Zur Injektivität eines durch die Normresteabbildung induzierten Homomorphismus

Die Arbeit schließt eine Lücke im Preprint 'On the spinor norm and A_0(X, K_1) for quadrics' von Markus Rost. Die Ergebnisse von Rost wurden von Vladimir Voevodsky beim Beweis der Milnor-Vermutung benutzt

Cruise Report RV Heincke HE560

The primary aim of this expedition was to investigate the spatial and temporal distribution, the ecology and physiology, as well as competition of co-occurring gadoid species (Atlantic cod, Polar cod, haddock) in the communities of Arctic and Atlantic influence around Svalbard. We sampled the benthic and pelagic communities (including plankton) on the shallow shelf regions of Svalbard to estimate the effects of climate change on Arctic ecosystems to obtain a picture of the entire system structure and function for a long-term monitoring program of the ‘Atlantification’ of the Svalbard region. We assessed the potential impact of changes in trophic interaction (predator-prey relations) of Atlantic cod (Gadus morhua), Polar cod (Boreogadus saida), haddock (Melanogrammus aeglefinus) and decapod crabs on the productivity and stability of benthic and pelagic communities in Arctic ecosystems, into which their distribution ranges now extend due to ocean warming. In addition to a stock assessment and distribution analysis of gadoid fish and decapod crabs, we aimed to obtain specimens of these species in the Atlantic and polar waters around Svalbard, which were transported alive back to Germany. Laboratory experiments under scenarios of climate change at the Alfred Wegener Institute then provided (and still provide) further insight into capacities for adaptation, performance and interaction of selected species of the Arctic ecosystem around Svalbard. The results will on the one hand be used in an international Norwegian-German project and the pan-Arctic data management system (Piepenburg et al. 2011), on the other hand they will flow into fisheries modelling at the University of Hamburg, the Thuenen Institute and socio-economic modelling approaches that build on the German ocean acidification project BIOACID (www.bioacid.de)

Influence of Age on Postoperative Neurological Outcomes after Surgery of Acute Type A Aortic Dissection

BackgroundAcute type A aortic dissection (AAAD) is considered a fatal disease which requires an emergent surgical intervention. This study focuses onthe neurological outcome after surgical repair in cases of AAAD in comparison between elderly and young patients.Methodsa retrospective analysis of 368 consecutive patients who underwent emergency surgery of ascending aorta in moderate hypothermic circulatory arrest (MHCA) (20-24 °C) and antegrade cerebral perfusion after AAAD between 2001 and 2016. Patients were divided into two groups: those aged 75 years and older (68 (18.5%)) and those younger than 75 years (300 (81.5%)).ResultsComparing both groups, average age was 79.0 ± 3.2 vs. 59.2 ± 10.7 years (p < 0.001); female gender represents 58.8% of elderly patients vs. 28.7% in younger patients (p < 0.001). Intraoperatively, cardiopulmonary bypass time (155 min (131; 187) vs. 171 min (137; 220); p = 0.012), cross-clamping time (79 min (60; 105) vs. 93 min (71; 134); p = 0.001] and circulatory arrest time (29 min (22; 40) vs. 33 min (26; 49); p = 0.011) were significantly shorter in elderly than younger group. Postoperatively, there was no significant difference in delirium (11.8% vs. 20.5%; p = 0.0968) or stroke (11.8% vs. 16.1%; p = 0.369). The 30-day mortality was satisfactory for both groups but significantly higher in the elderly group (27.9% vs. 14.3%; p = 0.007).ConclusionThe current study concluded that surgical treatment of AAAD in elderly patients can be applied safely without increasing risk of neurological complication. However, minimizing operation time may help limit the occurrence of postoperative neurological complication

Active Infective Native and Prosthetic Valve Endocarditis: Short- and Long-Term Outcomes of Patients after Surgical Treatment

