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Michael Gausa

Bio: Michael Gausa is an academic researcher from Bielefeld University. The author has contributed to research in topics: Aerosol & Sun photometer. The author has an hindex of 17, co-authored 35 publications receiving 1012 citations.

Papers
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Journal ArticleDOI
TL;DR: In this paper, large sets of filtered actinometer, filtered pyrheliometer and Sun photometer measurements have been carried out over the past 30 years by various groups at different Arctic and Antarctic sites and...
Abstract: Large sets of filtered actinometer, filtered pyrheliometer and Sun photometer measurements have been carried out over the past 30 years by various groups at different Arctic and Antarctic sites and ...

203 citations

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TL;DR: In this paper, photoelectrons (PE) from jet-cooled mass-identified silver and palladium cluster anions were detached by UV laser light and energy-analysed in a time-of-flight (TOF) electron spectrometer of the magnetic-bottle type.
Abstract: Photoelectrons (PE) from jet-cooled mass-identified silver and palladium cluster anions (number of atoms, n⩽ 21) were detached by UV laser light and energy-analysed in a time-of-flight (TOF) electron spectrometer of the magnetic-bottle type. For palladium PE threshold energies smoothly increase with n; for Ag, they show clear evidence of shell effects as well as an ‘even–odd oscillation’. The PE energy spectra are strongly structured, the structures being attributed to transitions involving the neutral ground states as well as contributions of low-lying excited neutral states. For silver the results can, in part, be qualitatively understood in terms of a delocalized electron Fermi-gas within the ellipsoidal deformed cluster. This picture fails for the more localized d electrons of palladium. For a thorough interpretation more elaborate calculations are necessary. The first results are available for alkali-metal clusters and will be compared to the silver and copper data.

104 citations

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TL;DR: In this article, the authors show the four-dimensional (4-D) distribution of the Eyjafjallajokull volcanic cloud in the troposphere over Europe as observed by EARLINET during the entire volcanic event (15 April-26 May 2010).
Abstract: . The eruption of the Icelandic volcano Eyjafjallajokull in April–May 2010 represents a "natural experiment" to study the impact of volcanic emissions on a continental scale. For the first time, quantitative data about the presence, altitude, and layering of the volcanic cloud, in conjunction with optical information, are available for most parts of Europe derived from the observations by the European Aerosol Research Lidar NETwork (EARLINET). Based on multi-wavelength Raman lidar systems, EARLINET is the only instrument worldwide that is able to provide dense time series of high-quality optical data to be used for aerosol typing and for the retrieval of particle microphysical properties as a function of altitude. In this work we show the four-dimensional (4-D) distribution of the Eyjafjallajokull volcanic cloud in the troposphere over Europe as observed by EARLINET during the entire volcanic event (15 April–26 May 2010). All optical properties directly measured (backscatter, extinction, and particle linear depolarization ratio) are stored in the EARLINET database available at http://www.earlinet.org . A specific relational database providing the volcanic mask over Europe, realized ad hoc for this specific event, has been developed and is available on request at http://www.earlinet.org . During the first days after the eruption, volcanic particles were detected over Central Europe within a wide range of altitudes, from the upper troposphere down to the local planetary boundary layer (PBL). After 19 April 2010, volcanic particles were detected over southern and south-eastern Europe. During the first half of May (5–15 May), material emitted by the Eyjafjallajokull volcano was detected over Spain and Portugal and then over the Mediterranean and the Balkans. The last observations of the event were recorded until 25 May in Central Europe and in the Eastern Mediterranean area. The 4-D distribution of volcanic aerosol layering and optical properties on European scale reported here provides an unprecedented data set for evaluating satellite data and aerosol dispersion models for this kind of volcanic events.

