Thermal effects in the ultrarelativistic two-stream instability

The dispersion relation for longitudinal waves in a one-dimensional ultrarelativistic plasma is calculated. Analytical and numerical results for the growth rate and frequency of the two-stream instability are presented as a function of the energy spread in the denser stream when the dilute stream is cold. The case of energy spreads in both beams is investigated numerically: it is found that relatively small energy spreads in both streams can lead to suppression of the instability.     

The Mordor Alkaline Igneous Complex,Central Australia: PGE-enriched disseminated sulfide layers in cumulates from a lamprophyric magma

The Mordor Alkaline Igneous Complex (MAIC) is a composite intrusion comprising a body of syenite and a funnel-shaped layered mafic–ultramafic intrusion of lamprophyric parentage, the Mordor Mafic–Ultramafic Intrusion or MMUI. The MMUI is highly unusual among intrusions of lamprophyric or potassic parentage in containing primary magmatic platinum-group element (PGE)-enriched sulfides. The MMUI sequence consists largely of phlogopite-rich pyroxenitic cumulates, with an inward dipping conformable layer of olivine-bearing cumulates divisible into a number of cyclic units. Stratiform-disseminated sulfide accumulations are of two types: disseminated layers at the base of cyclic units, with relatively high PGE tenors; and patchy PGE-poor disseminations within magnetite-bearing upper parts of cyclic units. Sulfide-enriched layers at cycle bases contain anomalous platinum group element contents with grades up to 1.5 g/t Pt+Pd+Au over 1-m intervals, returning to background values of low parts per billion (ppb) on a meter scale. They correspond to reversals in normal fractionation trends and are interpreted as the result of new magma influxes into a continuously replenished magma chamber. Basal layers have decoupled Cu and PGE peaks reflecting increasing PGE tenors up-section, due to increasing R factors during the replenishment episode, or progressive mixing of between resident PGE-poor magma and more PGE-enriched replenishing magma. The presence of PGE enriched sulfides in cumulates from a lamprophyric magma implies that low-degree partial melts do not necessarily leave sulfides and PGEs in the mantle restite during partial melting. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

High resolution paleoenvironmental and chronological investigations of Norse landnám at Tasiusaq, Eastern Settlement, Greenland

High-resolution paleoenvironmental data from a peat profile with a small pollen source area are used to reconstruct the impacts of landnám on vegetation and soils at a Norse farm complex (∅2 at Tasiusaq) comprising two farms in the Eastern Settlement of Greenland. Analyses include the AMS ¹⁴C dating of plant macrofossil samples and the use of Bayesian radiocarbon calibration to construct improved age-depth models for Norse cultural horizons. The onset of a regional landnám may be indicated by the clearance of Betula pubescens woodland immediately prior to local settlement. The latter is dated to AD 950-1020 (2σ) and is characterised by possible burning of Betula glandulosa scrub to provide grassland pasture for domestic stock. Clearance and grazing resulted in accelerated levels of soil erosion at a westerly farm. This was followed by an easterly migration of settlement and agriculture. Site constraints prevent an assessment of the demise of the easterly farm, but pressures of overgrazing and land degradation may have been the major factors responsible for the abandonment of the earlier farm.     

Basement–cover relationships of the Kalak Nappe Complex, Arctic Norwegian Caledonides and constraints on Neoproterozoic terrane assembly in the North Atlantic region

The Kalak Nappe Complex (KNC) has been regarded as Baltica passive margin metasediments telescoped eastwards onto the Baltic (Fennoscandian) Shield during the Caledonian Orogeny. Recent studies have questioned this interpretation, instead pointing to a Neoproterozoic exotic origin. In an effort to resolve this controversy we present a Sm–Nd and U–Th–Pb study of gnessic units, traditionally considered as the depositional basement, along with cover rock sediments and intrusives. Late Palaeoproterozoic gneisses now beneath the KNC were deposited after 1948 ± 33 Ma, before intrusion of the Tjukkfjellet Granite at 1796 ± 3 Ma, and were affected by later melting events at 1765 ± 9 and 1727 ± 9 Ma. These gneisses are interpreted as part of the Baltic Shield and underlie the KNC across a tectonic contact. An unconformity between psammites of the KNC and other paragneisses previously considered as its Precambrian basement is reinterpreted as a modified sedimentary contact between Neoproterozoic metasediments. These metasediments have statistically very similar detrital zircon populations with grains as young as 1034 ± 22, 1025 ± 32 and 1014 ± 14 Ma. The results indicate that the KNC sediments were deposited during the Neoproterozoic in basins along the Laurentian margin of eastern Rodinia and were not connected to Baltica via a depositional basement. Dating of the 851 ± 5 Ma Eidvågvatnet and 853 ± 4 Ma Nordneset granites shows that intrusive material associated with the Porsanger Orogeny (c. 850 Ma) affected a considerable region of the upper KNC terrane. Later Neoproterozoic events at 711 ± 6, 687 ± 12 and 617 ± 6 Ma are also recognised the latest of which may be an expression of rifting. Since early Neoproterozoic magmatism (c. 840–690 Ma) is unknown in Baltica, these results support an exotic origin for the KNC terranes.     

