Weiji: Globale Dimensionen des Ersten Weltkrieges

Es gehört heute schon fast zum guten Ton, sich in Publikationen zur Geschichte des Ersten Weltkrieges nicht mehr nur auf Europa zu beschränken, sondern auch andere Teile der Welt in den Blick zu nehmen. Das zeigen jüngst Publikationen von Oliver Janz oder Jörn Leonhard. In diesem Vortrag sollen die nicht europäischen Teile der Welt nun aber die europäischen nicht einfach ergänzen, sie sollen vielmehr im Zentrum stehen. Ausgehend vom chinesischen Wort weiji, welches aus den beiden Schriftzeichen wei für Gefahr oder Risiko und ji für Chance oder Gelegenheit besteht, soll in diesem Vortrag mit Blick auf globalgeschichtliche Überlegungen danach gefragt werden, was den Ersten Weltkrieg wirklich zum ersten Weltkrieg macht. In einem weiteren Teilen werden dann aussereuropäische Kriegsschauplätze in Togo, Samoa, Neuguinea und dem Pazifik, in China, Deutsch Südwestafrika und Kamerun, im Osmanischen Reich sowie in Ostafrika kurz vorgestellt, um zu zeigen, dass auch mit Blick auf die Kampfhandlungen nicht nur Europa Schauplatz war und dass der Krieg dort sogar länger dauerte als in Europa selbst. Unter dem Titel Yigong Daibing – Arbeiter statt Soldaten widmet sich der dritte Teil des Vortrages der Mobilisierung aussereuropäischer Arbeiter aus drei Ländern, nämlich Australien, China und Südafrika. In allen Fällen ging es sicherlich darum, damit dem Arbeitskräftemangel auf Seiten der Ententemächte zu begegnen, zumindest langfristig bedeutsamer waren aber das Wissen und die Fertigkeiten, welche die Arbeiter am Ende des Krieges in ihre Länder zurückbrachten. Ebenso wichtig war auch die Tatsache, dass die Behörden der betreffenden Länder mit der Entsendung der Arbeiter auch eigene Absichten verfolgten, so im Fall Australiens mit Blick auf den Aufbau einer eigenen Rüstungsindustrie, im Fall Chinas mit Blick auf die Aufwertung des Status des eigenen Landes auf der internationalen Bühne und im Fall Südafrikas um die Aufstellung bewaffneter schwarzer Einheiten im Land im Zeichen der Rassentrennung zu verhindern. Die Hoffnungen der einzelnen Arbeiter erfüllten sich nur selten und vor allem nicht in dem von ihnen gewünschten Tempo, die durch sie bewirkten politischen, wirtschaftlichen und/oder sozialen Veränderungen waren aber durchaus nachhaltig. Der letzte Aspekt, der im Vortrag angesprochen wird, ist die globale Ernährungskrise der Jahre 1916/17, die in der Forschung lange Zeit zu wenig beachtet wurde, dies zumindest mit Blick auf ihre globale Dimension. Dies ist eigentlich erstaunlich, denn die Lebensmittelversorgung war vor 1914 durch einen sich verstärkenden transnationalen, wenn nicht globalen Austausch geprägt. Trotzdem hatte sich auf die daraus resultierenden Folgen kaum eine kriegführende Macht ausreichend vorbereitet. Im Krieg musste daher häufig improvisiert werden, was der Entente insgesamt wesentlich besser gelang als den Mittelmächten, auch weil sie in diesem Bereich wesentlich mehr zu investieren bereit war.

„Als Christ, als Theologe, als Geschichtsschreiber, als Bürger kann ich diese Lehre nicht annehmen.“ Altkatholische Argumentation gegen die Dogmen des Ersten Vatikanischen Konzils

Als sich der altkatholische Protest gegen die Dogmen des Ersten Vatikanischen Konzils von 1870 formierte, brachten die Altkatholiken ganz unterschiedliche Argumente vor: Zum Teil argumentierten sie juristisch, dem Konzil habe die nötige Freiheit in Diskussion und Entscheidung gefehlt; sie griffen die Stringenz der Schrift- und Traditionsargumente der Befürwortre der Dogmen an und versuchten zu zeiten, dass Schrift und Tradition eher eine gegenteilige Ansicht favorisieren würden; aber sie argumentierten auch politisch. Der Vortrag zeichnet diese unterschiedlichen Argumentationslinien nach.

Estimating the prevalence of comorbid conditions and their effect on health care costs in patients with diabetes mellitus in Switzerland.

