@article{SteinCoulibalyBalimaetal.2020, author = {Stein, Katharina and Coulibaly, Drissa and Balima, Larba Hubert and Goetze, Dethardt and Linsenmair, Karl Eduard and Porembski, Stefan and Stenchly, Kathrin and Theodorou, Panagiotis}, title = {Plant-pollinator networks in savannas of Burkina Faso, West Africa}, series = {Diversity}, volume = {13}, journal = {Diversity}, number = {1}, issn = {1424-2818}, doi = {10.3390/d13010001}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-220157}, year = {2020}, abstract = {West African savannas are severely threatened with intensified land use and increasing degradation. Bees are important for terrestrial biodiversity as they provide native plant species with pollination services. However, little information is available regarding their mutualistic interactions with woody plant species. In the first network study from sub-Saharan West Africa, we investigated the effects of land-use intensity and climatic seasonality on plant-bee communities and their interaction networks. In total, we recorded 5686 interactions between 53 flowering woody plant species and 100 bee species. Bee-species richness and the number of interactions were higher in the low compared to medium and high land-use intensity sites. Bee- and plant-species richness and the number of interactions were higher in the dry compared to the rainy season. Plant-bee visitation networks were not strongly affected by land-use intensity; however, climatic seasonality had a strong effect on network architecture. Null-model corrected connectance and nestedness were higher in the dry compared to the rainy season. In addition, network specialization and null-model corrected modularity were lower in the dry compared to the rainy season. Our results suggest that in our study region, seasonal effects on mutualistic network architecture are more pronounced compared to land-use change effects. Nonetheless, the decrease in bee-species richness and the number of plant-bee interactions with an increase in land-use intensity highlights the importance of savanna conservation for maintaining bee diversity and the concomitant provision of ecosystem services.}, language = {en} } @article{PeixotoBentmannRuessmannetal.2020, author = {Peixoto, Thiago R. F. and Bentmann, Hendrik and R{\"u}ßmann, Philipp and Tcakaev, Abdul-Vakhab and Winnerlein, Martin and Schreyeck, Steffen and Schatz, Sonja and Vidal, Raphael Crespo and Stier, Fabian and Zabolotnyy, Volodymyr and Green, Robert J. and Min, Chul Hee and Fornari, Celso I. and Maaß, Henriette and Vasili, Hari Babu and Gargiani, Pierluigi and Valvidares, Manuel and Barla, Alessandro and Buck, Jens and Hoesch, Moritz and Diekmann, Florian and Rohlf, Sebastian and Kall{\"a}ne, Matthias and Rossnagel, Kai and Gould, Charles and Brunner, Karl and Bl{\"u}gel, Stefan and Hinkov, Vladimir and Molenkamp, Laurens W. and Friedrich, Reinert}, title = {Non-local effect of impurity states on the exchange coupling mechanism in magnetic topological insulators}, series = {NPJ Quantum Materials}, volume = {5}, journal = {NPJ Quantum Materials}, doi = {10.1038/s41535-020-00288-0}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-230686}, year = {2020}, abstract = {Since the discovery of the quantum anomalous Hall (QAH) effect in the magnetically doped topological insulators (MTI) Cr:(Bi,Sb)\(_2\)Te\(_3\) and V:(Bi,Sb)\(_2\)Te\(_3\), the search for the magnetic coupling mechanisms underlying the onset of ferromagnetism has been a central issue, and a variety of different scenarios have been put forward. By combining resonant photoemission, X-ray magnetic circular dichroism and density functional theory, we determine the local electronic and magnetic configurations of V and Cr impurities in (Bi,Sb)\(_2\)Te\(_3\). State-of-the-art first-principles calculations find pronounced differences in their 3d densities of states, and show how these impurity states mediate characteristic short-range pd exchange interactions, whose strength sensitively varies with the position of the 3d states relative to the Fermi level. Measurements on films with varying host stoichiometry support this trend. Our results explain, in an unified picture, the origins of the observed magnetic properties, and establish the essential role of impurity-state-mediated exchange interactions in the magnetism of MTI.}, language = {en} } @article{MairBiskupKressetal.2020, author = {Mair, Dorothea and Biskup, Saskia and Kress, Wolfram and Abicht, Angela and Br{\"u}ck, Wolfgang and Zechel, Sabrina and Knop, Karl Christian and Koenig, Fatima Barbara and Tey, Shelisa and Nikolin, Stefan and Eggermann, Katja and Kurth, Ingo and Ferbert, Andreas and Weis, Joachim}, title = {Differential diagnosis of vacuolar myopathies in the NGS era}, series = {Brain Pathology}, volume = {30}, journal = {Brain Pathology}, number = {5}, doi = {10.1111/bpa.12864}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-216048}, pages = {877 -- 896}, year = {2020}, abstract = {Altered autophagy accompanied by abnormal autophagic (rimmed) vacuoles detectable by light and electron microscopy is a common denominator of many familial and sporadic non-inflammatory muscle diseases. Even in the era of next generation sequencing (NGS), late-onset vacuolar myopathies remain a diagnostic challenge. We identified 32 adult vacuolar myopathy patients from 30 unrelated families, studied their clinical, histopathological and ultrastructural characteristics and performed genetic testing in index patients and relatives using Sanger sequencing and NGS including whole exome sequencing (WES). We established a molecular genetic diagnosis in 17 patients. Pathogenic mutations were found in genes typically linked to vacuolar myopathy (GNE, LDB3/ZASP, MYOT, DES and GAA), but also in genes not regularly associated with severely altered autophagy (FKRP, DYSF, CAV3, COL6A2, GYG1 and TRIM32) and in the digenic facioscapulohumeral muscular dystrophy 2. Characteristic histopathological features including distinct patterns of myofibrillar disarray and evidence of exocytosis proved to be helpful to distinguish causes of vacuolar myopathies. Biopsy validated the pathogenicity of the novel mutations p.(Phe55*) and p.(Arg216*) in GYG1 and of the p.(Leu156Pro) TRIM32 mutation combined with compound heterozygous deletion of exon 2 of TRIM32 and expanded the phenotype of Ala93Thr-caveolinopathy and of limb-girdle muscular dystrophy 2i caused by FKRP mutation. In 15 patients no causal variants were detected by Sanger sequencing and NGS panel analysis. In 12 of these cases, WES was performed, but did not yield any definite mutation or likely candidate gene. In one of these patients with a family history of muscle weakness, the vacuolar myopathy was eventually linked to chloroquine therapy. Our study illustrates the wide phenotypic and genotypic heterogeneity of vacuolar myopathies and validates the role of histopathology in assessing the pathogenicity of novel mutations detected by NGS. In a sizable portion of vacuolar myopathy cases, it remains to be shown whether the cause is hereditary or degenerative.}, language = {en} }