Measurements ofthe 197Au(n, γ) crosssectionupto100keV at the CSNSBack-nfacility

The neutron capture cross section of 197 Au was measured using the time-of-flight(TOF)technique at the Back-n facility of the China Spallation Neutron Source(CSNS)in the 1 eV to 100 keV range.Prompt c-rays originating from neutron-induced capture events were detected by four C_(6)D_(6) liquid scintillator detectors.Pulse height weighting technology(PHWT)was used to analyze the data.The results are in good agreement with ENDF/B-VIII.0,CENDL-3.1,and other evaluated libraries in the resonance region,and in agreement with both n TOF and GELINA experimental data in the 5–100 keV range.Finally,the resonance peaks in the energy range from 1eV to 1 keV were fitted by the SAMMY R-matrix code.

Measurements of the ^(107)Ag neutron capture cross sections with pulse height weighting technique at the CSNS Back-n facility

Silver indium cadmium(Ag–In–Cd) control rod is widely used in pressurized water reactor nuclear power plants,and it is continuously consumed in a high neutron flux environment. The mass ratio of ^(107)Ag in the Ag–In–Cd control rod is 41.44%. To accurately calculate the consumption value of the control rod, a reliable neutron reaction cross section of the ^(107)Ag is required. Meanwhile,^(107)Ag is also an important weak r nucleus. Thus, the cross sections for neutron induced interactions with ^(107)Ag are very important both in nuclear energy and nuclear astrophysics. The(n, γ) cross section of ^(107)Ag has been measured in the energy range of 1–60 eV using a back streaming white neutron beam line at China spallation neutron source. The resonance parameters are extracted by an R-matrix code. All the cross section of ^(107)Ag and resonance parameters are given in this paper as datasets. The datasets are openly available at http://www.doi.org/10.11922/sciencedb.j00113.00010.

New experimental measurement of^(nat)Se(n,γ)cross section between 1 eV to 1 keV at the CSNS Back-n facility

The^(74)Se is one of 35 p-nuclei,and^(82)Se is a r-process only nucleus,and their(n,γ)cross sections are vital input parameters for nuclear astrophysics reaction network calculations.The neutron capture cross section in the resonance range of isotopes and even natural selenium samples has not been measured.Promptγ-rays originating from neutron-induced capture events were detected by four C_(6)D_(6) liquid scintillator detectors at the Back-n facility of China Spallation Neutron Source(CSNS).The pulse height weighting technique(PHWT)was used to analyze the data in the 1 e V to 100 ke V region.The deduced neutron capture cross section was compared with ENDF/B-VIII.0,JEFF-3.2,and JENDL-4.0,and some differences were found.Resonance parameters were extracted by the R-matrix code SAMMY in the 1 e V-1 ke V region.All the cross sections ofnatSe and resonance parameters are given in the datasets.The datasets are openly available at http://www.doi.org/10.11922/sciencedb.j00113.00019.

Effects of Vitrification on the Imprinted Gene Snrpn in Neonatal Placental Tissue

Objective:To investigate the effects of vitrification on the expression of the imprinted gene Snrpn in neonatal placental tissue.Methods:Neonatal placental tissue was collected from women with natural pregnancy(control group)and from women in assisted reproductive technology(ART)pregnancy group,following fresh and vitrified embryo transfer(fresh group and vitrified group,respectively).Snrpn mRNA expression and SNRPN protein levels in placental tissue from these three groups were assessed by real-time reverse transcription polymerase chain reaction and Western blot,respectively.DNA methylation in the Snrpn promoter region was analyzed by bisulfite-pyrosequencing.Results:The expression of Snrpn mRNA and SNRPN protein was found to be higher in placental tissue from the fresh and vitrified ART groups,compared to the control group.There was no significant difference in SNRPN gene or protein expression between the fresh and vitrified groups.DNA methylation at the Snrpn promoter region was not significantly different between these three groups.Conclusions:Human ART may alter the transcriptional expression and protein levels of the imprinted gene Snrpn.However,compared to other ART methods,vitrification may not aggravate or reduce this effect.Moreover,the altered expression of Snrpn is likely not directly related to DNA methylation of the Snrpn promoter region.