Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

Search Results (11)

Search Parameters:
Keywords = H-like helium

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
17 pages, 6413 KB  
Article
Anomaly in Methane Concentrations on Co To Island (Northern Vietnam): Results from the 2024 Underground Water Research
by Andrei Kholmogorov, Nadezhda Syrbu, Renat Shakirov, Le Duc Anh, Le Dinh Nam, Elena Maltseva, Hitoshi Tomaru, Elena Khazanova, Anastasia Voitovskaya, Irina Isaeva, Ngo Bich Huong, Tran Hoang Yen and Trinh Hoai Thu
Geosciences 2026, 16(4), 138; https://doi.org/10.3390/geosciences16040138 - 26 Mar 2026
Viewed by 1144
Abstract
The northern Vietnam shelf, particularly the area adjacent to the Red River Fault Zone, is characterized by complex geology and active neotectonics. However, the patterns of degassing and the origins of hydrocarbon gases in this region remain poorly understood. In particular, the potential [...] Read more.
The northern Vietnam shelf, particularly the area adjacent to the Red River Fault Zone, is characterized by complex geology and active neotectonics. However, the patterns of degassing and the origins of hydrocarbon gases in this region remain poorly understood. In particular, the potential links between deep-seated fluid migration, fault systems, and gas anomalies in island groundwater systems have not been systematically investigated. This study presents preliminary results of dissolved methane, its homologues (C2–C5), helium, hydrogen, and carbon dioxide measurements in groundwater from Co To Island (Northern Vietnam), with the aim of identifying gas origins and assessing structural controls on fluid migration. A significant methane anomaly was discovered, with concentrations reaching up to 10% by volume in the northwestern part of the island. The hydrocarbon homologous series is traced up to pentane (C5), and CO2 content is also elevated, with a maximum of 5.4%. The average He concentration of 10.8 ppm significantly exceeds atmospheric equilibrium values, with maximum recorded concentrations of 18 ppm for He and 34.5 ppm for H2. Stable carbon isotope analysis of methane (δ13C-CH4 values ranging from −50.2‰ to −49.7‰ VPDB), combined with the presence of a complete C1–C5 hydrocarbon series and elevated mantle/crustal tracers (He, H2), indicates a predominantly thermogenic/metamorphogenic origin for the gases, ruling out a purely biogenic source. The spatial distribution of anomalies is structurally controlled, closely associated with the NE-SW trending Co To Fault system and its intersections with subsidiary faults, as corroborated by recent electrical resistivity tomography data. These findings indicate intensive, focused gas leakage from a deep-seated source, likely related to thermogenic/metamorphic processes and active fault-mediated degassing. The results highlight the significant hydrocarbon potential of the region and underscore the critical role of neotectonic activity in controlling fluid migration pathways in island aquifer systems. Full article
(This article belongs to the Section Geochemistry)
Show Figures