91 citations

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TL;DR: In this article, the decay phase of an unprecedented, record-breaking stratospheric perturbation caused by wildfire smoke is reported and discussed in terms of geometrical, optical, and microphysical aerosol properties.
Abstract: . Six months of stratospheric aerosol observations with the European Aerosol Research Lidar Network (EARLINET) from August 2017 to January 2018 are presented. The decay phase of an unprecedented, record-breaking stratospheric perturbation caused by wildfire smoke is reported and discussed in terms of geometrical, optical, and microphysical aerosol properties. Enormous amounts of smoke were injected into the upper troposphere and lower stratosphere over fire areas in western Canada on 12 August 2017 during strong thunderstorm–pyrocumulonimbus activity. The stratospheric fire plumes spread over the entire Northern Hemisphere in the following weeks and months. Twenty-eight European lidar stations from northern Norway to southern Portugal and the eastern Mediterranean monitored the strong stratospheric perturbation on a continental scale. The main smoke layer (over central, western, southern, and eastern Europe) was found at heights between 15 and 20 km since September 2017 (about 2 weeks after entering the stratosphere). Thin layers of smoke were detected at heights of up to 22–23 km. The stratospheric aerosol optical thickness at 532 nm decreased from values > 0.25 on 21–23 August 2017 to 0.005–0.03 until 5–10 September and was mainly 0.003–0.004 from October to December 2017 and thus was still significantly above the stratospheric background (0.001–0.002). Stratospheric particle extinction coefficients (532 nm) were as high as 50–200 Mm −1 until the beginning of September and on the order of 1 Mm −1 (0.5–5 Mm −1 ) from October 2017 until the end of January 2018. The corresponding layer mean particle mass concentration was on the order of 0.05–0.5 µ g m −3 over these months. Soot particles (light-absorbing carbonaceous particles) are efficient ice-nucleating particles (INPs) at upper tropospheric (cirrus) temperatures and available to influence cirrus formation when entering the tropopause from above. We estimated INP concentrations of 50–500 L −1 until the first days in September and afterwards 5–50 L −1 until the end of the year 2017 in the lower stratosphere for typical cirrus formation temperatures of − 55 ∘ C and an ice supersaturation level of 1.15. The measured profiles of the particle linear depolarization ratio indicated a predominance of nonspherical smoke particles. The 532 nm depolarization ratio decreased slowly with time in the main smoke layer from values of 0.15–0.25 (August–September) to values of 0.05–0.10 (October–November) and 0.05 (December–January). The decrease of the depolarization ratio is consistent with aging of the smoke particles, growing of a coating around the solid black carbon core (aggregates), and thus change of the shape towards a spherical form. We found ascending aerosol layer features over the most southern European stations, especially over the eastern Mediterranean at 32–35 ∘ N, that ascended from heights of about 18–19 to 22–23 km from the beginning of October to the beginning of December 2017 (about 2 km per month). We discuss several transport and lifting mechanisms that may have had an impact on the found aerosol layering structures.

71 citations

Journal ArticleDOI
TL;DR: In this paper, photoelectrons from mass-identified anion bunches are detached by laser light and undergo energy analysis in a magnetic bottle-type time-of-flight spectrometer.
Abstract: Aluminium cluster anions (A12) are produced by laser vaporization without additional ionization and cooled by supersonic expansion. Photoelectrons from mass-identified anion bunches (n=2...25) are detached by laser light (hv = 3.68 eV) and undergo energy analysis in a magnetic bottle-type time-of-flight spectrometer. The measurements provide information about the electronic excitation energies from ionic ground states to neutral states of the clusters. In contrast to bulk aluminium these cluster photoelectron spectra partially have well-resolved bands which originate from low-lying excited bands. For small clusters, especially the aluminium dimer and trimer, quantum-chemical calculations will be compared to the measurements. The electron affinity size dependence of larger clusters shows conclusive evidence for "shell" effects.

