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All sourcesNASA NTRSDOE OSTI
DOE OSTI2011

PERIODIC VARIABILITY OF LOW-MASS STARS IN SLOAN DIGITAL SKY SURVEY STRIPE 82

We present a catalog of periodic stellar variability in the 'Stripe 82' region of the Sloan Digital Sky Survey. After aggregating and re-calibrating catalog-level data from the survey, we ran a period-finding algorithm (Supersmoother) on all point-source light curves. We used color selection to identify systems that are likely to contain low-mass stars, in particular M dwarfs and white dwarfs. In total, we found 207 candidates, the vast majority of which appear to be in eclipsing binary systems. The catalog described in this paper includes 42 candidate M dwarf/white dwarf pairs, four white dwarf pairs, 59 systems whose colors indicate they are composed of two M dwarfs and whose light-curve shapes suggest they are in detached eclipsing binaries, and 28 M dwarf systems whose light-curve shapes suggest they are in contact binaries. We find no detached systems with periods longer than 3 days, thus the majority of our sources are likely to have experienced orbital spin-up and enhanced magnetic activity. Indeed, 26 of 27 M dwarf systems that we have spectra for show signs of chromospheric magnetic activity, far higher than the 24% seen in field stars of the same spectral type. We also find binaries composed of stars that bracket the expected boundary between partially and fully convective interiors, which will allow the measurement of the stellar mass-radius relationship across this transition. The majority of our contact systems have short orbital periods, with small variance (0.02 days) in the sample near the observed cutoff of 0.22 days. The accumulation of these stars at short orbital period suggests that the process of angular momentum loss, leading to period evolution, becomes less efficient at short periods. These short-period systems are in a novel regime for studying the effects of orbital spin-up and enhanced magnetic activity, which are thought to be the source of discrepancies between mass-radius predictions and measurements of these properties in eclipsing binaries.

79 ASTRONOMY AND ASTROPHYSICS↗
DOE OSTI2015

WE-G-207-05: Relationship Between CT Image Quality, Segmentation Performance, and Quantitative Image Feature Analysis

Purpose: Segmentation quality can affect quantitative image feature analysis. The objective of this study is to examine the relationship between computed tomography (CT) image quality, segmentation performance, and quantitative image feature analysis. Methods: A total of 90 pathology proven breast lesions in 87 dedicated breast CT images were considered. An iterative image reconstruction (IIR) algorithm was used to obtain CT images with different quality. With different combinations of 4 variables in the algorithm, this study obtained a total of 28 different qualities of CT images. Two imaging tasks/objectives were considered: 1) segmentation and 2) classification of the lesion as benign or malignant. Twenty-three image features were extracted after segmentation using a semi-automated algorithm and 5 of them were selected via a feature selection technique. Logistic regression was trained and tested using leave-one-out-cross-validation and its area under the ROC curve (AUC) was recorded. The standard deviation of a homogeneous portion and the gradient of a parenchymal portion of an example breast were used as an estimate of image noise and sharpness. The DICE coefficient was computed using a radiologist’s drawing on the lesion. Mean DICE and AUC were used as performance metrics for each of the 28 reconstructions. The relationship between segmentation and classification performance under different reconstructions were compared. Distributions (median, 95% confidence interval) of DICE and AUC for each reconstruction were also compared. Results: Moderate correlation (Pearson’s rho = 0.43, p-value = 0.02) between DICE and AUC values was found. However, the variation between DICE and AUC values for each reconstruction increased as the image sharpness increased. There was a combination of IIR parameters that resulted in the best segmentation with the worst classification performance. Conclusion: There are certain images that yield better segmentation or classification performance. The best segmentation Result does not necessarily lead to the best classification Result. This work has been supported in part by grants from the NIH R21-EB015053. R Nishikawa is receives royalties form Hologic, Inc.