Figure 1

22 pages, 5394 KB  
Article
Unveiling the Variability and Chemical Composition of AL Col
by Surath C. Ghosh, Santosh Joshi, Samrat Ghosh, Athul Dileep, Otto Trust, Mrinmoy Sarkar, Jaime Andrés Rosales Guzmán, Nicolás Esteban Castro-Toledo, Oleg Malkov, Harinder P. Singh, Kefeng Tan and Sarabjeet S. Bedi
Galaxies 2025, 13(4), 93; https://doi.org/10.3390/galaxies13040093 - 14 Aug 2025
Viewed by 1848
Abstract
In this study, we present analysis of TESS photometry, spectral energy distribution (SED), high-resolution spectroscopy, and spot modeling of the α2 CVn-type star AL Col (HD 46462). The primary objective is to determine its fundamental physical parameters and investigate its surface activity [...] Read more.
In this study, we present analysis of TESS photometry, spectral energy distribution (SED), high-resolution spectroscopy, and spot modeling of the α2 CVn-type star AL Col (HD 46462). The primary objective is to determine its fundamental physical parameters and investigate its surface activity characteristics. Using TESS short-cadence (120 s) SAP flux, we identified a rotational frequency of 0.09655 d1 (Prot=10.35733 d). Wavelet analysis reveals that while the amplitudes of the harmonic components vary over time, the strength of the primary rotational frequency remains stable. A SED analysis of multi-band photometric data yields an effective temperature (Teff) of 11,750 K. High-resolution spectroscopic observations covering wavelengthrange 4500–7000 Å provide refined estimates of Teff = 13,814 ± 400 K, logg = 4.09 ± 0.08 dex, and υsini = 16 ± 1 km s−1. Abundance analysis shows solar-like composition of O ii, Mg ii, S ii, and Ca ii, while helium is under-abundant by 0.62 dex. Rare earth elements (REEs) exhibit over-abundances of up to 5.2 dex, classifying the star as an Ap/Bp-type star. AL Col has a radius of R=3.74±0.48R, with its H–R diagram position estimating a mass of M=4.2±0.2M and an age of 0.12±0.01 Gyr, indicating that the star has slightly evolved from the main sequence. The TESS light curves were modeled using a three-evolving-spot configuration, suggesting the presence of differential rotation. This star is a promising candidate for future investigations of magnetic field diagnostics and the vertical stratification of chemical elements in its atmosphere. Full article
(This article belongs to the Special Issue Stellar Spectroscopy, Molecular Astronomy and Atomic Astronomy)
Show Figures

Figure 1

19 pages, 3870 KB  
Article
Gliding Arc Plasma Synthesis of MnO2 Nanomaterials for Catalytic Oxidation of Benzene: Effect of Plasmagenic Gas
by Franck W. Boyom-Tatchemo, François Devred, Elie Acayanka, Georges Kamgang-Youbi, Samuel Laminsi and Eric M. Gaigneaux
Catalysts 2025, 15(5), 451; https://doi.org/10.3390/catal15050451 - 5 May 2025
Cited by 4 | Viewed by 1273
Abstract
MnO2 nanostructures were successfully synthesized via the reduction of KMnO4 solutions using the gliding arc plasma (Plasma Glidarc) approach. Here, we highlight the effect of different plasmagenic gases, such as moist air (atmospheric air), dry air, nitrogen (N2) or [...] Read more.
MnO2 nanostructures were successfully synthesized via the reduction of KMnO4 solutions using the gliding arc plasma (Plasma Glidarc) approach. Here, we highlight the effect of different plasmagenic gases, such as moist air (atmospheric air), dry air, nitrogen (N2) or oxygen (O2). The obtained materials were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), nitrogen physisorption and scanning electron microscopy (SEM). The crystalline structures of obtained MnO2 polymorphs are mainly γ-MnO2 and α-MnO2, regardless of the feeding gas. The main reactive species, in addition to nitrogenous species like NO· radical generated with moist air, dry air or N2 gas, other oxygenated species such as H2O2 (E°(O2/H2O2) = 0.69 V) are produced with O2 able to reduce KMnO4 solution (E°(KMnO4/MnO2) = 1.70 V). Helium gas did not allow for the plasma reduction of the KMnO4 solution, even after 60 min of exposure. Furthermore, gas humidification did not significantly affect the precipitation time or the properties of plasma-synthesized MnO2. Atmospheric humidified air appears to be the best plasmagenic gas, as it allows for a shorter synthesis time and leads to a large specific surface area. All plasma-synthesized MnO2 showed good activity during the catalytic oxidation of benzene. The use of different MnO2 polymorphs (α-, δ- and γ-MnO2) showed that, in addition to the specific surface area, the crystalline structure significantly affects the catalytic oxidation of benzene. K+ species inserted within the MnO2 structure allow for their stability during the catalytic process. This work highlights the possibility to use different plasmagenic gases to prepare MnO2 nanostructures through plasma glidarc for the catalytic oxidation of benzene. Full article
(This article belongs to the Special Issue Nanocatalysts in Energy and Environmental Applications)
Show Figures

