Alteration of Trace Lead Isotopic Ratios by Postore Metamorphic and Hydrothermal Activity

1973 ◽  
Vol 10 (12) ◽  
pp. 1782-1789 ◽  
Author(s):  
G. L. Cumming ◽  
P. J. Gudjurgis

Isotope analyses on leads in iron sulfides and trace galenas from two deposits (Big Ledge, British Columbia and Quemont Mine, Quebec) suggest that variations in the isotopic composition may be influenced by postmineralization alteration of ore. It is postulated that when the ore has been subject to regional metamorphism after emplacement, the metamorphism has homogenized the lead isotope ratios throughout the ore body as appears to have happened at Big Ledge, whereas, if postore activity is limited to minor hydrothermal alteration, as at Quemont, then the lead may be left with a wide range of isotopic composition.

1983 ◽  
Vol 20 (10) ◽  
pp. 1521-1527
Author(s):  
W. F. Slawson

Twelve new lead isotope analyses of samples from the West and East Shasta districts, California are presented. The measured isotopic ratios 206Pb/204Pb versus 207Pb/204Pb exhibit a good linear trend with a slope of 0.1794 ± 0.0066. Arguments are presented that the two-stage ages calculated from this slope are not real events. It is suggested the linear array is due to fortuitous addition of contaminants to the volcanogenic mineralizations. Thus common lead isotopes are possibly better geochemical tracers than they are geochronometers. This may be particularly true in cases where the total lead content is low.


1987 ◽  
Vol 24 (10) ◽  
pp. 2089-2098 ◽  
Author(s):  
John N. Aleinikoff ◽  
Cynthia Dusel-Bacon ◽  
Helen L. Foster ◽  
Warren J. Nokleberg

Common lead isotopic compositions have been determined on feldspars from meta-igneous rocks from nine tectono-stratigraphic terranes or subterranes in east-central Alaska. Most of the terranes have distinct and well-defined signatures in terms of isotopic composition; thus, most can be distinguished on conventional lead isotopic diagrams. Lead isotopic ratios provide evidence for (1) possible sources for the igneous rocks, (2) time of metamorphism, (3) correlation of terrane fragments, and (4) delineation of juxtaposed terranes. Determination of lead isotopic ratios from igneous rocks can be useful in characterizing tectono-stratigraphic terranes (as to mantle or crustal origin) and in correlation, particularly where terrane relationships are enigmatic.


1986 ◽  
Vol 23 (10) ◽  
pp. 1603-1614 ◽  
Author(s):  
A. James Macdonald ◽  
Marek J. Kreczmer ◽  
Stephen E. Kesler

Discovered in 1553, the Fresnillo mine in central Mexico has produced approximately 18 t Au, 8830 t Ag, 690 000 t Pb, 925 600 t Zn, and 74 000 t Cu (data for production from 1921 to 1984 inclusive). Ore has been mined from an oxide capping near surface and from unoxidized veins, mantos, and chimneys to a depth of 1 km along a strike length of 4 km. Ore zones at depth, in the northwest portion of the mine, are spatially related to a quartz monzonite porphyry stock, which intrudes a sequence of Mesozoic marine sediments that is overlain by terrestrial rhyolites. Manto and chimney mineralization followed development of skarn around the intrusion and was cut, in turn, by the veins that contain the bulk of the ore. The veins cut the quartz monzonite stock. Manto and chimney mineralization is characterized by partial replacement of the Mesozoic sedimentary rocks with axinite, hedenbergite, quartz, carbonate, sulphides, sulphosalts, sulpharsenides, and sulphantimonides. Brecciation preceded replacement in the chimney bodies. One of the largest replacement orebodies, the Cueva Santa Branch Manto in the central part of the mine, contains an orthogonal fracture set formed during antiformal folding. Trends in grade distribution throughout the manto follow the orthogonal fractures, which are filled by quartz and sulphides. Silver/base-metal ratios show marked peaks where manto mineralization abuts against major veins. Fluid-inclusion filling temperatures and salinities are high in ore zones adjacent to the quartz monzonite stock at a depth of 1 km: mean filling temperature is approximately 320 °C (range 230–370 °C), salinity ranges from 4 to 12 eq. wt.% NaCl. Fluid inclusions from ore near surface exhibit lower filling temperatures (a mean of 235 °C and a range of 210–290 °C) and lower salinity (< 1 eq. wt.% NaCl). The data are consistent with a reduction in temperature and with dilution as the hydrothermal fluids flowed away from the intrusive porphyry.δ34S values for sphalerite, galena, and chalcopyrite from deeper and intermediate levels in the mine range from −6.1 to −3.5‰. Calculated δ34SΣS is approximately 0‰, suggesting a magmatic sulphur source. Lead isotopic ratios obtained from galena-bearing vein, manto, and chimney samples throughout the mine fall on a line defined by 34 deposits in northern Mexico with slope of 0.092 ± 0.017 in the 208Pb/204Pb versus 207Pb/204Pb system. The lead data indicate that felsic igneous processes extracted the metal from a Precambrian basement source; this was followed by concentration within mineralized zones during hydrothermal activity.