68 citations


Cited by
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TL;DR: While the book is a standard fixture in most chemical and physical laboratories, including those in medical centers, it is not as frequently seen in the laboratories of physician's offices (those either in solo or group practice), and I believe that the Handbook can be useful in those laboratories.
Abstract: There is a special reason for reviewing this book at this time: it is the 50th edition of a compendium that is known and used frequently in most chemical and physical laboratories in many parts of the world. Surely, a publication that has been published for 56 years, withstanding the vagaries of science in this century, must have had something to offer. There is another reason: while the book is a standard fixture in most chemical and physical laboratories, including those in medical centers, it is not as frequently seen in the laboratories of physician's offices (those either in solo or group practice). I believe that the Handbook can be useful in those laboratories. One of the reasons, among others, is that the various basic items of information it offers may be helpful in new tests, either physical or chemical, which are continuously being published. The basic information may relate

2,493 citations

Journal ArticleDOI
TL;DR: In this paper, a review of the experimental methods for the production of free nanoclusters is presented, along with theoretical and simulation issues, always discussed in close connection with the experimental results.
Abstract: The structural properties of free nanoclusters are reviewed. Special attention is paid to the interplay of energetic, thermodynamic, and kinetic factors in the explanation of cluster structures that are actually observed in experiments. The review starts with a brief summary of the experimental methods for the production of free nanoclusters and then considers theoretical and simulation issues, always discussed in close connection with the experimental results. The energetic properties are treated first, along with methods for modeling elementary constituent interactions and for global optimization on the cluster potential-energy surface. After that, a section on cluster thermodynamics follows. The discussion includes the analysis of solid-solid structural transitions and of melting, with its size dependence. The last section is devoted to the growth kinetics of free nanoclusters and treats the growth of isolated clusters and their coalescence. Several specific systems are analyzed.

1,563 citations

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TL;DR: Theoretical D determination of Electron Affinities and Statistical Analysis of DFT Results ThroughComparisons to Experiment and Other theoretical Methods and Specific Theoretical Successes 251E.
Abstract: I. Introduction and Scope 231A. Definitions of Atomic Electron Affinities 233B. Definitions of Molecular Electron Affinities 233II. Experimental Photoelectron Electron Affinities 235A. Historical Background 235B. The Photoeffect 236C. Experimental Methods 237D. Time-of-Flight Negative Ion PhotoelectronSpectroscopy239E. Some Thermochemical Uses of ElectronAffinities241F. Layout of Table 10: ExperimentalPhotoelectron Electron Affinities242III. Theoretical Determination of Electron Affinities 242A. Historical Background 2421. Theoretical Predictions of Atomic ElectronAffinities2422. Theoretical Predictions of MolecularElectron Affinities243B. Present Status of Theoretical Electron AffinityPredictions243C. Basis Sets and Theoretical Electron Affinities 244D. Density Functional Theory (DFT) andElectron Affinities245E. Layout of Tables 8 and 9: Theoretical DFTElectron Affinities247F. Details of Density Functional MethodsEmployed in Tables 8 and 9247IV. Discussion and Observations 248A. Statistical Analysis of DFT Results ThroughComparisons to Experiment and OtherTheoretical Methods248B. Theoretical EAs for Species with UnknownExperimental EAs251C. On the Applicability of DFT to Anions and theFuture of DFT EA Predictions251D. Specific Theoretical Successes 251E. Interesting Problems 2521. C

1,137 citations

Journal ArticleDOI
TL;DR: In this paper, the authors discuss the possibility to use thin, well-ordered oxide films as supports for the study of deposited metal particles, which offers the advantage to permit the unrestricted application of all experimental methods, which rely on a good electrical or thermal conductivity of the sample, like PES, LEED, STM or TDS.

900 citations

Journal ArticleDOI
TL;DR: The field of cluster research can trace its origins back to the mid-nineteenth century when early studies of colloids, aerosols, and nucleation phenomena were reported.
Abstract: The field of cluster research can trace its origins back to the mid-nineteenth century when early studies of colloids, aerosols, and nucleation phenomena were reported. The field underwent a resurgence of interest several decades ago when well-defined clusters were observed in supersonic expansions that could be investigated using mass spectrometers. The advent of the laser provided a new dimension, enabling detailed spectroscopic observations through the probing of systems of varying size and degree of solvation. Modern interest derives from recognition that interrogating clusters provides a way of studying the energetics and dynamics of intermediate states of matter as cluster systems evolve from the gas toward the condensed state. Herein, we endeavor to highlight some of the significant advances which have been made during the past several decades that have led to a nearly explosive growth of interest in the field of cluster science. Finally, we conclude that the field will continue to expand through i...

631 citations