249 research outputs found

    Do drivers of biodiversity change differ in importance across marine and terrestrial systems — Or is it just different research communities' perspectives?

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    Cross-system studies on the response of different ecosystems to global change will support our understanding of ecological changes. Synoptic views on the planet's two main realms, the marine and terrestrial, however, are rare, owing to the development of rather disparate research communities.We combined questionnaires and a literature review to investigate howthe importance of anthropogenic drivers of biodiversity change differs amongmarine and terrestrial systems and whether differences perceived by marine vs. terrestrial researchers are reflected by the scientific literature. This included asking marine and terrestrial researchers to rate the relevance of different drivers of global change for either marine or terrestrial biodiversity. Land use and the associated loss of natural habitatswere rated as most important in the terrestrial realm,while the exploitation of the sea by fishing was rated as most important in the marine realm. The relevance of chemicals, climate change and the increasing atmospheric concentration of CO2 were rated differently for marine and terrestrial biodiversity respectively. Yet, our literature review provided less evidence for such differences leading to the conclusion that while the history of the use of land and sea differs, impacts of global change are likely to become increasingly similar

    Simultaneous in Situ Measurements of Small-Scale Structures in Neutral, Plasma, and Atomic Oxygen Densities During the WADIS Sounding Rocket Project

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    In this paper we present an overview of measurements conducted during the WADIS-2 rocket campaign. We investigate the effect of small-scale processes like gravity waves and turbulence on the distribution of atomic oxygen and other species in the mesosphere–lower thermosphere (MLT) region. Our analysis suggests that density fluctuations of atomic oxygen are coupled to fluctuations of other constituents, i.e., plasma and neutrals. Our measurements show that all measured quantities, including winds, densities, and temperatures, reveal signatures of both waves and turbulence. We show observations of gravity wave saturation and breakdown together with simultaneous measurements of generated turbulence. Atomic oxygen inside turbulence layers shows two different spectral behaviors, which might imply a change in its diffusion properties

    Anisotropy enhanced X-ray scattering from solvated transition metal complexes

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    Time-resolved X-ray scattering patterns from photoexcited molecules in solution are in many cases anisotropic at the ultrafast time scales accessible at X-ray Free Electron Lasers (XFELs). This anisotropy arises from the interaction of a linearly polarized UV-vis pump laser pulse with the sample, which induces anisotropic structural changes that can be captured by femtosecond X-ray pulses. In this work we describe a method for quantitative analysis of the anisotropic scattering signal arising from an ensemble of molecules and we demonstrate how its use can enhance the structural sensitivity of the time-resolved X-ray scattering experiment. We apply this method on time-resolved X-ray scattering patterns measured upon photoexcitation of a solvated di-platinum complex at an XFEL and explore the key parameters involved. We show that a combined analysis of the anisotropic and isotropic difference scattering signals in this experiment allows a more precise determination of the main photoinduced structural change in the solute, i.e. the change in Pt-Pt bond length, and yields more information on the excitation channels than the analysis of the isotropic scattering only. Finally, we discuss how the anisotropic transient response of the solvent can enable the determination of key experimental parameters such as the Instrument Response Function.Comment: Accepted for publication in Journal of Synchrotron Radiatio

    Cold-water corals in the Bay of Biscay - occurrences and distribution in space and time (TransBiscay) - Cruise No. M84/5, May 31 - June 21, 2011, Vigo (Spain) - Brest (France)

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    The scientific objectives of METEOR cruise M84/5 focused on the measurement and analysis of the environmental controls of modern and fossil cold-water coral growth along a transect in the Bay of Biscay. In four working areas we successfully deployed lander systems and CTD/Ro’s to document the physical and hydrochemical characteristics of bottom water masses and the water column in general. These are used to shed light on potential linkages to modern cold-water coral growth and distribution. These investigations were flanked by plankton tows in surface waters. The base for all investigations was a thorough hydroacoustic survey to characterize potential cold-water coral bearing areas with living colonies. Based on these maps we deployed all video-guided gear such as the OFOS-video sled, the TV grab, and the lander systems. Benthic assemblages and sedimentary structures have been documented and sampled with the OFOS and a box corer. Simultaneously, genetic samples of the living coral material were taken for additional studies. Furthermore, we have taken gravity cores to investigate the paleoceanographic conditions as well as the timing of cold-water coral colonization in the Bay of Biscay. Along with the coring efforts, a detailed sampling and study of porewater properties was performed. An additional aim of this cruise was to investigate the influence of boundary exchange processes on the Neodymium isotopy in bottom waters along the pathway of the Mediterranean Outflow water (MOW) by taking multiple samples with the CTD/Ro. The new data and samples of this METEOR cruise will provide the framework to investigate the timing of cold-water coral colonization in the Bay of Biscay, as well as its interplay with the ambient hydrography and geochemistry. This successful cruise has provided the basis to investigate the scientific aims of this expedition in great detail

    Atomistic characterization of the active-site solvation dynamics of a model photocatalyst

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    The interactions between the reactive excited state of molecular photocatalysts and surrounding solvent dictate reaction mechanisms and pathways, but are not readily accessible to conventional optical spectroscopic techniques. Here we report an investigation of the structural and solvation dynamics following excitation of a model photocatalytic molecular system [Ir 2 (dimen) 4 ] 2+, where dimen is para-diisocyanomenthane. The time-dependent structural changes in this model photocatalyst, as well as the changes in the solvation shell structure, have been measured with ultrafast diffuse X-ray scattering and simulated with Born-Oppenheimer Molecular Dynamics. Both methods provide direct access to the solute-solvent pair distribution function, enabling the solvation dynamics around the catalytically active iridium sites to be robustly characterized. Our results provide evidence for the coordination of the iridium atoms by the acetonitrile solvent and demonstrate the viability of using diffuse X-ray scattering at free-electron laser sources for studying the dynamics of photocatalysis
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