1997 ◽  
Vol 506 ◽  
Author(s):  
H. Isobe ◽  
H. Hidaka ◽  
T. Ohnuki

ABSTRACTLead, the final decay product of uranium, is found in natural uranium ore deposits. The isotope composition of lead in uranium-bearing minerals reflects their age and the migration behavior of lead. Secondary Ion Mass Spectroscopy (SIMS) can be used to analyze the isotopic composition of minerals. SIMS analysis of lead contained in the Koongarra uranium deposit, Australia, revealed that uraninite and uranyl minerals with different chemical composition in the primary ore region have homogeneous lead isotope, from the highest grade area to a uranyl silicate zone at a distance of 6.1m. Uranyl minerals, which have good crystallinity and retain stoichiometric composition, have “old” lead isotope composition identical to that of uraninite. Uranyl minerals keep exchanging lead with ground water in the primary ore region through metamictization and recrystallization by alpha-decay damage. Sulfide minerals just outside the primary ore body contain only radiogenic lead with an isotopic composition different from that of uranium minerals. Lead that migrated from the primary ore body formed sulfide minerals in a specific geological event. Since then, lead produced from uranium decay has been retained in the primary ore body, in spite of recrystallization of uranyl minerals and exchange and homogenization of lead isotopes. Uranium minerals may retain minor elements despite intense alpha-decay dose.


1998 ◽  
Vol 29 (1) ◽  
pp. 1-20 ◽  
Author(s):  
Peter Raben ◽  
Wilfred H. Theakstone

Marked vertical variations of ions and oxygen isotopes were present in the snowpack at the glacier Austre Okstindbreen during the pre-melting phase in 1995 at sites between 825 m and 1,470 m above sea level. As the first meltwater percolated from the top of the pack, ions were moved to a greater depth, but the isotopic composition remained relatively unchanged. Ions continued to move downwards through the pack during the melting phase, even when there was little surface melting and no addition of liquid precipitation. The at-a-depth correlation between ionic concentrations and isotopic ratios, strong in the pre-melting phase, weakened during melting. In August, concentrations of Na+ and Mg2+ ions in the residual pack were low and vertical variations were slight; 18O enrichment had occurred. The difference of the time at which melting of the snowpack starts at different altitudes influences the input of ions and isotopes to the underlying glacier.


2021 ◽  
Vol 37 ◽  
pp. 102970
Author(s):  
Takeshi Minami ◽  
Akinori Takeuchi ◽  
Setsuo Imazu ◽  
Masayoshi Okuyama ◽  
Yu Higashikage ◽  
...  

1995 ◽  
Vol 311 (2) ◽  
pp. 141-151 ◽  
Author(s):  
W. Chisholm ◽  
K.J.R. Rosman ◽  
C.F. Boutron ◽  
J.P. Candelone ◽  
S. Hong

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