2,373 research outputs found

    Hybrid LSTM and Encoder-Decoder Architecture for Detection of Image Forgeries

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    With advanced image journaling tools, one can easily alter the semantic meaning of an image by exploiting certain manipulation techniques such as copy-clone, object splicing, and removal, which mislead the viewers. In contrast, the identification of these manipulations becomes a very challenging task as manipulated regions are not visually apparent. This paper proposes a high-confidence manipulation localization architecture which utilizes resampling features, Long-Short Term Memory (LSTM) cells, and encoder-decoder network to segment out manipulated regions from non-manipulated ones. Resampling features are used to capture artifacts like JPEG quality loss, upsampling, downsampling, rotation, and shearing. The proposed network exploits larger receptive fields (spatial maps) and frequency domain correlation to analyze the discriminative characteristics between manipulated and non-manipulated regions by incorporating encoder and LSTM network. Finally, decoder network learns the mapping from low-resolution feature maps to pixel-wise predictions for image tamper localization. With predicted mask provided by final layer (softmax) of the proposed architecture, end-to-end training is performed to learn the network parameters through back-propagation using ground-truth masks. Furthermore, a large image splicing dataset is introduced to guide the training process. The proposed method is capable of localizing image manipulations at pixel level with high precision, which is demonstrated through rigorous experimentation on three diverse datasets

    The Insoluble Carbonaceous Material of CM Chondrites as Possible Source of Discrete Organics During the Asteroidal Aqueous Phase

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    The larger portion of the organic carbon in carbonaceous chondrites (CC) is present as a complex and heterogeneous macromolecular material that is insoluble in acids and most solvents (IOM). So far, it has been analyzed only as a whole by microscopy (TEM) and spectroscopy (IR, NMR, EPR), which have offered and overview of its chemical nature, bonding, and functional group composition. Chemical or pyrolytic decomposition has also been used in combination with GC-MS to identify individual compounds released by these processes. Their value in the recognition of the original IOM structure resides in the ability to properly interpret the decomposition pathways for any given process. We report here a preliminary study of IOM from the Murray meteorite that combines both the analytical approaches described above, under conditions that would realistically model the IOM hydrothermal exposure in the meteorite parent body. The aim is to document the possible release of water and solvent soluble organics, determine possible changes in NMR spectral features, and ascertain, by extension, the effect of this loss on the frame of the IOM residue. Additional information is included in the original extended abstract

    Quantum decoherence of a charge qubit in a spin-fermion model

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    We consider quantum decoherence in solid-state systems by studying the transverse dynamics of a single qubit interacting with a fermionic bath and driven by external pulses. Our interest is in investigating the extent to which the lost coherence can be restored by the application of external pulses to the qubit. We show that the qubit evolution under various pulse sequences can be mapped onto Keldysh path integrals. This approach allows a simple diagrammatic treatment of different bath excitation processes contributing to qubit decoherence. We apply this theory to the evolution of the qubit coupled to the Andreev fluctuator bath in the context of widely studied superconducting qubits. We show that charge fluctuations within the Andreev-fluctuator model lead to a 1/f noise spectrum with a characteristic temperature depedence. We discuss the strategy for suppression of decoherence by the application of higher-order (beyond spin echo) pulse sequences.Comment: 7 pages, 4 figures; extended version (accepted to Phys. Rev. B

    Generating intravital super-resolution movies with conventional microscopy reveals actin dynamics that construct pioneer axons

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    Super-resolution microscopy is broadening our in-depth understanding of cellular structure. However, super-resolution approaches are limited, for numerous reasons, from utilization in longer-term intravital imaging. We devised a combinatorial imaging technique that combines deconvolution with stepwise optical saturation microscopy (DeSOS) to circumvent this issue and image cells in their native physiological environment. Other than a traditional confocal or two-photon microscope, this approach requires no additional hardware. Here, we provide an open-access application to obtain DeSOS images from conventional microscope images obtained at low excitation powers. We show that DeSOS can be used in time-lapse imaging to generate super-resolution movies in zebrafish. DeSOS was also validated in live mice. These movies uncover that actin structures dynamically remodel to produce a single pioneer axon in a 'top-down' scaffolding event. Further, we identify an F-actin population - stable base clusters - that orchestrate that scaffolding event. We then identify that activation of Rac1 in pioneer axons destabilizes stable base clusters and disrupts pioneer axon formation. The ease of acquisition and processing with this approach provides a universal technique for biologists to answer questions in living animals

