11,072 research outputs found

    Generalised Umbral Moonshine

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    Umbral moonshine describes an unexpected relation between 23 finite groups arising from lattice symmetries and special mock modular forms. It includes the Mathieu moonshine as a special case and can itself be viewed as an example of the more general moonshine phenomenon which connects finite groups and distinguished modular objects. In this paper we introduce the notion of generalised umbral moonshine, which includes the generalised Mathieu moonshine [Gaberdiel M.R., Persson D., Ronellenfitsch H., Volpato R., Commun. Number Theory Phys. 7 (2013), 145-223] as a special case, and provide supporting data for it. A central role is played by the deformed Drinfel'd (or quantum) double of each umbral finite group GG, specified by a cohomology class in H3(G,U(1))H^3(G,U(1)). We conjecture that in each of the 23 cases there exists a rule to assign an infinite-dimensional module for the deformed Drinfel'd double of the umbral finite group underlying the mock modular forms of umbral moonshine and generalised umbral moonshine. We also discuss the possible origin of the generalised umbral moonshine

    Experimental Verification of Acoustic Waveform and VSP Seismic Tube Wave Measurements of Fracture Permeability

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    A variety of established and experimental geophysical techniques was used to measure the vertical distribution of fracture permeability in a 229-meter deep borehole penetrating schist and quartz monzonite near Mirror Lake, New Hampshire. The distribution of fractures in the borehole was determined by acoustic borehole televiewer and other geophysical logs. Fracture permeability was estimated by application of two experimental methods: (1) Analysis of tube-wave-amplitude attenuation in acoustic full-waveform logs; and (2) interpretation of tube waves generated in vertical seismic profiles. Independent information on fracture permeability was obtained by means of packer-isolation flow tests and flowmeter measurement of vertical velocity distributions during pumping in the same borehole. Both experimental methods and packer-isolation-flow tests and flowmeter data indicated a single, near horizontal zone of permeability intersecting the borehole at a depth of about 45 meters. Smaller values of transmissivity were indicated for other fractures at deeper depths, with details of fracture response related to the apparent volume of rock represented by the individual measurements. Tube-wave amplitude attenuation in full-waveform acoustic logs, packer-isolation flow tests, and flowmeter measurements during pumping indicated transmissivity values for the upper permeability zone within the range of 0.6 to 10.0 centimeters squared per second. Vertical seismic-profile data indicated a relative distribution of fracture permeability in agreement with the other methods; however, the calculated values of transmissivity appeared to be too small. This disagreement is attributed to oversimplification of the model for fracture-zone compressibility used in the analysis of vertical seismic-profile data

    An Army of Me: Sockpuppets in Online Discussion Communities

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    In online discussion communities, users can interact and share information and opinions on a wide variety of topics. However, some users may create multiple identities, or sockpuppets, and engage in undesired behavior by deceiving others or manipulating discussions. In this work, we study sockpuppetry across nine discussion communities, and show that sockpuppets differ from ordinary users in terms of their posting behavior, linguistic traits, as well as social network structure. Sockpuppets tend to start fewer discussions, write shorter posts, use more personal pronouns such as "I", and have more clustered ego-networks. Further, pairs of sockpuppets controlled by the same individual are more likely to interact on the same discussion at the same time than pairs of ordinary users. Our analysis suggests a taxonomy of deceptive behavior in discussion communities. Pairs of sockpuppets can vary in their deceptiveness, i.e., whether they pretend to be different users, or their supportiveness, i.e., if they support arguments of other sockpuppets controlled by the same user. We apply these findings to a series of prediction tasks, notably, to identify whether a pair of accounts belongs to the same underlying user or not. Altogether, this work presents a data-driven view of deception in online discussion communities and paves the way towards the automatic detection of sockpuppets.Comment: 26th International World Wide Web conference 2017 (WWW 2017

    Room-temperature multiferroic hexagonal LuFeO3_3 films

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    The crystal and magnetic structures of single-crystalline hexagonal LuFeO3_3 films have been studied using x-ray, electron and neutron diffraction methods. The polar structure of these films are found to persist up to 1050 K; and the switchability of the polar behavior is observed at room temperature, indicating ferroelectricity. An antiferromagnetic order was shown to occur below 440 K, followed by a spin reorientation resulting in a weak ferromagnetic order below 130 K. This observation of coexisting multiple ferroic orders demonstrates that hexagonal LuFeO3_3 films are room-temperature multiferroics

    On CP Asymmetries in Two-, Three- and Four-Body D Decays

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    Indirect and direct CP violations have been established in K_L and B_d decays. They have been found in two-body decay channels -- with the exception of K_L to pi^+ pi^- e^+ e^- transitions. Evidence for direct CP asymmetry has just appeared in LHCb data on A_{CP}(D^0 to K^+ K^-) - A_{CP}(D^0 to pi^+ pi^-) with 3.5 sigma significance. Manifestations of New Dynamics (ND) can appear in CP asymmetries just below experimental bounds. We discuss D^{\pm}_{(s)}, D^0/\bar D^0 and D_L/D_S transitions to 2-, 3- and 4-body final states with a comment on predictions for inclusive vs. exclusive CP asymmetries. In particular we discuss T asymmetries in D to h_1 h_2 l^+ l^- in analogy with K_L to pi^+ pi^- e^+ e^- transitions due to interference between M1, internal bremsstrahlung and possible E1 amplitudes. Such an effect depends on the strength of CP violation originating from the ND -- as discussed here for Little Higgs Models with T parity and non-minimal Higgs sectors -- but also in the interferences between these amplitudes even in the Standard Model (SM). More general lessons can be learnt for T asymmetries in non-leptonic D decays like D to h_1h_2 h_3 h_4. Such manifestations of ND can be tested at LHCb and other Super-Flavour Factories like the projects at KEK near Tokyo and at Tor Vergata/Frascati near Rome.Comment: 27 pages, 6 figures. Revised with current results from LHCb and HFAG and further interpretation

    Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

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    Background: Congenital dilatation of the bile-duct (CDD) is a rare, mostly sporadic, disorder that results in bile retention with severe associated complications. CDD affects mainly Asians. To our knowledge, no genetic study has ever been conducted. Methods: We aim to identify genetic risk factors by a “trio-based” exome-sequencing approach, whereby 31 CDD probands and their unaffected parents were exome-sequenced. Seven-hundred controls from the local population were used to detect gene-sets significantly enriched with rare variants in CDD patients. Results: Twenty-one predicted damaging de novo variants (DNVs; 4 protein truncating and 17 missense) were identified in several evolutionarily constrained genes (p < 0.01). Six genes carrying DNVs were associated with human developmental disorders involving epithelial, connective or bone morphologies (PXDN, RTEL1, ANKRD11, MAP2K1, CYLD, ACAN) and four linked with cholangio- and hepatocellular carcinomas (PIK3CA, TLN1 CYLD, MAP2K1). Importantly, CDD patients have an excess of DNVs in cancer-related genes (p < 0.025). Thirteen genes were recurrently mutated at different sites, forming compound heterozygotes or functionally related complexes within patients. Conclusions: Our data supports a strong genetic basis for CDD and show that CDD is not only genetically heterogeneous but also non-monogenic, requiring mutations in more than one genes for the disease to develop. The data is consistent with the rarity and sporadic presentation of CDD
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