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Teleconnection in the martian atmosphere during the 2001 planet-encircling dust storm
Introduction: In July 2001 (Martian year 25), Mars was enshrouded by a thick veil of dust which lasted for several months and obscured the observation of its surface to spacecraft cameras and ground-based telescopes. The emergence and rapid evolution (within a few days) of multiple, isolated, regional dust storms which eventually attained planetary scale extent were observed by NASA’s Mars Global Surveyor (MGS) spacecraft using high resolution camera images and the thermal profiles and dust opacity measurements pro-vided by the Thermal Emission Spectrometer (TES) [1, 2].
We have applied a technique used in Terrestrial meteorology (sequential data assimilation, [3]) to ob-tain a complete, four-dimensional evolution of all the atmospheric variables during the period of this planet-encircling dust storm, even those which were not di-rectly observed by the MGS satellite, such as surface pressure and winds. We assimilated TES nadir-pointing thermal profiles and total dust opacities in a global circulation model of the Martian atmosphere, developed jointly by the University of Oxford and the Open University in the United Kingdom, with the col-laboration of the Laboratoire de Météorologie Dyna-mique in Paris (UK-MGCM) [4, 5, 6]
Radiative decays of light vector mesons in a quark level linear sigma model
We calculate the P0 to gamma gamma, V0 to P0 gamma and V0to V'0 gamma gamma
decays in the framework of a U(3)xU(3) linear sigma model which includes
constituent quarks. For the first two decays this approach improves results
based on the anomalous Wess-Zumino term, with contributions due to SU(3)
symmetry breaking and vector mixing. The phi to (omega,rho) gamma gamma decays
are dominated by resonant eta' exchange . Our calculation for the later decays
improves and update similar calculations in the -closely related- framework of
vector meson dominance. We obtain BR(phi to rho gamma gamma)=2.5x10^{-5} and
BR(phi to omega gamma gamma)=2.8x10^{-6} within the scope of the
high-luminosity phi factories.Comment: 8 pages, submitted to Phys. Rev.
Late Cenozoic tephrostratigraphy offshore the southern Central American Volcanic Arc: 1. Tephra ages and provenance
We studied the tephra inventory of 18 deep sea drill sites from six DSDP/ODP legs (Legs 84, 138, 170, 202, 205, 206) and two IODP legs (Legs 334 and 344) offshore the southern Central American Volcanic Arc (CAVA). Eight drill sites are located on the incoming Cocos plate and ten drill sites on the continental slope of the Caribbean plate. In total we examined ∼840 ash-bearing horizons and identified ∼650 of these as primary ash beds of which 430 originated from the CAVA. Correlations of ash beds were established between marine cores and with terrestrial tephra deposits, using major and trace element glass compositions with respect to relative stratigraphic order. As a prerequisite for marine-terrestrial correlations we present a new geochemical data set for significant Neogene and Quaternary Costa Rican tephras. Moreover, new Ar/Ar ages for marine tephras have been determined and marine ash beds are also dated using the pelagic sedimentation rates. The resulting correlations and provenance analyses build a tephrochronostratigraphic framework for Costa Rica and Nicaragua that covers the last >8 Myr. We define 39 correlations of marine ash beds to specific tephra formations in Costa Rica and Nicaragua; from the 4.15 Ma Lower Sandillal Ignimbrite to the 3.5 ka Rincón de la Vieja Tephra from Costa Rica, as well as another 32 widely distributed tephra layers for which their specific region of origin along Costa Rica and Nicaragua can be constrained
A biochemical hypothesis on the formation of fingerprints using a turing patterns approach
<p>Abstract</p> <p>Background</p> <p>Fingerprints represent a particular characteristic for each individual. Characteristic patterns are also formed on the palms of the hands and soles of the feet. Their origin and development is still unknown but it is believed to have a strong genetic component, although it is not the only thing determining its formation. Each fingerprint is a papillary drawing composed by papillae and rete ridges (crests). This paper proposes a phenomenological model describing fingerprint pattern formation using reaction diffusion equations with Turing space parameters.</p> <p>Results</p> <p>Several numerical examples were solved regarding simplified finger geometries to study pattern formation. The finite element method was used for numerical solution, in conjunction with the Newton-Raphson method to approximate nonlinear partial differential equations.</p> <p>Conclusions</p> <p>The numerical examples showed that the model could represent the formation of different types of fingerprint characteristics in each individual.</p
Hypothyroidism Enhances Tumor Invasiveness and Metastasis Development
11 pages, 9 figures.[Background]: Whereas there is increasing evidence that loss of expression and/or function of the thyroid hormone receptors (TRs) could result in a selective advantage for tumor development, the relationship between thyroid hormone levels and human cancer is a controversial issue. It has been reported that hypothyroidism might be a possible risk factor for liver and breast cancer in humans, but a lower incidence of breast carcinoma has been also reported in hypothyroid patients
[Methodology/Principal Findings]: In this work we have analyzed the influence of hypothyroidism on tumor progression and metastasis development using xenografts of parental and TRβ1–expressing human hepatocarcinoma (SK-hep1) and breast cancer cells (MDA-MB-468). In agreement with our previous observations tumor invasiveness and metastasis formation was strongly repressed when TRβ–expressing cells were injected into euthyroid nude mice. Whereas tumor growth was retarded when cells were inoculated into hypothyroid hosts, tumors had a more mesenchymal phenotype, were more invasive and metastatic growth was enhanced. Increased aggressiveness and tumor growth retardation was also observed with parental cells that do not express TRs.