BackgroundActive infective endocarditis (IE) is a serious disease associated with high mortality. The current study represents our experience over 18 years with surgical treatment for active infective native and prosthetic valve endocarditis (INVE, IPVE).MethodAnalysis of 413 patients (171 with IPVE vs. 242 with INVE) who underwent cardiac surgery due to IE between 2002 and 2020.ResultsPatients with IPVE were significantly older (64.9 ± 13.2 years vs. 58.3 ± 15.5 years; p < 0.001) with higher EuroSCORE II (21.2 (12.7; 41.8) vs. 6.9 (3.0; 17.0); p < 0.001)) and coronary heart disease (50.6% vs. 38.0%; p < 0.011). Preoperative embolization was significantly higher within INVE (35.5% vs. 16.4%; p < 0.001) with high incidence of cerebral embolization (18.6% vs. 7.6%; p = 0.001) and underwent emergency curative surgery than the IPVE group (19.6% vs. 10.6%; p < 0.001). However, patients with IPVE were significantly represented with intracardiac abscess (44.4% vs.15.7%; p < 0.001). Intraoperatively, the duration of surgery was expectedly significantly higher in the IPVE group (356 min vs. 244 min.; p = 0.001) as well as transfusion of blood (4 units (0-27) vs. 2 units (0-14); p < 0.001). Post-operatively, the incidence of bleeding was markedly higher within the IPVE group (700 mL (438; 1163) vs. 500 mL (250; 1075); p = 0.005). IPVE required significantly more permanent pacemakers (17.6% vs. 7.5%: p = 0.002). The 30-day mortality was higher in the IPVE group (24.6% vs. 13.2%; p < 0.003).ConclusionPatients with INVE suffered from a higher incidence of cerebral embolization and neurological deficits than patients with IPVE. Surgical treatment in INVE is performed mostly as an emergency indication. However, patients with IPVE were represented commonly with intracardiac abscess, and had a higher indication of pacemaker implantation. The short- and long-term mortality rate among those patients was still high

Towards a global understanding of vegetation-climate dynamics at multiple timescales

Funding Information: Acknowledgements. This paper has been realized within the Earth System Data Lab project funded by the European Space Agency. The authors acknowledge Lina Fürst for initiation of the preliminary study laying the foundation for this project. The authors acknowledge support from Ulrich Weber for data management and preprocessing. Lina M. Estupinan-Suarez acknowledges the support of the DAAD and its Graduate School Scholarship Programme (57395813). Nora Linscheid acknowledges the support of the TUM Graduate School. Lina M. Estupinan-Suarez and Nora Linscheid acknowledge the continuous support of the International Max Planck Research School for Global Biogeochemical Cycles. Felix Cre-mer acknowledges the support of the German Research Foundation project HyperSense (grant no. TH 1435/4-1). Publisher Copyright: © Author(s) 2020. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.Climate variables carry signatures of variability at multiple timescales. How these modes of variability are reflected in the state of the terrestrial biosphere is still not quantified or discussed at the global scale. Here, we set out to gain a global understanding of the relevance of different modes of variability in vegetation greenness and its covariability with climate. We used > 30 years of remote sensing records of the normalized difference vegetation index (NDVI) to characterize biosphere variability across timescales from submonthly oscillations to decadal trends using discrete Fourier decomposition. Climate data of air temperature (Tair) and precipitation (Prec) were used to characterize atmosphere-biosphere covariability at each timescale. Our results show that short-term (intra-annual) and longerterm (interannual and longer) modes of variability make regionally highly important contributions to NDVI variability: short-term oscillations focus in the tropics where they shape 27% of NDVI variability. Longer-term oscillations shape 9% of NDVI variability, dominantly in semiarid shrublands. Assessing dominant timescales of vegetation-climate covariation, a natural surface classification emerges which captures patterns not represented by conventional classifications, especially in the tropics. Finally, we find that correlations between variables can differ and even invert signs across timescales. For southern Africa for example, correlation between NDVI and Tair is positive for the seasonal signal but negative for short-term and longer-term oscillations, indicating that both short- and long-term temperature anomalies can induce stress on vegetation dynamics. Such contrasting correlations between timescales exist for 15% of vegetated areas for NDVI with Tair and 27% with Prec, indicating global relevance of scale-specific climate sensitivities. Our analysis provides a detailed picture of vegetation-climate covariability globally, characterizing ecosystems by their intrinsic modes of temporal variability. We find that (i) correlations of NDVI with climate can differ between scales, (ii) nondominant subsignals in climate variables may dominate the biospheric response, and (iii) possible links may exist between short-term and longer-term scales. These heterogeneous ecosystem responses on different timescales may depend on climate zone and vegetation type, and they are to date not well understood and do not always correspond to transitions in dominant vegetation types. These scale dependencies can be a benchmark for vegetation model evaluation and for comparing remote sensing products.publishersversionpublishe

