835 research outputs found
Optical Flow in Mostly Rigid Scenes
The optical flow of natural scenes is a combination of the motion of the
observer and the independent motion of objects. Existing algorithms typically
focus on either recovering motion and structure under the assumption of a
purely static world or optical flow for general unconstrained scenes. We
combine these approaches in an optical flow algorithm that estimates an
explicit segmentation of moving objects from appearance and physical
constraints. In static regions we take advantage of strong constraints to
jointly estimate the camera motion and the 3D structure of the scene over
multiple frames. This allows us to also regularize the structure instead of the
motion. Our formulation uses a Plane+Parallax framework, which works even under
small baselines, and reduces the motion estimation to a one-dimensional search
problem, resulting in more accurate estimation. In moving regions the flow is
treated as unconstrained, and computed with an existing optical flow method.
The resulting Mostly-Rigid Flow (MR-Flow) method achieves state-of-the-art
results on both the MPI-Sintel and KITTI-2015 benchmarks.Comment: 15 pages, 10 figures; accepted for publication at CVPR 201
Regulation of annexins following infection like tissue damage – investigated by 2-dimensional gel electrophoresis.
Sensitivity of Antarctic Urospora penicilliformis (Ulotrichales, Chlorophyta) to ultraviolet radiation is life stage dependent
The sensitivity of different life stages of the eulittoral green alga Urospora penicilliformis (Roth) Aresch. to ultraviolet radiation (UVR) was examinedin the laboratory. Gametophytic filaments and propagules (zoospores and gametes) released from filaments were separately exposed to different fluence of radiation treatments consisting of PAR (P = 400700 nm), PAR + ultraviolet A (UVA) (PA, UVA = 320400 nm), and PAR + UVA + ultraviolet B (UVB) (PAB, UVB = 280320 nm). Photophysiological indices (ETRmax, Ek, and a) derived from rapid light curves were measured in controls, while photosynthetic efficiency and amount of DNA lesions in terms of cyclobutane pyrimidine dimers (CPDs) were measured after exposure to radiation treatments and after recovery in low PAR; pigments of propagules were quantified after exposure treatment only. The photosynthetic conversion efficiency (a) and photosynthetic capacity (rETRmax) were higher in gametophytes compared with the propagules. The propagules were slightly more sensitive to UVB-induced DNA damage; however, both life stages of the eulittoral inhabiting turf alga were not severely affected by the negative impacts of UVR. Exposure to a maximum of 8 h UVR caused mild effects on the photochemical efficiency of PSII and induced minimal DNA lesions in both the gametophytes and propagules. Pigment concentrations were not significantly different between PAR-exposed and PAR + UVRexposed propagules. Our data showed that U. penicilliformis from the Antarctic is ratherinsensitive to the applied UVR. This amphi-equatorial species possesses different protective mechanisms that can cope with high UVR in coldtemperatewaters of both hemispheres and in polar regions under conditions of increasing UVR as a consequence of further reduction of stratosphericozone
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Alpha1 -adrenergic stimulation selectively enhances endothelium-mediated vasodilation in rat cremaster arteries.
