9 research outputs found
Effect of processing temperature on the texture and shear mechanical properties of diffusion bonded Ti-6Al-4V multilayer laminates
Two multilayer materials based on Ti-6Al-4V alloy have been processed by diffusion bonding at two different temperatures [1023 K and 1173 K (750 °C and 900 °C)]. The influence of the processing temperature on microstructure, texture, and mechanical properties of the two multilayer materials has been analyzed. Scanning electron microscopy, X-ray diffraction, electron backscatter diffraction, and shear tests have been used as experimental techniques. The multilayer laminate processed at the lowest temperature of 1023 K (750 °C) exhibits mainly transversal texture in the longitudinal plane, which provides an anisotropic mechanical behavior, showing higher shear modulus and maximum shear strength under one of the shear test directions considered. In contrast, diffusion bonding at 1173 K (900 °C) leads to basal/transversal texture because of the partial α → β → α transformation, which provides more isotropic mechanical properties. Accordingly, this laminate shows similar shear modulus and maximum shear strength in different shear test orientationsFinancial support from MICINN (Projects MAT2009-14452 and MAT2012-38962)Peer reviewe
Reorganization of a deeply incised drainage: role of deformation, sedimentation and groundwater flow
Deeply incised drainage networks are thought to be robust and not easily
modified, and are commonly used as passive markers of horizontal strain.
Yet, reorganizations (rearrangements) appear in the geologic record. We
provide field evidence of the reorganization of a Miocene drainage
network in response to strike-slip and vertical displacements in
Guatemala. The drainage was deeply incised into a 50-km-wide orogen
located along the North America-Caribbean plate boundary. It rearranged
twice, first during the Late Miocene in response to transpressional
uplift along the Polochic fault, and again in the Quaternary in response
to transtensional uplift along secondary faults. The pattern of
reorganization resembles that produced by the tectonic defeat of rivers
that cross growing tectonic structures. Compilation of remote sensing
data, field mapping, sediment provenance study, grain-size analysis and
Ar(40)/Ar(39) dating from paleovalleys and their fill reveals that the
classic mechanisms of river diversion, such as river avulsion over
bedrock, or capture driven by surface runoff, are not sufficient to
produce the observed diversions. The sites of diversion coincide
spatially with limestone belts and reactivated fault zones, suggesting
that solution-triggered or deformation-triggered permeability have
helped breaching of interfluves. The diversions are also related
temporally and spatially to the accumulation of sediment fills in the
valleys, upstream of the rising structures. We infer that the breaching
of the interfluves was achieved by headward erosion along tributaries
fed by groundwater flow tracking from the valleys soon to be captured.
Fault zones and limestone belts provided the pathways, and the aquifers
occupying the valley fills provided the head pressure that enhanced
groundwater circulation. The defeat of rivers crossing the rising
structures results essentially from the tectonically enhanced activation
of groundwater flow between catchments
All Small Nuclear RNAs (snRNAs) of the [U4/U6.U5] Tri-snRNP Localize to Nucleoli; Identification of the Nucleolar Localization Element of U6 snRNA
Previously, we showed that spliceosomal U6 small nuclear RNA (snRNA) transiently passes through the nucleolus. Herein, we report that all individual snRNAs of the [U4/U6.U5] tri-snRNP localize to nucleoli, demonstrated by fluorescence microscopy of nucleolar preparations after injection of fluorescein-labeled snRNA into Xenopus oocyte nuclei. Nucleolar localization of U6 is independent from [U4/U6] snRNP formation since sites of direct interaction of U6 snRNA with U4 snRNA are not nucleolar localization elements. Among all regions in U6, the only one required for nucleolar localization is its 3′ end, which associates with the La protein and subsequently during maturation of U6 is bound by Lsm proteins. This 3′-nucleolar localization element of U6 is both essential and sufficient for nucleolar localization and also required for localization to Cajal bodies. Conversion of the 3′ hydroxyl of U6 snRNA to a 3′ phosphate prevents association with the La protein but does not affect U6 localization to nucleoli or Cajal bodies