    Mapping accretion and its variability in the young open cluster NGC 2264: a study based on u-band photometry

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    We aim at characterizing the accretion properties of several hundred members of the star-forming cluster NGC 2264 (3 Myr). We performed a deep u,g,r,i mapping and a simultaneous u+r monitoring of the region with CFHT/MegaCam in order to directly probe the accretion process from UV excess measurements. Photometric properties and stellar parameters are determined homogeneously for about 750 monitored young objects, spanning the mass range 0.1-2 Mo. About 40% are classical (accreting) T Tauri stars, based on various diagnostics (H_alpha, UV and IR excesses). The remaining non-accreting members define the (photospheric+chromospheric) reference UV emission level over which flux excess is detected and measured. We revise the membership status of cluster members based on UV accretion signatures and report a new population of 50 CTTS candidates. A large range of UV excess is measured for the CTTS population, varying from a few 0.1 to 3 mag. We convert these values to accretion luminosities and obtain mass accretion rates ranging from 1e-10 to 1e-7 Mo/yr. Taking into account a mass-dependent detection threshold for weakly accreting objects, we find a >6sigma correlation between mass accretion rate and stellar mass. A power-law fit, properly accounting for upper limits, yields M_acc \propto M^{1.4+/-0.3}. At any given stellar mass, we find a large spread of accretion rates, extending over about 2 orders of magnitude. The monitoring of the UV excess on a timescale of a couple of weeks indicates that its variability typically amounts to 0.5 dex, much smaller than the observed spread. We suggest that a non-negligible age spread across the cluster may effectively contribute to the observed spread in accretion rates at a given mass. In addition, different accretion mechanisms (like, e.g., short-lived accretion bursts vs. more stable funnel-flow accretion) may be associated to different M_acc regimes.Comment: 24 pages, 21 figures, accepted for publication in Astronomy & Astrophysic

    Targeting fibroblast activation protein in tumor stroma with chimeric antigen receptor T cells can inhibit tumor growth and augment host immunity without severe toxicity.

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    The majority of chimeric antigen receptor (CAR) T-cell research has focused on attacking cancer cells. Here, we show that targeting the tumor-promoting, nontransformed stromal cells using CAR T cells may offer several advantages. We developed a retroviral CAR construct specific for the mouse fibroblast activation protein (FAP), comprising a single-chain Fv FAP [monoclonal antibody (mAb) 73.3] with the CD8α hinge and transmembrane regions, and the human CD3ζ and 4-1BB activation domains. The transduced muFAP-CAR mouse T cells secreted IFN-γ and killed FAP-expressing 3T3 target cells specifically. Adoptively transferred 73.3-FAP-CAR mouse T cells selectively reduced FAP(hi) stromal cells and inhibited the growth of multiple types of subcutaneously transplanted tumors in wild-type, but not FAP-null immune-competent syngeneic mice. The antitumor effects could be augmented by multiple injections of the CAR T cells, by using CAR T cells with a deficiency in diacylglycerol kinase, or by combination with a vaccine. A major mechanism of action of the muFAP-CAR T cells was the augmentation of the endogenous CD8(+) T-cell antitumor responses. Off-tumor toxicity in our models was minimal following muFAP-CAR T-cell therapy. In summary, inhibiting tumor growth by targeting tumor stroma with adoptively transferred CAR T cells directed to FAP can be safe and effective, suggesting that further clinical development of anti-human FAP-CAR is warranted

    Medical Physics Practice Guidelines ‐ The AAPM’s minimum practice recommendations for medical physicists

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/135373/1/acm20001c.pd
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