178 research outputs found

    Shallow stratigraphic control on pockmark distribution in north temperate estuaries

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    This paper is not subject to U.S. copyright. The definitive version was published in Marine Geology 329-331 (2012): 34-45, doi:10.1016/j.margeo.2012.09.006.Pockmark fields occur throughout northern North American temperate estuaries despite the absence of extensive thermogenic hydrocarbon deposits typically associated with pockmarks. In such settings, the origins of the gas and triggering mechanism(s) responsible for pockmark formation are not obvious. Nor is it known why pockmarks proliferate in this region but do not occur south of the glacial terminus in eastern North America. This paper tests two hypotheses addressing these knowledge gaps: 1) the region's unique sea-level history provided a terrestrial deposit that sourced the gas responsible for pockmark formation; and 2) the region's physiography controls pockmarks distribution. This study integrates over 2500 km of high-resolution swath bathymetry, Chirp seismic reflection profiles and vibracore data acquired in three estuarine pockmark fields in the Gulf of Maine and Bay of Fundy. Vibracores sampled a hydric paleosol lacking the organic-rich upper horizons, indicating that an organic-rich terrestrial deposit was eroded prior to pockmark formation. This observation suggests that the gas, which is presumably responsible for the formation of the pockmarks, originated in Holocene estuarine sediments (loss on ignition 3.5–10%), not terrestrial deposits that were subsequently drowned and buried by mud. The 7470 pockmarks identified in this study are non-randomly clustered. Pockmark size and distribution relate to Holocene sediment thickness (r2 = 0.60), basin morphology and glacial deposits. The irregular underlying topography that dictates Holocene sediment thickness may ultimately play a more important role in temperate estuarine pockmark distribution than drowned terrestrial deposits. These results give insight into the conditions necessary for pockmark formation in nearshore coastal environments.Graduate support for Brothers came from a Maine Economic Improvement Fund Dissertation Fellowship

    Loss of CIC promotes mitotic dysregulation and chromosome segregation defects

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    Background: CIC is a transcriptional repressor inactivated by loss-of-function mutations in several cancer types, including gliomas, lung cancers, and gastric adenocarcinomas. CIC alterations and/or loss of CIC activity have been associated with poorer outcomes and more aggressive phenotypes across cancer types, which is consistent with the notion that CIC functions as a tumour suppressor across a wide range of contexts. Results: Using mammalian cells lacking functional CIC, we found that CIC deficiency was associated with chromosome segregation (CS) defects, resulting in chromosomal instability and aneuploidy. These CS defects were associated with transcriptional dysregulation of spindle assembly checkpoint and cell cycle regulators. We also identified novel CIC interacting proteins, including core members of the SWI/SNF complex, and showed that they cooperatively regulated the expression of genes involved in cell cycle regulation. Finally, we showed that loss of CIC and ARID1A cooperatively increased CS defects and reduced cell viability. Conclusions: Our study ascribes a novel role to CIC as an important regulator of the cell cycle and demonstrates that loss of CIC can lead to chromosomal instability and aneuploidy in human and murine cells through defects in CS, providing insight into the underlying mechanisms of CIC's increasingly apparent role as a "pan-cancer" tumour suppressor

    Gold(I) Fluorohalides: Theory and Experiment

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    The anionic trifluoromethylgold(I) derivatives [CF3AuX]βˆ’, which have been prepared and isolated as their [PPh4]+ salts in good yield, undergo thermally induced difluorocarbene extrusion in the gas phase, giving rise to the mixed gold(I) fluorohalide complexes [Fβˆ’Auβˆ’X]βˆ’ (X=Cl, Br, I). These triatomic species have been detected by tandem mass spectrometry (MS2) experiments and their properties have been analyzed by DFT methods. The CF2 extrusion mechanism from the Auβˆ’CF3 moiety serves as a model for the CF2 insertion into the Auβˆ’F bond, since both reactivity channels are connected by the microreversibility principle

    Mechanical behavior of concrete prisms reinforced with steel and GFRP bar systems

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    Being immune to corrosion, and having a tensile strength up to three times higher than structural steel, glass fiber reinforced polymer (GFRP) bars are suitable for reinforcing concrete structures exposed to aggressive environmental conditions. However, a relatively low elasticity modulus of GFRP bars (in respect to the steel) favors the occurrence of relatively large deformability of cracked reinforced concrete. Lack of ductility and degradation of properties under high temperature can be also identified as debilities of GFRP bars over steel ones. Combining GFRP and steel bars can be a suitable solution to overcoming these concerns. Nevertheless, the application of such hybrid reinforcement systems requires reliable material models. The influence of the relative area of GFRP and steel bars on the tensile capacity of cracked concrete (generally known as tension-stiffening effect), was never investigated from the experimental point of view, mainly crossing results from different tools on the assessment of the cracking process. This paper experimentally investigates deformations and cracking behavior of concrete prisms reinforced with steel bars and GFRP bars in different combinations. The test results of 11 elements are reported. A tensile stress-strain diagram is conceptually proposed for modelling the tension-stiffening effect in elements with such hybrid combination of the reinforcement. The cracking process in terms of crack width and crack spacing is analyzed considering the hybrid reinforcement particularities and a preliminary approach is proposed for the prediction of the crack width for this type of reinforced concrete elementsResearch Council of Lithuania (Research Project S-MIP-17-62). The second author also 590 wish to acknowledge the support provided by FCT through the PTDC/ECM591 EST/1882/2014 projec

