3,682 research outputs found
Fiber-Flux Diffusion Density for White Matter Tracts Analysis: Application to Mild Anomalies Localization in Contact Sports Players
We present the concept of fiber-flux density for locally quantifying white
matter (WM) fiber bundles. By combining scalar diffusivity measures (e.g.,
fractional anisotropy) with fiber-flux measurements, we define new local
descriptors called Fiber-Flux Diffusion Density (FFDD) vectors. Applying each
descriptor throughout fiber bundles allows along-tract coupling of a specific
diffusion measure with geometrical properties, such as fiber orientation and
coherence. A key step in the proposed framework is the construction of an FFDD
dissimilarity measure for sub-voxel alignment of fiber bundles, based on the
fast marching method (FMM). The obtained aligned WM tract-profiles enable
meaningful inter-subject comparisons and group-wise statistical analysis. We
demonstrate our method using two different datasets of contact sports players.
Along-tract pairwise comparison as well as group-wise analysis, with respect to
non-player healthy controls, reveal significant and spatially-consistent FFDD
anomalies. Comparing our method with along-tract FA analysis shows improved
sensitivity to subtle structural anomalies in football players over standard FA
measurements
Re-circumscription of the mimosoid genus Entada including new combinations for all species of the phylogenetically nested Elephantorrhiza (Leguminosae, Caesalpinioideae, mimosoid clade)
Recent phylogenomic analyses of 997 nuclear genes support the long-held view that the genus Entada is congeneric with Elephantorrhiza. Entada is resolved as monophyletic only if the genus Elephantorrhiza is subsumed within it. The two genera were distinguished solely by relatively minor differences in the mode of dehiscence of the fruits (a craspedium separating into one-seeded endocarp segments in Entada versus a craspedium with the whole fruit valve breaking away from the persistent replum in Elephantorrhiza) and the craspedial fruit type itself provides a shared synapomorphy for the re-circumscribed Entada. Here, we provide a synopsis of Entada, including 11 new combinations in total, for the eight species, one subspecies and one variety previously placed in Elephantorrhiza, as well as a new combination for a subspecies of Entada rheedei Spreng. not previously dealt with when Entada pursaetha DC. was placed in synonymy. These new combinations are: Entada burkei (Benth.) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada elephantina (Burch.) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada goetzei (Harms) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada goetzei subsp. lata (Brenan & Brummitt) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada obliqua (Burtt Davy) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada praetermissa (J.H. Ross) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada rangei (Harms) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada rheedei subsp. sinohimalensis (Grierson & D.G. Long) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada schinziana (Dinter) S.A. O’Donnell & G.P. Lewis, comb. nov.; Entada woodii (E. Phillips) S.A. O’Donnell & G.P. Lewis, comb. nov.; and Entada woodii var. pubescens (E. Phillips) S.A. O’Donnell & G.P. Lewis, comb. nov. We provide a revised circumscription of the genus Entada which now comprises 40 species distributed pantropically, with the greatest diversity of species in tropical Africa. We present a complete taxonomic synopsis, including a map showing the global distribution of the genus and photographs showing variation amongst species in habit, foliage, flowers and fruits. A short discussion about extrafloral nectaries, mainly observed in the Madagascan species, is presented
Charm and Bottom Semileptonic Decays
We review the present status of theoretical attempts to calculate the
semileptonic charm and bottom decays and then present a calculation of these
decays in the light--front frame at the kinematic point . This allows us
to evaluate the form factors at the same value of , even though the
allowed kinematic ranges for charm and bottom decays are very different. Also,
at this kinematic point the decay is given in terms of only one form factor
. For the ratio of the decay rates given by the E653 collaboration we
show that the determination of the ratio of the Cabibbo--Kobayashi--Maskawa
(CKM) matrix elements is consistent with that obtained from the unitarity
constraint. At present, though, the unitarity method still has greater
accuracy. Since comparisons of the semileptonic decays into and either
electrons or muons will be available soon from the E791 Fermilab experiment, we
also look at the massive muon case. We show that for a range of the
symmetry breaking is small even though the contributions of the
various helicity amplitudes becomes more complicated. For decays, the decay
at involves an extra form factor
coming from the photon contribution and so is not amenable to the same kind of
analysis, leaving only the decay as a
possibility. As the mass of the decaying particle increases we note that the
symmetry becomes badly broken at .Comment: Latex, 19 pages, two figures are attached, a minor change in the
manuscript related to thi
A consistent treatment for pion form factors in space-like and time-like regions
We write down some relevant matrix elements for the scattering and decay
processes of the pion by considering a quark-meson vertex function. The pion
charge and transition form factors , , and
are extracted from these matrix elements using a relativistic
quark model on the light-front. We found that, the form factors and
in the space-like region agree well with experiment.
Furthermore, the branching ratios of all observed decay modes of the neutral
pion, that are related to the form factors and
in the time-like region, are all consistent with the data as
well. Additionally, in the time-like region, which deals with the
nonvalence contribution, is also discussed.Comment: 24 pages, 6 figures, to appear in Phys. Rev.
CE19010
The WESPAS survey program is the consolidation of two existing survey programs carried out by FEAS. The Malin Shelf herring acoustic survey has been carried out annually since 2008 and reports on the annual abundance of summer feeding aggregations of herring to the west of Scotland and to the north and west of Ireland from 54°N to 58°30’N. The boarfish survey was carried out from 2011 using a chartered fishing vessel and reports on the abundance of spawning aggregations of boarfish from 47°N to 57°N. In 2016 both surveys were combined and carried out onboard the RV Celtic Explorer over a 42 day period providing synoptic coverage of shelf waters from 47°N northwards to 58°30’N
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