Graphical abstract

18 pages, 5304 KB  
Article
Stable Isotope Evaluation of Geothermal Gases from the Kızıldere and Tekke Hamam Geothermal Fields, Western Anatolia, Turkey
by Selin Süer, Thomas Wiersberg, Nilgün Güleç and Fausto Grassa
Geosciences 2022, 12(12), 452; https://doi.org/10.3390/geosciences12120452 - 9 Dec 2022
Cited by 5 | Viewed by 3427
Abstract
Volatiles transported from the Earth’s interior to the surface through permeable faults provide insights on the gas composition of deep reservoirs, mixing and migration processes, and can also be applied as gas-geothermometer. Here, we present carbon (δ13C), hydrogen (δ2H) [...] Read more.
Volatiles transported from the Earth’s interior to the surface through permeable faults provide insights on the gas composition of deep reservoirs, mixing and migration processes, and can also be applied as gas-geothermometer. Here, we present carbon (δ13C), hydrogen (δ2H) and nitrogen (δ15N) isotopic data of CO2, CH4, and N2 from gas samples collected from the Kızıldere and Tekke Hamam geothermal fields, located along the eastern segment of the Büyük Menderes Graben, Turkey. The stable isotopic composition of carbon (δ13C) ranges from +0.30 to +0.99‰ (PDB) for CO2 from Kızıldere and is slightly more variable (−0.95 to +1.3‰) in samples from Tekke Hamam. Carbon isotope data in combination with CO2/3He data reveal that ~97% (Tekke Hamam) to ~99% (Kızıldere) of CO2 derives from limestone sources, with the residual CO2 being magmatic in origin with no evidence for CO2 from organic sources. The slightly higher contribution of limestone-derived CO2 in Kızıldere, compared to Tekke Hamam can be attributed to the higher temperatures of the Kızıldere reservoir and resulting amplified fluid–limestone interaction, as well as helium depletion during phase separation for Kızıldere samples. In contrast to the carbon isotopic composition of CO2, the δ13C values of methane from Kızıldere and Tekke Hamam are clearly distinct and vary between −23.6 and −20.8‰ for Kızıldere and −34.4 and −31.7‰ for Tekke Hamam, respectively. The δ2H-CH4 composition is also distinct, measured as −126.7‰ for Kızıldere and −143.3‰ for Tekke Hamam. CO2-CH4 carbon isotope geothermometry calculations based on the isotopic fractionation of δ13C between the dominant component CO2 and the minor component CH4 reveals temperatures 20–40 °C and 100–160 °C higher than the bottom–hole temperatures measured for Tekke Hamam and Kızıldere, respectively. Based on the CO2-CH4 carbon isotope disequilibrium, unusual high methane concentrations of ~0.3 to 0.4 vol.-% and CH4/3He-δ13C-CH4 relationships we suggest thermal decomposition of late (Tekke Hamam) to over-mature (Kızıldere) organic matter and, to some extent, also abiogenic processes as principal source of methane. The N2/36Ar ratios of most samples reveal the existence of a non–atmospheric nitrogen component within the gas mixture issuing from both fields, in addition to a constant contribution of atmospheric derived nitrogen accompanied into the system via the meteoric recharge of the geothermal system. Based on the δ15N isotopic ratios (varying between −4.44‰ and 4.54‰), the non–atmospheric component seems to be a mixture of both sedimentary (crustal organic) and mantle nitrogen. The thick Pliocene sedimentary sequence covering the metamorphic basement is the likely major source for the thermogenic content of CH4 and crustal N2 gas content in the samples. Full article
(This article belongs to the Special Issue Geogases in Fault Zones)
Show Figures