BACKGROUND Estimating the prevalence of comorbidities and their associated costs in patients with diabetes is fundamental to optimizing health care management. This study assesses the prevalence and health care costs of comorbid conditions among patients with diabetes compared with patients without diabetes. Distinguishing potentially diabetes- and nondiabetes-related comorbidities in patients with diabetes, we also determined the most frequent chronic conditions and estimated their effect on costs across different health care settings in Switzerland. METHODS Using health care claims data from 2011, we calculated the prevalence and average health care costs of comorbidities among patients with and without diabetes in inpatient and outpatient settings. Patients with diabetes and comorbid conditions were identified using pharmacy-based cost groups. Generalized linear models with negative binomial distribution were used to analyze the effect of comorbidities on health care costs. RESULTS A total of 932,612 persons, including 50,751 patients with diabetes, were enrolled. The most frequent potentially diabetes- and nondiabetes-related comorbidities in patients older than 64 years were cardiovascular diseases (91%), rheumatologic conditions (55%), and hyperlipidemia (53%). The mean total health care costs for diabetes patients varied substantially by comorbidity status (US$3,203-$14,223). Patients with diabetes and more than two comorbidities incurred US$10,584 higher total costs than patients without comorbidity. Costs were significantly higher in patients with diabetes and comorbid cardiovascular disease (US$4,788), hyperlipidemia (US$2,163), hyperacidity disorders (US$8,753), and pain (US$8,324) compared with in those without the given disease. CONCLUSION Comorbidities in patients with diabetes are highly prevalent and have substantial consequences for medical expenditures. Interestingly, hyperacidity disorders and pain were the most costly conditions. Our findings highlight the importance of developing strategies that meet the needs of patients with diabetes and comorbidities. Integrated diabetes care such as used in the Chronic Care Model may represent a useful strategy.

Species richness, but not phylogenetic diversity, influences community biomass production and temporal stability in a re-examination of 16 grassland biodiversity studies

* Hundreds of experiments have now manipulated species richness (SR) of various groups of organisms and examined how this aspect of biological diversity influences ecosystem functioning. Ecologists have recently expanded this field to look at whether phylogenetic diversity (PD) among species, often quantified as the sum of branch lengths on a molecular phylogeny leading to all species in a community, also predicts ecological function. Some have hypothesized that phylogenetic divergence should be a superior predictor of ecological function than SR because evolutionary relatedness represents the degree of ecological and functional differentiation among species. But studies to date have provided mixed support for this hypothesis. * Here, we reanalyse data from 16 experiments that have manipulated plant SR in grassland ecosystems and examined the impact on above-ground biomass production over multiple time points. Using a new molecular phylogeny of the plant species used in these experiments, we quantified how the PD of plants impacts average community biomass production as well as the stability of community biomass production through time. * Using four complementary analyses, we show that, after statistically controlling for variation in SR, PD (the sum of branches in a molecular phylogenetic tree connecting all species in a community) is neither related to mean community biomass nor to the temporal stability of biomass. These results run counter to past claims. However, after controlling for SR, PD was positively related to variation in community biomass over time due to an increase in the variances of individual species, but this relationship was not strong enough to influence community stability. * In contrast to the non-significant relationships between PD, biomass and stability, our analyses show that SR per se tends to increase the mean biomass production of plant communities, after controlling for PD. The relationship between SR and temporal variation in community biomass was either positive, non-significant or negative depending on which analysis was used. However, the increases in community biomass with SR, independently of PD, always led to increased stability. These results suggest that PD is no better as a predictor of ecosystem functioning than SR. * Synthesis. Our study on grasslands offers a cautionary tale when trying to relate PD to ecosystem functioning suggesting that there may be ecologically important trait and functional variation among species that is not explained by phylogenetic relatedness. Our results fail to support the hypothesis that the conservation of evolutionarily distinct species would be more effective than the conservation of SR as a way to maintain productive and stable communities under changing environmental conditions.

