353 research outputs found
The unintegrated gluon distribution from the CCFM equation
The gluon distribution f(x, k_t^2,mu^2), unintegrated over the transverse
momentum k_t of the gluon, satisfies the angular-ordered CCFM equation which
interlocks the dependence on the scale k_t with the scale \mu of the probe. We
show how, to leading logarithmic accuracy, the equation can be simplified to a
single scale problem. In particular we demonstrate how to determine the
two-scale unintegrated distribution f(x,k_t^2,mu^2) from knowledge of the
integrated gluon obtained from a unified scheme embodying both BFKL and DGLAP
evolution.Comment: 16 pages LaTeX, 3 eps figure
Gluon- vs. Sea quark-Shadowing
We calculate the shadowing of sea quarks and gluons and show that the
shadowing of gluons is {\it not} simply given by the sea quark shadowing,
especially at small . The calculations are done in the lab frame approach by
using the generalized vector meson dominance model. Here the virtual photon
turns into a hadronic fluctuation long before the nucleus. The subsequent
coherent interaction with more than one nucleon in the nucleus leads to the
depletion known as shadowing. A
comparison of the shadowing of quarks to E665 data for and
shows good agreement.Comment: 9 pages, 3 eps figure
High Energy Quark-Antiquark Elastic scattering with Mesonic Exchange
We studies the high energy elastic scattering of quark anti-quark with an
exchange of a mesonic state in the channel with .
Both the normalization factor and the Regge trajectory can be calculated in
PQCD in cases of fixed (non-running) and running coupling constant. The
dependence of the Regge trajectory on the coupling constant is highly
non-linear and the trajectory is of order of in the interesting physical
range.Comment: 29 page
Theoretical issues of small physics
The perturbative QCD predictions concerning deep inelastic scattering at low
are summarized. The theoretical framework based on the leading log
resummation and factorization theorem is described and some recent
developments concerning the BFKL equation and its generalization are discussed.
The QCD expectations concerning the small behaviour of the spin dependent
structure function are briefly summarized and the importance of
the double logarithmic terms which sum contributions containing the leading
powers of is emphasised. The role of studying final states
in deep inelastic scattering for revealing the details of the underlying
dynamics at low is pointed out and some dedicated measurements, like deep
inelastic scattering accompanied by an energetic jet, the measurement of the
transverse energy flow etc., are briefly discussed.Comment: 17 pages, LATEX, 7 uuencoded eps figures include
Deep inelastic events containing a forward photon as a probe of small dynamics
We calculate the rate of producing deep inelastic events containing an
energetic isolated forward photon at HERA. We quantify the enhancement arising
from the leading gluon emissions with a view to using such events to
identify the underlying dynamics.Comment: 11 pages, Latex, 7 ps figure
The CCFM Monte Carlo generator CASCADE
CASCADE is a full hadron level Monte Carlo event generator for e-p, gamma-p
and p-p_bar processes, which uses the CCFM evolution equation for the initial
state cascade in a backward evolution approach supplemented with off-shell
matrix elements for the hard scattering. A detailed program description is
given, with emphasis on parameters the user wants to change and common block
variables which completely specify the generated events.Comment: Program manual, 14 page
Structure Functions of the Nucleon and their Interpretation
The current status of measurements of the nucleon structure functions and
their understanding is reviewed. The fixed target experiments E665, CCFR and
NMC and the HERA experiments H1 and ZEUS are discussed in some detail. The
extraction of parton momentum distribution functions from global fits is
described, with particular attention paid to much improved information on the
gluon momentum distribution. The status of alpha_s measurements from deep
inelastic data is reviewed. Models and non-perturbative approaches for the
parton input distributions are outlined. The impact on the phenomenology of QCD
of the data at very low values of the Bjorken x variable is discussed in
detail. Recent advances in the understanding of the transition from deep
inelastic scattering to photoproduction are summarised. Some brief comments are
