11,205 research outputs found

    The Accuracy of Subhalo Detection

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    With the ever increasing resolution of N-body simulations, accurate subhalo detection is becoming essential in the study of the formation of structure, the production of merger trees and the seeding of semi-analytic models. To investigate the state of halo finders, we compare two different approaches to detecting subhaloes; the first based on overdensities in a halo and the second being adaptive mesh refinement. A set of stable mock NFW dark matter haloes were produced and a subhalo was placed at different radii within a larger halo. SUBFIND (a Friends-of-Friends based finder) and AHF (an adaptive mesh based finder) were employed to recover the subhalo. As expected, we found that the mass of the subhalo recovered by SUBFIND has a strong dependence on the radial position and that neither halo finder can accurately recover the subhalo when it is very near the centre of the halo. This radial dependence is shown to be related to the subhalo being truncated by the background density of the halo and originates due to the subhalo being defined as an overdensity. If the subhalo size is instead determined using the peak of the circular velocity profile, a much more stable value is recovered. The downside to this is that the maximum circular velocity is a poor measure of stripping and is affected by resolution. For future halo finders to recover all the particles in a subhalo, a search of phase space will need to be introduced.Comment: 9 pages, 7 figures, accepted for publication in MNRA

    Palladium, platinum, and gold distribution in serpentinite seamounts in the Mariana and Izu-Bonin forearcs: evidence from Leg 125 fluids and serpentinites

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    Palladium, platinum, and gold were analyzed for 20 interstitial water samples from Leg 125. No Pd or Pt was detected in fluids from serpentinite muds from Conical Seamount in the Mariana forearc, indicating that low-temperature seawater-peridotite interaction does not mobilize these elements into the serpentinizing fluids to levels above 0.10 parts per billion (ppb) in solution. However, Au may be mobilized in high pH solutions. In contrast, fluids from vitric-rich clays on the flanks of the Torishima Seamount in the Izu-Bonin forearc have Pd values of between 4.0 and 11.8 nmol/L, Pt values between 2.3 and 5.0 nmol/L and Au values between 126.9 and 1116.9 pmol/L. The precious metals are mobilized, and possibly adsorbed onto clay mineral surfaces, during diagenesis and burial of the volcanic-rich clays. Desorption during squeezing of the sediments may produce the enhanced precious metal concentrations in the analyzed fluids. The metals are mobilized in the fluids probably as neutral hydroxide, bisulfide, and ammonia complexes. Pt/Pd ratios are between 0.42 and 2.33, which is much lower than many of the potential sources for Pt and Pd but is consistent with the greater solubility of Pd compared with Pt in most natural low-temperature fluids

    Palladium, platinum, and gold distribution in serpentinite seamounts in the Mariana and Izu-Bonin forearcs: evidence from Leg 125 fluids and serpentinites

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    Palladium, platinum, and gold were analyzed for 20 interstitial water samples from Leg 125. No Pd or Pt was detected in fluids from serpentinite muds from Conical Seamount in the Mariana forearc, indicating that low-temperature seawater-peridotite interaction does not mobilize these elements into the serpentinizing fluids to levels above 0.10 parts per billion (ppb) in solution. However, Au may be mobilized in high pH solutions. In contrast, fluids from vitric-rich clays on the flanks of the Torishima Seamount in the Izu-Bonin forearc have Pd values of between 4.0 and 11.8 nmol/L, Pt values between 2.3 and 5.0 nmol/L and Au values between 126.9 and 1116.9 pmol/L. The precious metals are mobilized, and possibly adsorbed onto clay mineral surfaces, during diagenesis and burial of the volcanic-rich clays. Desorption during squeezing of the sediments may produce the enhanced precious metal concentrations in the analyzed fluids. The metals are mobilized in the fluids probably as neutral hydroxide, bisulfide, and ammonia complexes. Pt/Pd ratios are between 0.42 and 2.33, which is much lower than many of the potential sources for Pt and Pd but is consistent with the greater solubility of Pd compared with Pt in most natural low-temperature fluids

    The turn to international protection: Examining the relationship between humanitarian intervention and internal displacement

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    This study examines the relationship between two phenomena that are products of the move towards increased international protection during the 1990s

    Trace element geochemistry of peridotites from the Izu-Bonin-Mariana Forearc, Leg 125

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    Trace element analyses (first-series transition elements, Ti, Rb, Sr, Zr, Y, Nb, and REE) were carried out on whole rocks and minerals from 10 peridotite samples from both Conical Seamount in the Mariana forearc and Torishima Forearc Seamount in the Izu-Bonin forearc using a combination of XRF, ID-MS, ICP-MS, and ion microprobe. The concentrations of incompatible trace elements are generally low, reflecting the highly residual nature of the peridotites and their low clinopyroxene content (n ratios in the range of 0.05-0.25; several samples show possible small positive Eu anomalies. LREE enrichment is common to both seamounts, although the peridotites from Conical Seamount have higher (La/Ce)n ratios on extended chondrite-normalized plots, in which both REEs and other trace elements are organized according to their incompatibility with respect to a harzburgitic mantle. Comparison with abyssal peridotite patterns suggests that the LREEs, Rb, Nb, Sr, Sm, and Eu are all enriched in the Leg 125 peridotites, but Ti and the HREEs exhibit no obvious enrichment. The peridotites also give positive anomalies for Zr and Sr relative to their neighboring REEs. Covariation diagrams based on clinopyroxene data show that Ti and the HREEs plot on an extension of an abyssal peridotite trend to more residual compositions. However, the LREEs, Rb, Sr, Sm, and Eu are displaced off this trend toward higher values, suggesting that these elements were introduced during an enrichment event. The axis of dispersion on these plots further suggests that enrichment took place during or after melting and thus was not a characteristic of the lithosphere before subduction. Compared with boninites sampled from the Izu-Bonin-Mariana forearc, the peridotites are significantly more enriched in LREEs. Modeling of the melting process indicates that if they represent the most depleted residues of the melting events that generated forearc boninites they must have experienced subsolidus enrichment in these elements, as well as in Rb, Sr, Zr, Nb, Sm, and Eu. The lack of any correlation with the degree of serpentinization suggests that low-temperature fluids were not the prime cause of enrichment. The enrichment in the high-field-strength elements also suggests that at least some of this enrichment may have involved melts rather than aqueous fluids. Moreover, the presence of the hydrous minerals magnesio-hornblende and tremolite and the common resorption of orthopyroxene indicate that this high-temperature peridotite-fluid interaction may have taken place in a water-rich environment in the forearc following the melting event that produced the boninites. The peridotites from Leg 125 may therefore contain a record of an important flux of elements into the mantle wedge during the initial formation of forearc lithosphere. Ophiolitic peridotites with these characteristics have not yet been reported, perhaps because the precise equivalents to the serpentinite seamounts have not been analyzed

    Integrals of Motion for Critical Dense Polymers and Symplectic Fermions

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    We consider critical dense polymers L(1,2){\cal L}(1,2). We obtain for this model the eigenvalues of the local integrals of motion of the underlying Conformal Field Theory by means of Thermodynamic Bethe Ansatz. We give a detailed description of the relation between this model and Symplectic Fermions including the indecomposable structure of the transfer matrix. Integrals of motion are defined directly on the lattice in terms of the Temperley Lieb Algebra and their eigenvalues are obtained and expressed as an infinite sum of the eigenvalues of the continuum integrals of motion. An elegant decomposition of the transfer matrix in terms of a finite number of lattice integrals of motion is obtained thus providing a reason for their introduction.Comment: 53 pages, version accepted for publishing on JSTA

    Introduction: The emergence of ‘trans’

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