420 research outputs found
Udsædsbårne sygdomme i økologisk såsæd - betydning og skadetærskler
Det økologiske projekt ORGSEED har givet ny viden om skadetærsklerne for de vigtigste udsædsbårne sygdomme i korn og ærter. I projektets sidste del vil disse tærskelværdier blive vurderet med henblik på justering. Sammenholdt med nye metoder til bestemmelse af den faktiske forekomst af udsædsbårne sygdomme, vil det give en mere sikker karakterisering af den økologiske såsæd og hermed mindre unødig kassation
Strength Reduction in Electrical and Elastic Networks
Particular aspects of problems ranging from dielectric breakdown to metal
insu- lator transition can be studied using electrical o elastic networks. We
present an expression for the mean breakdown strength of such networks.First,
we intro- duce a method to evaluate the redistribution of current due to the
removal of a finite number of elements from a hyper-cubic network of
conducatances.It is used to determine the reduction of breakdown strength due
to a fracture of size .Numerical analysis is used to show that the
analogous reduction due to random removal of elements from electrical and
elastic networks follow a similar form.One possible application, namely the use
of bone density as a diagnostic tools for osteorosporosis,is discussed.Comment: one compressed file includes: 9 PostScrpt figures and a text fil
Using Nonlinear Response to Estimate the Strength of an Elastic Network
Disordered networks of fragile elastic elements have been proposed as a model
of inner porous regions of large bones [Gunaratne et.al., cond-mat/0009221,
http://xyz.lanl.gov]. It is shown that the ratio of responses of such
a network to static and periodic strain can be used to estimate its ultimate
(or breaking) stress. Since bone fracture in older adults results from the
weakening of porous bone, we discuss the possibility of using as a
non-invasive diagnostic of osteoporotic bone.Comment: 4 pages, 4 figure
Cross-Correlation Studies with CMB Polarization Maps
The free-electron population during the reionized epoch rescatters CMB
temperature quadrupole and generates a now well-known polarization signal at
large angular scales. While this contribution has been detected in the
temperature-polarization cross power spectrum measured with WMAP data, due to
the large cosmic variance associated with anisotropy measurements at tens of
degree angular scales only limited information related to reionization, such as
the optical depth to electron scattering, can be extracted. The inhomogeneities
in the free-electron population lead to an additional secondary polarization
anisotropy contribution at arcminute scales. While the fluctuation amplitude,
relative to dominant primordial fluctuations, is small, we suggest that a
cross-correlation between arcminute scale CMB polarization data and a tracer
field of the high redshift universe, such as through fluctuations captured by
the 21 cm neutral Hydrogen background or those in the infrared background
related to first proto-galaxies, may allow one to study additional details
related to reionization. For this purpose, we discuss an optimized higher order
correlation measurement, in the form of a three-point function, including
information from large angular scale CMB temperature anisotropies in addition
to arcminute scale polarization signal related to inhomogeneous reionization.
We suggest that the proposed bispectrum can be measured with a substantial
signal-to-noise ratio and does not require all-sky maps of CMB polarization or
that of the tracer field. A measurement such as the one proposed may allow one
to establish the epoch when CMB polarization related to reionization is
generated and to address if the universe was reionized once or twice.Comment: 13 pages, 7 figures; Version in press with Phys. Rev.
Landscape Features Impact on Soil Available Water, Corn Biomass, and Gene Expression during the Late Vegetative Stage
Crop yields at summit positions of rolling landscapes often are lower than backslope yields. The differences in plant response may be the result of many different factors. We examined corn (Zea mays L.) plant productivity, gene expression, soil water, and nutrient availability in two landscape positions located in historically high (backslope) and moderate (summit and shoulder) yielding zones to gain insight into plant response differences. Growth characteristics, gene expression, and soil parameters (water and N and P content) were determined at the V12 growth stage of corn. At tassel, plant biomass, N content, 13C isotope discrimination (Δ), and soil water was measured. Soil water was 35% lower in the summit and shoulder compared with the lower backslope plots. Plants at the summit had 16% less leaf area, biomass, and N and P uptake at V12 and 30% less biomass at tassel compared with plants from the lower backslope. Transcriptome analysis at V12 indicated that summit and shoulder-grown plants had 496 downregulated and 341 upregulated genes compared with backslope-grown plants. Gene set and subnetwork enrichment analyses indicated alterations in growth and circadian response and lowered nutrient uptake, wound recovery, pest resistance, and photosynthetic capacity in summit and shoulder-grown plants. Reducing plant populations, to lessen demands on available soil water, and applying pesticides, to limit biotic stress, may ameliorate negative water stress responses
Large-scale pathways-based association study in amyotrophic lateral sclerosis