Outcome of Unilateral Pulmonary Edema after Minimal-Invasive Mitral Valve Surgery: 10-Year Follow-Up

The study was approved by the institutional review board (IRB) at the University Medical Center Campus Kiel, Kiel, Germany (reference number: AZ D 559/18) and registered at the German Clinical Trials Register (reference number: DRKS00022222). Objective Unilateral pulmonary edema (UPE) is a complication after minimally invasive mitral valve surgery (MIMVS). We analyzed the impact of this complication on the short- and long-term outcome over a 10-year period. Methods We retrospectively observed 393 MIMVS patients between 01/2009 and 12/2019. The primary endpoint was a radiographically and clinically defined UPE within the first postoperative 24 h, secondary endpoints were 30-day and long-term mortality and the percentage of patients requiring ECLS. Risk factors for UPE incidence were evaluated by logistic regression, and risk factors for mortality in the follow-up period were assessed by Cox regression. Results Median EuroSCORE II reached 0.98% in the complete MIMVS group. Combined 30-day and in-hospital mortality after MIMVS was 2.0% with a 95, 93 and 77% survival rate after 1, 3 and 10 years. Seventy-two (18.3%) of 393 patients developed a UPE 24 h after surgery. Six patients (8.3%) with UPE required an extracorporeal life-support system. Logistic regression analysis identified a higher creatinine level, a worse LV function, pulmonary hypertension, intraoperative transfusion and a longer aortic clamp time as predictors for UPE. Combined in hospital mortality and 30-day mortality was slightly but not significantly higher in the UPE group (4.2 vs. 1.6%; p = 0.17). Predictors for mortality during follow-up were age ≥ 70 years, impaired RVF, COPD, drainage loss ≥ 800 mL and length of ventilation ≥ 48 h. During a median follow-up of 4.6 years, comparable survival between UPE and non-UPE patients was seen in our analysis after 5 years (89 vs. 88%; p = 0.98)

The actin family member Arp6 and the histone variant H2A.Z are required for spatial positioning of chromatin in chicken cell nuclei

The spatial organization of chromatin in the nucleus contributes to genome function and is altered during the differentiation of normal and tumorigenic cells. Although nuclear actin-related proteins (Arps) have roles in the local alteration of chromatin structure, it is unclear whether they are involved in the spatial positioning of chromatin. In the interphase nucleus of vertebrate cells, gene-dense and gene-poor chromosome territories (CTs) are located in the center and periphery, respectively. We analyzed chicken DT40 cells in which Arp6 had been knocked out conditionally, and showed that the radial distribution of CTs was impaired in these knockout cells. Arp6 is an essential component of the SRCAP chromatin remodeling complex, which deposits the histone variant H2A.Z into chromatin. The redistribution of CTs was also observed in H2A.Z-deficient cells for gene-rich microchromosomes, but to lesser extent for gene-poor macrochromosomes. These results indicate that Arp6 and H2A.Z contribute to the radial distribution of CTs through different mechanisms. Microarray analysis suggested that the localization of chromatin to the nuclear periphery per se is insufficient for the repression of most genes

The actin family member Arp6 and the histone variant H2A.Z are required for spatial positioning of chromatin in chicken cell nuclei

The spatial organization of chromatin in the nucleus contributes to genome function and is altered during the differentiation of normal and tumorigenic cells. Although nuclear actin-related proteins (Arps) have roles in the local alteration of chromatin structure, it is unclear whether they are involved in the spatial positioning of chromatin. In the interphase nucleus of vertebrate cells, gene-dense and gene-poor chromosome territories (CTs) are located in the center and periphery, respectively. We analyzed chicken DT40 cells in which Arp6 had been knocked out conditionally, and showed that the radial distribution of CTs was impaired in these knockout cells. Arp6 is an essential component of the SRCAP chromatin remodeling complex, which deposits the histone variant H2A.Z into chromatin. The redistribution of CTs was also observed in H2A.Z-deficient cells for gene-rich microchromosomes, but to lesser extent for gene-poor macrochromosomes. These results indicate that Arp6 and H2A.Z contribute to the radial distribution of CTs through different mechanisms. Microarray analysis suggested that the localization of chromatin to the nuclear periphery per se is insufficient for the repression of most genes

