New perspectives on evolutionary medicine: the relevance of microevolution for human health and disease

Evolutionary medicine (EM) is a growing field focusing on the evolutionary basis of human diseases and their changes through time. To date, the majority of EM studies have used pure theories of hominin macroevolution to explain the present-day state of human health. Here, we propose a different approach by addressing more empirical and health-oriented research concerning past, current and future microevolutionary changes of human structure, functions and pathologies. Studying generation-to-generation changes of human morphology that occurred in historical times, and still occur in present-day populations under the forces of evolution, helps to explain medical conditions and warns clinicians that their current practices may influence future humans. Also, analyzing historic tissue specimens such as mummies is crucial in order to address the molecular evolution of pathogens, of the human genome, and their coadaptations.Frank Jakobus Rühli and Maciej Henneber

Paleospecies as cognitive construct: The meme of “Homo floresiensis”

Creation and subsequent abandonment of a number of earlier species considered human ancestors: Eoanthropus dawsoni, Hesperopithecus haroldcooki, Homo gardarensis and Ramapithecus punjabicus is presented using cases from the history of science. This review indicates that the fossil evidence for these species has been questionable from the beginning but that mental images – memes – they invoked were attractive to students of human evolution and as such persisted even if not confirmed by further finds, with new research still being disputed. Against this background the status of the recent construction of the hominin species “Homo floresiensis” is discussed showing that despite dubious interpretations of the objective data and a relatively long time of non-confirmation due to paucity of newly discovered skeletal remains, the “species” still exists in minds of scholars and in the scientific literature extending into textbooks

Assessing plant diversity and composition in grasslands across spatial scales: the standardised EDGG sampling methodology

This paper presents the details of the EDGG sampling methodology and its underlying rationales. The methodology has been applied during EDGG Research Expeditions and EDGG Field Workshops since 2009, and has been subsequently adopted by various other researchers. The core of the sampling are the EDGG Biodiversity Plots, which are 100‐m2 squares comprising, in two opposite corners, nested‐plot series of 0.0001, 0.001, 0.01, 0.1, 1 and 10 m2 square plots, in which all terricolous vascular plants, bryophytes and lichens are recorded using the shoot presence method. In the 10‐m2 plots, species cover is also estimated as a percentage and various environmental and structural parameters are recorded. Usually the EDGG Biodiversity Plots are complemented by the sampling of additional 10 m2 normal plots with the same parameters as the 10‐m2 corners of the first, allowing coverage of a greater environmental diversity and the achievement of higher statistical power in the subsequent analyses for this important grain size. The EDGG sampling methodology has been refined over the years, while its core has turned out to generate high‐quality, standardised data in an effective manner, which facilitates a multitude of analyses. In this paper we provide the current versions of our guidelines, field forms and data entry spreadsheets, as open‐access Online Resources to facilitate the easy implementation of this methodology by other researchers. We also discuss potential future additions and modifications to the approach, among which the most promising are the use of stratified‐random methods to a priori localise the plots and ideas to sample invertebrate taxa on the same plots and grain sizes, such as grasshoppers (Orthoptera) and vegetation‐dwelling spiders (Araneae). As with any other method, the EDGG sampling methodology is not ideal for every single purpose, but with its continuous improvements and its flexibility, it is a good multi‐ purpose approach. A particularly advantageous element, lacking in most other sampling schemes, including classical phytosociogical sampling, is the multi‐scale and multi‐taxon approach, which provides data that allow for deeper understanding of the generalities and idiosyncrasies of biodiversity patterns and their underlying drivers across scales and taxa

MODELLING AND PROGNOSIS OF COMPETITIVE PERFORMANCES IN ELITE SWIMMING

The study demonstrates that the performance of an elite female swimmer in the finals of the 200 m backstroke at the Olympic Games 2000 in Sydney can be predicted by means of the nonlinear mathematical method of a neural back-propagation network. The analysis included the performance output data of 19 competitions prior to the Olympics within a time period of 95 successive weeks and the training input data of the last four weeks prior to each competition. The training data were divided into two phases: (1) a two-week taper cycle, and (2) an earlier two-week high load cycle. The trained neural network was not only able to model the 19 competitive performances, but also to predict the performance in the semi final of the Olympic Games in Sydney on the basis of the two sets of training data during the preparation before that specific competition

