Optimization by Smoothed Bandpass Calibration in Radio Spectroscopy

We have developed the Smoothed Bandpass Calibration (SBC) method and the best suitable scan pattern to optimize radio spectroscopic observations. Adequate spectral smoothing is applied to the spectrum toward OFF-source blank sky adjacent to a target source direction for the purpose of bandpass correction. Because the smoothing process reduces noise, the integration time for OFF-source scans can be reduced keeping the signal-to-noise ratio. Since the smoothing is not applied to ON-source scans, the spectral resolution for line features is kept. An optimal smoothing window is determined by bandpass flatness evaluated by Spectral Allan Variance (SAV). An efficient scan pattern is designed to the OFF-source scans within the bandpass stability timescale estimated by Time-based Allan Variance (TAV). We have tested the SBC using the digital spectrometer, VESPA, on the VERA Iriki station. For the targeted noise level of 5e-4 as a ratio to the system noise, the optimal smoothing window was 32 - 60 ch in the whole bandwidth of 1024 ch, and the optimal scan pattern was designed as a sequence of 70-s ON + 10-s OFF scan pairs. The noise level with the SBC was reduced by a factor of 1.74 compared with the conventional method. The total telescope time to achieve the goal with the SBC was 400 s, which was 1/3 of 1200 s required by the conventional way. Improvement in telescope time efficiency with the SBC was calculated as 3x, 2x and 1.3x for single-beam, dual-beam, and on-the-fly (OTF) scans, respectively. The SBC works to optimize scan patterns for observations from now, and also works to improve signal-to-noise ratios of archival data if ON- and OFF-source spectra are individually recorded, though the efficiency depends on the spectral stability of the receiving system.Comment: 12 pages, 11 figures, to appear in the Publications of Astronomical Society of Japan, Vol.64, No.

Single Transverse-Spin Asymmetry in Large PTP_T Open Charm Production at an Electron-Ion Collider

We discuss the single transverse-spin asymmetry (SSA) to be observed in the $D$-meson production with large transverse-momentum in semi-inclusive deep inelastic scattering, $e p^\uparrow \rightarrow e D X$. This contribution is embodied as a twist-3 mechanism in the collinear factorization, which is induced by purely gluonic correlation inside the transversely-polarized nucleon, in particular, by the three-gluon correlation effects. The complete formula for the corresponding SSA in the leading-order QCD is expressed in terms of the four independent gluonic correlation functions and reveals the five independent structures with respect to the dependence on the azimuthal angle for the produced $D$-meson. We present the numerical calculations of the SSA formula at the kinematics relevant to a future Electron Ion Collider.Comment: 16 pages, 7 figure

Verifiable identification condition for nonignorable nonresponse data with categorical instrumental variables

We consider a model identification problem in which an outcome variable contains nonignorable missing values. Statistical inference requires a guarantee of the model identifiability to obtain estimators enjoying theoretically reasonable properties such as consistency and asymptotic normality. Recently, instrumental or shadow variables, combined with the completeness condition in the outcome model, have been highlighted to make a model identifiable. However, the completeness condition may not hold even for simple models when the instrument is categorical. We propose a sufficient condition for model identifiability, which is applicable to cases where establishing the completeness condition is difficult. Using observed data, we demonstrate that the proposed conditions are easy to check for many practical models and outline their usefulness in numerical experiments and real data analysis

ミトコンドリア タンパクシツ ゼンクタイ ユソウ ソウチ 29kDa タンパクシツ ノ cDNA クローニング ト ソノ キノウ カイセキ

A cDNA clone for the 29 kDa protein, a putative component of the import machinery of rat liver mitochondrial precursor proteins, was isolated from a rat liver cDNA library.　The nucleotide sequence showed that an open reading frame encodes a polypeptide of 284 amino acid residues, with a molecular weight of 33,345. The N-terminal portion of this protein has a 35mer-peptide with the typical features of a mitochondrial presequence. The molecular weight of the mature form was calculated to be 29,579.　The peptide, composed of sixteen amino acids, was synthesized chemically based on the amino acid sequence of this protein and was used as an antigen to prepare antibody.　This antibody specifically recognized the 29 kDa protein and inhibited the import of mitochondrial precursor proteins. Furthermore, the 29 kDa protein formed a complex with a precursor proteins on its way to the mitochondrial matrix. These results strongly suggest that the 29 kDa protein is a component of the import machinery.　Key words ：Mitochondria, protein precursor, protein impor