Three-dimensional super-resolution microscopy of the inactive X chromosome territory reveals a collapse of its active nuclear compartment harboring distinct Xist RNA foci

Background: A Xist RNA decorated Barr body is the structural hallmark of the compacted inactive X territory in female mammals. Using super resolution three-dimensional structured illumination microscopy (3D-SIM) and quantitative image analysis, we compared its ultrastructure with active chromosome territories (CTs) in human and mouse somatic cells, and explored the spatio-temporal process of Barr body formation at onset of inactivation in early differentiating mouse embryonic stem cells (ESCs). Results: We demonstrate that all CTs are composed of structurally linked chromatin domain clusters (CDCs). In active CTs the periphery of CDCs harbors low-density chromatin enriched with transcriptionally competent markers, called the perichromatin region (PR). The PR borders on a contiguous channel system, the interchromatin compartment (IC), which starts at nuclear pores and pervades CTs. We propose that the PR and macromolecular complexes in IC channels together form the transcriptionally permissive active nuclear compartment (ANC). The Barr body differs from active CTs by a partially collapsed ANC with CDCs coming significantly closer together, although a rudimentary IC channel system connected to nuclear pores is maintained. Distinct Xist RNA foci, closely adjacent to the nuclear matrix scaffold attachment factor-A (SAF-A) localize throughout Xi along the rudimentary ANC. In early differentiating ESCs initial Xist RNA spreading precedes Barr body formation, which occurs concurrent with the subsequent exclusion of RNA polymerase II (RNAP II). Induction of a transgenic autosomal Xist RNA in a male ESC triggers the formation of an `autosomal Barr body' with less compacted chromatin and incomplete RNAP II exclusion. Conclusions: 3D-SIM provides experimental evidence for profound differences between the functional architecture of transcriptionally active CTs and the Barr body. Basic structural features of CT organization such as CDCs and IC channels are however still recognized, arguing against a uniform compaction of the Barr body at the nucleosome level. The localization of distinct Xist RNA foci at boundaries of the rudimentary ANC may be considered as snap-shots of a dynamic interaction with silenced genes. Enrichment of SAF-A within Xi territories and its close spatial association with Xist RNA suggests their cooperative function for structural organization of Xi

Acetylcholine Neurotransmitter Receptor Densities in the Striatum of Hemiparkinsonian Rats Following Botulinum Neurotoxin-A Injection

Cholinergic neurotransmission has a pivotal function in the caudate-putamen, and is highly associated with the pathophysiology of Parkinson's disease. Here, we investigated long-term changes in the densities of the muscarinic receptor subtypes M1, M2, M3 (mAchRs) and the nicotinic receptor subtype α4β2 (nAchRs) in the striatum of the 6-OHDA-induced hemiparkinsonian (hemi-PD) rat model using quantitative in vitro receptor autoradiography. Hemi-PD rats exhibited an ipsilateral decrease in striatal mAchR densities between 6 and 16%. Moreover, a massive and constant decrease in striatal nAchR density by 57% was found. A second goal of the study was to disclose receptor-related mechanisms for the positive motor effect of intrastriatally injected Botulinum neurotoxin-A (BoNT-A) in hemi-PD rats in the apomorphine rotation test. Therefore, the effect of intrastriatally injected BoNT-A in control and hemi-PD rats on mAchR and nAchR densities was analyzed and compared to control animals or vehicle-injected hemi-PD rats. BoNT-A administration slightly reduced interhemispheric differences of mAchR and nAchR densities in hemi-PD rats. Importantly, the BoNT-A effect on striatal nAchRs significantly correlated with behavioral testing after apomorphine application. This study gives novel insights of 6-OHDA-induced effects on striatal mAchR and nAchR densities, and partly explains the therapeutic effect of BoNT-A in hemi-PD rats on a cellular level