Crystal orientation effects during ion microprobe U-Pb analysis of baddeleyite

We show that Pb-206/U-238 ratios measured in baddeleyite by ion microprobe vary significantly (up to +/- 10% or more) and systematically with the rela tive orientation of the baddeleyite crystal structure and the primary ion b eam. Low dispersion between multiple analyses of single crystals demonstrat es that it is possible to measure undispersed Pb-206/U-238 ratios in multi- grain baddeleyite samples if all material is in a single orientation. Owing to the small size of most crystals and their ubiquitous polysynthetic {100 } twinning, however, it is extremely difficult to arrange a reasonable numb er of crystals in identical orientations for analysis. These orientation ef fects constitute an intractable problem, and place unacceptable limits on t he accuracy and precision that can be obtained for Pb-206/U-238 in baddeley ite by ion microprobe techniques. Comparisons with isotope dilution measure ments indicate that any Pb isotope discrimination during analysis of baddel eyite by ion microprobe is negligible, and there is no evidence that Pb iso tope ratios vary with crystal orientation. Although the precision of Pb-207 /Pb-206 ages decreases for younger samples, rocks younger than 1 Ga can be dated precisely if the baddeleyite is enriched sufficiently in uranium and if enough analyses are performed. We speculate that orientation effects in baddeleyite might involve channelling of primary ions into the crystal, emi ssion of secondary ions along preferred directions, and/or differential ion isation of secondary species. No orientation-related differences in Pb-206/ U-238 were detected during ion microprobe analysis of zircon or monazite. ( C) 2000 Elsevier Science B.V. All rights reserved.