238 research outputs found
D'atri spaces of type k and related classes of geometries concerning jacobi operators
In this article we continue the study of the geometry of -D'Atri spaces,
( denotes the dimension of the manifold) began by
the second author. It is known that -D'Atri spaces, are related
to properties of Jacobi operators along geodesics, since she has shown
that , are invariant
under the geodesic flow for any unit tangent vector . Here, assuming that
the Riemannian manifold is a D'Atri space, we prove in our main result that
is also invariant under the geodesic flow if . In addition, other properties of Jacobi operators related to the
Ledger conditions are obtained and they are used to give applications to
Iwasawa type spaces. In the class of D'Atri spaces of Iwasawa type, we show two
different characterizations of the symmetric spaces of noncompact type: they
are exactly the -spaces and on the other hand they are -D'Atri
spaces for some In the last case, they are -D'Atri for all
as well. In particular, Damek-Ricci spaces that are -D'Atri
for some are symmetric.
Finally, we characterize -D'Atri spaces for all as the -spaces (geodesic symmetries preserve the principal curvatures of
small geodesic spheres). Moreover, applying this result in the case of 4%
-dimensional homogeneous spaces we prove that the properties of being a D'Atri
(1-D'Atri) space, or a 3-D'Atri space, are equivalent to the property of being
a -D'Atri space for all .Comment: 19 pages. This paper substitute the previous one where one Theorem
has been deleted and one section has been adde
Spectral geometry of the Steklov problem on orbifolds
We consider how the geometry and topology of a compact -dimensional Riemannian orbifold with boundary relates to its Steklov spectrum. In two dimensions, motivated by work of A. Girouard, L. Parnovski, I. Polterovich and D. Sher in the manifold setting, we compute the precise asymptotics of the Steklov spectrum in terms of only boundary data. As a consequence, we prove that the Steklov spectrum detects the presence and number of orbifold singularities on the boundary of an orbisurface and it detects the number each of smooth and singular boundary components. Moreover, we find that the Steklov spectrum also determines the lengths of the boundary components modulo an equivalence relation, and we show by examples that this result is the best possible. We construct various examples of Steklov isospectral Riemannian orbifolds which demonstrate that these two-dimensional results do not extend to higher dimensions. In addition, we give two- imensional examples which show that the Steklov spectrum does \emph{not} detect the presence of interior singularities nor does it determine the orbifold Euler characteristic. In fact, a flat disk is Steklov isospectral to a cone. In another direction, we obtain upper bounds on the Steklov eigenvalues of a Riemannian orbifold in terms of the isoperimetric ratio and a conformal invariant. We generalize results of B. Colbois, A. El Soufi and A. Girouard, and the fourth author to the orbifold setting; in the process, we gain a sharpness result on these bounds that was not evident in the manifold setting. In dimension two, our eigenvalue bounds are solely in terms of the orbifold Euler characteristic and the number each of smooth and singular boundary components
Stability and enzymatic studies with omeprazole: hydroxypropyl-β-cyclodextrin
The original publication is available at www.springerlink.com. A publicação original está disponível em www.springerlink.comOmeprazole (OME) exhibits low stability to light, heat and humidity. In stress conditions OME stability should improve under inclusion complex form with hydroxypropyl-b-cyclodextrin (HPbCD). Stability of OME, its physical mixture (PM) with HPbCD and OME:HPbCD inclusion complex was assessed during 60 days. The inclusion complexes were prepared by kneading and freezedrying techniques and characterized by differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). A molecular modelling was also held to predict the most probable tridimensional conformation of inclusion complex OME:HPbCD. The inhibitory activity of free and complexed OME on selected enzymes, namely, papain (protease model of the proton pump) and acetylcholinesterase (enzyme present in cholinergic neurons and also involved in Alzheimer’s disease) was compared. The results obtained show that HPbCD do not protect against OME degradation, in any prepared powder, in the presence of light, heat and humidity. This may indicate that the reactive group of OME is not included in the HPbCD cavity.