Sporadic amyotrophic lateral sclerosis (ALS), a devastating neurodegenerative disease, most likely results from complex genetic and environmental interactions. Although a number of association studies have been performed in an effort to find genetic components of sporadic ALS, most of them resulted in inconsistent findings due to a small number of genes investigated in relatively small sample sizes, while the replication of results was rarely attempted. Defects in retrograde axonal transport, vesicle trafficking and xenobiotic metabolism have been implicated in neurodegeneration and motor neuron death both in human disease and animal models. To assess the role of common genetic variation in these pathways in susceptibility to sporadic ALS, we performed a pathway-based candidate gene case-control association study with replication. Furthermore, we determined reliability of whole genome amplified DNA in a large-scale association study. In the first stage of the study, 1277 putative functional and tagging SNPs in 134 genes spanning 8.7 Mb were genotyped in 822 British sporadic ALS patients and 872 controls using whole genome amplified DNA. To detect variants with modest effect size and discriminate among false positive findings 19 SNPs showing a trend of association in the initial screen were genotyped in a replication sample of 580 German sporadic ALS patients and 361 controls. We did not detect strong evidence of association with any of the genes investigated in the discovery sample (lowest uncorrected P-value 0.00037, lowest permutation corrected P-value 0.353). None of the suggestive associations was replicated in a second sample, further excluding variants with moderate effect size. We conclude that common variation in the investigated pathways is unlikely to have a major effect on susceptibility to sporadic ALS. The genotyping efficiency was only slightly decreased (∼1%) and genotyping quality was not affected using whole genome amplified DNA. It is reliable for large scale genotyping studies of diseases such as ALS, where DNA sample collections are limited because of low disease prevalence and short survival time. © 2007 The Author(s)
Breakup reaction models for two- and three-cluster projectiles
Breakup reactions are one of the main tools for the study of exotic nuclei,
and in particular of their continuum. In order to get valuable information from
measurements, a precise reaction model coupled to a fair description of the
projectile is needed. We assume that the projectile initially possesses a
cluster structure, which is revealed by the dissociation process. This
structure is described by a few-body Hamiltonian involving effective forces
between the clusters. Within this assumption, we review various reaction
models. In semiclassical models, the projectile-target relative motion is
described by a classical trajectory and the reaction properties are deduced by
solving a time-dependent Schroedinger equation. We then describe the principle
and variants of the eikonal approximation: the dynamical eikonal approximation,
the standard eikonal approximation, and a corrected version avoiding Coulomb
divergence. Finally, we present the continuum-discretized coupled-channel
method (CDCC), in which the Schroedinger equation is solved with the projectile
continuum approximated by square-integrable states. These models are first
illustrated by applications to two-cluster projectiles for studies of nuclei
far from stability and of reactions useful in astrophysics. Recent extensions
to three-cluster projectiles, like two-neutron halo nuclei, are then presented
and discussed. We end this review with some views of the future in
breakup-reaction theory.Comment: Will constitute a chapter of "Clusters in Nuclei - Vol.2." to be
published as a volume of "Lecture Notes in Physics" (Springer
Near-Infrared Spectral Monitoring of Triton with IRTF/SpeX II: Spatial Distribution and Evolution of Ices
This report arises from an ongoing program to monitor Neptune's largest moon
Triton spectroscopically in the 0.8 to 2.4 micron range using IRTF/SpeX. Our
objective is to search for changes on Triton's surface as witnessed by changes
in the infrared absorption bands of its surface ices N2, CH4, H2O, CO, and CO2.
We have recorded infrared spectra of Triton on 53 nights over the ten
apparitions from 2000 through 2009. The data generally confirm our previously
reported diurnal spectral variations of the ice absorption bands (Grundy &
Young 2004). Nitrogen ice shows a large amplitude variation, with much stronger
absorption on Triton's Neptune-facing hemisphere. We present evidence for
seasonal evolution of Triton's N2 ice: the 2.15 micron absorption band appears
to be diminishing, especially on the Neptune-facing hemisphere. Although it is
mostly dissolved in N2 ice, Triton's CH4 ice shows a very different
longitudinal variation from the N2 ice, challenging assumptions of how the two
ices behave. Unlike Triton's CH4 ice, the CO ice does exhibit longitudinal
variation very similar to the N2 ice, implying that CO and N2 condense and
sublimate together, maintaining a consistent mixing ratio. Absorptions by H2O
and CO2 ices show negligible variation as Triton rotates, implying very uniform
and/or high latitude spatial distributions for those two non-volatile ices.Comment: 22 pages, 13 figures, 5 tables, to appear in Icaru
Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G>C Variant in SMN2
Spinal muscular atrophy (SMA) is a severe neuromuscular disorder caused by biallelic loss or pathogenic variants in the SMN1 gene. Copy number and modifier intragenic variants in SMN2, an almost identical paralog gene of SMN1, are known to influence the amount of complete SMN proteins. Therefore, SMN2 is considered the main phenotypic modifier of SMA, although genotype-phenotype correlation is not absolute. We present eleven unrelated SMA patients with milder phenotypes carrying the c.859G>C-positive modifier variant in SMN2. All were studied by a specific NGS method to allow a deep characterization of the entire SMN region. Analysis of two homozygous cases for the variant allowed us to identify a specific haplotype, Smn2-859C.1, in association with c.859G>C. Two other cases with the c.859G>C variant in their two SMN2 copies showed a second haplotype, Smn2-859C.2, in cis with Smn2-859C.1, assembling a more complex allele. We also identified a previously unreported variant in intron 2a exclusively linked to the Smn2-859C.1 haplotype (c.154-1141G>A), further suggesting that this region has been ancestrally conserved. The deep molecular characterization of SMN2 in our cohort highlights the importance of testing c.859G>C, as well as accurately assessing the SMN2 region in SMA patients to gain insight into the complex genotype-phenotype correlations and improve prognostic outcomes
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