Back to Search Start Over

Differential behavior of components of the 238U-206Pb and 235U-207Pb isotopic systems in polymineralic U ores.

Authors :
Golubev, V.
Chernyshev, I.
Source :
Geochemistry International; Apr2009, Vol. 47 Issue 4, p321-328, 8p
Publication Year :
2009

Abstract

U-Pb systems were examined in samples (ranging from 4 to 10 cm<superscript>3</superscript> in volume) of ore material taken from along a 3.5-m profile across a zone of U mineralization exposed in an underground mine at the Strel’tsovskoe U deposit in eastern Transbaikalia. The behaviors of two isotopic U-Pb systems (<superscript>238</superscript>U-<superscript>206</superscript>Pb and <superscript>235</superscript>U-<superscript>207</superscript>Pb) are principally different in all samples from our profile. While the individual samples are characterized by a vast scatter of their T(<superscript>206</superscript>Pb/<superscript>238</superscript>U) age values (from 112 to 717 Ma), the corresponding T(<superscript>207</superscript>Pb/<superscript>235</superscript>U) values vary much less significantly (from 127 to 142 Ma) and are generally close to the true age of the U mineralization. The main reason for the distortion of the U-Pb system is the long-lasting (for tens of million years) migration of intermediate decay products in the <superscript>238</superscript>U-<superscript>206</superscript>Pb(RD<superscript>238</superscript>U) in the samples. This process resulted in the loss of RD<superscript>238</superscript>U from domains with high U concentrations and the subsequent accommodation of RD<superscript>238</superscript>U at sites with low U concentrations. The long-term effect of these opposite processes resulted in a deficit or excess of <superscript>206</superscript>Pb as the final product of <superscript>238</superscript>U decay. The loss or migration of RD<superscript>238</superscript>U are explained by the occurrence of pitchblende in association with U oxides that have higher Si and OH concentrations than those in the pitchblende and a higher <superscript>+6</superscript>U/<superscript>+4</superscript>U ratio. The finely dispersed character of the mineralization and the loose or metamict texture of the material are the principal prerequisites for RD<superscript>238</superscript>U loss and an excess of <superscript>206</superscript>Pb in adjacent domains with low U concentrations. Domains with low U contents in the zone with U mineralization serve as geochemical barriers (because of sulfides contained in them) at which long-lived RD<superscript>238</superscript>U(<superscript>226</superscript>Ra, <superscript>210</superscript>Po, <superscript>210</superscript>Bi, and <superscript>210</superscript>Pb) were accommodated and subsequently caused an excess of <superscript>206</superscript>Pb. The <superscript>235</superscript>U-<superscript>207</superscript>Pb system remained closed because of the much briefer lifetime of the <superscript>235</superscript>U decay products. This may account for the significant discrepancies between the T(<superscript>206</superscript>Pb/<superscript>238</superscript>U) and T(<superscript>207</superscript>Pb/<superscript>235</superscript>U) age values. RD<superscript>238</superscript>U was most probably lost via the migration of radioisotopes at the middle part and end of the <superscript>238</superscript>U family (starting with <superscript>226</superscript>Ra). The heavy Th, Pa, and U radioisotopes (<superscript>234</superscript>Th, <superscript>234</superscript>Pa, <superscript>234</superscript>U, and <superscript>230</superscript>Th) that occur closer to the beginning of <superscript>238</superscript>U decay, before <superscript>226</superscript>Ra, only relatively insignificantly participated in the process. Our results show that the loss and migration of RD<superscript>238</superscript>U are, under certain conditions, the main (or even the only) process responsible for the distortion of the U-Pb system. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00167029
Volume :
47
Issue :
4
Database :
Complementary Index
Journal :
Geochemistry International
Publication Type :
Academic Journal
Accession number :
49569319
Full Text :
https://doi.org/10.1134/S0016702909040016