This fact is supported by molecular modelling data, which demonstrated that 2-pyridylmethyl group of OME is not included into the cyclodextrin cavity. In relation to enzymatic assays it was observed that free OME and OME in the binary systems showed identical inhibitory activity on papain and acethylcolinesterase, concluding that HPbCD do not affect OME activity on these two enzymes
Cell Type–dependent Requirement for PIP Box–regulated Cdt1 Destruction During S Phase
Previous studies have shown that Cdt1 overexpression in cultured cells can trigger re-replication, but not whether CRL4Cdt2-triggered destruction of Cdt1 is required for normal mitotic cell cycle progression in vivo. We demonstrate that PIP box–mediated destruction of Cdt1Dup during S phase is necessary for the cell division cycle in Drosophila
Fidelity Variants of RNA Dependent RNA Polymerases Uncover an Indirect, Mutagenic Activity of Amiloride Compounds
In a screen for RNA mutagen resistance, we isolated a high fidelity RNA dependent RNA polymerase (RdRp) variant of Coxsackie virus B3 (CVB3). Curiously, this variant A372V is also resistant to amiloride. We hypothesize that amiloride has a previously undescribed mutagenic activity. Indeed, amiloride compounds increase the mutation frequencies of CVB3 and poliovirus and high fidelity variants of both viruses are more resistant to this effect. We hypothesize that this mutagenic activity is mediated through alterations in intracellular ions such as Mg2+ and Mn2+, which in turn increase virus mutation frequency by affecting RdRp fidelity. Furthermore, we show that another amiloride-resistant RdRp variant, S299T, is completely resistant to this mutagenic activity and unaffected by changes in ion concentrations. We show that RdRp variants resist the mutagenic activity of amiloride via two different mechanisms: 1) increased fidelity that generates virus populations presenting lower basal mutation frequencies or 2) resisting changes in divalent cation concentrations that affect polymerase fidelity. Our results uncover a new antiviral approach based on mutagenesis
Tectono-stratigraphic response of the Sandino Forearc Basin (N-Costa Rica and W-Nicaragua) to episodes of rough crust and oblique subduction
The southern Central American active margin is a world-class site where past and
present subduction processes have been extensively studied. Tectonic erosion/accretion
and oblique/orthogonal subduction are thought to alternate in space and time
along the Middle American Trench. These processes may cause various responses
in the upper plate, such as uplift/subsidence, deformation, and volcanic arc migration/
shut-off. We present an updated stratigraphic framework of the Late Cretaceous–
Cenozoic Sandino Forearc Basin (SFB) which provides evidence of
sedimentary response to tectonic events. Since its inception, the basin was predominantly
filled with deep-water volcaniclastic deposits. In contrast, shallow-water
deposits appeared episodically in the basin record and are considered as tectonic
event markers. The SFB stretches for about 300 km and varies in thickness from
5 km (southern part) to about 16 km (northern part). The drastic, along-basin, thickness
variation appears to be the result of (1) differential tectonic evolutions and (2)
differential rates of sediment supply. (1) The northern SFB did not experience major
tectonic events. In contrast, the reduced thickness of the southern SFB (5 km) is the
result of at least four uplift phases related to the collision/accretion of bathymetric
reliefs on the incoming plate: (i) the accretion of a buoyant oceanic plateau (Nicoya
Complex) during the middle Campanian; (ii) the collision of an oceanic plateau (?)
