Early Mesoproterozoic evolution of midcontinental Laurentia: Defining the geon 14 Baraboo orogeny

New geochronologic data from midcontinental Laurentia demonstrate that emplacement of the 1476-1470 Ma Wolf River granitic batholith was not an isolated igneous event,but was accompanied by regional metamorphism,deformation,and sedimentation.Evidence for such metamorphism and deformation is best seen in siliciclastic sedimentary rocks of the Baraboo Interval,which were deposited closely following the1.65-1.63 Ga Mazatzal orogeny.In Baraboo Interval strata,muscovite parallel to slatey cleavage,in hydrothermal veins,in quartzite breccia,and in metamorphosed paleosol yielded ~(40)Ar/~(39)Ar plateau age s of 1493-1465 Ma.In addition,U-Th-total Pb dating of neoblastic overgrowths on detrital monazite gave an age of 1488±20 Ma,and recrystallized hematite in folded metapelite gave a mean U/Th-He age of 1411± 39 Ma.Post-Baraboo,arkosic polymictic conglomerate,which contains detrital zircon with a minimum peak age of 1493 Ma,was intruded by a 1470 Ma granite porphyry at the northeastern margin of the Wolf River batholith.This episode of magmatism,regional deformation and metamorphism,and sedimentation,which is designated herein as the Baraboo orogeny,provides a midcontinental link between the Picuris orogeny to the southwe st and the Pinware orogeny to the northeast,completing the extent of early Mesoproterozoic(Calymmian) orogenesis for 5000 km along the southern margin of Laurentia.This transcontinental orogen is unique among Precambrian orogenies for its great width(～1600 km),the predominance of ferroan granites derived from partial melting of lower continental crust,and the prevalence of re gional high T-P metamorphism related to advective heating by granitic magmas emplaced in the middle to upper crust.     

Iron biomineralization by anaerobic neutrophilic iron-oxidizing bacteria

Minerals formed by bio-oxidation of ferrous iron (Fe(II)) at neutral pH, their association with bacterial ultrastructures as well as their impact on the metabolism of iron-oxidizing bacteria remain poorly understood. Here, we investigated iron biomineralization by the anaerobic nitrate-dependent iron-oxidizing bacterium Acidovorax sp. strain BoFeN1 in the presence of dissolved Fe(II) using electron microscopy and Scanning Transmission X-ray Microscopy (STXM). All detected minerals consisted mainly of amorphous iron phosphates, but based on their morphology and localization, three types of precipitates could be discriminated: (1) mineralized filaments at distance from the cells, (2) globules of 100 ± 25 nm in diameter, at the cell surface and (3) a 40-nm thick mineralized layer within the periplasm. All of those phases were shown to be intimately associated with organic molecules. Periplasmic encrustation was accompanied by an accumulation of protein moieties. In the same way, exopolysaccharides were associated with the extracellular mineralized filaments. The evolution of cell encrustation was followed by TEM over the time course of a culture: cell encrustation proceeded progressively, with rapid precipitation in the periplasm (in a few tens of minutes), followed by the formation of surface-bound globules. Moreover, we frequently observed an asymmetric mineral thickening at the cell poles. In parallel, the evolution of iron oxidation was quantified by STXM: iron both contained in the bacteria and in the extracellular precipitates reached complete oxidation within 6 days. While a progressive oxidation of Fe in the bacteria and in the medium could be observed, spatial redox (oxido-reduction state) heterogeneities were detected at the cell poles and in the extracellular precipitates after 1 day. All these findings provide new information to further the understanding of molecular processes involved in iron biomineralization by anaerobic iron-oxidizing bacteria and offer potential signatures of those metabolisms that can be looked for in the geological record.     

X-ray absorption fine structure study of As(V) and Se(IV) sorption complexes on hydrous Mn oxides