Figure 1

22 pages, 4873 KB  
Article
Cyclohexylammonium Hexaisothiocyanatonickelate(II) Dihydrate as a Single-Source Precursor for High Surface Area Nickel Oxide and Sulfide Nanocrystals
by Mohamed F. Aly Aboud, Abdulmalik M. BinTaleb, Hamdi Ben Yahia, Abdelhamid Albaid, Sultan Albishi, Rasheed Arasheed, Ibrahim Albinali, Fahad Albaqi, Khalid Anojaidi, Fahad Alqahtani, Asma M. Alenad, Kamal Taha and Abdulaziz Bagabas
Crystals 2022, 12(3), 315; https://doi.org/10.3390/cryst12030315 - 23 Feb 2022
Cited by 1 | Viewed by 4595
Abstract
Cyclohexylammonium hexaisothiocyanatonickelate(II) dihydrate, (C6H11NH3)4[Ni(NCS)6]·2H2O, was synthesized, for the first time, by a four-step method in a yield of 95%. The compound was fully characterized by elemental microanalysis, Fourier transform infrared (FTIR), [...] Read more.
Cyclohexylammonium hexaisothiocyanatonickelate(II) dihydrate, (C6H11NH3)4[Ni(NCS)6]·2H2O, was synthesized, for the first time, by a four-step method in a yield of 95%. The compound was fully characterized by elemental microanalysis, Fourier transform infrared (FTIR), ultraviolet-visible-near infrared (UV-Vis-NIR), and nuclear magnetic resonance (NMR) spectroscopy and thermogravimetry. A single crystal X-ray diffraction (SXRD) gave the monoclinic space group P21/c with a = 15.8179 (5) Å, b = 10.6222 (3) Å, c = 13.8751 (4) Å, β = 109.362 (1)°, V = 2199.45 (11) Å3, Z = 2 (T = 293 K) for this novel hybrid organic–inorganic compound. The title compound was employed as a single-source precursor for the synthesis of mesoporous, high surface area nickel oxide (53 Å; 452 m2/g) and nickel sulfide (46 Å; 220 m2/g) via pyrolysis under air at 550 °C or helium atmosphere at 500 °C, respectively. X-ray powder diffraction (XRPD) demonstrated the nanocrystalline nature of both NiO and NiS with an average crystallite size of 16 and 54 nm, respectively. Scanning electron microscope (SEM) indicated the formation of agglomerated, quasi-spherical particles of nickel oxide and agglomerated flake-like structures of nickel sulfide. The high surface area, porosity, and nanocrystallinity of both NiO and NiS, obtained via this approach, are promising for a wide spectrum of applications. Full article
(This article belongs to the Special Issue New Trends in Crystals at Saudi Arabia)
Show Figures

Figure 1

22 pages, 5162 KB  
Article
Influence of Thermal and Mechanical Stimuli on the Behavior of Al-CAU-13 Metal–Organic Framework
by Michael T. Wharmby, Felicitas Niekiel, Jannik Benecke, Steve Waitschat, Helge Reinsch, Dominik Daisenberger, Norbert Stock and Pascal G. Yot
Nanomaterials 2020, 10(9), 1698; https://doi.org/10.3390/nano10091698 - 28 Aug 2020
Cited by 4 | Viewed by 4472
Abstract
The response of the metal–organic framework aluminum-1,4-cyclohexanedicarboxylate or Al-CAU-13 (CAU: Christian Albrecht University) to the application of thermal and mechanical stimuli was investigated using synchrotron powder X-ray diffraction (SPXRD). Variable temperature in situ SPXRD data, over the range 80–500 K, revealed a complex [...] Read more.
The response of the metal–organic framework aluminum-1,4-cyclohexanedicarboxylate or Al-CAU-13 (CAU: Christian Albrecht University) to the application of thermal and mechanical stimuli was investigated using synchrotron powder X-ray diffraction (SPXRD). Variable temperature in situ SPXRD data, over the range 80–500 K, revealed a complex evolution of the structure of the water guest containing Al-CAU-13•H2O, the dehydration process from ca. 310 to 370 K, and also the evolution of the guest free Al-CAU-13 structure between ca. 370 and 500 K. Rietveld refinement allowed this complexity to be rationalized in the different regions of heating. The Berman thermal Equation of State was determined for the two structures (Al-CAU-13•H2O and Al-CAU-13). Diamond anvil cell studies at elevated pressure (from ambient to up to ca. 11 GPa) revealed similarities in the structural responses on application of pressure and temperature. The ability of the pressure medium to penetrate the framework was also found to be important: non-penetrating silicone oil caused pressure induced amorphization, whereas penetrating helium showed no plastic deformation of the structure. Third-order Vinet equations of state were calculated and show Al-CAU-13•H2O is a hard compound for a metal–organic framework material. The mechanical response of Al-CAU-13, with tetramethylpyrazine guests replacing water, was also investigated. Although the connectivity of the structure is the same, all the linkers have a linear e,e-conformation and the structure adopts a more open, wine-rack-like arrangement, which demonstrates negative linear compressibility (NLC) similar to Al-MIL-53 and a significantly softer mechanical response. The origin of this variation in behavior is attributed to the different linker conformation, demonstrating the influence of the S-shaped a,a-conformation on the response of the framework to external stimuli. Full article
(This article belongs to the Special Issue Thermo-Mechanical Properties of Metal Organic Frameworks)
Show Figures

