4,704 research outputs found
Time lower bounds for nonadaptive turnstile streaming algorithms
We say a turnstile streaming algorithm is "non-adaptive" if, during updates,
the memory cells written and read depend only on the index being updated and
random coins tossed at the beginning of the stream (and not on the memory
contents of the algorithm). Memory cells read during queries may be decided
upon adaptively. All known turnstile streaming algorithms in the literature are
non-adaptive.
We prove the first non-trivial update time lower bounds for both randomized
and deterministic turnstile streaming algorithms, which hold when the
algorithms are non-adaptive. While there has been abundant success in proving
space lower bounds, there have been no non-trivial update time lower bounds in
the turnstile model. Our lower bounds hold against classically studied problems
such as heavy hitters, point query, entropy estimation, and moment estimation.
In some cases of deterministic algorithms, our lower bounds nearly match known
upper bounds
COST COMPARISONS OF ALTERNATIVE METHODS FOR PROCESSING RECYCLED WASTE NEWSPAPERS INTO FARM-ANIMAL BEDDING
The United States is facing a seemingly overwhelming problem of how to dispose of its solid waste. For disposal solutions to be viable, they must be environmentally sound and economically viable. Processing waste newspapers for farm-animal bedding offers a successful partial solution that meets both criteria. Centralized newspaper chopping is found to cost less than on-farm chopping. Both chopped and unchopped waste newspapers can be economically transported considerable distances. The use of waste newspapers for animal bedding is economically attractive at the farm level and can provide a partial solution to the solid-waste disposal problem.Environmental Economics and Policy, Livestock Production/Industries,
Photoelectron diffraction: from phenomenological demonstration to practical tool
The potential of photoelectron diffractionâexploiting the coherent interference of directly-emitted and elastically scattered components of the photoelectron wavefield emitted from a core level of a surface atom to obtain structural informationâwas first appreciated in the 1970s. The first demonstrations of the effect were published towards the end of that decade, but the method has now entered the mainstream armoury of surface structure determination. This short review has two objectives: First, to outline the way that the idea emerged and the way this evolved in my own collaboration with Neville Smith and his colleagues at Bell Labs in the early years: Second, to provide some insight into the current state-of-the art in application of (scanned-energy mode) photoelectron diffraction to address two key issue in quantitative surface structure determination, namely, complexity and precision. In this regard a particularly powerful aspect of photoelectron diffraction is its elemental and chemical-state specificity
The (2â3Ă3)rect. phase of alkylthiolate self-assembled monolayers on Au(111): a symmetry-constrained structural solution
Low-energy electron-diffraction (LEED) patterns of the Au(111)(2â3Ă3)rect.-butylthiolate surface phase (a structure also seen in longer alkane chain thiolate self-assembled monolayers) show missing diffracted beams characteristic of glide symmetry, but do not show the larger set of missing beams found in surface x-ray diffraction (SXRD). The difference can be attributed to the greatly enhanced role of multiple scattering in LEED, but the combination of symmetry constraints placed on possible structural models by the observed SXRD and LEED beam extinctions greatly reduces the number of possible structural models. Only three such models are identified, one of which is clearly incompatible with other published experimental data. The relative merits of the remaining models, both involving Au adatom-thiolate moieties, are discussed in the light of the results of previous experimental studies
The local adsorption site of methylthiolate on Au(1 1 1): Bridge or atop?
Measurements of the local adsorption geometry of the S head-group atom in the Au(1 1 1)(â3 Ă â3)R30°âCH3S surface have been made using normal incidence X-ray standing waves (NIXSW) and S 1s scanned-energy mode photoelectron diffraction on the same surface preparations. The results confirm that the local adsorption site is atop an Au atom in a bulk-continuation site with a SâAu bondlength of 2.42 ± 0.02 Ă
, and that there can be no significant fraction of coadsorbed bridging species as recently proposed in a combined molecular dynamics/experimental study by Mazzarello et al. [R. Mazzarello, A. Cossaro, A. Verdini, R. Rousseau, L. Casalis, M.F. Danisman, L. Floreano, S. Scandolo, A. Morgante, G. Scoles, Phys. Rev. Lett. 98 (2007) 016102]. The results do not, however, clearly distinguish the different local reconstruction (adatom) models proposed for this surface
Local methylthiolate adsorption geometry on Au(111) from photoemission core-level shifts
The local adsorption structure of methylthiolate in the ordered Au(111)-(â3Ăâ3)R30° phase has been investigated using core-level-shift measurements of the surface and bulk components of the Au 4f7/2 photoelectron binding energy. The amplitude ratio of the core-level-shift components associated with surface Au atoms that are, and are not, bonded to the thiolate is found to be compatible only with the previously proposed Au-adatom-monothiolate moiety in which the thiolate is bonded atop Au adatoms in hollow sites, and not on an unreconstructed surface, or in Au-adatom-dithiolate species
Exoplanets imaging with a Phase-Induced Amplitude Apodization Coronagraph - I. Principle
Using 2 aspheric mirrors, it is possible to apodize a telescope beam without
losing light or angular resolution: the output beam is produced by
``remapping'' the entrance beam to produce the desired light intensity
distribution in a new pupil. We present the Phase-Induced Amplitude Apodization
Coronagraph (PIAAC) concept, which uses this technique, and we show that it
allows efficient direct imaging of extrasolar terrestrial planets with a
small-size telescope in space. The suitability of the PIAAC for exoplanet
imaging is due to a unique combination of achromaticity, small inner working
angle (about 1.5 ), high throughput, high angular resolution and
large field of view. 3D geometrical raytracing is used to investigate the
off-axis aberrations of PIAAC configurations, and show that a field of view of
more than 100 in radius is available thanks to the correcting
optics of the PIAAC. Angular diameter of the star and tip-tilt errors can be
compensated for by slightly increasing the size of the occulting mask in the
focal plane, with minimal impact on the system performance. Earth-size planets
at 10 pc can be detected in less than 30s with a 4m telescope. Wavefront
quality requirements are similar to classical techniques.Comment: 35 pages, 16 figures, Accepted for publication in Ap
The local adsorption structure of benzene on Si(001)-(2 Ă 1): a photoelectron diffraction investigation
Scanned-energy mode C 1s photoelectron diffraction has been used to investigate the local adsorption geometry of benzene on Si(001) at saturation coverage and room temperature. The results show that two different local bonding geometries coexist, namely the 'standard butterfly' (SB) and 'tilted bridge' (TB) forms, with a composition of 58 ± 29% of the SB species. Detailed structural parameter values are presented for both species including SiâC bond lengths. On the basis of published measurements of the rate of conversion of the SB to the TB form on this surface, we estimate that the timescale of our experiment is sufficient for achieving equilibrium, and in this case our results indicate that the difference in the Gibbs free energy of adsorption, ÎG(TB)âÎG(SB), is in the range â0.023 to +0.049 eV. We suggest, however, that the relative concentration of the two species may also be influenced by a combination of steric effects influencing the kinetics, and a sensitivity of the adsorption energies of the adsorbed SB and TB forms to the nature of the surrounding benzene molecules
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