[Conclusions/Significance]: These results show that changes in the stromal cells secondary to host hypothyroidism can modulate tumor progression and metastatic growth independently of the presence of TRs on the tumor cells. On the other hand, the finding that hypothyroidism can affect differentially tumor growth and invasiveness can contribute to the explanation of the confounding reports on the influence of thyroidal status in human cancer.This work was supported by grants BFU2007-62402 from MEC; RD06/0020/0036 from FIS and from the EU Project CRESCENDO (FP6-018652.Peer reviewe
Extrinsic Magnetotransport Phenomena in Ferromagnetic Oxides
This review is focused on extrinsic magnetotransport effects in ferromagnetic
oxides. It consists of two parts; the second part is devoted to an overview of
experimental data and theoretical models for extrinsic magnetotransport
phenomena. Here a critical discussion of domain-wall scattering is given.
Results on surfacial and interfacial magnetism in oxides are presented.
Spin-polarized tunnelling in ferromagnetic junctions is reviewed and
grain-boundary magnetoresistance is interpreted within a model of
spin-polarized tunnelling through natural oxide barriers. The situation in
ferromagnetic oxides is compared with data and models for conventional
ferromagnets. The first part of the review summarizes basic material
properties, especially data on the spin-polarization and evidence for
half-metallicity. Furthermore, intrinsic conduction mechanisms are discussed.
An outlook on the further development of oxide spin-electronics concludes this
review.Comment: 133 pages, 47 figures, submitted to Rep. Prog. Phy
The PREDICT study uncovers three clinical courses of acutely decompensated cirrhosis that have distinct pathophysiology
Background & Aims: Acute decompensation (AD) of cirrhosis is defined as the acute development of ascites, gastrointestinal hemorrhage, hepatic encephalopathy, infection or any combination thereof, requiring hospitalization. The presence of organ failure(s) in patients with AD defines acute-on-chronic liver failure (ACLF). The PREDICT study is a European, prospective, observational study, designed to characterize the clinical course of AD and to identify predictors of ACLF. Methods: A total of 1,071 patients with AD were enrolled. We collected detailed pre-specified information on the 3-month period prior to enrollment, and clinical and laboratory data at enrollment. Patients were then closely followed up for 3 months. Outcomes (liver transplantation and death) at 1 year were also recorded. Results: Three groups of patients were identified. Pre-ACLF patients (n = 218) developed ACLF and had 3-month and 1-year mortality rates of 53.7% and 67.4%, respectively. Unstable decompensated cirrhosis (UDC) patients (n = 233) required ≥1 readmission but did not develop ACLF and had mortality rates of 21.0% and 35.6%, respectively. Stable decompensated cirrhosis (SDC) patients (n = 620) were not readmitted, did not develop ACLF and had a 1-year mortality rate of only 9.5%. The 3 groups differed significantly regarding the grade and course of systemic inflammation (high-grade at enrollment with aggravation during follow-up in pre-ACLF; low-grade at enrollment with subsequent steady-course in UDC; and low-grade at enrollment with subsequent improvement in SDC) and the prevalence of surrogates of severe portal hypertension throughout the study (high in UDC vs. low in pre-ACLF and SDC). Conclusions: Acute decompensation without ACLF is a heterogeneous condition with 3 different clinical courses and 2 major pathophysiological mechanisms: systemic inflammation and portal hypertension. Predicting the development of ACLF remains a major future challenge. ClinicalTrials.gov number: NCT03056612. Lay summary: Herein, we describe, for the first time, 3 different clinical courses of acute decompensation (AD) of cirrhosis after hospital admission. The first clinical course includes patients who develop acute-on-chronic liver failure (ACLF) and have a high short-term risk of death – termed pre-ACLF. The second clinical course (unstable decompensated cirrhosis) includes patients requiring frequent hospitalizations unrelated to ACLF and is associated with a lower mortality risk than pre-ACLF. Finally, the third clinical course (stable decompensated cirrhosis), includes two-thirds of all patients admitted to hospital with AD – patients in this group rarely require hospital admission and have a much lower 1-year mortality risk
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