Graphical abstract

11 pages, 1705 KB  
Article
A Synchrotron Mössbauer Spectroscopy Study of a Hydrated Iron-Sulfate at High Pressures
by Tyler Perez, Gregory J. Finkelstein, Olivia Pardo, Natalia V. Solomatova and Jennifer M. Jackson
Minerals 2020, 10(2), 146; https://doi.org/10.3390/min10020146 - 8 Feb 2020
Cited by 4 | Viewed by 5922
Abstract
Szomolnokite is a monohydrated ferrous iron sulfate mineral, FeSO4·H2O, where the ferrous iron atoms are in octahedral coordination with four corners shared with SO4 and two with H2O groups. While somewhat rare on Earth, szomolnokite has [...] Read more.
Szomolnokite is a monohydrated ferrous iron sulfate mineral, FeSO4·H2O, where the ferrous iron atoms are in octahedral coordination with four corners shared with SO4 and two with H2O groups. While somewhat rare on Earth, szomolnokite has been detected on the surface of Mars along with several other hydrated sulfates and is suggested to occur near the surface of Venus. Previous measurements have characterized the local environment of the iron atoms in szomolnokite using Mössbauer spectroscopy at a range of temperatures and 1 bar. Our study represents a step towards understanding the electronic environment of iron in szomolnokite under compression at 300 K. Using a hydrostatic helium pressure-transmitting medium, we explored the pressure dependence of iron’s site-specific behavior in a synthetic szomolnokite powdered sample up to 95 GPa with time-domain synchrotron Mössbauer spectroscopy. At 1 bar, the Mössbauer spectrum is well described by two Fe2+-like sites and no ferric iron, consistent with select conventional Mössbauer spectra evaluations. At pressures below 19 GPa, steep gradients in the hyperfine parameters are most likely due to a structural phase transition. At 19 GPa, a fourth site is required to explain the time spectrum with increasing fractions of a low quadrupole splitting site, which could indicate the onset of another transition. Above 19 GPa we present three different models, including those with a high- to low-spin transition, that provide reasonable scenarios of electronic environment changes of the iron in szomolnokite with pressure. We summarize the complex range of Fe2+ spin transition characteristics at high-pressures by comparing szomolnokite with previous studies on ferrous-iron bearing phases. Full article
(This article belongs to the Special Issue Mineral Physics—In Memory of Orson Anderson)
Show Figures

Figure 1

20 pages, 2366 KB  
Article
Charge Transfer, Complexes Formation and Furan Fragmentation Induced by Collisions with Low-Energy Helium Cations
by Tomasz J. Wasowicz, Marta Łabuda and Boguslaw Pranszke
Int. J. Mol. Sci. 2019, 20(23), 6022; https://doi.org/10.3390/ijms20236022 - 29 Nov 2019
Cited by 13 | Viewed by 4437
Abstract
The present work focuses on unraveling the collisional processes leading to the fragmentation of the gas-phase furan molecules under the He+ and He2+ cations impact in the energy range 5–2000 eV. The presence of different mechanisms was identified by the analysis [...] Read more.
The present work focuses on unraveling the collisional processes leading to the fragmentation of the gas-phase furan molecules under the He+ and He2+ cations impact in the energy range 5–2000 eV. The presence of different mechanisms was identified by the analysis of the optical fragmentation spectra measured using the collision-induced emission spectroscopy (CIES) in conjunction with the ab initio calculations. The measurements of the fragmentation spectra of furan were performed at the different kinetic energies of both cations. In consequence, several excited products were identified by their luminescence. Among them, the emission of helium atoms excited to the 1s4d 1D2, 3D1,2,3 states was recorded. The structure of the furan molecule lacks an He atom. Therefore, observation of its emission lines is spectroscopic evidence of an impact reaction occurring via relocation of the electronic charge between interacting entities. Moreover, the recorded spectra revealed significant variations of relative band intensities of the products along with the change of the projectile charge and its velocity. In particular, at lower velocities of He+, the relative cross-sections of dissociation products have prominent resonance-like maxima. In order to elucidate the experimental results, the calculations have been performed by using a high level of quantum chemistry methods. The calculations showed that in both impact systems two collisional processes preceded fragmentation. The first one is an electron transfer from furan molecules to cations that leads to the neutralization and further excitation of the cations. The second mechanism starts from the formation of the He−C4H4O+/2+ temporary clusters before decomposition, and it is responsible for the appearance of the narrow resonances in the relative cross-section curves. Full article
(This article belongs to the Special Issue Radiation-Induced Damage to DNA)
Show Figures