    A semi-implicit discrete-continuum coupling method for porous media based on the effective stress principle at finite strain

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    Abstract: A finite strain multiscale hydro-mechanical model is established via an extended Hill–Mandel condition for two-phase porous media. By assuming that the effective stress principle holds at unit cell scale, we established a micro-to-macro transition that links the micromechanical responses at grain scale to the macroscopic effective stress responses, while modeling the fluid phase only at the macroscopic continuum level. We propose a dual-scale semi-implicit scheme, which treats macroscopic responses implicitly and microscopic responses explicitly. The dual-scale model is shown to have good convergence rate, and is stable and robust. By inferring effective stress measure and poro-plasticity parameters, such as porosity, Biot’s coefficient and Biot’s modulus from micro-scale simulations, the multiscale model is able to predict effective poro-elasto-plastic responses without introducing additional phenomenological laws. The performance of the proposed framework is demonstrated via a collection of representative numerical examples. Fabric tensors of the representative elementary volumes are computed and analyzed via the anisotropic critical state theory when strain localization occurs. Keywords: Multiscale poromechanics; Semi-implicit scheme; Homogenization; Discrete-continuum coupling; DEM–FEM; Anisotropic critical stat

    Loss of CIC promotes mitotic dysregulation and chromosome segregation defects

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    Background: CIC is a transcriptional repressor inactivated by loss-of-function mutations in several cancer types, including gliomas, lung cancers, and gastric adenocarcinomas. CIC alterations and/or loss of CIC activity have been associated with poorer outcomes and more aggressive phenotypes across cancer types, which is consistent with the notion that CIC functions as a tumour suppressor across a wide range of contexts. Results: Using mammalian cells lacking functional CIC, we found that CIC deficiency was associated with chromosome segregation (CS) defects, resulting in chromosomal instability and aneuploidy. These CS defects were associated with transcriptional dysregulation of spindle assembly checkpoint and cell cycle regulators. We also identified novel CIC interacting proteins, including core members of the SWI/SNF complex, and showed that they cooperatively regulated the expression of genes involved in cell cycle regulation. Finally, we showed that loss of CIC and ARID1A cooperatively increased CS defects and reduced cell viability. Conclusions: Our study ascribes a novel role to CIC as an important regulator of the cell cycle and demonstrates that loss of CIC can lead to chromosomal instability and aneuploidy in human and murine cells through defects in CS, providing insight into the underlying mechanisms of CIC's increasingly apparent role as a "pan-cancer" tumour suppressor

    The Antiquity and Evolutionary History of Social Behavior in Bees

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    A long-standing controversy in bee social evolution concerns whether highly eusocial behavior has evolved once or twice within the corbiculate Apidae. Corbiculate bees include the highly eusocial honey bees and stingless bees, the primitively eusocial bumble bees, and the predominantly solitary or communal orchid bees. Here we use a model-based approach to reconstruct the evolutionary history of eusociality and date the antiquity of eusocial behavior in apid bees, using a recent molecular phylogeny of the Apidae. We conclude that eusociality evolved once in the common ancestor of the corbiculate Apidae, advanced eusociality evolved independently in the honey and stingless bees, and that eusociality was lost in the orchid bees. Fossil-calibrated divergence time estimates reveal that eusociality first evolved at least 87 Mya (78 to 95 Mya) in the corbiculates, much earlier than in other groups of bees with less complex social behavior. These results provide a robust new evolutionary framework for studies of the organization and genetic basis of social behavior in honey bees and their relatives

    Palladium–mediated organofluorine chemistry

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    ProducciΓ³n CientΓ­ficaThe substitution of fluorine for hydrogen in a molecule may result in profound changes in its properties and behaviour. Fluorine does not introduce special steric constraints since the F atom has a small size. However, the changes in bond polarity and the possibility of forming hydrogen bonds with other hydrogen donor fragments in the same or other molecules, may change the solubility and physical properties of the fluorinated compound when compared to the non-fluorinated one. Fluorine forms strong bonds to other elements and this ensures a good chemical stability. Altogether, fluorinated compounds are very attractive in materials chemistry and in medicinal chemistry, where many biologically active molecules and pharmaceuticals do contain fluorine in their structure and this has been shown to be essential for their activityJunta de Castilla y LeΓ³n (programa de apoyo a proyectos de investigaciΓ³n – Ref. VA302U13)Junta de Castilla y LeΓ³n (programa de apoyo a proyectos de investigaciΓ³n – Ref. VA256U13

    The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment

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    Autism and schizophrenia share a history of diagnostic conflation that was not definitively resolved until the publication of the DSM-III in 1980. Though now recognized as heterogeneous disorders with distinct developmental trajectories and dissociative features, much of the early nosological confusion stemmed from apparent overlap in certain areas of social dysfunction. In more recent years, separate but substantial literatures have accumulated for autism and schizophrenia demonstrating that abnormalities in social cognition directly contribute to the characteristic social deficits of both disorders. The current paper argues that direct comparison of social cognitive impairment can highlight shared and divergent mechanisms underlying pathways to social dysfunction, a process that can provide significant clinical benefit by informing the development of tailored treatment efforts. Thus, while the history of diagnostic conflation between autism and schizophrenia may have originated in similarities in social dysfunction, the goal of direct comparisons is not to conflate them once again but rather to reveal distinctions that illuminate disorder-specific mechanisms and pathways that contribute to social cognitive impairment
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