made on the recent HERA measurements of the ep NC and CC cross-sections at very
high Q2.Comment: 196 pages, 79 figures, uses ijmpa.sty and psfig.tex (included
Respiration-averaged CT versus standard CT attenuation maps for correction of the 18F-NaF uptake in hybrid PET/CT
BACKGROUND: To evaluate the impact of respiratory-averaged computed tomography attenuation correction (RACTAC) compared to standard single-phase computed tomography attenuation correction (CTAC) map, on the quantitative measures of coronary atherosclerotic lesions of (18)F-sodium fluoride ((18)F-NaF) uptake in hybrid positron emission tomography and computed tomography (PET/CT). METHODS: This study comprised 23 patients who underwent (18)F-NaF coronary PET in a hybrid PET/CT system. All patients had a standard single-phase CTAC obtained during free-breathing and a 4D cine-CT scan. From the cine-CT acquisition, RACTAC maps were obtained by averaging all images acquired over 5 seconds. PET reconstructions using either CTAC or RACTAC were compared. The quantitative impact of employing RACTAC was assessed using maximum target-to-background (TBR(MAX)) and coronary microcalcification activity (CMA). Statistical differences were analyzed using reproducibility coefficients and Bland-Altman plots. RESULTS: In 23 patients, we evaluated 34 coronary lesions using CTAC and RACTAC reconstructions. There was good agreement between CTAC and RACTAC for TBR(MAX) (median [Interquartile range]): CTAC= 1.65[1.23â2.38], RACTAC= 1.63[1.23â2.33], p=0.55), with coefficient of reproducibility of 0.18, and CMA: CTAC= 0.10 [0â1.0], RACTAC= 0.15[0â1.03], p=0.55 with coefficient of reproducibility of 0.17 CONCLUSION: Respiratory-averaged and standard single-phase attenuation correction maps provide similar and reproducible methods of quantifying coronary (18)F-NaF uptake on PET/CT
Bats of Saint Martin, French West Indies/Sint Maarten, Netherlands Antilles
Six species of bats have been previously reported from the Antillean island of Saint Martin/Sint MaartenâArtibeus jamaicensis, Brachyphylla cavernarum, Molossus molossus, Tadarida brasiliensis, Noctilio leporinus, and Myotis nigricans nesopolus. Our field research reported herein documents an additional three species of bats from the island for the first timeâMonophyllus plethodon, Ardops nichollsi, and Natalus stramineus. Re-examination of the single voucher of Myotis nigricans nesopolus has led us to exclude this species from the fauna of Saint Martin/Sint Maarten. Based on our field research and the study of specimens housed in museum collections, we present information on the eight species of bats that we have documented as occurring on Saint Martin/Sint Maarten. The average rate of fruit bat captures on Saint Martin/Sint Maarten (0.92 bats per net-nightâ BNN) falls towards the lower end of the range (0.65-2.47 BNN) reported from nearby islands in the northern Lesser Antilles and below the range (2.20-5.93 BNN) reported for mainland populations of Neotropical fruit bats. We discuss possible causes of these decreased population levels and we express some concerns about the future conservation status of the chiropteran fauna of the island
Bats of Barbados
The chiropteran fauna of Barbados includes representatives of four families â Noctilionidae, Phyllostomidae, Vespertilionidae, and Molossidae â including 1 piscivore (Noctilio leporinus), 1 omnivore (Brachyphylla cavernarum), 1 pollenivore/nectarivore (Monophyllus plethodon), 1 frugivore (Artibeus jamaicensis), and 2 insectivorous species (Myotis nyctor and Molossus molossus). Despite an early report, we believe that preponderance of the evidence available at this time is that E. fuscus is not part of the fauna of Barbados. The Barbadian chiropteran fauna of 6 species is much smaller than those on the four neighboring Lesser Antillean islands to the west and north. We believe that this is primarily the result of two factorsâgeological age and geographic isolation. Our work indicates that populations of the 6 species of bats on Barbados are in good condition in all cases, but only for Artibeus jamaicensis and Molossus molossus are the populations large enough to not be of ongoing concern. The maintenance of the chiropteran fauna can best be served by three management actions â preservation of caves and associated gullies, forests, and hydrological systems
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