Figure 1

18 pages, 3009 KB  
Article
Helium-Induced Changes in Circulating Caveolin in Mice Suggest a Novel Mechanism of Cardiac Protection
by Nina C. Weber, Jan M. Schilling, Moritz V. Warmbrunn, Mehul Dhanani, Raphaela Kerindongo, Jamila Siamwala, Young Song, Alice E. Zemljic-Harpf, McKenzie J. Fannon, Markus W. Hollmann, Benedikt Preckel, David M. Roth and Hemal H. Patel
Int. J. Mol. Sci. 2019, 20(11), 2640; https://doi.org/10.3390/ijms20112640 - 29 May 2019
Cited by 15 | Viewed by 4699
Abstract
The noble gas helium (He) induces cardioprotection in vivo through unknown molecular mechanisms. He can interact with and modify cellular membranes. Caveolae are cholesterol and sphingolipid-enriched invaginations of the plasma-membrane-containing caveolin (Cav) proteins that are critical in protection of the heart. Mice (C57BL/6J) [...] Read more.
The noble gas helium (He) induces cardioprotection in vivo through unknown molecular mechanisms. He can interact with and modify cellular membranes. Caveolae are cholesterol and sphingolipid-enriched invaginations of the plasma-membrane-containing caveolin (Cav) proteins that are critical in protection of the heart. Mice (C57BL/6J) inhaled either He gas or adjusted room air. Functional measurements were performed in the isolated Langendorff perfused heart at 24 h post He inhalation. Electron paramagnetic resonance spectrometry (EPR) of samples was carried out at 24 h post He inhalation. Immunoblotting was used to detect Cav-1/3 expression in whole-heart tissue, exosomes isolated from platelet free plasma (PFP) and membrane fractions. Additionally, transmission electron microscopy analysis of cardiac tissue and serum function and metabolomic analysis were performed. In contrast to cardioprotection observed in in vivo models, the isolated Langendorff perfused heart revealed no protection after He inhalation. However, levels of Cav-1/3 were reduced 24 h after He inhalation in whole-heart tissue, and Cav-3 was increased in exosomes from PFP. Addition of serum to muscle cells in culture or naïve ventricular tissue increased mitochondrial metabolism without increasing reactive oxygen species generation. Primary and lipid metabolites determined potential changes in ceramide by He exposure. In addition to direct effects on myocardium, He likely induces the release of secreted membrane factors enriched in caveolae. Our results suggest a critical role for such circulating factors in He-induced organ protection. Full article
Show Figures

