108 research outputs found
Entropy production of cyclic population dynamics
Entropy serves as a central observable in equilibrium thermodynamics.
However, many biological and ecological systems operate far from thermal
equilibrium. Here we show that entropy production can characterize the behavior
of such nonequilibrium systems. To this end we calculate the entropy production
for a population model that displays nonequilibrium behavior resulting from
cyclic competition. At a critical point the dynamics exhibits a transition from
large, limit-cycle like oscillations to small, erratic oscillations. We show
that the entropy production peaks very close to the critical point and tends to
zero upon deviating from it. We further provide analytical methods for
computing the entropy production which agree excellently with numerical
simulations.Comment: 4 pages, 3 figures and Supplementary Material. To appear in Phys.
Rev. Lett.
Nations under God: How Church–State Relations Shape Christian Responses to Right-Wing Populism in Germany and the United States
Right-wing populists across many western countries have markedly intensified their references to Christianity in recent years. However, Christian communities’ reactions to such developments often vary significantly, ranging from disproportionate support in some countries to outspoken opposition in others. This paper explores the role of structural factors, and in particular of Church–State relations, in accounting for some of these differences. Specifically, this article explores how Church–State relations in Germany and the United States have produced different incentives and opportunity structures for faith leaders when facing right-wing populism. Based on quantitative studies, survey data, and 31 in-depth elite interviews, this research suggests that whereas Germany’s system of “benevolent neutrality” encourages highly centralised churches whose leaders perceive themselves as integral part and defenders of the current system, and are therefore both willing and able to create social taboos against right-wing populism, America’s “Wall of separation” favours a de-centralised religious marketplace, in which church leaders are more prone to agree with populists’ anti-elitist rhetoric, and face higher costs and barriers against publicly condemning right-wing populism. Taking such structural factors into greater account when analysing Christian responses to right-wing populism is central to understanding current and future dynamics between politics and religion in western democracies.</jats:p
Pyrrolidinium chloride
The title compound, C4H10N+·Cl−, was obtained as a decomposition product from 2,6-bis(pyrrolidinyl)pyridine. The anion lies on the same cristallographic mirror plane as the N atom of the cation, the complete cation being generated by mirror symmetry. The anions and cations are connected by N+—H⋯Cl− hydrogen bonds into chains along [100]. The pyrrolidinium cation is puckered in an envelope conformation E
N1
The edge of neutral evolution in social dilemmas
The functioning of animal as well as human societies fundamentally relies on
cooperation. Yet, defection is often favorable for the selfish individual, and
social dilemmas arise. Selection by individuals' fitness, usually the basic
driving force of evolution, quickly eliminates cooperators. However, evolution
is also governed by fluctuations that can be of greater importance than fitness
differences, and can render evolution effectively neutral. Here, we investigate
the effects of selection versus fluctuations in social dilemmas. By studying
the mean extinction times of cooperators and defectors, a variable sensitive to
fluctuations, we are able to identify and quantify an emerging 'edge of neutral
evolution' that delineates regimes of neutral and Darwinian evolution. Our
results reveal that cooperation is significantly maintained in the neutral
regimes. In contrast, the classical predictions of evolutionary game theory,
where defectors beat cooperators, are recovered in the Darwinian regimes. Our
studies demonstrate that fluctuations can provide a surprisingly simple way to
partly resolve social dilemmas. Our methods are generally applicable to
estimate the role of random drift in evolutionary dynamics.Comment: 17 pages, 4 figure
Estimation of conversion factors for wood stacks in landings and their influencing parameters: a comprehensive literature review for America and Europe
In commercial transaction of stacked roundwood, the estimation of the stack net volume plays a key role. One generalized method to determine the net volume is using conversion factors that relate the gross and net volumes. In this literature review the developed methods to estimate the conversion factors as well as their influencing parameters were analyzed based on 153 references from America and Europe. According to the results, 48 different methods (including their variants) for estimating the conversion factors were developed. The newest methods enabled their accurate determination inexpensively, e.g., photo-optical methods or 3D simulation models. The analyzed references revealed that 30 parameters influence the conversion factors. Based on this comprehensive review, each stakeholder involved in the roundwood supply chain can know which method is used for estimating the conversion factors in the analyzed territories and which influencing parameters should be considered when purchasing roundwood in order to accurately assess the solid wood content in the stacks
Neutrophil “plucking” on megakaryocytes drives platelet production and boosts cardiovascular disease
Intravascular neutrophils and platelets collaborate in maintaining host integrity, but their interaction can also trigger thrombotic complications. We report here that cooperation between neutrophil and platelet lineages extends to the earliest stages of platelet formation by megakaryocytes in the bone marrow. Using intravital microscopy, we show that neutrophils "plucked" intravascular megakaryocyte extensions, termed proplatelets, to control platelet production. Following CXCR4-CXCL12-dependent migration towards perisinusoidal megakaryocytes, plucking neutrophils actively pulled on proplatelets and triggered myosin light chain and extracellular-signal-regulated kinase activation through reactive oxygen species. By these mechanisms, neutrophils accelerate proplatelet growth and facilitate continuous release of platelets in steady state. Following myocardial infarction, plucking neutrophils drove excessive release of young, reticulated platelets and boosted the risk of recurrent ischemia. Ablation of neutrophil plucking normalized thrombopoiesis and reduced recurrent thrombosis after myocardial infarction and thrombus burden in venous thrombosis. We establish neutrophil plucking as a target to reduce thromboischemic events