60 APPLIED LIFE SCIENCES↗
DOE OSTI2019

Nonlinear saturation and oscillations of collisionless zonal flows

Abstract In homogeneous drift-wave turbulence, zonal flows (ZFs) can be generated via a modulational instability (MI) that either saturates monotonically or leads to oscillations of the ZF energy at the nonlinear stage. This dynamics is often attributed as the predator–prey oscillations induced by ZF collisional damping; however, similar dynamics is also observed in collisionless ZFs, in which case a different mechanism must be involved. Here, we propose a semi-analytic theory that explains the transition between the oscillations and saturation of collisionless ZFs within the quasilinear Hasegawa–Mima model. By analyzing phase-space trajectories of DW quanta (driftons) within the geometrical-optics (GO) approximation, we argue that the parameter that controls this transition is N ∼ γ MI / ω DW , where γ MI is the MI growth rate and ω DW is the linear DW frequency. We argue that at N ≪ 1, ZFs oscillate due to the presence of so-called passing drifton trajectories, and we derive an approximate formula for the ZF amplitude as a function of time in this regime. We also show that at N ≳ 1, the passing trajectories vanish and ZFs saturate monotonically, which can be attributed to phase mixing of higher-order sidebands. A modification of N that accounts for effects beyond the GO limit is also proposed. These analytic results are tested against both quasilinear and fully-nonlinear simulations. They also explain the earlier numerical results by Connaughton et al (2010 J. Fluid Mech. 654 207) and Gallagher et al (2012 Phys. Plasmas 19 122115) and offer a different perspective on what the control parameter actually is that determines the transition from the oscillations to saturation of collisionless ZFs.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2019

Nonlinear saturation and oscillations of collisionless zonal flows

In homogeneous drift-wave (DW) turbulence, zonal flows (ZFs) can be generated via a modulational instability (MI) that either saturates monotonically or leads to oscillations of the ZF energy at the nonlinear stage. This dynamics is often attributed as the predator-prey oscillations induced by ZF collisional damping; however, similar dynamics is also observed in collisionless ZFs, in which case a different mechanism must be involved. Here, we propose a semi-analytic theory that explains the transition between the oscillations and saturation of collisionless ZFs within the quasilinear Hasegawa-Mima model. By analyzing phase-space trajectories of DW quanta (driftons) within the geometrical-optics (GO) approximation, we argue that the parameter that controls this transition is N ~ \gamma_MI/\omega_DW, where \gamma_MI is the MI growth rate and \omega_DW is the linear DW frequency. We argue that at N << 1, ZFs oscillate due to the presence of so-called passing drifton trajectories, and we derive an approximate formula for the ZF amplitude as a function of time in this regime. We also show that at N >~ 1, the passing trajectories vanish and ZFs saturate monotonically, which can be attributed to phase mixing of higher-order sidebands. A modification of N that accounts for effects beyond the GO limit is also proposed. These analytic results are tested against both quasilinear and fully-nonlinear simulations. They also explain the earlier numerical results by Connaughton et al. [J. Fluid Mech. 654, 207 (2010)] and Gallagher et al. [Phys. Plasmas 19, 122115 (2012)] and offer a revised perspective on what the control parameter is that determines the transition from the oscillations to saturation of collisionless ZFs.

collisionless zonal flows, modulational instabilit↗
DOE OSTI2020

Characterization and CST Batch Contact Equilibrium Testing of Modified Tank 9H Process Supernate Samples in Support of TCCR

