Gravity recovery and climate experiment (GRACE)-derived temporal gravity variations can be resolved within the µgal (10 −8 m/s 2 ) range, if we restrict the spatial resolution to a half-wavelength of about 1,500 km and the temporal resolution to 1 month. For independent validations, a comparison with ground gravity measurements is of fundamental interest. For this purpose, data from selected superconducting gravimeter (SG) stations forming the Global Geodynamics Project (GGP) network are used. For comparison, GRACE and SG data sets are reduced for the same known gravity effects due to Earth and ocean tides, pole tide and atmosphere. In contrast to GRACE, the SG also measures gravity changes due to load-induced height variations, whereas the satellite-derived models do not contain this effect. For a solid spherical harmonic decomposition of the gravity field, this load effect can be modelled using degreedependent load Love numbers, and this effect is added to the P. Schwintzer has deceased. satellite-derived models. After reduction of the known gravity effects from both data sets, the remaining part can mainly be assumed to represent mass changes in terrestrial water storage. Therefore, gravity variations derived from global hydrological models are applied to verify the SG and GRACE results. Conversely, the hydrology models can be checked by gravity variations determined from GRACE and SG observations. Such a comparison shows quite a good agreement between gravity variation derived from SG, GRACE and hydrology models, which lie within their estimated error limits for most of the studied SG locations. It is shown that the SG gravity variations (point measurements) are representative for a large area within the µgal accuracy, if local gravity effects are removed. The individual discrepancies between SG, GRACE and hydrology models may give hints for further investigations of each data series.
Context. The tenuous nitrogen (N2) atmosphere on Pluto undergoes strong seasonal effects due to high obliquity and orbital eccentricity, and has recently (July 2015) been observed by the New Horizons spacecraft. Aims. The main goals of this study are (i) to construct a well calibrated record of the seasonal evolution of surface pressure on Pluto and (ii) to constrain the structure of the lower atmosphere using a central flash observed in 2015. Methods. Eleven stellar occultations by Pluto observed between 2002 and 2016 are used to retrieve atmospheric profiles (density, pressure, temperature) between altitude levels of ~5 and ~380 km (i.e. pressures from ~ 10 μbar to 10 nbar). Results. (i) Pressure has suffered a monotonic increase from 1988 to 2016, that is compared to a seasonal volatile transport model, from which tight constraints on a combination of albedo and emissivity of N2 ice are derived. (ii) A central flash observed on 2015 June 29 is consistent with New Horizons REX profiles, provided that (a) large diurnal temperature variations (not expected by current models) occur over Sputnik Planitia; and/or (b) hazes with tangential optical depth of ~0.3 are present at 4–7 km altitude levels; and/or (c) the nominal REX density values are overestimated by an implausibly large factor of ~20%; and/or (d) higher terrains block part of the flash in the Charon facing hemisphere.
We present results from a multi-chord Pluto stellar occultation observed on 2015 June 29 from New Zealand and Australia. This occurred only two weeks before the NASA New Horizons flyby of the Pluto system and serves as a useful comparison between ground-based and space results. We find that Pluto's atmosphere is still expanding, with a significant pressure increase of 5 ± 2% since 2013 and a factor of almost three since 1988. This trend rules out, as of today, an atmospheric collapse associated with Pluto's recession from the Sun. A central flash, a rare occurrence, was observed from several sites in New Zealand. The flash shape and amplitude are compatible with a spherical and transparent atmospheric layer of roughly 3 km in thickness whose base lies at about 4 km above Pluto's surface, and where an average thermal gradient of about 5 K km−1 prevails. We discuss the possibility that small departures between the observed and modeled flash are caused by local topographic features (mountains) along Pluto's limb that block the stellar light. Finally, using two possible temperature profiles, and extrapolating our pressure profile from our deepest accessible level down to the surface, we obtain a possible range of 11.9–13.7 μbar for the surface pressure.
Abstract. We report here experimental results for the electron ionization of large superfluid helium nanodroplets with sizes of about 10 5 atoms that are doped with valine and clusters of valine. Spectra of both cations and anions were monitored with high-resolution time-of-flight mass spectrometry (mass resolution >4000). Clear series of peaks with valine cluster sizes up to at least 40 and spaced by the mass of a valine molecule are visible in both the cation and anion spectra. Ion efficiency curves are presented for selected cations and anions at electron energies up to about 40 eV and these provide insight into the mode of ion formation. The measured onset of 24.59 eV for cations is indicative of valine ionization by He + whereas broad resonances at 2, 10 and 22 eV (and beyond) in the formation of anions speak to the occurrence of various modes of dissociative electron attachment by collisions with electrons or He* − and the influence of droplet size on the relative importance of these processes. Comparisons are also made with gas phase results and these provide insight into a matrix effect within the superfluid helium nanodroplet.
Abstract.We explore the formation of C60 sodium and C60 cesium complexes in superfluid helium nanodroplets. Anomalies in mass spectra of these doped droplets reveal anomalies in the stability of ions. (C60)mCs + n ions (m 6) are particularly abundant if they contain n = 6m + 1 cesium atoms; (C60)mCs 2+ n dications (m 3 or 5) are abundant if n = 6m + 2. These findings are consistent with the notion that alkali metal atoms (A) transfer their valence electrons into the three-fold degenerate lowest unoccupied orbital of C60, resulting in particularly stable C60A6 building blocks. However, (C60)4Cs 2+ n dications display an entirely different pattern; instead of an expected anomaly at n = 6 × 4 + 2 = 26 we observe a strong odd-even alternation starting at n = 6. Also surprising is the effect of adding one H2O or CO2 molecule to (C60)mCsn mono-or dications; anomalies shift by two units as if the impurity were acting as an acceptor for two valence electrons from the alkali metal atoms.
Adsorption of helium on free, negatively charged fullerenes is studied in this work. Helium nanodroplets have been doped with fullerenes and ionised by electron attachment. For suitable experimental conditions, C − 60 and C − 70 anions are found to be complexed with a large number of helium atoms. Prominent anomalies in the ion abundances indicate the high stability of the commensurate 1 × 1 phase in which all hollow adsorption sites are occupied by one atom each. The adsorption energy for an additional helium atom is about 40% less than for atoms in the commensurate layer, similar to our previous findings for fullerene cations and in agreement with theoretical dissociation energies. Similarly, an anomaly in the adsorption energy occurs when 60 helium atoms are attached to C − 60 or 65 to C − 70 . For C 60 , the anomaly coincides with the one observed for cationic complexes but for C 70 it does not. Implications of these features are discussed in light of several theoretical studies of neutral and positively charged helium-fullerene complexes.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
334 Leonard St
Brooklyn, NY 11211
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.