Crustal structure between the Knipovich Ridge and the Van Mijenfjorden (Svalbard)

The Alfred Wegener Institute of Polar and Marine Research, the University of Bergenand the Hokkaido University acquired new seismic refraction data along a transect fromthe Knipovich Ridge to the inner Van Mijenfjorden in southern Svalbard. A close spacing ofon- and offshore receivers and a dense marine shot pattern provide the data for a high resolutionp-wave velocity model for geological interpretation. Additional new seismic reflection data(University of Bergen) yield structural information for a more reliable analysis.Crustal thickness along the Van Mijenfjorden is 33 to 34 km. Seismic velocities of 5.0 km/sare observed within the upper crustal section of the Tertiary Central Spitsbergen Basin.A Paleozoic sedimentary basin with a depth of 8 to 10 km is associated with the Nordfjorden Block.The seismic velocities are up to 6.0 km/s. Paleozoic sedimentary rocks are expected furtherto the west of the Hornsund Lineament since seismic velocities reveal a similar range here.West of the Bellsund the continental crust thins gradually over a 90 km wide rifted zone.The velocity structure within this section is very complex and comprises zones of decreasedvelocities below the West Spitsbergen Fold Belt (down to 20 km depth) and slightly elevatedvelocities (7.2 km/s) at the crust-mantle transition. The first structure is interpreted as intensivelyfractured rocks linked to post-Late Paleocene transpressive orogenic activity and subsequentlyaffected by transtension during break-up from Greenland. The faster deep-crustal velocities aresupposed to express magmatic intrusions of an unidentified origin. Melts could either be channelled by theSpitsbergen Shear Zone from more distant sources, or originate in magmatic interaction between the northern Knipovich Ridgeand the neighbouring young rifted crust.Oceanic crust each side of the Knipovich Ridge is thin (~3.5 km) and is characterised by theabsence of oceanic layer 3 (3.5/4.1 to 4.7 km/s). The oceanic section exhibits zones of verythin crust (~1 km) that are interpreted as fracture zones. Beneath these we observed decreasedmantle velocities (~7.3 km/s) indicating probable serpentinization of peridotites along thesefracture zones. Thickness variations further provide information about the segmentationand magma supply along the northern Knipovich Ridge

Regulatory feedback cycle of the insulin-degrading enzyme and the amyloid precursor protein intracellular domain: Implications for Alzheimer's disease

One of the major pathological hallmarks of Alzheimer´s disease (AD) is an accumulation of amyloid-β (Aβ) in brain tissue leading to formation of toxic oligomers and senile plaques. Under physiological conditions, a tightly balanced equilibrium between Aβ-production and -degradation is necessary to prevent pathological Aβ-accumulation. Here, we investigate the molecular mechanism how insulin-degrading enzyme (IDE), one of the major Aβ-degrading enzymes, is regulated and how amyloid precursor protein (APP) processing and Aβ-degradation is linked in a regulatory cycle to achieve this balance. In absence of Aβ-production caused by APP or Presenilin deficiency, IDE-mediated Aβ-degradation was decreased, accompanied by a decreased IDE activity, protein level, and expression. Similar results were obtained in cells only expressing a truncated APP, lacking the APP intracellular domain (AICD) suggesting that AICD promotes IDE expression. In return, APP overexpression mediated an increased IDE expression, comparable results were obtained with cells overexpressing C50, a truncated APP representing AICD. Beside these genetic approaches, also AICD peptide incubation and pharmacological inhibition of the γ-secretase preventing AICD production regulated IDE expression and promoter activity. By utilizing CRISPR/Cas9 APP and Presenilin knockout SH-SY5Y cells results were confirmed in a second cell line in addition to mouse embryonic fibroblasts. In vivo, IDE expression was decreased in mouse brains devoid of APP or AICD, which was in line with a significant correlation of APP expression level and IDE expression in human postmortem AD brains. Our results show a tight link between Aβ-production and Aβ-degradation forming a regulatory cycle in which AICD promotes Aβ-degradation via IDE and IDE itself limits its own production by degrading AICD

Coordination of opposing sex-specific and core muscle groups regulates male tail posture during Caenorhabditis elegans male mating behavior

Background To survive and reproduce, animals must be able to modify their motor behavior in response to changes in the environment. We studied a complex behavior of Caenorhabditis elegans, male mating behavior, which provided a model for understanding motor behaviors at the genetic, molecular as well as circuit level. C. elegans male mating behavior consists of a series of six sub-steps: response to contact, backing, turning, vulva location, spicule insertion, and sperm transfer. The male tail contains most of the sensory structures required for mating, in addition to the copulatory structures, and thus to carry out the steps of mating behavior, the male must keep his tail in contact with the hermaphrodite. However, because the hermaphrodite does not play an active role in mating and continues moving, the male must modify his tail posture to maintain contact. We provide a better understanding of the molecular and neuro-muscular pathways that regulate male tail posture during mating. Results Genetic and laser ablation analysis, in conjunction with behavioral assays were used to determine neurotransmitters, receptors, neurons and muscles required for the regulation of male tail posture. We showed that proper male tail posture is maintained by the coordinated activity of opposing muscle groups that curl the tail ventrally and dorsally. Specifically, acetylcholine regulates both ventral and dorsal curling of the male tail, partially through anthelmintic levamisole-sensitive, nicotinic receptor subunits. Male-specific muscles are required for acetylcholine-driven ventral curling of the male tail but dorsal curling requires the dorsal body wall muscles shared by males and hermaphrodites. Gamma-aminobutyric acid activity is required for both dorsal and ventral acetylcholine-induced curling of the male tail and an inhibitory gamma-aminobutyric acid receptor, UNC-49, prevents over-curling of the male tail during mating, suggesting that cross-inhibition of muscle groups helps maintain proper tail posture. Conclusion Our results demonstrated that coordination of opposing sex-specific and core muscle groups, through the activity of multiple neurotransmitters, is required for regulation of male tail posture during mating. We have provided a simple model for regulation of male tail posture that provides a foundation for studies of how genes, molecular pathways, and neural circuits contribute to sensory regulation of this motor behavior