Cr-spinel/olivine and Cr-spinel/liquid nickel partition coefficients from natural samples

The Nernst partition coefficient of nickel (D^Ni) between Cr-spinel and silicate melt in natural systems has been investigated using mid-ocean ridge basalts (MORB) and other volcanic rocks. The Cr-spinel/olivine D^Ni values in volcanic rocks are between 1.2 and 0.3, indicating that the Cr-spinel/liquid D^Ni values vary from slightly higher to significantly lower than the olivine/liquid D^Ni values in natural systems. The Cr-spinel/liquid D^Ni values from the MORB samples vary between 6 and 11, slightly higher than those from the S-bearing experiments of Satari et al. [Satari P., Brenan J. M., Horn I. and McDonough W. F. (2002) Experimental constraints on the sulfide- and chromite-silicate melt partitioning behavior of rhenium and platinum-group elements. Economic Geology97, 385-398]. The results of the MORB samples and the experiments of Satari et al. (2002) indicate a negative correlation between the Cr-spinel/liquid D^Ni and the X_Cr values in Cr-spinels (Cr cation number on the basis of 3 total cations in the spinel structure). Variations of Cr-spinel/liquid D^Ni values with Cr-spinel compositions can be estimated from an empirical equation based on the results of the MORB samples and the experiments by Satari et al. (2002). The choice of Cr-spinel/liquid D^Ni = 10 for numerical modeling by Righter et al. [Righter K., Leeman W. P. and Hervig R. L. (2006) Partitioning of Ni, Co, and V between spinel-structured oxides and silicate melts: importance of spinel composition. Chemical Geology227, 1-25] is reasonable for basaltic systems. For picritic and komatiitic systems a lower value of ∼5 is more appropriate.     

Iron isotope fractionation in subterranean estuaries

Dissolved Fe concentrations in subterranean estuaries, like their river-seawater counterparts, are strongly controlled by non-conservative behavior during mixing of groundwater and seawater in coastal aquifers. Previous studies at a subterranean estuary of Waquoit Bay on Cape Cod, USA demonstrate extensive precipitation of groundwater-borne dissolved ferrous iron and subsequent accumulation of iron oxides onto subsurface sands. Waquoit Bay is thus an excellent natural laboratory to assess the mechanisms of Fe-isotope fractionation in redox-stratified environments and determine potential Fe-isotope signatures of groundwater sources to coastal seawater. Here, we report Fe isotope compositions of iron-coated sands and porewaters beneath the intertidal zone of Waquoit Bay. The distribution of pore water Fe shows two distinct sources of Fe: one residing in the upward rising plume of Fe-rich groundwater and the second in the salt-wedge zone of pore water. The groundwater source has high Fe(II) concentration consistent with anoxic conditions and yield δ⁵⁶Fe values between 0.3 and −1.3‰. In contrast, sediment porewaters occurring in the mixing zone of the subterranean estuary have very low δ⁵⁶Fe values down to −5‰. These low δ⁵⁶Fe values reflect Fe-redox cycling and result from the preferential retention of heavy Fe-isotopes onto newly formed Fe-oxyhydroxides. Analysis of Fe-oxides precipitated onto subsurface sands in two cores from the subterranean estuary revealed strong δ⁵⁶Fe and Fe concentration gradients over less than 2m, yielding an overall range of δ⁵⁶Fe values between −2 and 1.5‰. The relationship between Fe concentration and δ⁵⁶Fe of Fe-rich sands can be modeled by the progressive precipitation of Fe-oxides along fluid flow through the subterranean estuary. These results demonstrate that large-scale Fe isotope fractionation (up to 5‰) can occur in subterranean estuaries, which could lead to coastal seawater characterized by very low δ⁵⁶Fe values relative to river values.     

The effect of As, Co, and Ni impurities on pyrite oxidation kinetics: Batch and flow-through reactor experiments with synthetic pyrite

Pyrite samples synthesized with As, Co, or Ni impurities and without added impurities were oxidized in batch and mixed flow-through reactors in the presence of 1 mM ferric iron, at pH 2. Six samples from each dopant population were used to provide a statistically robust comparison; two natural samples from Leadville, CO (major impurities Pb, As, Bi, Ag, Zn) and Elba, Italy (Co, As) were also included. In each experiment, three reaction progress variables were monitored: ferric iron, ferrous iron, and sulfate. The pyrite samples with impurities have average oxidation rates that are faster than the undoped samples, with As- and Co-doped pyrite having the highest rates. As, Co, and Ni were released to solution in accordance with their concentrations in the solid samples. As concentrations in the batch reactor experiments tended to remain constant, in contrast to Co and Ni, which increased over time. Initial rates, calculated from the batch reactor experiments, were faster than the steady-state rates calculated from the mixed flow-through reactor experiments. Apparent rates calculated using sulfate were faster than apparent rates calculated using ferric and ferrous iron, reflecting oxidation of ferrous iron in solution by dissolved oxygen. The results imply that impurities in pyrite do contribute to its reactivity, in agreement with studies using electrochemical methods. Oxidation rate differences among pyrite samples with different impurities are probably too small to warrant explicit consideration in environmental modeling applications, but are important to understanding pyrite oxidation mechanisms and semiconducting properties.