An Adaptable and Scalable Generator of Distributed Massive MIMO Baseband Processing Systems

Journal of Signal Processing Systems - This paper presents an algorithm-adaptable, scalable, and platform-portable generator for massive multiple-input multiple-output (MIMO) baseband processing...     

Short communication: Risk factors for sonographically detectable udder edema in overbagged cows at dairy shows

At dairy cow shows, the appearance of the udder is very important. To show cows at their best, udders are often presented in an overbagged state by extending milking intervals before the show. This practice represents an animal welfare issue because it is associated with behavior changes (e.g., excessive abduction and decreased eating time) and may affect the health of the animal. The aim of the current study was to determine the association between various parameters (e.g., milk yield, days in milk, milking procedures, or administration of nonsteroidal anti-inflammatory drugs, steroids, or diuretics) and the sonographically detectable udder edema score. Data were collected from the show catalogs, by interviewing the exhibitors, by analyzing official veterinary treatment protocols and official milking data, via laboratory analysis of blood samples, and by sonographic examinations of the udders at the show. For sonographically detectable udder edema scoring, 3 scans were taken, 1 on each fore quarter and 1 incorporating both rear quarters at the level of the median suspensory ligament. For grading the scans, a scoring system of 4 grades (score 0 = no edema, 1 = slight edema, 2 = moderate edema, 3 = severe edema) was used. Data from 321 cows of different breeds were collected at 4 highly competitive Swiss dairy shows (shows A–D) between January and September 2017. To determine risk factors for sonographically detectable udder edema, data were analyzed with 2 different logistic regression models. In model 1, the odds ratios were 3.33 (milking intervals of ≥16 h vs. <14 h), 3.84 (show A vs. show C), and 7.39 (dairy breeds vs. dual-purpose breeds). Milking intervals of dairy breeds were significantly higher than those of dual-purpose breeds. In model 2, milking interval was the only significant risk factor with an odds ratio of 9.00 for milking intervals of ≥16 h. Only the milking intervals represented a relevant risk factor in both models; therefore, we concluded that the previously described sonographic udder edema scoring is a useful technique for detecting overbagged udders at dairy shows. Its routine implementation may improve cow welfare at dairy shows.     

Freezing of aqueous specimens: an X-ray diffraction study

The effects on water of two cooling methods, immersion in a liquid cryogen and high-pressure freezing, were studied by X-ray cryodiffraction on different sucrose solutions. The nature of the ice formed by each method depends on both the sucrose concentration and the specimen thickness. In order to compare the two methods, we mainly studied specimens having a thickness of 0.2 mm. Under these conditions, freezing by immersion gives rise to hexagonal (IH), cubic (IC) and amorphous (IV) ices when the sucrose concentration (weight/weight) has a value within the range 0–30%, 30–60%, 60% and higher, respectively. The temperature of the phase transitions IV–IC, IC–IH depends on the sucrose concentration. High-pressure freezing gives rise to two specific forms of ice: an amorphous and a crystalline ice (ice III). Ice III is observed when pure water samples are high-pressure frozen provided that the sample temperature does not rise above −150 °C. Above this temperature, ice III transforms into hexagonal ice. Amorphous ice is formed when the sucrose concentration is higher than 20%. The amorphous ice formed under high pressure has a similar, but not identical, X-ray diffraction pattern to that of amorphous ice formed at atmospheric pressure. While the X-ray diffraction pattern of amorphous ice formed at atmospheric pressure (IV) shows a broad ring at a position corresponding to 0.37 nm, that of high-pressure amorphous ice (IVHP) shows a broader ring, located at 0.35 nm. IVHP presents a phase transition (IVHP–IV) at temperatures that depend on the sucrose concentration. We also observed that some precautions have to be taken in order to minimize the alcohol contamination of high-pressure frozen samples. The ice-phase diagram presented in this paper should be taken into account in all methods dedicated to the structural study of frozen biological specimens.     

Chemoselective Hydrogenation of α,β‐Unsaturated Nitriles

The chemoselective hydrogenation of cinnamonitrile to 3‐phenylallylamine proceeds with up to 80% selectivity at conversions of >90% with Raney cobalt and up to 60% selectivity with Raney nickel catalysts. Best results were obtained with a doped Raney cobalt catalyst (RaCo/Cr/Ni/Fe 2724) in ammonia saturated methanol at 100 °C and 80 bar. Major problems are the formation of hydrocinnamonitrile and of secondary amines, and overreduction to 3‐phenylpropylamine. Important parameters are the catalyst type and composition, the solvent type and the presence and concentration of ammonia. The catalytic system tolerates functional groups like OH, OMe, Cl, CO, but not aromatic nitro groups. Preliminary experiments indicate that other unsaturated nitriles with di‐ or trisubstituted CC bonds are also suitable substrates.     

