Major- and trace-element characterization, expanded distribution, and a new chronology for the latest Pleistocene Glacier Peak tephras in western North America

2009 ◽  
Vol 71 (2) ◽  
pp. 201-216 ◽  
Author(s):  
Stephen C. Kuehn ◽  
Duane G. Froese ◽  
Paul E. Carrara ◽  
Franklin F. Foit ◽  
Nicholas J.G. Pearce ◽  
...  

AbstractThe Glacier Peak tephra beds are among the most widespread and arguably some of the most important late Pleistocene chronostratigraphic markers in western North America. These beds represent a series of closely-spaced Plinian and sub-Plinian eruptions from Glacier Peak, Washington. The two most widespread beds, Glacier Peak ‘G’ and ‘B’, are reliably distinguished by their glass major and trace element abundances. These beds are also more broadly distributed than previously considered, covering at least 550,000 and 260,000 km2, respectively. A third bed, the Irvine bed, known only from southern Alberta, is similar in its major-element composition to the Glacier Peak G bed, but it shows considerable differences in trace element concentrations. The Irvine bed is likely considerably older than the G and B tephras and probably records an additional Plinian eruption, perhaps also from Glacier Peak but from a different magma than G through B. A review of the published radiocarbon ages, new ages in this study, and consideration in a Bayesian framework suggest that the widespread G and B beds are several hundred years older than widely assumed. Our revised age is about 11,600 14C yr BP or a calibrated age (at 2 sigma) of 13,710–13,410 cal yr BP.

The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.


2016 ◽  
Vol 154 (1) ◽  
pp. 68-86 ◽  
Author(s):  
PRANJIT HAZARIKA ◽  
DEWASHISH UPADHYAY ◽  
KAMAL LOCHAN PRUSETH

AbstractMica pegmatites from the Bihar Mica Belt contain three distinct generations of tourmaline. The major-element composition, substitution vectors and trajectories within each group are different, which indicates that the three types of tourmalines are not a part of one evolutionary series. Rather, the differences in their chemistries as well their mutual microtextural relations, can be best explained by growth of tourmaline from pegmatitic melts followed by episodic re-equilibration during discrete geological events. The euhedral, coarse-grained brown type I tourmaline cores have relatively high Ca, Mg (XMgc. 0.37) and Al with correlated variation in Sr, Sc, Ti, Zr, Y, Cr, Pb and Rare Earth elements (REEs). They are inferred to have crystallized from pegmatitic melts. Monazites included within these tourmalines give chemical ages of 1290−1242 Ma interpreted to date the crystallization of the pegmatitic tourmaline. The bluish type II and greyish type III tourmalines with low Ca and Mg contents (XMg = 0.16−0.27) and high Zn, Sn, Nb, Ta and Na, formed by pseudomorphic partial replacement of the pegmatitic tourmaline via fluid-mediated coupled dissolution–reprecipitation, are ascribed to a hydrothermal origin. The ages obtained from monazites included in these tourmalines indicate two alteration events at c. 1100 Ma and c. 950 Ma. The correlated variation of Ca, Mg and Fe and the trace elements Sr, Sn, Sc, Zn and REE within the tourmalines indicates that the trace-element concentrations of tourmaline are controlled not only by the fluid chemistry but also by coupled substitutions with major-element ions.


2003 ◽  
Vol 40 (8) ◽  
pp. 1027-1051 ◽  
Author(s):  
D Canil ◽  
D J Schulze ◽  
D Hall ◽  
B C Hearn Jr. ◽  
S M Milliken

This study presents major and trace element data for 243 mantle garnet xenocrysts from six kimberlites in parts of western North America. The geochemical data for the garnet xenocrysts are used to infer the composition, thickness, and tectonothermal affinity of the mantle lithosphere beneath western Laurentia at the time of kimberlite eruption. The garnets record temperatures between 800 and 1450°C using Ni-in-garnet thermometry and represent mainly lherzolitic mantle lithosphere sampled over an interval from about 110–260 km depth. Garnets with sinuous rare-earth element patterns, high Sr, and high Sc/V occur mainly at shallow depths and occur almost exclusively in kimberlites interpreted to have sampled Archean mantle lithosphere beneath the Wyoming Province in Laurentia, and are notably absent in garnets from kimberlites erupting through the Proterozoic Yavapai Mazatzal and Trans-Hudson provinces. The similarities in depths of equilibration, but differing geochemical patterns in garnets from the Cross kimberlite (southeastern British Columbia) compared to kimberlites in the Wyoming Province argue for post-Archean replacement and (or) modification of mantle beneath the Archean Hearne Province. Convective removal of mantle lithosphere beneath the Archean Hearne Province in a "tectonic vise" during the Proterozoic terminal collisions that formed Laurentia either did not occur, or was followed by replacement of thick mantle lithosphere that was sampled by kimberlite in the Triassic, and is still observed there seismically today.


AMBIO ◽  
2014 ◽  
Vol 43 (7) ◽  
pp. 878-890 ◽  
Author(s):  
Olof Regnell ◽  
Mark Elert ◽  
Lars Olof Höglund ◽  
Anna Helena Falk ◽  
Anders Svensson

Radiocarbon ◽  
2012 ◽  
Vol 54 (3-4) ◽  
pp. 351-358 ◽  
Author(s):  
Mitsuru Okuno ◽  
Masayuki Torii ◽  
Hideto Naruo ◽  
Yoko Saito-Kokubu ◽  
Tetsuo Kobayashi

Four late Pleistocene tephra layers—Tane I (Tn1), II (Tn2), III (Tn3), and IV (Tn4) in ascending order—are intercalated between widespread tephras, Kikai-Tozurahara (K-Tz: 95 ka) and Aira-Tn (AT: 30 cal kBP), on Tanegashima Island, in southern Japan. Paleolithic ruins such as the Yokomine C and Tatikiri archaeological sites were excavated from the loam layer between the Tn4 and Tn3 tephras. To refine the chronological framework on the island, we conducted accelerator mass spectrometry (AMS) radiocarbon dating for 2 paleosol and 6 charcoal samples related with the late Pleistocene tephras and the Yokomine C archaeological site. The obtained 14C dates are consistent with the stratigraphy in calendar years, 33 cal kBP for Tn4, 40 cal kBP for Tn3, and >50 cal kBP for Tn2 and Tn1. The charcoal dates from Yokomine C, 32–38 cal kBP, not only constrain the age of Tn4 and Tn3 ashes, but also serve as a possible date for the site. We also measured the major element compositions of volcanic glass shards with EDS-EPMA to characterize these tephras. Although we could not find a possible correlative for Tn3 and Tn4 ashes using major element oxides of the glass shards, i.e. 75–76 wt% in SiO2, the glass chemistry obtained in this study will be valuable in correlating these tephras with their source volcanoes in the near future.


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