X-ray absorption fine structure (XAFS) spectroscopic analysis at the As, Se, and Mn K-edges was used to study arsenate [As(V)O₄³⁻] and selenite [Se(IV)O₃²⁻] sorption complexes on the synthetic hydrous manganese oxides (HMOs) vernadite (δ-MnO₂) and K-birnessite (nominal composition: K₄Mn₁₄O₂₇ · 9H₂O). No significant changes were observed in sorption complex structure as a function of sorbent, pH (5 to 8), surface coverage (0.04 to 0.73 μmol/m²), or reaction time (5 to 22 h) in the arsenate or selenite systems. In the arsenate/HMO system, extended XAFS parameters indicate an average second-neighbor As(V) coordination of 2.0 ± 0.4 Mn at an average distance of 3.16 ± 0.01 Å, which is consistent with formation of As(V)O₄ sorption complexes sharing corners with two adjacent Mn(IV)O₆ surface species (i.e., bidentate, binuclear). In the selenite/HMO system, selenite surface complexes are surrounded by two shells of Mn atoms, which could represent two different adsorption complexes or a precipitate. The first shell consists of 1.6 ± 0.4 Mn at 3.07 ± 0.01 Å, which is consistent with the selenite anion forming bidentate (mononuclear) edge-sharing complexes with Mn(II)O₆ or Mn(III)O₆ octahedra. The second shell consists of 1.4 ± 0.4 Mn at 3.49 ± 0.03 Å, consistent with selenite forming monodentate, corner-sharing complexes with Mn(II)O₆ or Mn(III)O₆ octahedra. Pauling bond valence analysis that uses the extended XAFS-derived bond lengths for As(V)-O, Se(IV)-O, and Mn-O bonds indicates that the proposed surface complexes of selenite and arsenate on HMOs should be stable. Although a nearly identical Se(IV) coordination environment is found in a crystalline Mn(II)-Se(IV) precipitate (which has a structure similar to that of MnSeO₃ · H₂O), there are significant differences in the X-ray absorption near-edge structure and extended XAFS spectra of this precipitate and the selenite/HMO sorption samples. These differences coupled with transmission electron microscopy results suggest that if a precipitate is present it lacks long-range order characteristic of crystalline MnSeO₃ · H₂O.     

Assessing subcontinental lithospheric mantle sources for basalts: Neogene volcanism in the Pacific Northwest,USA as a test case

Many objections have been raised as to the ability of subcontinental lithospheric mantle to produce voluminous amounts of basalt, because this upper part of the mantle is thought to be refractory, and the geotherm is rarely above the peridotite solidus at these depths under continents. However, in the Pacific Northwest of the USA during the Neogene, the subcontinental lithospehric mantle has been proposed as a key source for basalts erupted within the northern Basin and Range, and for the Columbia River flood basalts erupted on the Columbia Plateau. An alternative explanation to melting in the subcontinental lithospheric mantle, which equally well explains the chemical compositions thought to originate there, is that these magmas were contaminated by crust of varying ages. Calc-alkaline lavas, which occupy the Blue Mountains in the center of this region, hold clues to the latter process. Their elevated trace element ratios (e.g., Ba/Zr, K₂O/P₂O₅), coupled with differentiation indicators such as Mg? [molar Mg/(Mg?+?Fe)], and Sr, Nd, and Pb isotopic compositions, can most reasonably be explained by crustal contamination. Appraisal of continental peridotite xenolith data indicates that high trace element ratios such as Ba/Zr in continental basalts cannot result from melting in the subcontinental lithospheric mantle. Instead, as with the calc-alkaline lavas, these high ratios in the tholeiites most likely indicate crustal contamination. Furthermore, the peridotite xenoliths do not have a relative depletion in Nb and Ta that is observed in most of the lavas within the region. Relatively minor volumes of tholeiites erupted in late Neogene times in the northern Basin and Range (Hi-Mg olivine tholeiites) and Columbia Plateau (Saddle Mountains basalts), are the only lavas which have trace element and isotopic compositions consistent with being derived from, or largely interacting with a subcontinental lithospheric mantle in the Pacific Northwest. In contrast to the prior studies, we suggest that the mantle sources for most of the basalts in this region were ultimately beneath the lithospheric mantle.     

MEG Investigation of Low Pressure Silica — Shell model for polarization

We present a two-shell polarization model for the α-quartz and α-cristobalite structures. By allowing for polarization, we correct problems encountered in purely ionic bonding treatments of tetrahedrally coordinated silica phases. The shell model predicts zero pressure structures in very good agreement with experiment using no empirical parameters. The behavior of the shell model α-quartz lattice upon compression shows dramatic improvement over the distorted, rigid lattice given by the ionic model.     

Cultural sediment analyses and transitions in early fishing activity at Langenesværet,Vesterålen,Northern Norway

The development of specialized and commercial fishing activity in the island archipelago of Lofoten and Vesterålen in northern Norway is a critical foundation from which to understand the subsequent spread of commercial fishing across the north Atlantic region during the medieval and early modern period. One little understood aspect of this development is the relationship between medieval commercial fishing stations (fiskevaer) and earlier fishing activity. In this article, cultural sediment deposits at Langenesværet, Vesterålen, Northern Norway provide an opportunity to examine this relationship and its implications for current historical models of fishing development in northern Norway and the north Atlantic region. Conventional and AMS radiocarbon dating techniques are used to establish a chronology for the deposits, while activities associated with the sediments are characterized using thin‐section micromorphology supported by proton induced X‐ray emission spectrometry (PIXE). The results suggest that the site commenced formation as early as ca. 3000 B.C. and that the site was first used for specialized fishing activity from the early centuries A.D. The medieval commercial fiskevaer settlement at Langenesværet was introduced to an area that had a longstanding tradition of specialised fishing activity. © 2000 John Wiley & Sons, Inc.