Graphical abstract

16 pages, 2020 KB  
Article
Detrimental Effects of Helium Ion Irradiation on Cognitive Performance and Cortical Levels of MAP-2 in B6D2F1 Mice
by Jacob Raber, Eileen Ruth S. Torres, Tunde Akinyeke, Joanne Lee, Sydney J. Weber Boutros, Mitchell S. Turker and Amy Kronenberg
Int. J. Mol. Sci. 2018, 19(4), 1247; https://doi.org/10.3390/ijms19041247 - 20 Apr 2018
Cited by 22 | Viewed by 5594
Abstract
The space radiation environment includes helium (4He) ions that may impact brain function. As little is known about the effects of exposures to 4He ions on the brain, we assessed the behavioral and cognitive performance of C57BL/6J × DBA2/J F1 [...] Read more.
The space radiation environment includes helium (4He) ions that may impact brain function. As little is known about the effects of exposures to 4He ions on the brain, we assessed the behavioral and cognitive performance of C57BL/6J × DBA2/J F1 (B6D2F1) mice three months following irradiation with 4He ions (250 MeV/n; linear energy transfer (LET) = 1.6 keV/μm; 0, 21, 42 or 168 cGy). Sham-irradiated mice and mice irradiated with 21 or 168 cGy showed novel object recognition, but mice irradiated with 42 cGy did not. In the passive avoidance test, mice received a slight foot shock in a dark compartment, and latency to re-enter that compartment was assessed 24 h later. Sham-irradiated mice and mice irradiated with 21 or 42 cGy showed a higher latency on Day 2 than Day 1, but the latency to enter the dark compartment in mice irradiated with 168 cGy was comparable on both days. 4He ion irradiation, at 42 and 168 cGy, reduced the levels of the dendritic marker microtubule-associated protein-2 (MAP-2) in the cortex. There was an effect of radiation on apolipoprotein E (apoE) levels in the hippocampus and cortex, with higher apoE levels in mice irradiated at 42 cGy than 168 cGy and a trend towards higher apoE levels in mice irradiated at 21 than 168 cGy. In addition, in the hippocampus, there was a trend towards a negative correlation between MAP-2 and apoE levels. While reduced levels of MAP-2 in the cortex might have contributed to the altered performance in the passive avoidance test, it does not seem sufficient to do so. The higher hippocampal and cortical apoE levels in mice irradiated at 42 than 168 cGy might have served as a compensatory protective response preserving their passive avoidance memory. Thus, there were no alterations in behavioral performance in the open filed or depressive-like behavior in the forced swim test, while cognitive impairments were seen in the object recognition and passive avoidance tests, but not in the contextual or cued fear conditioning tests. Taken together, the results indicate that some aspects of cognitive performance are altered in male mice exposed to 4He ions, but that the response is task-dependent. Furthermore, the sensitive doses can vary within each task in a non-linear fashion. This highlights the importance of assessing the cognitive and behavioral effects of charged particle exposure with a variety of assays and at multiple doses, given the possibility that lower doses may be more damaging due to the absence of induced compensatory mechanisms at higher doses. Full article
(This article belongs to the Special Issue Advances and Challenges in Biomolecular Radiation Research)
Show Figures

Graphical abstract

33 pages, 556 KB  
Article
Radiative Rates and Electron Impact Excitation Rates for Transitions in He II
by Kanti M. Aggarwal, Akinori Igarashi, Francis P. Keenan and Shinobu Nakazaki
Atoms 2017, 5(2), 19; https://doi.org/10.3390/atoms5020019 - 2 May 2017
Cited by 5 | Viewed by 4772
Abstract
We report calculations of energy levels, radiative rates, collision strengths and effective collision strengths for transitions among the lowest 25 levels of the n 5 configurations of He II. The general-purpose relativistic atomic structure package (grasp) and Dirac atomic R-matrix [...] Read more.
We report calculations of energy levels, radiative rates, collision strengths and effective collision strengths for transitions among the lowest 25 levels of the n 5 configurations of He II. The general-purpose relativistic atomic structure package (grasp) and Dirac atomic R-matrix code (darc) are adopted for the calculations. Radiative rates, oscillator strengths and line strengths are reported for all electric dipole (E1), magnetic dipole (M1), electric quadrupole (E2) and magnetic quadrupole (M2) transitions among the 25 levels. Furthermore, collision strengths and effective collision strengths are listed for all 300 transitions among the above 25 levels over a wide energy (temperature) range up to 9 Ryd (10 5.4 K). Comparisons are made with earlier available results, and the accuracy of the data is assessed. Full article
(This article belongs to the Section Atomic, Molecular and Nuclear Spectroscopy and Collisions)
Show Figures

Figure 1

Back to TopTop