The Effective Particle-Hole Interaction and the Optical Response of Simple Metal Clusters

Following Sham and Rice [L. J. Sham, T. M. Rice, Phys. Rev. 144 (1966) 708] the correlated motion of particle-hole pairs is studied, starting from the general two-particle Greens function. In this way we derive a matrix equation for eigenvalues and wave functions, respectively, of the general type of collective excitation of a N-particle system. The interplay between excitons and plasmons is fully described by this new set of equations. As a by-product we obtain - at least a-posteriori - a justification for the use of the TDLDA for simple-metal clusters.Comment: RevTeX, 15 pages, 5 figures in uufiles format, 1 figure avaible from [email protected]

Kinks in the Kondo problem

We find the exact quasiparticle spectrum for the continuum Kondo problem of $k$ species of electrons coupled to an impurity of spin $S$. In this description, the impurity becomes an immobile quasiparticle sitting on the boundary. The particles are ``kinks'', which can be thought of as field configurations interpolating between adjacent wells of a potential with $k+1$ degenerate minima. For the overscreened case $k>2S$, the boundary has this kink structure as well, which explains the non-integer number of boundary states previously observed. Using simple arguments along with the consistency requirements of an integrable theory, we find the exact elastic $S$-matrix for the quasiparticles scattering among themselves and off of the boundary. This allows the calculation of the exact free energy, which agrees with the known Bethe ansatz solution.Comment: 9 pages +1 figur

Kinetic Roughening in Surfaces of Crystals Growing on Disordered Substrates

Substrate disorder effects on the scaling properties of growing crystalline surfaces in solidification or epitaxial deposition processes are investigated. Within the harmonic approach there is a phase transition into a low-temperature (low-noise) superrough phase with a continuously varying dynamic exponent z>2 and a non-linear response. In the presence of the KPZ nonlinearity the disorder causes the lattice efects to decay on large scales with an intermediate crossover behavior. The mobility of the rough surface hes a complex dependence on the temperature and the other physical parameters.Comment: 13 pages, 2 figures (not included). Submitted to Phys. Rev. Letts. Use Latex twic

Self-regulation of ice flow varies across the ablation area in South-West Greenland

The concept of a positive feedback between ice flow and enhanced melt rates in a warmer climate fuelled the debate regarding the temporal and spatial controls on seasonal ice acceleration. Here we combine melt, basal water pressure and ice velocity data. Using 20 years of data covering the whole ablation area, we show that there is not a strong positive correlation between annual ice velocities and melt rates. Annual velocities even slightly decreased with increasing melt. Results also indicate that melt variations are most important for velocity variations in the upper ablation zone up to the equilibrium line altitude. During the extreme melt in 2012, a large velocity response near the equilibrium line was observed, highlighting the possibility of meltwater to have an impact even high on the ice sheet. This may lead to an increase of the annual ice velocity in the region above S9 and requires further monitoring

The level of air pollution in the impact zone of coal-fired power plant (Karaganda City) using the data of geochemical snow survey (Republic of Kazakhstan)

Coal-fired power plants emissions impact the air quality and human health. Of great significance is assessment of solid airborne particles emissions from those plants and distance of their transportation. The article presents the results of air pollution assessment in the zone of coal-fired power plant (Karaganda City) using snow survey. Based on the mass of solid airborne particles deposited in snow, time of their deposition on snow at the distance from 0.5 to 4.5 km a value of dust load has been determined. It is stated that very high level of pollution is observed at the distance from 0.5 to 1 km. there is a trend in decrease of dust burden value with the distance from the stacks of coal-fired power plant that may be conditioned by the particle size and washing out smaller ash particles by ice pellets forming at freezing water vapour in stacks of the coal-fired power plant. Study in composition of solid airborne particles deposited in snow has shown that they mainly contain particulates of underburnt coal, Al-Si- rich spheres, Fe-rich spheres, and coal dust. The content of the particles in samples decreases with the distance from the stacks of the coal-fired power plant

North Pacific-wide spreading of isotopically heavy nitrogen during the last deglaciation: Evidence from the western Pacific

Sedimentary delta(15) N records in two IMAGES cores (MD012404 and MD012403) retrieved from the Okinawa Trough (OT) in the western North Pacific reveal deglacial increases with two peaks occurring during the Bolling/Allerod and the Preboreal/early Holocene periods. These peaks are synchronous with previously reported delta(15) N peaks in the Eastern Tropical North Pacific, although the amplitudes (from 3.8 to 5.8%) are much smaller in the OT. Similar delta(15) N values for the last glacial maximum and the late-Holocene observed by us at a site far from the present-day zones of water-column denitrification (WCD) indicate that the mean N-15/N-14 of nitrate in the upper ocean did not differ much between the two climate states. The accumulation rate of organic carbon and total sulfur content are used as indices of the local WCD potential. The results suggest that enhancement of global WCD rather than local denitrification should be responsible for the deglacial maxima of sedimentary delta(15) N in the Okinawa Trough. Our data could provide additional constraints to better understand changes in nitrogen budget during the glacial to interglacial transition.National Science Council of Taiwan [NSC 96-2611-M-001-005]; State Key Laboratory of Marine Environmental Science, ; Xiamen University, Xiame