Wafer-Scale Epitaxial Modulation of Quantum Dot Density

Precise control of the properties of semiconductor quantum dots (QDs) is vital for creating novel devices for quantum photonics and advanced opto-electronics. Suitable low QD-density for single QD devices and experiments are challenging to control during epitaxy and are typically found only in limited regions of the wafer. Here, we demonstrate how conventional molecular beam epitaxy (MBE) can be used to modulate the density of optically active QDs in one- and two- dimensional patterns, while still retaining excellent quality. We find that material thickness gradients during layer-by-layer growth result in surface roughness modulations across the whole wafer. Growth on such templates strongly influences the QD nucleation probability. We obtain density modulations between 1 and 10 QDs/${\mu}m^{2}$ and periods ranging from several millimeters down to at least a few hundred microns. This novel method is universal and expected to be applicable to a wide variety of different semiconductor material systems. We apply the method to enable growth of ultra-low noise QDs across an entire 3-inch semiconductor wafer

Wafer-scale epitaxial modulation of quantum dot density

Precise control of the properties of semiconductor quantum dots (QDs) is vital for creating novel devices for quantum photonics and advanced opto-electronics. Suitable low QD-densities for single QD devices and experiments are challenging to control during epitaxy and are typically found only in limited regions of the wafer. Here, we demonstrate how conventional molecular beam epitaxy (MBE) can be used to modulate the density of optically active QDs in one- and two- dimensional patterns, while still retaining excellent quality. We find that material thickness gradients during layer-by-layer growth result in surface roughness modulations across the whole wafer. Growth on such templates strongly influences the QD nucleation probability. We obtain density modulations between 1 and 10 QDs/µm2 and periods ranging from several millimeters down to at least a few hundred microns. This method is universal and expected to be applicable to a wide variety of different semiconductor material systems. We apply the method to enable growth of ultra-low noise QDs across an entire 3-inch semiconductor wafer

Complete Genome Sequence of Mycoplasma suis and Insights into Its Biology and Adaption to an Erythrocyte Niche

Mycoplasma suis, the causative agent of porcine infectious anemia, has never been cultured in vitro and mechanisms by which it causes disease are poorly understood. Thus, the objective herein was to use whole genome sequencing and analysis of M. suis to define pathogenicity mechanisms and biochemical pathways. M. suis was harvested from the blood of an experimentally infected pig. Following DNA extraction and construction of a paired end library, whole-genome sequencing was performed using GS-FLX (454) and Titanium chemistry. Reads on paired-end constructs were assembled using GS De Novo Assembler and gaps closed by primer walking; assembly was validated by PFGE. Glimmer and Manatee Annotation Engine were used to predict and annotate protein-coding sequences (CDS). The M. suis genome consists of a single, 742,431 bp chromosome with low G+C content of 31.1%. A total of 844 CDS, 3 single copies, unlinked rRNA genes and 32 tRNAs were identified. Gene homologies and GC skew graph show that M. suis has a typical Mollicutes oriC. The predicted metabolic pathway is concise, showing evidence of adaptation to blood environment. M. suis is a glycolytic species, obtaining energy through sugars fermentation and ATP-synthase. The pentose-phosphate pathway, metabolism of cofactors and vitamins, pyruvate dehydrogenase and NAD+ kinase are missing. Thus, ribose, NADH, NADPH and coenzyme A are possibly essential for its growth. M. suis can generate purines from hypoxanthine, which is secreted by RBCs, and cytidine nucleotides from uracil. Toxins orthologs were not identified. We suggest that M. suis may cause disease by scavenging and competing for host' nutrients, leading to decreased life-span of RBCs. In summary, genome analysis shows that M. suis is dependent on host cell metabolism and this characteristic is likely to be linked to its pathogenicity. The prediction of essential nutrients will aid the development of in vitro cultivation systems

Crustal and basin evolution of the southwestern Barents Sea: from Caledonian orogeny to continental breakup

A new generation of aeromagnetic data documents the post-Caledonide rift evolution of the southwestern Barents Sea (SWBS) from the Norwegian mainland up to the continent-ocean transition. We propose a geological and tectonic scenario of the SWBS in which the Caledonian nappes and thrust sheets, well-constrained onshore, swing from a NE-SW trend onshore Norway to NW-SE/NNW-SSE across the SWBS platform area. On the Finnmark and Bjarmeland platforms, the dominant inherited magnetic basement pattern may also reflect the regional and post-Caledonian development of the late Paleozoic basins. Farther west, the pre-breakup rift system is characterized by the Loppa and Stappen Highs, which are interpreted as a series of rigid continental blocks (ribbons) poorly thinned as compared to the adjacent grabens and sag basins. As part of the complex western rift system, the Bjørnøya Basin is interpreted as a propagating system of highly thinned crust, which aborted in late Mesozoic time. This thick Cretaceous sag basin is underlain by a deep-seated high-density body, interpreted as exhumed high-grade metamorphic lower crust. The abortion of this propagating basin coincides with a migration and complete reorganization of the crustal extension toward a second necking zone defined at the level of the western volcanic sheared margin and proto-breakup axis. The abortion of the Bjørnøya Basin may be partly explained by its trend oblique to the regional, inherited, structural grain, revealed by the new aeromagnetic compilation, and by the onset of further weakening later sustained by the onset of magmatism to the west