Éditeur(s) : HAL CCSD Elsevier
Résumé : LA-ICP-MS and SIMS U–Pb analyses have been performed on detrital zircon grains from four heavy mineral rich metasediments collected at different levels of the Nathorst Land Group (Eleonore Bay Supergroup, Greenland). Zircons from high-grade samples collected in the sillimanite and migmatite zones exhibit modifications to their structure, which are lacking in grains from a low-grade sample (0.3 GPa and 350–400 °C). In the sillimanite zone (0.5 GPa, 650 °C), thin discontinuous rims (<20 μm) plating detrital zircon grains document a metamorphic overgrowth during the Caledonian event dated at 428 ± 25 Ma (2σ). In the migmatite zone (0.4 GPa, 700 °C), zircons underwent severe recrystallisation processes but no new zircon growth. Ilmenite, which constitutes over 50% of the heavy mineral layers, underwent recrystallisation in both high-grade samples and is likely to represent the main source of Zr available for growth of zircon rims in the sillimanite zone. However, in the migmatite zone sample, the metamorphic conditions allowed titanite overgrowth around ilmenite, which acted as a sink for Zr and inhibited new zircon growth. 207Pb/206Pb ages for 152 detrital zircons broadly range between 2800 and 990 Ma. The detrital zircon age signature is characterized by the large predominance of late Paleoproterozoic (1.85–1.60 Ga) grains in all analysed samples and by lesser amounts of Archean (2.7–2.8 Ga) and Mesoproterozoic (1.2–1.0 Ga) zircons. The overall age range indicates that detritus can be sourced from the Labradorian and Makkovikian provinces of northeastern Laurentia. The youngest grain analysed (987 ± 18 Ma) indicates that deposition took place during the Neoproterozoic, in a post-Grenvillian sedimentary environment and was likely coeval with the Mid-Neoproterozoic episode of aborted rifting that affected the eastern margin of Laurentia. The lack of detritus originating from Amazonia or Baltica, placed adjacent to Laurentia during the early stages of Rodinia fragmentation, suggests that these two continental landmasses did not constitute a topographic high during the Neoproterozoic or that the Mid-Neoproterozoic rifting opened toward an open ocean to the north of a combined Laurentia/Baltica, thus resulting in a general south to north direction of transport of the sediments.
ISSN: 0301-9268

hal-00407204
https://hal.archives-ouvertes.fr/hal-00407204
DOI : 10.1016/j.precamres.2007.01.002

Éditeur(s) : HAL CCSD Springer Verlag (Germany) Springer Verlag
Résumé : International audience
Peridotite xenoliths erupted by alkali basaltic volcanoes in the western Pannonian Basin can be divided into two fundamentally contrasting groups. Geochemical characteristics of the abundant protogranular, porphyroclastic and equigranular nodules suggest that these samples originate from an old consolidated and moderately depleted lithospheric mantle domain. In contrast, the geochemical features of the worldwide rare, but in the Pannonian Basin relatively abundant, poikilitic xenoliths attest to a more complex evolution. It has been argued that the origin of the peculiar texture and chemistry may be intimately linked to melt/rock reactions at successively decreasing liquid volumes in a porous melt flow system. The most likely site where such reactions can take place is the asthenosphere-lithosphere boundary. In this context, poikilitic xenoliths may provide petrological and geochemical evidence for reactions between magmatic liquids issued from the uprising asthenosphere and the solid mantle rocks of the lithosphere. These reactions are important agents of the thermal erosion of the lithosphere; thus, they could have considerably contributed to the thinning of the lithosphere in the Pannonian region. We suggest that in the Pannonian Basin, there could be a strong relation between the unusual abundance of poikilitic mantle xenoliths and the strongly eroded lithosphere.
ISSN: 0010-7999

hal-01107421
https://hal.archives-ouvertes.fr/hal-01107421
DOI : 10.1007/s00410-014-1054-y

Éditeur(s) : HAL CCSD Elsevier Masson
Résumé : Ten international laboratories participated in an inter-laboratory comparison of a fossil bone composite with the objective of producing a matrix and structure-matched reference material for studies of the bio-mineralization of ancient fossil bone. We report the major and trace element compositions of the fossil bone composite, using in-situ method as well as various wet chemical digestion techniques. For major element concentrations, the intra-laboratory analytical precision (%RSDr) ranges from 7 to 18%, with higher percentages for Ti and K. The %RSDr are smaller than the inter-laboratory analytical precision (%RSDR; <15-30%). Trace element concentrations vary by similar to 5 orders of magnitude (0.1 mg kg(-1) for Th to 10,000 mg kg(-1) for Ba). The intra-laboratory analytical precision %RSDr varies between 8 and 45%. The reproducibility values (%RSDR) range from 13 to <50%, although extreme value >100% was found for the high field strength elements (Hf, Th, Zr, Nb). The rare earth element (REE) concentrations, which vary over 3 orders of magnitude, have %RSDr and %RSDR values at 8-15% and 20-32%, respectively. However, the REE patterns (which are very important for paleo-environmental, taphonomic and paleo-oceanographic analyses) are much more consistent. These data suggest that the complex and unpredictable nature of the mineralogical and chemical composition of fossil bone makes it difficult to set-up and calibrate analytical instruments using conventional standards, and may result in non-spectral matrix effects. We propose an analytical protocol that can be employed in future inter-laboratory studies to produce a certified fossil bone geochemical standard. (C) 2007 Elsevier B.V. All rights reserved.
ISSN: 0003-2670

hal-00407629
https://hal.archives-ouvertes.fr/hal-00407629
DOI : 10.1016/j.aca.2007.08.015