Parkinson's disease age at onset genome-wide association study : Defining heritability, genetic loci, and α-synuclein mechanisms

Background Increasing evidence supports an extensive and complex genetic contribution to PD. Previous genome-wide association studies (GWAS) have shed light on the genetic basis of risk for this disease. However, the genetic determinants of PD age at onset are largely unknown. Objectives To identify the genetic determinants of PD age at onset. Methods Using genetic data of 28,568 PD cases, we performed a genome-wide association study based on PD age at onset. Results We estimated that the heritability of PD age at onset attributed to common genetic variation was similar to 0.11, lower than the overall heritability of risk for PD (similar to 0.27), likely, in part, because of the subjective nature of this measure. We found two genome-wide significant association signals, one at SNCA and the other a protein-coding variant in TMEM175, both of which are known PD risk loci and a Bonferroni-corrected significant effect at other known PD risk loci, GBA, INPP5F/BAG3, FAM47E/SCARB2, and MCCC1. Notably, SNCA, TMEM175, SCARB2, BAG3, and GBA have all been shown to be implicated in alpha-synuclein aggregation pathways. Remarkably, other well-established PD risk loci, such as GCH1 and MAPT, did not show a significant effect on age at onset of PD. Conclusions Overall, we have performed the largest age at onset of PD genome-wide association studies to date, and our results show that not all PD risk loci influence age at onset with significant differences between risk alleles for age at onset. This provides a compelling picture, both within the context of functional characterization of disease-linked genetic variability and in defining differences between risk alleles for age at onset, or frank risk for disease. (c) 2019 International Parkinson and Movement Disorder SocietyPeer reviewe

DNM1 encephalopathy: A new disease of vesicle fission.

ObjectiveTo evaluate the phenotypic spectrum caused by mutations in dynamin 1 (DNM1), encoding the presynaptic protein DNM1, and to investigate possible genotype-phenotype correlations and predicted functional consequences based on structural modeling.MethodsWe reviewed phenotypic data of 21 patients (7 previously published) with DNM1 mutations. We compared mutation data to known functional data and undertook biomolecular modeling to assess the effect of the mutations on protein function.ResultsWe identified 19 patients with de novo mutations in DNM1 and a sibling pair who had an inherited mutation from a mosaic parent. Seven patients (33.3%) carried the recurrent p.Arg237Trp mutation. A common phenotype emerged that included severe to profound intellectual disability and muscular hypotonia in all patients and an epilepsy characterized by infantile spasms in 16 of 21 patients, frequently evolving into Lennox-Gastaut syndrome. Two patients had profound global developmental delay without seizures. In addition, we describe a single patient with normal development before the onset of a catastrophic epilepsy, consistent with febrile infection-related epilepsy syndrome at 4 years. All mutations cluster within the GTPase or middle domains, and structural modeling and existing functional data suggest a dominant-negative effect on DMN1 function.ConclusionsThe phenotypic spectrum of DNM1-related encephalopathy is relatively homogeneous, in contrast to many other genetic epilepsies. Up to one-third of patients carry the recurrent p.Arg237Trp variant, which is now one of the most common recurrent variants in epileptic encephalopathies identified to date. Given the predicted dominant-negative mechanism of this mutation, this variant presents a prime target for therapeutic intervention

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

Background Classifying pathogenicity of missense variants represents a major challenge in clinical practice during the diagnoses of rare and genetic heterogeneous neurodevelopmental disorders (NDDs). While orthologous gene conservation is commonly employed in variant annotation, approximately 80% of known disease-associated genes belong to gene families. The use of gene family information for disease gene discovery and variant interpretation has not yet been investigated on a genome-wide scale. We empirically evaluate whether paralog-conserved or non-conserved sites in human gene families are important in NDDs. Methods Gene family information was collected from Ensembl. Paralog-conserved sites were defined based on paralog sequence alignments; 10,068 NDD patients and 2078 controls were statistically evaluated for de novo variant burden in gene families. Results We demonstrate that disease-associated missense variants are enriched at paralog-conserved sites across all disease groups and inheritance models tested. We developed a gene family de novo enrichment framework that identified 43 exome-wide enriched gene families including 98 de novo variant carrying genes in NDD patients of which 28 represent novel candidate genes for NDD which are brain expressed and under evolutionary constraint. Conclusion This study represents the first method to incorporate gene family information into a statistical framework to interpret variant data for NDDs and to discover new NDD-associated genes