TY  - JOUR
A1  - Stein, Katharina
A1  - Coulibaly, Drissa
A1  - Balima, Larba Hubert
A1  - Goetze, Dethardt
A1  - Linsenmair, Karl Eduard
A1  - Porembski, Stefan
A1  - Stenchly, Kathrin
A1  - Theodorou, Panagiotis
T1  - Plant-pollinator networks in savannas of Burkina Faso, West Africa
JF  - Diversity
N2  - 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.
KW  - bees
KW  - community composition
KW  - connectance
KW  - land-use intensity
KW  - modularity
KW  - mutualism
KW  - number of interactions
KW  - seasonality
KW  - woody plant richness
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-220157
SN  - 1424-2818
VL  - 13
IS  - 1
ER  - 
TY  - JOUR
A1  - Peixoto, Thiago R. F.
A1  - Bentmann, Hendrik
A1  - Rüßmann, Philipp
A1  - Tcakaev, Abdul-Vakhab
A1  - Winnerlein, Martin
A1  - Schreyeck, Steffen
A1  - Schatz, Sonja
A1  - Vidal, Raphael Crespo
A1  - Stier, Fabian
A1  - Zabolotnyy, Volodymyr
A1  - Green, Robert J.
A1  - Min, Chul Hee
A1  - Fornari, Celso I.
A1  - Maaß, Henriette
A1  - Vasili, Hari Babu
A1  - Gargiani, Pierluigi
A1  - Valvidares, Manuel
A1  - Barla, Alessandro
A1  - Buck, Jens
A1  - Hoesch, Moritz
A1  - Diekmann, Florian
A1  - Rohlf, Sebastian
A1  - Kalläne, Matthias
A1  - Rossnagel, Kai
A1  - Gould, Charles
A1  - Brunner, Karl
A1  - Blügel, Stefan
A1  - Hinkov, Vladimir
A1  - Molenkamp, Laurens W.
A1  - Friedrich, Reinert
T1  - Non-local effect of impurity states on the exchange coupling mechanism in magnetic topological insulators
JF  - NPJ Quantum Materials
N2  - 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.
KW  - shape-truncation functions
KW  - semiconductors
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-230686
VL  - 5
ER  - 
TY  - JOUR
A1  - Mair, Dorothea
A1  - Biskup, Saskia
A1  - Kress, Wolfram
A1  - Abicht, Angela
A1  - Brück, Wolfgang
A1  - Zechel, Sabrina
A1  - Knop, Karl Christian
A1  - Koenig, Fatima Barbara
A1  - Tey, Shelisa
A1  - Nikolin, Stefan
A1  - Eggermann, Katja
A1  - Kurth, Ingo
A1  - Ferbert, Andreas
A1  - Weis, Joachim
T1  - Differential diagnosis of vacuolar myopathies in the NGS era
JF  - Brain Pathology
N2  - 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.
KW  - autophagy
KW  - FSHD
KW  - glycogenin 1
KW  - muscular dystrophy
KW  - myofibrillar myopathy
KW  - next generation sequencing (NGS)
KW  - Pompe disease
KW  - sarcotubular myopathy
KW  - TRIM32
KW  - vacuolar myopathy
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-216048
VL  - 30
IS  - 5
SP  - 877
EP  - 896
ER  -