681 research outputs found
Numerical modeling of REE fractionation patterns in fluorapatite from the olympic dam deposit (South Australia)
Trace element signatures in apatite are used to study hydrothermal processes due to the ability of this mineral to chemically record and preserve the impact of individual hydrothermal events. Interpretation of rare earth element (REE)-signatures in hydrothermal apatite can be complex due to not only evolving fO2, fS2 and fluid composition, but also to variety of different REE-complexes (Cl-, F-, P-, SO4, CO3, oxide, OH− etc.) in hydrothermal fluid, and the significant differences in solubility and stability that these complexes exhibit. This contribution applies numerical modeling to evolving REE-signatures in apatite within the Olympic Dam iron-oxide-copper-gold deposit, South Australia with the aim of constraining fluid evolution. The REE-signatures of three unique types of apatite from hydrothermal assemblages that crystallized under partially constrained conditions have been numerically modeled, and the partitioning coefficients between apatite and fluid calculated in each case. Results of these calculations replicate the measured data well and show a transition from early light rare earth element (LREE)- to later middle rare earth element (MREE)-enriched apatite, which can be achieved by an evolution in the proportions of different REE-complexes. Modeling also efficiently explains the switch from REE-signatures with negative to positive Eu-anomalies. REE transport in hydrothermal fluids at Olympic Dam is attributed to REE–chloride complexes, thus explaining both the LREE-enriched character of the deposit and the relatively LREE-depleted nature of later generations of apatite. REE deposition may, however, have been induced by a weakening of REE–Cl activity and subsequent REE complexation with fluoride species. The conspicuous positive Eu-anomalies displayed by later apatite with are attributed to crystallization from high pH fluids characterized by the presence of Eu3+ species.Sasha Krneta, Cristiana L. Ciobanu, Nigel J. Cook and Kathy J. Ehri
Biased allosteric modulation at the CaS receptor engendered by structurally diverse calcimimetics
Background and Purpose
Clinical use of cinacalcet in hyperparathyroidism is complicated by its tendency to induce hypocalcaemia, arising partly from activation of calcium-sensing receptors (CaS receptors) in the thyroid and stimulation of calcitonin release. CaS receptor allosteric modulators that selectively bias signalling towards pathways that mediate desired effects [e.g. parathyroid hormone (PTH) suppression] rather than those mediating undesirable effects (e.g. elevated serum calcitonin), may offer better therapies.
Experimental Approach
We characterized the ligand-biased profile of novel calcimimetics in HEK293 cells stably expressing human CaS receptors, by monitoring intracellular calcium (Ca2+i) mobilization, inositol phosphate (IP)1 accumulation, ERK1/2 phosphorylation (pERK1/2) and receptor expression.
Key Results
Phenylalkylamine calcimimetics were biased towards allosteric modulation of Ca2+i mobilization and IP1 accumulation. S,R-calcimimetic B was biased only towards IP1 accumulation. R,R-calcimimetic B and AC-265347 were biased towards IP1 accumulation and pERK1/2. Nor-calcimimetic B was unbiased. In contrast to phenylalkylamines and calcimimetic B analogues, AC-265347 did not promote trafficking of a loss-of-expression, naturally occurring, CaS receptor mutation (G670E).
Conclusions and Implications
The ability of R,R-calcimimetic B and AC-265347 to bias signalling towards pERK1/2 and IP1 accumulation may explain their suppression of PTH levels in vivo at concentrations that have no effect on serum calcitonin levels. The demonstration that AC-265347 promotes CaS receptor receptor signalling, but not trafficking reveals a novel profile of ligand-biased modulation at CaS receptors The identification of allosteric modulators that bias CaS receptor signalling towards distinct intracellular pathways provides an opportunity to develop desirable biased signalling profiles in vivo for mediating selective physiological responses
Distributed phase-covariant cloning with atomic ensembles via quantum Zeno dynamics
We propose an interesting scheme for distributed orbital state quantum
cloning with atomic ensembles based on the quantum Zeno dynamics. These atomic
ensembles which consist of identical three-level atoms are trapped in distant
cavities connected by a single-mode integrated optical star coupler. These
qubits can be manipulated through appropriate modulation of the coupling
constants between atomic ensemble and classical field, and the cavity decay can
be largely suppressed as the number of atoms in the ensemble qubits increases.
The fidelity of each cloned qubit can be obtained with analytic result. The
present scheme provides a new way to construct the quantum communication
network.Comment: 5 pages, 4 figure
Strings on conifolds from strong coupling dynamics, part I
A method to solve various aspects of the strong coupling expansion of the
superconformal field theory duals of AdS_5 x X geometries from first principles
is proposed. The main idea is that at strong coupling the configurations that
dominate the low energy dynamics of the field theory compactified on a three
sphere are given by certain non-trivial semi-classical configurations in the
moduli space of vacua.
We show that this approach is self-consistent and permits one to express most
of the dynamics in terms of an effective N=4 SYM dynamics. This has the
advantage that some degrees of freedom that move the configurations away from
moduli space can be treated perturbatively, unifying the essential low energy
dynamics of all of these theories. We show that with this formalism one can
compute the energies of strings in the BMN limit in the Klebanov-Witten theory
from field theory considerations, matching the functional form of results found
using AdS geometry. This paper also presents various other technical results
for the semiclassical treatment of superconformal field theories.Comment: 52 pages, JHEP3 styl
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