic and Cambrian clastic sequence, transported as part of the ore fluid and then deposited in the ore-stage arsenian pyrite and fluorite. The second model is based on the observation that the Pb isotope characteristics of the ore-stage minerals also are found in some Ordovician to Devonian calcareous and siliciclastic rocks. Hence, ore-stage Pb could have been derived locally and simply concentrated during the ore stage. Critical to the second model is the removal of all high 206 Pb/ 204 Pb (>20) material during alteration. It Also requires the retention of only the low 206 Pb/ 204 Pb component of the Ordovician to Devonian sedimentary rocks. This critical step is possible only if the high 206 Pb/ 204 Pb values are contained in readily dissolvable mineral phases, whereas the low 206 Pb/ 204 Pb values are found only in refractory minerals that released Pb during a final alteration stage just prior deposition of auriferous arsenian pyrite. Distinguishing between Pb transported with the ore fluid or inherited from the site of mineral deposition is not straightforward; however, it is simpler to explain the Pb isotope compositions of ore-stage arsenian pyrite and fluorite in two different but spatially related Carlin - type deposits ( Getchell and Turquoise Ridge ) with different host rocks by input of Pb with the ore fluid . Once the limited Pb in the hydrothermal fluid was exhausted by incorporation in ore-stage arsenian pyrite or other ore-stage minerals, Pb from the second source , the Ordovician to Devonian sedimentary rock sequences, became available for incorporation in some but not all of the late-stage sulfide minerals.

Nevada↗

On geological interpretations of crystal size distributions: Constant vs. proportionate growth

Geological interpretations of crystal size distributions (CSDs) depend on understanding the crystal growth laws that generated the distributions. Most descriptions of crystal growth, including a population-balance modeling equation that is widely used in petrology, assume that crystal growth rates at any particular time are identical for all crystals, and, therefore, independent of crystal size. This type of growth under constant conditions can be modeled by adding a constant length to the diameter of each crystal for each time step. This growth equation is unlikely to be correct for most mineral systems because it neither generates nor maintains the shapes of lognormal CSDs, which are among the most common types of CSDs observed in rocks. In an alternative approach, size-dependent (proportionate) growth is modeled approximately by multiplying the size of each crystal by a factor, an operation that maintains CSD shape and variance, and which is in accord with calcite growth experiments. The latter growth law can be obtained during supply controlled growth using a modified version of the Law of Proportionate Effect (LPE), an equation that simulates the reaction path followed by a CSD shape as mean size increases.

American Mineralogist↗