The Tank Closure Cesium Removal (TCCR) system uses ion exchange columns filled with crystalline silicotitanate (CST) media to process radioactive waste solutions for the removal of ¹³⁷Cs. TCCR currently focuses on dissolving Savannah River Site (SRS) radioactive tank waste (primarily sodium saltcake solids) within Tank 10H followed by at-tank ion exchange column treatment. Two supernate batches from Tank 10H have been processed through the TCCR unit and processing of a third batch is expected soon. After processing of this supernate batch, plans are to replace the CST columns and process dissolved salt solution from Tank 9H through Tank 10H and then through the new CST columns installed in the TCCR unit. The new columns are expected to contain either a media similar to an archived CST batch (IE-911) or the R9120-B CST media used in the current TCCR columns (the two materials are fundamentally the same; just different specifications, product names, and preconditioning steps). Samples of Tank 9H dissolved saltcake were received at the Savannah River National Laboratory (SRNL) and characterized. The Tank 9H supernate contained a high sodium concentration (~9.6 M Na⁺) and will require dilution to near 6 M [Na⁺] prior to processing through the TCCR unit. The cesium concentration in Tank 9H is currently significantly higher than was observed with Tank 10H. Three dilutions of the Tank 9H supernate were conducted to mimic possible dilutions that could be conducted in the tank farm prior to TCCR processing using inhibited water, sodium hydroxide, and sodium nitrate solutions. Dilution #1 was prepared by diluting the Tank 9H supernate by a factor of 1.6 with inhibited water, Dilution #2 was prepared by diluting the Tank 9H supernate by a factor of 3.7 with a mixed sodium hydroxide/sodium nitrate diluent, and Dilution #3 was prepared by also diluting by a factor of 3.7 but with sodium hydroxide only. All three dilutions have similar Na⁺ concentrations (~6 M), but Dilutions #2 and #3 contain significantly less cesium. Major and key minor components of the diluted Tank 9H supernate samples are provided in Table ES-1. Batch contact equilibrium tests were conducted with the Tank 9H dilutions and the two different CST media batches being considered for use in the new TCCR columns. Results are summarized in Table ES-2 and compared to ZAM model predictions. The highest cesium distribution coefficient and percent removal were observed with Dilution #3. IE-911 CST (an archived CST media batch) was more effective at removing cesium than the more recently prepared R9120-B CST media, though both media samples removed >88% of the cesium and the differences may not be statistically different considering the overall uncertainty. Based on the results, maximum cesium loadings were calculated for each CST media type and Tank 9H dilution. In general, maximum cesium loadings from dilutions of this supernate batch are quite high (approaching 0.1 mmol total Cs⁺/g CST for Dilution #1). The highest calculated maximum ¹³⁷Cs loading for the Tank 9H dilutions using the ZAM model with input of the tank compositions and batch contact results was 207 Ci/kg CST (Dilution #1 with IE-911 CST). In all cases, higher maximum cesium loading values were predicted for IE-911 CST versus R9120-B, although the differences varied considerably between the dilutions. The maximum loading value for IE-911 CST with Tank 9H Dilution #1 was only 7% higher than the maximum loading for R9120-B. The maximum loading value for IE-911 CST with Dilution #3 was 24% higher than the maximum loading for R9120-B. Dilution #2 was intermediate between these values. Note that these maximum loading values are the theoretical calculated values, and actual operating conditions will cause differences. A CST binder dilution (correction) factor near 0.7 (relative to pure powder CST) was required for each batch contact test with IE-911 engineered CST using the three Tank 9H dilutions. Correction factors calculated for R9120-B CST ranged from 0.56 to 0.66 for the three dilutions. Following the batch contact tests, the CST samples were isolated from the Tank 9H solution, washed, dried, and digested in acid following established procedures. The analysis results are provided in Table ES-3. Total cesium loading values determined by CST digestion were similar to the calculated loading values based on solution analysis (Table ES-2) for all samples. In addition, the CST was observed to load calcium (R9120-B sample only), iron, strontium, lead, uranium, and plutonium after contact with the waste supernate, as has been observed previously.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2017

Excess Li-Ion Storage on Reconstructed Surfaces of Nanocrystals To Boost Battery Performance

Abstract. Due to the enhanced kinetic properties, nanocrystallites have received much attention as potential electrode materials for energy storage. However, because of the large specific surface areas of nanocrystallites, they usually suffer from decreased energy density, reduced cycling stability and total electrode capacity. In this work, we report a size-dependent excess capacity beyond the theoretical value of 170 mAhg-1 in a special carbon coated LiFePO4 composite cathode material, which delivers capacities of 191.2 and 213.5 mAhg-1 with the mean particle sizes of 83 nm and 42 nm, respectively. Moreover, this LiFePO4 composite also shows excellent cycling stability and high rate performance. Our further experimental tests and ab initio calculations reveal that the excess capacity comes from the charge passivation for which the C-O-Fe bonds would lead to charge redistribution on the surface of LiFePO4 and hence to enhance the bonding interaction between surface O atoms and Li-ions. The surface reconstruction for excess Li-ion storage makes full use of the large specific surface area for the nanocrystallites, which can maintain the fast Li-ion transport and enhance the capacity greatly that the nanocrystallites usually suffers.

Duan, Yandong↗
DOE OSTI2019

Evaluation of Low-cost, Full HD, CMOS Cameras for Use in the Calcine Retrieval Project - 19530