Heterogeneous Enantioselective Hydrogenation of Activated Ketones Catalyzed by Modified Pt‐Catalysts: A Systematic Structure‐Selectivity Study

A systematic structure‐selectivity study was carried out for the enantioselective hydrogenation of activated ketones with chirally modified Pt/Al₂O₃ catalysts. For this, 18 modifiers containing an extended aromatic system able to form a strong adsorption complex with the Pt surface, and a suitable chiral group with an amino function capable to interact with the keto group of the substrate ( HCd, Qd, HCn, Qn , and semi‐synthetic derivatives, as well as synthetic analogues) were prepared and tested on 8 different activated ketones in AcOH and toluene under standard conditions. It was found that relatively small structural changes of the substrate and/or modifier structures strongly affected the enantioselectivity, and that no “best” modifier exists for all substrates. The highest ees for all substrates were obtained with quinuclidine‐derived modifiers in combination with naphthalene or quinoline rings, either in AcOH (substrates 1 – 5 and 8 , all carrying an sp³ carbon next to the keto group) or toluene ( 6 and 7 , with an sp² carbon next to the ketone). The presence and nature of the substituent R' at the quinuclidine significantly affected the ee (positive and negative effects). Certain combinations of an aromatic system and an amino function were preferred: For the quinuclidine moiety, quinoline and to a somewhat lesser extent naphthalene were a better match, while for the pyrrolidinylmethyl group anthracene was better suited. Methylation of the OH group often had a positive effect for hydrogenations in AcOH but not in toluene. With the exception of 8 , higher ees were obtained for the Cd / Qn series [leading to (R)‐products] than for the Cn / Qd series [leading to (S)‐products]. In several cases, opposite structure‐selectivity trends were detected when comparing reactions in toluene and AcOH, indicating a significant influence of the solvent.     

A state space analysis of propose-and-revise

A central research topic in the area of knowledge engineering is the reuse of problem-solving methods for developing knowledge based systems. For being able to reuse a problem-solving method it is important to know under which restrictions a problem-solving method is appropriate to solve a given problem. This paper describes the problem-solving method propose-and-revise as well as the way this problem-solving method searches in its problem space for a solution. A quantitative analysis of the efficiency of this search process is given. Additionally, task and domain specific properties and restrictions and their influence on the efficiency of the search process are considered. For these purposes an instance of the problem-solving method is transformed to a corresponding instance of a Stanford Research Institute Problem Solver (STRIPS) planning system. Then the problem-solving method is considered as an additional control strategy for such a planning system. By this way the various insights and analysis results which are available in the area of planning systems may be exploited for the analysis of problem-solving methods. ©1999 John Wiley & Sons, Inc.     

Hydroxylamine as a Source for Nitric Oxide in Metal‐Free 2,2,6,6‐ Tetramethylpiperidine N‐Oxyl Radical (TEMPO) Catalyzed Aerobic Oxidation of Alcohols

The communication reports on the metal‐free 2,2,6,6‐tetramethylpiperidine N‐oxyl radical (TEMPO) catalyzed aerobic oxidation of various alcohols to aldehydes and ketones. A novel catalyst system that uses 1–4 mol% of TEMPO in combination with 4–6 mol% of aqueous hydroxylamine is introduced. No other additives are necessary and corrosive by‐products are not formed during oxidation. Nitric oxide which is important for the catalytic cycle is generated in situ by reaction of the hydroxylamine with TEMPO. A catalytic cycle for the overall oxidation process is suggested.     

In Situ Characterization of Lattice Structure Evolution during Phase Transformation of Zr‐2.5Nb

The α–β phase transformation behavior of Zr‐2.5Nb (in mass%) has been characterized in real time during an in situ neutron diffraction experiment. The Zr‐2.5Nb material in the current study consists, at room temperature, of α‐Zr phase (hcp) and two β phases (bcc), a Nb rich β‐Nb phase and retained, Zr rich, β‐Zr(Nb) phase. It is suggested that this is related to a quench off the equilibrium solubility of Nb atoms in the Zr bcc unit cells. Vegard's law combined with thermal expansion is applied to calculate the composition of the β‐phase, which is compared with the phase diagram, revealing the system's kinetic behavior for approaching equilibrium.     

Electronic sputtering of Gd3Ga5O12 and Y3Fe5O12 garnets: Yield, stoichiometry and comparison to track formation

The results of present paper have shown that sputtering of yttrium iron garnet (Y₃Fe₅O₁₂) under swift heavy ions in the electronic energy loss regime is non-stoichiometric. Here we are presenting additional experimental results for gadolinium gallium garnet (Gd₃Ga₅O₁₂) as target. The irradiations were performed with different ions (⁵⁰Cr (589 MeV), ⁸⁶Kr (195 MeV) and ¹⁸¹Ta (400 MeV)) impinging perpendicularly to the surface. As earlier, the sputtering yield was determined by collecting the emitted gadolinium and gallium atoms on a thin aluminium foil, placed upstream above the target and analyzing the Al catcher by Rutherford backscattering. Also for Gd₃Ga₅O_12, the emission of Gd and Ga is non-stoichiometric. Sputtering appears above a critical electronic stopping power of S_th = 11.6 ± 1.5 keV/nm, which is larger than the threshold for track formation, in agreement with other amorphisable materials. In addition, the angular distribution of the sputtered species was measured for Y₃Fe₅O₁₂ and Gd₃Ga₅O₁₂ using 200 MeV Au ions impinging the surface at 20° relatively to the surface. For the two garnets the ratio of Y/Fe (and Gd/Ga) varies with the angle of emitted species and the stoichiometry seems to be preserved only for an emission perpendicular to the surface.