We have systematically investigated how vascular smooth muscle α1 -adrenoceptor activation impacts endothelium-mediated vasodilation in isolated, myogenically active, rat cremaster muscle 1A arteries. Cannulated cremaster arteries were pressurized intraluminally to 70 mmHg to induce myogenic tone, and exposed to vasoactive agents via bath superfusion at 34°C. Smooth muscle membrane potential was measured via sharp microelectrode recordings in pressurized, myogenic arteries. The α1 -adrenergic agonist phenylephrine (25-100 nmol/L) produced further constriction of myogenic arteries, but did not alter the vasorelaxant responses to acetylcholine (0.3 μmol/L), SKA-31 (an activator of endothelial Ca2+ -dependent K+ channels) (3 μmol/L) or sodium nitroprusside (10 μmol/L). Exposure to 0.25-1 μmol/L phenylephrine or 1 μmol/L norepinephrine generated more robust constrictions, and also enhanced the vasodilations evoked by acetylcholine and SKA-31, but not by sodium nitroprusside. In contrast, the thromboxane receptor agonist U46619 (250 nmol/L) dampened responses to all three vasodilators. Phenylephrine exposure depolarized myogenic arteries, and mimicking this effect with 4-aminopyridine (1 mmol/L) was sufficient to augment the SKA-31-evoked vasodilation. Inhibition of L-type Ca2+ channels by 1 μmol/L nifedipine decreased myogenic tone, phenylephrine-induced constriction and prevented α1 -adrenergic enhancement of endothelium-evoked vasodilation; these latter deficits were overcome by exposure to 3 and 10 μmol/L phenylephrine. Mechanistically, augmentation of ACh-evoked dilation by phenylephrine was dampened by eNOS inhibition and abolished by blockade of endothelial KCa channels. Collectively, these data suggest that increasing α1 -adrenoceptor activation beyond a threshold level augments endothelium-evoked vasodilation, likely by triggering transcellular signaling between smooth muscle and the endothelium. Physiologically, this negative feedback process may serve as a "brake" to limit the extent of vasoconstriction in the skeletal microcirculation evoked by the elevated sympathetic tone
Competitive Collaboration: Joint Unsupervised Learning of Depth, Camera Motion, Optical Flow and Motion Segmentation
We address the unsupervised learning of several interconnected problems in
low-level vision: single view depth prediction, camera motion estimation,
optical flow, and segmentation of a video into the static scene and moving
regions. Our key insight is that these four fundamental vision problems are
coupled through geometric constraints. Consequently, learning to solve them
together simplifies the problem because the solutions can reinforce each other.
We go beyond previous work by exploiting geometry more explicitly and
segmenting the scene into static and moving regions. To that end, we introduce
Competitive Collaboration, a framework that facilitates the coordinated
training of multiple specialized neural networks to solve complex problems.
Competitive Collaboration works much like expectation-maximization, but with
neural networks that act as both competitors to explain pixels that correspond
to static or moving regions, and as collaborators through a moderator that
assigns pixels to be either static or independently moving. Our novel method
integrates all these problems in a common framework and simultaneously reasons
about the segmentation of the scene into moving objects and the static
background, the camera motion, depth of the static scene structure, and the
optical flow of moving objects. Our model is trained without any supervision
and achieves state-of-the-art performance among joint unsupervised methods on
all sub-problems.Comment: CVPR 201
T-Duality of Green-Schwarz Superstrings on AdS(d) x S(d) x M(10-2d)
We verify the self-duality of Green-Schwarz supercoset sigma models on AdS backgrounds (d=2,3,5) under combined bosonic and fermionic
T-dualities without gauge fixing kappa symmetry. We also prove this property
for superstrings on AdS (d=2,3) described by
supercoset sigma models with the isometries governed by the exceptional Lie
supergroups (d=2) and
(d=3), which requires an additional T-dualisation along one of the spheres.
Then, by taking into account the contribution of non-supercoset fermionic modes
(up to the second order), we provide evidence for the T-self-duality of the
complete type IIA and IIB Green-Schwarz superstring theory on AdS (d=2,3) backgrounds with Ramond-Ramond fluxes. Finally,
applying the Buscher-like rules to T-dualising supergravity fields, we prove
the T-self-duality of the whole class of the AdS
superbackgrounds with Ramond-Ramond fluxes in the context of supergravity.Comment: v2: 57 pages, 1 figure, typos fixed and clarifications added, version
to appear in JHE
Scattering in AdS2/CFT1 and the BES phase
We study worldsheet scattering for the type IIA superstring in AdS 2 ×S 2 ×T 6. Using the Green-Schwarz action to quartic order in fermions we take the near-BMN limit, where as in the AdS3/CFT2 case there are both massive and massless excitations. For the massive excitations we compute all possible tree-level processes, and show that these agree with a truncated version of the exact AdS 5 × S 5 S-matrix. We also compute several S-matrix elements involving massless excitations. At one loop we find that the dressing phase is the same Hernándes-López phase appearing in AdS5/CFT4. We see the same phase when calculating this by semiclassical means using the PSU(1, 1
2)/U(1)2 coset sigma model, for which we can also study the scattering of fermions. This supports the conjecture that the all-loop dressing phase is again the BES phase, rather than a new phase like that seen in AdS3/CFT2
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