Abstract Despite being a prominent continental-scale feature, the late Mesoproterozoic North American Midcontinent Rift did not result in the break-up of Laurentia, and subsequently underwent structural inversion. The timing of inversion is critical for constraining far-field effects of orogenesis and processes associated with the rift's failure. The Keweenaw fault in northern Michigan (USA) is a major thrust structure associated with rift inversion; it places ca. 1093 Ma rift volcanic rocks atop the post-rift Jacobsville Formation, which is folded in its footwall. Previous detrital zircon (DZ) U-Pb geochronology conducted by laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) assigned a ca. 950 Ma maximum age to the Jacobsville Formation and led researchers to interpret its deposition and deformation as postdating the ca. 1090–980 Ma Grenvillian Orogeny. In this study, we reproduced similar DZ dates using LA-ICP-MS and then dated 19 of the youngest DZ grains using high-precision chemical abrasion–isotope dilution–thermal ionization mass spectrometry (CA-ID-TIMS). The youngest DZ dated by CA-ID-TIMS at 992.51 ± 0.64 Ma (2σ) redefines the maximum depositional age of the Jacobsville Formation and overlaps with a U-Pb LA-ICP-MS date of 985.5 ± 35.8 Ma (2σ) for late-kinematic calcite veins within the brecciated Keweenaw fault zone. Collectively, these data are interpreted to constrain deposition of the Jacobsville Formation and final rift inversion to have occurred during the 1010–980 Ma Rigolet Phase of the Grenvillian Orogeny, following an earlier phase of Ottawan inversion. Far-field deformation propagated >500 km into the continental interior during the Ottawan and Rigolet phases of the Grenvillian Orogeny. 
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                            Apatites for destruction: Reference apatites from Morocco and Brazil for U-Pb petrochronology and Nd and Sr isotope geochemistry
                        
                    
    
            In situ apatite U-Pb petrochronology and Sr-Nd isotope geochemistry requires well-characterized and matrix-matched references materials (RMs), yet only a few suitable apatite RMs are currently available. To ameliorate this issue, we determined the U-Pb, Sm-Nd, and Sr isotopic and elemental compositions of a suite of prospective apatite RMs using isotope dilution (ID) TIMS and laser ablation (LA) ICP-MS. The two RMs, from Morocco (MRC-1) and Brazil (BRZ-1), are cm-sized and available in significant quantities. The U-Pb ID-TIMS data yield an isochron age of 153.3 ± 0.2 Ma for MRC-1. This age is consistent with laser ablation split stream ICP-MS (LASS) analyses that produce an isochron age of 152.7 ± 0.6 Ma. The weighted mean of ID-TIMS analyses for 143Nd/144Nd analyses is 0.512677 ± 3, for 147Sm/144Nd is 0.10923 ± 9, and for 87Sr/86Sr is 0.707691 ± 2. The range and mean of TIMS Sm-Nd isotopic data are reproducible by LA-ICP-MS, but laser ablation Sr data are consistently offset towards more radiogenic values. For BRZ-1 apatite, ID-TIMS U-Pb analyses are dispersed, but a subset of the data yields a coherent age intercept of 2078 ± 13 Ma. The vast majority of LASS spot transects across the apatite produce an isochron that define a younger age of 2038 ± 14 Ma. We interpret this as incorporation of cryptic, younger altered domains within BRZ-1. Discordant U-Pb spot analyses are associated with chemically distinct cracks, likely a result of fluid infiltration. The weighted means of ID-TIMS analyses of BRZ-1 yield 143Nd/144Nd = 0.510989 ± 5, 147Sm/144Nd = 0.10152 ± 8, and 87Sr/86Sr = 0.709188 ± 3. The distribution of Nd isotopic compositions of this RM measured by LA-MC-ICP-MS analyses are comparable to TIMS analyses. By contrast, 87Sr/86Sr measurements by LA-ICP-MS are inaccurate and exhibit large uncertainties, but this RM can be useful for empirically correcting in situ 87Sr/86Sr measurements. The data indicate that MRC-1 apatite may serve well as a U-Pb, Sm-Nd, and Sr RM, whereas BRZ-1 apatite has the most potential as a Sm-Nd RM. These potential RMs provide new benchmarks for in situ apatite chemical analyses and inter-laboratory calibrations. 
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                            - PAR ID:
- 10313860
- Editor(s):
- Chauvel, Catherine
- Date Published:
- Journal Name:
- Chemical geology
- Volume:
- 590
- ISSN:
- 0009-2541
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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