Models of hybridization during range expansions and their application to recent human evolution

Several lines of genetic, archeological and paleontological evidence suggest that anatomically modern humans (Homo sapiens) colonized the world in the last 60,000 years by a series of migrations originating from Africa (e.g. Liu et al., 2006; Handley et al., 2007; Prugnolle, Manica, and Balloux, 2005; Ramachandran et al. 2005; Li et al. 2008; Deshpande et al. 2009; Mellars, 2006a, b; Lahr and Foley, 1998; Gravel et al., 2011; Rasmussen et al., 2011). With the progress of ancient DNA analysis, it has been shown that archaic humans hybridized with modern humans outside Africa. Recent direct analyses of fossil nuclear DNA have revealed that 1–4 percent of the genome of Eurasian has been likely introgressed by Neanderthal genes (Green et al., 2010; Reich et al., 2010; Vernot and Akey, 2014; Sankararaman et al., 2014; Prufer et al., 2014; Wall et al., 2013), with Papua New Guineans and Australians showing even larger levels of admixture with Denisovans (Reich et al., 2010; Skoglund and Jakobsson, 2011; Reich et al., 2011; Rasmussen et al., 2011). It thus appears that the past history of our species has been more complex than previously anticipated (Alves et al., 2012), and that modern humans hybridized several times with local hominins during their expansion out of Africa, but the exact mode, time and location of these hybridizations remain to be clarifi ed (Ibid.; Wall et al., 2013). In this context, we review here a general model of admixture during range expansion, which lead to some predictions about expected patterns of introgression that are relevant to modern human evolution.

Biodiversity increases the resistance of ecosystem productivity to climate extremes

It remains unclear whether biodiversity buffers ecosystems against climate extremes, which are becoming increasingly frequent worldwide. Early results suggested that the ecosystem productivity of diverse grassland plant communities was more resistant, changing less during drought, and more resilient, recovering more quickly after drought, than that of depauperate communities. However, subsequent experimental tests produced mixed results. Here we use data from 46 experiments that manipulated grassland plant diversity to test whether biodiversity provides resistance during and resilience after climate events. We show that biodiversity increased ecosystem resistance for a broad range of climate events, including wet or dry, moderate or extreme, and brief or prolonged events. Across all studies and climate events, the productivity of low-diversity communities with one or two species changed by approximately 50% during climate events, whereas that of high-diversity communities with 16–32 species was more resistant, changing by only approximately 25%. By a year after each climate event, ecosystem productivity had often fully recovered, or overshot, normal levels of productivity in both high- and low-diversity communities, leading to no detectable dependence of ecosystem resilience on biodiversity. Our results suggest that biodiversity mainly stabilizes ecosystem productivity, and productivity-dependent ecosystem services, by increasing resistance to climate events. Anthropogenic environmental changes that drive biodiversity loss thus seem likely to decrease ecosystem stability, and restoration of biodiversity to increase it, mainly by changing the resistance of ecosystem productivity to climate events.

Global diversity, population stratification and selection of human copy number variation

In order to explore the diversity and selective signatures of duplication and deletion human copy number variants (CNVs), we sequenced 236 individuals from 125 distinct human populations. We observed that duplications exhibit fundamentally different population genetic and selective signatures than deletions and are more likely to be stratified between human populations. Through reconstruction of the ancestral human genome, we identify megabases of DNA lost in different human lineages and pinpoint large duplications that introgressed from the extinct Denisova lineage now found at high frequency exclusively in Oceanic populations. We find that the proportion of CNV base pairs to single nucleotide variant base pairs is greater among non-Africans than it is among African populations, but we conclude that this difference is likely due to unique aspects of non-African population history as opposed to differences in CNV load.

Plant diversity drives soil microbial biomass carbon in grasslands irrespective of global environmental change factors

Soil microbial biomass is a key determinant of carbon dynamics in the soil. Several studies have shown that soil microbial biomass significantly increases with plant species diversity, but it remains unclear whether plant species diversity can also stabilize soil microbial biomass in a changing environment. This question is particularly relevant as many global environmental change (GEC) factors, such as drought and nutrient enrichment, have been shown to reduce soil microbial biomass. Experiments with orthogonal manipulations of plant diversity and GEC factors can provide insights whether plant diversity can attenuate such detrimental effects on soil microbial biomass. Here, we present the analysis of 12 different studies with 14 unique orthogonal plant diversity × GEC manipulations in grasslands, where plant diversity and at least one GEC factor (elevated CO2, nutrient enrichment, drought, earthworm presence, or warming) were manipulated. Our results show that higher plant diversity significantly enhances soil microbial biomass with the strongest effects in long-term field experiments. In contrast, GEC factors had inconsistent effects with only drought having a significant negative effect. Importantly, we report consistent non-significant effects for all 14 interactions between plant diversity and GEC factors, which indicates a limited potential of plant diversity to attenuate the effects of GEC factors on soil microbial biomass. We highlight that plant diversity is a major determinant of soil microbial biomass in experimental grasslands that can influence soil carbon dynamics irrespective of GEC.