This paper describes results from radiation testing conducted on low-cost, commercial off-the-shelf, full high-definition (HD) resolution (1920 x 1080 p), complementary metal-oxide-semiconductor (CMOS) camera sensors. The purpose of the testing was to evaluate the sensors' suitability for use in the Calcine Retrieval Project by determining their image quality and life expectancy while operating in an ionizing radiation field of 20.0 Gy/h. The two camera sensors tested were the Axis FA1105 and Axis FA1125. These commercial camera sensors were designed for retail security surveillance and have no radiation-hardened (rad-hard) components. In addition to radiation testing, the sensors' field-of-view, resolution, and low-light image quality were tested at several target distances to ensure they meet project requirements. Testing was divided into two phases. During Phase 1, four FA1105 sensors and four FA1125 sensors were tested simultaneously without any shielding in radiation fields of 25.5 Gy/h and 49.3 Gy/h. In Phase 2, three FA1105 and five FA1125 sensors were shielded by 22.2 mm of lead and tested simultaneously in radiation fields of 26.8 Gy/h, 52.3 Gy/h, 143.0 Gy/h, 200.7 Gy/h, 404.6 Gy/h, and 2,317.5 Gy/h. Dose rate values were established using film dosimetry readings. Apertures in the shielding allowed for a 40-degree field of view while shielding all parts of the sensor except for directly in front of the CMOS sensor array. All testing was conducted at the Idaho Accelerator Center in Pocatello, Idaho, using a 450 keV X-ray generator. Sensor images were automatically captured at regular intervals throughout the testing for qualitative evaluation by the test team. Film dosimetry was placed near the sensors to record actual dose totals. The 450 keV setting generates X-ray radiation with an energy level close to the primary gamma energy level produced by the Cesium-137 isotope in the calcine, which is 662 keV. Results from Phase 1 indicate the sensors failed at an average cumulative dose of 226.3 Gy. For a given 20.0 Gy/h field this results in a mean time to failure (MTTF) of 11.3 hours. Recorded images from all sensors showed minimal image degradation due to radiation-induced noise. When the sensors finally failed, the failure mode was an abrupt loss of video. The image went black suggesting some other component in the sensor head besides the CMOS sensor array was responsible for the failure. During a portion of Phase 1 testing, a commercial, rad-hard camera was irradiated in the 25.5 Gy/h field along with the eight Axis FA series sensors. Image quality from the FA series sensors significantly outperformed the image quality of the rad-hard camera in radiation-induced noise tolerance, image resolution, and dynamic range. During Phase 2 testing, all sensors produced excellent images in radiation fields as high as 404.6 Gy/h. One FA1125 sensor was tested at the highest dose rate of 2,317.5 Gy/h. At this dose rate, the image was color shifted towards red and contained a significant amount radiation-induced noise. The sensor did not fail and was producing usable imagery after one hour, at which time the test was ended due to allotted beam-time at the test facility. Eighteen hours after X-rays were shut off, the sensor image returned to normal color and all eight sensors continued to operate without any visible, permanent image degradation. For Phase 2 testing, it was not possible to establish a MTTF since none of the shielded sensors failed during the allotted test time. However, given the highest cumulative dose of 4,142.1 Gy received by a shielded FA1125 sensor, a minimum life expectancy of 207 hours (8.6 days) is predicted while operating in a 20.0 Gy/h field. Test results indicate the radiation tolerance of the FA series sensor's CMOS array, along with the small form factor, full HD image quality, wide dynamic range, and Ethernet standard makes it suitable for short-term use in monitoring and visually documenting waste remediation efforts for the Calcine Retrieval Project at the INL. The sensor's low-cost of about $140 US, compared to commercial rad-hard cameras costing between $5,000 and $7,000 US each, allow them to be used as an affordable, disposable resource for many short-duration, radioactive waste remediation efforts where decontamination of an expensive, commercial rad-hard camera is undesirable or not possible. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2019