during the late Danian–Selandian; (iii) the collision/accretion of seamounts during
the late Eocene–early Oligocene; (iv) the collision of seamounts and ridges during
the Pliocene–Holocene. (2) The northwestward thickening of the SFB may have
been enhanced by high sediment supply in the Fonseca Gulf area which reflects
sourcing from wide, high relief drainage basins. In contrast, sedimentary input has
possibly been lower along the southern SFB, due to the proximity of the narrow,
lowland isthmus of southern Central America. Moreover, two phases of strongly
oblique subduction affected the margin, producing strike-slip faulting in the forearc
basin: (1) prior to the Farallon Plate breakup, an Oligocene transpressional phase
caused deformation and uplift of the basin depocenter, triggering shallowing-upward
of the Nicaraguan Isthmus in the central and northern SFB; (2) a Pleistocene–Holocene transtensional phase drives the NW-directed motion of a forearc sliver
and reactivation of the graben-bounding faults of the late Neogene Nicaraguan
Depression. We discuss arguments in favour of a Pliocene development of the
Nicaraguan Depression and propose that the Nicaraguan Isthmus, which is the
apparent rift shoulder of the depression, represents a structure inherited from the Oligocene
transpressional phase
Shells and humans: molluscs and other coastal resources from the earliest human occupations at the Mesolithic shell midden of El Mazo (Asturias, Northern Spain)
Human populations exploited coastal areas with intensity during the Mesolithic in Atlantic Europe, resulting in the accumulation of large shell middens. Northern Spain is one of the most prolific regions, and especially the so-called Asturian area. Large accumulations of shellfish led some scholars to propose the existence of intensification in the exploitation of coastal resources in the region during the Mesolithic. In this paper, shell remains (molluscs, crustaceans and echinoderms) from stratigraphic units 114 and 115 (dated to the early Mesolithic c. 9 kys cal BP) at El Mazo cave (Asturias, northern Spain) were studied in order to establish resource exploitation patterns and environmental conditions. Species representation showed that limpets, top shells and sea urchins were preferentially exploited. One-millimetre mesh screens were crucial in establishing an accurate minimum number of individuals for sea urchins and to determine their importance in exploitation patterns. Environmental conditions deduced from shell assemblages indicated that temperate conditions prevailed at the time of the occupation and the morphology of the coastline was similar to today (rocky exposed shores). Information recovered relating to species representation, collection areas and shell biometry reflected some evidence of intensification (reduced shell size, collection in lower areas of exposed shores, no size selection in some units and species) in the exploitation of coastal resources through time. However, the results suggested the existence of changes in collection strategies and resource management, and periods of intense shell collection may have alternated with times of shell stock recovery throughout the Mesolithic.This research was performed as part of the project “The human response to the global climatic change in a littoral zone: the case of the transition to the Holocene in the Cantabrian coast (10,000–5000 cal BC) (HAR2010-22115-C02-01)” funded by the Spanish Ministry of Economy and Competitiveness. AGE was funded by the University of Cantabria through a predoctoral grant and IGZ was funded by the Spanish Ministry of Economy and Competitiveness through a Juan de la Cierva grant. We also would like to thank the University of Cantabria and the IIIPC for providing support, David Cuenca-Solana, Alejandro García Moreno and Lucia Agudo Pérez for their help. We also thank Jennifer Jones for correcting the English. Comments from two anonymous reviewers helped to improve the paper
Why Are Outcomes Different for Registry Patients Enrolled Prospectively and Retrospectively? Insights from the Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF).
Background: Retrospective and prospective observational studies are designed to reflect real-world evidence on clinical practice, but can yield conflicting results. The GARFIELD-AF Registry includes both methods of enrolment and allows analysis of differences in patient characteristics and outcomes that may result. Methods and Results: Patients with atrial fibrillation (AF) and ≥1 risk factor for stroke at diagnosis of AF were recruited either retrospectively (n = 5069) or prospectively (n = 5501) from 19 countries and then followed prospectively. The retrospectively enrolled cohort comprised patients with established AF (for a least 6, and up to 24 months before enrolment), who were identified retrospectively (and baseline and partial follow-up data were collected from the emedical records) and then followed prospectively between 0-18 months (such that the total time of follow-up was 24 months; data collection Dec-2009 and Oct-2010). In the prospectively enrolled cohort, patients with newly diagnosed AF (≤6 weeks after diagnosis) were recruited between Mar-2010 and Oct-2011 and were followed for 24 months after enrolment. Differences between the cohorts were observed in clinical characteristics, including type of AF, stroke prevention strategies, and event rates. More patients in the retrospectively identified cohort received vitamin K antagonists (62.1% vs. 53.2%) and fewer received non-vitamin K oral anticoagulants (1.8% vs . 4.2%). All-cause mortality rates per 100 person-years during the prospective follow-up (starting the first study visit up to 1 year) were significantly lower in the retrospective than prospectively identified cohort (3.04 [95% CI 2.51 to 3.67] vs . 4.05 [95% CI 3.53 to 4.63]; p = 0.016). Conclusions: Interpretations of data from registries that aim to evaluate the characteristics and outcomes of patients with AF must take account of differences in registry design and the impact of recall bias and survivorship bias that is incurred with retrospective enrolment. Clinical Trial Registration: - URL: http://www.clinicaltrials.gov . Unique identifier for GARFIELD-AF (NCT01090362)
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