Evolution of modern humans is a result of self-amplifying feedbacks beginning in the Miocene and continuing without interruption until now

Humans are a part of the complex system of life. This consists of a multitude of feedbacks among all parts of living systems. In the case of human origins, many feedbacks became positive rather than homeostatic, thus producing self-amplifying effects in basic morphological and behavioural characteristics of emerging humans: erect bipedalism, social structure, tool-making, food procurement and environmental management, symbolic communication, sexuality, extended childhood, and mental capacities. These, plus many other human characteristics, changed gradually, though at varying rates, over the last 6 million years, producing directional variation in extant morphological and behavioural characteristics of what are considered modern humans. The change through time and geographic space of those characteristics is an ongoing dynamic process, thus it is futile to pose essentialist questions about the precise date and place of the modern human origins. Modernity is a process, not an endpoint

Gaining access to agency and structure in industrial marketing theory : a critical pluralist approach.

This article is concerned with gaining greater insight into the interplay between agency and structure in industrial marketing (IM) scholarship. The article’s intent is to embed Midgley’s notion of critical pluralism within this endeavour. The article commends the movement towards increased deployment of critical realism, but cautions against the dangers of creating further atomism in marketing theory by generating another paradigm of thought with strongly defended boundaries, impervious to outside influence. The article advances a case for critical pluralism within IM scholarship and offers a three-dimensional (theoretical, methodological and methodical) framework to aid this. The discussion demonstrates how critical pluralism can be deployed to gain insights into agency and structure using a number of ‘integrative’ theoretical perspectives

Effect of clonidine to prevent agitation in children after sevoflurane anaesthesia:a randomised placebo controlled multicentre trial

INTRODUCTION: Post-operative agitation (PA) is a common problem (20-70%) in children anaesthetised with sevoflurane. Clonidine is widely used off-label in children for several indications, including PA; but the current level of evidence is limited. Our aim is to investigate the impact of prophylactic intravenous (IV) clonidine administered at the end of surgery on the incidence and degree of PA. Furthermore, the pharmacokinetic profile of IV clonidine in children is not well established and our aim is to obtain pharmacokinetic data relating hereto. METHODS: This is a multicentre, randomised and blinded clinical trial in which we will be enrolling 380 children aged 1-5 years who are planned for anaesthesia with sevoflurane and fentanyl. Inclusion is based on computer-generated randomisation (1: 1) and stratified by age and site. The study drug is administered IV approximately 20 min. before the expected completion of surgery (intervention: clonidine 3 mu g per kg; placebo: equal quantity of saline). CONCLUSION: The primary outcome is PA measured on the Watcha scale. The secondary outcomes include post-operative pain relief and adverse effects, including a 30-day follow- up. In total, 40 children will be allocated to drug assay sampling, enabling a compartmental pharmacokinetic analysis

Effect of clonidine to prevent agitation in children after sevoflurane anaesthesia:a randomised placebo controlled multicentre trial

INTRODUCTION: Post-operative agitation (PA) is a common problem (20-70%) in children anaesthetised with sevoflurane. Clonidine is widely used off-label in children for several indications, including PA; but the current level of evidence is limited. Our aim is to investigate the impact of prophylactic intravenous (IV) clonidine administered at the end of surgery on the incidence and degree of PA. Furthermore, the pharmacokinetic profile of IV clonidine in children is not well established and our aim is to obtain pharmacokinetic data relating hereto. METHODS: This is a multicentre, randomised and blinded clinical trial in which we will be enrolling 380 children aged 1-5 years who are planned for anaesthesia with sevoflurane and fentanyl. Inclusion is based on computer-generated randomisation (1: 1) and stratified by age and site. The study drug is administered IV approximately 20 min. before the expected completion of surgery (intervention: clonidine 3 mu g per kg; placebo: equal quantity of saline). CONCLUSION: The primary outcome is PA measured on the Watcha scale. The secondary outcomes include post-operative pain relief and adverse effects, including a 30-day follow- up. In total, 40 children will be allocated to drug assay sampling, enabling a compartmental pharmacokinetic analysis