20 research outputs found
A larger agglutinated foraminifer originally described as a marine plant : the case of Arthrodendron Ulrich, 1904 (Foraminifera), its synonyms and homonyms
The large, agglutinated foraminiferal genus Aschemocella Vialov, 1966 (type species Aschemonella carpathica Neagu, 1964) and the body fossil Halysium Świdziński, 1934 (type species Halysium problematicum Świdziński, 1934) are herein synonymized with the genus Arthrodendron Ulrich, 1904 (type species A. diffusum Ulrich, 1904), a form originally described as a marine alga from Upper Cretaceous (Maastrichtian) flysch sediments of the Kodiak Formation of the Yakutat Group (formerly Yakutat Formation) on Pogibshi Island, Alaska. The species Aschemonella carpathica Neagu is regarded as a subjective junior synonym of Arthrodendron diffusum Ulrich, which is herein lectotypified and transferred to the Foraminifera
Following the Birth of a Nanoplasma Produced by an Ultrashort Hard-X-Ray Laser in Xenon Clusters
X-ray free-electron lasers (XFELs) made available a new regime of x-ray intensities, revolutionizing the ultrafast structure determination and laying the foundations of the novel field of nonlinear x-ray optics. Although earlier studies revealed nanoplasma formation when an XFEL pulse interacts with any nanometer-scale matter, the formation process itself has never been decrypted and its timescale was unknown. Here we show that time-resolved ion yield measurements combined with a near-infrared laser probe reveal a surprisingly ultrafast population (similar to 12 fs), followed by a slower depopulation (similar to 250 fs) of highly excited states of atomic fragments generated in the process of XFEL-induced nanoplasma formation. Inelastic scattering of Auger electrons and interatomic Coulombic decay are suggested as the mechanisms populating and depopulating, respectively, these excited states. The observed response occurs within the typical x-ray pulse durations and affects x-ray scattering, thus providing key information on the foundations of x-ray imaging with XFELs
Real-time observation of X-ray-induced intramolecular and interatomic electronic decay in CH2I2
The increasing availability of X-ray free-electron lasers (XFELs) has catalyzed the development of single-object structural determination and of structural dynamics tracking in realtime. Disentangling the molecular-level reactions triggered by the interaction with an XFEL pulse is a fundamental step towards developing such applications. Here we report real-time observations of XFEL-induced electronic decay via short-lived transient electronic states in the diiodomethane molecule, using a femtosecond near-infrared probe laser. We determine the lifetimes of the transient states populated during the XFEL-induced Auger cascades and find that multiply charged iodine ions are issued from short-lived (similar to 20 fs) transient states, whereas the singly charged ones originate from significantly longer-lived states (similar to 100 fs). We identify the mechanisms behind these different time scales: contrary to the short-lived transient states which relax by molecular Auger decay, the long-lived ones decay by an interatomic Coulombic decay between two iodine atoms, during the molecular fragmentation
\u3cem\u3e Rosalina marginata\u3c/em\u3e REUSS 1845 (Foraminifera) and its taxonomic position
The central idea of this article is the obligation of a micropaleontologist to respect without any doubt the rules and demands stipulated by the International Commission on Zoological Nomenclature (ICZN), in order to avoid taxonomical mistakes. An unusual example of confusion generated by disregard for the ICZN Code rules is the case of Rosalina marginata REUSS. The species Rosalina marginata REUSS, 1845 emend. REUSS, 1854 is here transferred to the genus Dicarinella. Other specimens illustrated as “Marginotruncana marginata” for example the “neotype” established by Jirova (1956) are placed in the new species Marginotruncana pseudomarginata nom. novum
Rectogerochammina eugubina nov. gen., nov. sp., a new agglutinated foraminifer from the Upper Cretaceous of Gubbio, Italy
Parures et objets d’art du Gravettien récent de Poiana Cireșului-Piatra Neamț (Roumanie)
International audienc
Following the Birth of a Nanoplasma Produced by an Ultrashort Hard-X-Ray Laser in Xenon Clusters
X-ray free-electron lasers (XFELs) made available a new regime of x-ray intensities, revolutionizing the ultrafast structure determination and laying the foundations of the novel field of nonlinear x-ray optics. Although earlier studies revealed nanoplasma formation when an XFEL pulse interacts with any nanometer-scale matter, the formation process itself has never been decrypted and its timescale was unknown. Here we show that time-resolved ion yield measurements combined with a near-infrared laser probe reveal a surprisingly ultrafast population (∼12 fs), followed by a slower depopulation (∼250 fs) of highly excited states of atomic fragments generated in the process of XFEL-induced nanoplasma formation. Inelastic scattering of Auger electrons and interatomic Coulombic decay are suggested as the mechanisms populating and depopulating, respectively, these excited states. The observed response occurs within the typical x-ray pulse durations and affects x-ray scattering, thus providing key information on the foundations of x-ray imaging with XFELs
Real-time observation of X-ray-induced intramolecular and interatomic electronic decay in CH2I2
The increasing availability of X-ray free-electron lasers (XFELs) has catalyzed the development of single-object structural determination and of structural dynamics tracking in real-time. Disentangling the molecular-level reactions triggered by the interaction with an XFEL pulse is a fundamental step towards developing such applications. Here we report real-time observations of XFEL-induced electronic decay via short-lived transient electronic states in the diiodomethane molecule, using a femtosecond near-infrared probe laser. We determine the lifetimes of the transient states populated during the XFEL-induced Auger cascades and find that multiply charged iodine ions are issued from short-lived (∼20 fs) transient states, whereas the singly charged ones originate from significantly longer-lived states (∼100 fs). We identify the mechanisms behind these different time scales: contrary to the short-lived transient states which relax by molecular Auger decay, the long-lived ones decay by an interatomic Coulombic decay between two iodine atoms, during the molecular fragmentation. © 2019, The Author(s)
Production of charged pions, kaons, and (anti-)protons in Pb-Pb and inelastic collisions at = 5.02 TeV
International audienceMid-rapidity production of , and ()p measured by the ALICE experiment at the LHC, in Pb-Pb and inelastic pp collisions at = 5.02 TeV, is presented. The invariant yields are measured over a wide transverse momentum () range from hundreds of MeV/ up to 20 GeV/. The results in Pb-Pb collisions are presented as a function of the collision centrality, in the range 090%. The comparison of the -integrated particle ratios, i.e. proton-to-pion (p/) and kaon-to-pion (K/) ratios, with similar measurements in Pb-Pb collisions at = 2.76 TeV show no significant energy dependence. Blast-wave fits of the spectra indicate that in the most central collisions radial flow is slightly larger at 5.02 TeV with respect to 2.76 TeV. Particle ratios (p/, K/) as a function of show pronounced maxima at 3 GeV/ in central Pb-Pb collisions. At high , particle ratios at 5.02 TeV are similar to those measured in pp collisions at the same energy and in Pb-Pb collisions at = 2.76 TeV. Using the pp reference spectra measured at the same collision energy of 5.02 TeV, the nuclear modification factors for the different particle species are derived. Within uncertainties, the nuclear modification factor is particle species independent for high and compatible with measurements at = 2.76 TeV. The results are compared to state-of-the-art model calculations, which are found to describe the observed trends satisfactorily