Nuclear Data Sheets for A=266,270,274,278,282,286,290,294,298☆

Spectroscopic information such as production, identification, half-lives, decay modes and possible excited states for experimentally known nuclides of mass numbers 266, 270, 274, 278, 282, 286, 290, 294, and 298 are presented together with the recommended values, superseding information and data in the previous ENSDF and NDS evaluation by 2005Gu33. No nuclides have yet been identified for A=302. In the last 14 years, large amounts of new and definitive data on the superheavy nuclides (SHN) have become available, thus changing almost entirely the landscape of nuclear data in this mass region, as also indicated by a number of recent review articles: 2017Og01, 2016Ho09, 2016Ho06 (for fission barriers), 2015Og05, 2015Og07, 2015Mo25, 2015OgZX, 2013Th02, and 2011Og07. See 2016Ka49 for IUPAC technical discussions for the discovery of Z=117 (Ts), Z=115 (Mc), Z=113 (Nh), 2001Ka70 and 2003Ka71 for Z=110-112, 2011Ba54 for Z≥113, 2009Ba62 for Z=112, and 2016Ka50 for Z=118 (Og). A special issue of Nuclear Physics A444 (2015) is devoted to research on superheavy elements (SHE) with 27 articles. In particular, see article by 2015Ko20 on mass spectrometric searches for superheavy elements in terrestrial matter. See also Proceedings of Nobel Symposium NS160 ‘Chemistry and Physics of Heavy and Superheavy Elements’ published in Eur. Phys. Jour. Web of Conferences 131 (2016), in particular 2016UtZZ, 2016DmZZ and 2016HoZY. See also 2016DuZX for future prospects of discovery of elements beyond Z=118 A=266: {sup 266}Db, {sup 266}Sg, {sup 266}Bh, {sup 266}Hs and {sup 266}Mt are the experimentally identified nuclides with A=266. Identification of {sup 266}Lr from α decay of {sup 270}Db has been proposed by 2014Kh04 from experiments at GSI, but complete details and analyses of all the four decay chains reported in this experiment have not yet been published, and discussion in 2015Og05 review article considering their work from Dubna (2013Og04, 2011Og04) and from GSI (2014Kh04) still concluded that {sup 270}Db decayed dominantly by SF mode, in contrast with dominant α decay mode proposed by 2014Kh04. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, RIKEN, and LBNL facilities: {sup 266}Db from the α-decay of {sup 282}Nh in two correlated decay chains at Dubna; {sup 266}Sg as α-daughter of {sup 270}Hs in 12 correlated decay chains at Dubna and GSI; {sup 266}Bh in α decay of {sup 278}Nh in three correlated decay chains observed at RIKEN, and also directly with one event in {sup 249}Bk({sup 22}Ne,5n) at LBNL, and with four events in {sup 243}Am({sup 26}Mg,3n) at HIRFL-Lanzhou; {sup 266}Hs as α-daughter of {sup 270}Ds at GSI in two different experiments, six correlated decays in the first, and 25 decay chains in the second experiment, the analysis of which has not been fully reported as yet; and {sup 266}Mt directly in {sup 209}Bi({sup 58}Fe,n) reaction at GSI in two different experiments, observing three events in the first experiment and 12 events in the second, also produced in {sup 208}Pb({sup 59}Co,n) reaction at LBNL, observing five correlated decay chains. See also 2000Ho27 for discussion on {sup 266}Sg and {sup 266}Mt. A=270: {sup 270}Db, {sup 270}Bh, {sup 270}Hs, {sup 270}Mt and {sup 270}Ds are the experimentally identified nuclides with A=270 are presented. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, and RIKEN: {sup 270}Db from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI; {sup 270}Bh as α great-granddaughter of {sup 282}Nh in two correlated decay chains observed at Dubna; {sup 270}Hs directly in {sup 248}Cm({sup 26}Mg,4n) reaction at GSI, and in {sup 226}Ra({sup 48}Ca,4n) reaction at Dubna; {sup 270}Mt as granddaughter of {sup 278}Ts in three correlated decay chains at RIKEN; and {sup 270}Ds directly in {sup 207}Pb({sup 64}Ni,n) at GSI in 33 correlated decay chains. A=274: {sup 274}Bh, {sup 274}Mt and {sup 274}Rg are the experimentally identified nuclides with A=274. Search for {sup 274}Ds in {sup 238}U({sup 40}Ar, 4n),E=5.7 MeV/nucleon reaction and subsequent α decays at GSI (1990Sc11) proved negative. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, and RIKEN: {sup 274}Bh from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 274}Mt produced as α daughter of {sup 282}Nh in two correlated decay chains observed at Dubna, and {sup 274}Rg as α daughter of {sup 278}Nh produced in three correlated decay chains at RIKEN. A=278: {sup 278}Mt, {sup 278}Rg and {sup 278}Nh are the experimentally identified nuclides with A=278. A very tentative evidence is provided for {sup 278}Bh and {sup 278}Hs from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL labs in the USA, GSI-SHIP facility, and RIKEN: {sup 278}Mt from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 278}Rg produced as α daughter of {sup 282}Nh in two correlated decay chains observed at Dubna, and {sup 278}Nh produced directly in three correlated decay chains at RIKEN. A=282: {sup 282}Rg, {sup 282}Cn and {sup 282}Nh are the experimentally identified nuclides with A=282. A very tentative evidence is provided for {sup 282}Mt and {sup 282}Ds from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 282}Rg in α decay chain of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 282}Cn produced in four ways at Dubna: independently in one correlated decay chain, as α daughter of {sup 286}Lv in 11 correlated decay chains, as α grand-daughter of {sup 290}Lv in 12 correlated decay chains, as α great-grand daughter of {sup 294}Og in four correlated decay chains, and {sup 282}Nh produced at Dubna directly in two correlated decay chains. A=286: {sup 286}Nh and {sup 286}Fl are the only experimentally identified nuclides with A=286. A very tentative evidence is provided for {sup 286}Rg and {sup 286}Cn from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. 2017Ka66 in experiments at RIKEN using GARIS separator interpret one correlated decay chain in three different ways, one involving possible production of {sup 294}Lv in {sup 248}Cm({sup 48}Ca,2n),E=261.6 MeV, and α decay to {sup 290}Fl which further decays to {sup 286}Cn. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 286}Nh as α grand-daughter of {sup 294}Ts in six correlated decay chains, and {sup 286}Fl produced in three ways: independently in 11 correlated decay chains, as α daughter of {sup 290}Lv in 12 correlated decay chains, and as α grand-daughter of {sup 294}Og in four correlated decay chains. A=290: {sup 290}Mc and {sup 290}Lv are the only experimentally identified nuclides with A=290. A tentative evidence is provided for {sup 290}Nh and {sup 290}Fl from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. 2017Ka66 in experiments at RIKEN using GARIS separator interpret one correlated decay chain in three different ways, one involving possible production of {sup 294}Lv in {sup 248}Cm({sup 48}Ca,2n),E=261.6 MeV, and α decay to {sup 290}Fl. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 290}Mc as α daughter of {sup 294}Ts in six correlated decay chains, and {sup 290}Lv produced in two ways, independently in 14 correlated decay chains, and as α daughter of {sup 294}Og in four correlated decay chains. A=294: {sup 294}Ts and {sup 294}Og are the only experimentally identified nuclides with A=294. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, with a total of six EVR-α-SF correlated decay chains observed for {sup 294}Ts and four for {sup 294}Og. Tentative identification of {sup 294}Lv is provided by 2017Ka66 from the observation one correlated event using GARIS-RIKEN facility, where this event is interpreted in three possible ways, two interpretations lead to production of {sup 293}Lv and successive odd-A nuclides of {sup 289}Fl, {sup 285}Cn and {sup 281}Ds, whereas the third prediction starts with the production of {sup 294}Lv and successive {sup 290}Fl and {sup 286}Cn nuclides. Search for {sup 294}Rg in natural gold materials (2011De03), and for {sup 294}Ds, {sup 294}Fl and {sup 294}Mc in natural Pt, Pb and Bi samples (2011De21) using accelerator mass spectroscopy (AMS) proved negative, with extremely low upper limits established. Also 1980St05 did not see any evidence for {sup 294}Ds in natural Pt sample using AMS. A=298: Search for {sup 298}120 through fusion-evaporation reaction at Dubna, and for {sup 298}Fl and {sup 298}Mc in natural Pt, Pb and Bi samples using accelerator mass spectroscopy (AMS) proved negative. Tentative assignment of three α-α-α decay chains by 2016Ho09 to {sup 299}120 in {sup 248}Cm({sup 54}Cr,3n){sup 299}120 at GSI was refuted by 2017He11, assigning these correlations to random events, instead. A=302: Fluorescent x rays from Z=120 element were observed by 2012Fr03 from compound nucleus {sup 302}120 produced in {sup 238}U({sup 64}Ni,X),E=6.6 MeV/nucleon at GANIL, and x-ray yields were measured, together with minimum average time deduced from x-ray multiplicity. The compound nucleus could decay by 3n- or 4n-channels to produce {sup 299}120 or {sup 298}120. 2012He05 and 2016Ho09 also produced {sup 302}120 compound nucleus in {sup 248}Cm({sup 54}Cr, xn){sup 302}120{sup *},E=6.035 MeV/nucleon; and {sup 238}U({sup 64}Ni,xn){sup 302}120{sup *},E=5.53 MeV/nucleon reactions using UNILAC at GSI. Three α-α-α correlated decays from {sup 248}Cm({sup 54}Cr,xn){sup 302}120{sup *} reaction were tentatively assigned by 2016Ho09 to {sup 299}120 decay, however, a detailed analysis by 2017He11 refuted this claim, ascribing these events to random sequences. There are no data tables for A=302.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