The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomes
Fine-structured multi-scaling long-range correlations in completely sequenced genomes—features, origin, and classification
The sequential organization of genomes, i.e. the relations between distant base pairs and regions within sequences, and its connection to the three-dimensional organization of genomes is still a largely unresolved problem. Long-range power-law correlations were found using correlation analysis on almost the entire observable scale of 132 completely sequenced chromosomes of 0.5 × 106 to 3.0 × 107 bp from Archaea, Bacteria, Arabidopsis thaliana, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Drosophila melanogaster, and Homo sapiens. The local correlation coefficients show a species-specific multi-scaling behaviour: close to random correlations on the scale of a few base pairs, a first maximum from 40 to 3,400 bp (for Arabidopsis thaliana and Drosophila melanogaster divided in two submaxima), and often a region of one or more second maxima from 105 to 3 × 105 bp. Within this multi-scaling behaviour, an additional fine-structure is present and attributable to codon usage in all except the human sequences, where it is related to nucleosomal binding. Computer-generated random sequences assuming a block organization of genomes, the codon usage, and nucleosomal binding explain these results. Mutation by sequence reshuffling destroyed all correlations. Thus, the stability of correlations seems to be evolutionarily tightly controlled and connected to the spatial genome organization, especially on large scales. In summary, genomes show a complex sequential organization related closely to their three-dimensional organization
Monogenic variants in dystonia: an exome-wide sequencing study
Background Dystonia is a clinically and genetically heterogeneous condition that occurs in isolation (isolated dystonia), in combination with other movement disorders (combined dystonia), or in the context of multisymptomatic phenotypes (isolated or combined dystonia with other neurological involvement). However, our understanding of its aetiology is still incomplete. We aimed to elucidate the monogenic causes for the major clinical categories of dystonia. Methods For this exome-wide sequencing study, study participants were identified at 33 movement-disorder and neuropaediatric specialty centres in Austria, Czech Republic, France, Germany, Poland, Slovakia, and Switzerland. Each individual with dystonia was diagnosed in accordance with the dystonia consensus definition. Index cases were eligible for this study if they had no previous genetic diagnosis and no indication of an acquired cause of their illness. The second criterion was not applied to a subset of participants with a working clinical diagnosis of dystonic cerebral palsy. Genomic DNA was extracted from blood of participants and whole-exome sequenced. To find causative variants in known disorder-associated genes, all variants were filtered, and unreported variants were classified according to American College of Medical Genetics and Genomics guidelines. All considered variants were reviewed in expert round-table sessions to validate their clinical significance. Variants that survived filtering and interpretation procedures were defined as diagnostic variants. In the cases that went undiagnosed, candidate dystonia-causing genes were prioritised in a stepwise workflow. Findings We sequenced the exomes of 764 individuals with dystonia and 346 healthy parents who were recruited between June 1, 2015, and July 31, 2019. We identified causative or probable causative variants in 135 (19%) of 728 families, involving 78 distinct monogenic disorders. We observed a larger proportion of individuals with diagnostic variants in those with dystonia (either isolated or combined) with coexisting non-movement disorder-related neurological symptoms (100 [45%] of 222;excepting cases with evidence of perinatal brain injury) than in those with combined (19 [19%] of 98) or isolated (16 [4%] of 388) dystonia. Across all categories of dystonia, 104 (65%) of the 160 detected variants affected genes which are associated with neurodevelopmental disorders. We found diagnostic variants in 11 genes not previously linked to dystonia, and propose a predictive clinical score that could guide the implementation of exome sequencing in routine diagnostics. In cases without perinatal sentinel events, genomic alterations contributed substantively to the diagnosis of dystonic cerebral palsy. In 15 families, we delineated 12 candidate genes. These include IMPDH2, encoding a key purine biosynthetic enzyme, for which robust evidence existed for its involvement in a neurodevelopmental disorder with dystonia. We identified six variants in IMPDH2, collected from four independent cohorts, that were predicted to be deleterious de-novo variants and expected to result in deregulation of purine metabolism. Interpretation In this study, we have determined the role of monogenic variants across the range of dystonic disorders, providing guidance for the introduction of personalised care strategies and fostering follow-up pathophysiological explorations
Prognostic impact of vitamin B6 metabolism in lung cancer
Patients with non-small cell lung cancer (NSCLC) are routinely treated with cytotoxic agents such as cisplatin. Through a genome-wide siRNA-based screen, we identified vitamin B6 metabolism as a central regulator of cisplatin responses in vitro and in vivo. By aggravating a bioenergetic catastrophe that involves the depletion of intracellular glutathione, vitamin B6 exacerbates cisplatin-mediated DNA damage, thus sensitizing a large panel of cancer cell lines to apoptosis. Moreover, vitamin B6 sensitizes cancer cells to apoptosis induction by distinct types of physical and chemical stress, including multiple chemotherapeutics. This effect requires pyridoxal kinase (PDXK), the enzyme that generates the bioactive form of vitamin B6. In line with a general role of vitamin B6 in stress responses, low PDXK expression levels were found to be associated with poor disease outcome in two independent cohorts of patients with NSCLC. These results indicate that PDXK expression levels constitute a biomarker for risk stratification among patients with NSCLC.publishedVersio
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