Schrumpfung und Urban Sprawl - analytische und planerische Problemstellungen

Das vorliegende UFZ-Diskussionspapier ist die Dokumentation des Workshops Schrumpfung und Urban Sprawl, der am 3. November 2003 am UFZ stattfand. Es führt damit eine Diskussions- und Forschungslinie fort, die in den 1990er Jahren durch Forscher und Praktiker aus unterschiedlichen Einrichtungen der Region Halle-Leipzig begründet wurde. Im Arbeitskreis Suburbanisierung wurden unter Koordination des UFZ disziplinäre Zugänge und praktische Erfahrungen zusammengeführt und daraus Handlungsempfehlungen abgeleitet. Zwischenzeitlich hat der Suburbanisierungsdruck, der noch Ende der 1990er Jahre konstatiert wurde, deutlich abgenommen nicht nur in der Region, sondern in ganz Ostdeutschland. Nichtsdestoweniger ist Suburbanisierung ein zentraler Gegenstand von raumbezogener Politik und räumlicher Planung geblieben und hat im Zusammenhang mit dem Thema Stadtumbau neue Relevanz gewonnen. So ist davon auszugehen, dass auch in der Region Halle-Leipzig die intensive Beschäftigung mit dem Problem der Suburbanisierung anhalten wird allerdings unter veränderten Vorzeichen. Im Mittelpunkt steht nunmehr die Frage, welche Anforderungen sich aus der Situation von demographischer und städtischer Schrumpfung für die wissenschaftliche und praktische Auseinandersetzung mit Suburbanisierung ergeben. So gilt es, unter anderem, zu klären, ob sich die Richtung von Sprawl unter Schrumpfungsbedingungen umkehrt, ob das Zusammenspiel von Schrumpfung und Sprawl zu einer neuen Stadtstruktur führt oder ob sich durch diese spezifische Situation die Segregationsmuster verändern. Auf dem Workshop selbst wurden vor allem die Möglichkeiten der Steuerung von Suburbanisierung bzw. Sprawl unter Schrumpfungsbedingungen behandelt. Dazu wurden Überlegungen und Ergebnisse, die im EU-Projekt URBS PANDENS am Fallbeispiel Leipzig gewonnen wurden, vorgestellt, diskutiert und mit Erfahrungen aus der Praxis bzw. aus einer anderen Region konfrontiert. Neben der empirischen Analyse spielt dabei ein im Rahmen von URBS PANDENS entwickeltes qualitatives Modell des Urban Sprawl eine zentrale Rolle. --

Adaptations and transformations of hunter-gatherers in forest environments: New archaeological and anthropological insights

Like any other living being, humans constantly influence their environment, be it intentionally or unintentionally. By extracting natural resources, they shape their environment and also that of plants and other animals. A great difference setting people apart from all other living beings is the ability to construct and develop their own niche intentionally, and the unique tool for this is cultural behaviour. Here, we discuss anthropogenic environmental changes of hunter-gatherers and present new palaeoecological and palynological data. The studies are framed with ethnoarchaeological data from Western Siberia to gain a better understanding of how different triggers lead to coping mechanisms. For archaeological implication, we use two Mesolithic case studies from Germany: One of them focuses on hazelnut economy around ancient Lake Duvensee, and the other broaches the issue of selective roe deer hunt and its consequences at the site of Friesack. We address the archaeological evidence from the perspective of active alteration and its consequences, starting our argumentation from a perspective of niche construction theory. This approach has rarely been applied to early Holocene hunter-gatherers in Northern Europe even though the available data render possible to discuss human–environment interaction from such a perspective. It is demonstrated that archaeological research has tools at hand that enables to detect anthropogenic niche construction. However, the ethnoarchaeological example shows limitations and archaeologically invisible triggers and consequent results of human adaptations. The critical revision of such perspectives based on empirical data provides a better understanding of social and environmental transformations in the early- and mid-Holocene

Early Postnatal but Not Late Adult Neurogenesis Is Impaired in the Pitx3-Mutant Animal Model of Parkinson's Disease

The generation of new neurons in the adult dentate gyrus has functional implications for hippocampal formation. Reduced hippocampal neurogenesis has been described in various animal models of hippocampal dysfunction such as dementia and depression, which are both common non-motor-symptoms of Parkinson's disease (PD). As dopamine plays an important role in regulating precursor cell proliferation, the loss of dopaminergic neurons in the substantia nigra (SN) in PD may be related to the reduced neurogenesis observed in the neurogenic regions of the adult brain: subventricular zone (SVZ) and dentate gyrus (DG). Here we examined adult hippocampal neurogenesis in the Pitx3-mutant mouse model of PD (aphakia mice), which phenotypically shows a selective embryonic degeneration of dopamine neurons within the SN and to a smaller extent in the ventral tegmental area (VTA). Proliferating cells were labeled with BrdU in aphakia mice and healthy controls from 3 to 42 weeks of age. Three weeks old mutant mice showed an 18% reduction of proliferating cells in the DG and of 26% in the SVZ. Not only proliferation but also the number of new neurons was impaired in young aphakia mice resulting in 33% less newborn cells 4 weeks after BrdU-labeling. Remarkably, however, the decline in the number of proliferating cells in the neurogenic regions vanished in older animals (8–42 weeks) indicating that aging masks the effect of dopamine depletion on adult neurogenesis. Region specific reduction in precursor cells proliferation correlated with the extent of dopaminergic degeneration in mesencephalic subregions (VTA and SN), which supports the theory of age- and region-dependent regulatory effects of dopaminergic projections. Physiological stimulation of adult neurogenesis by physical activity (wheel running) almost doubled the number of proliferating cells in the dentate gyrus of 8 weeks old aphakia mice to a number comparable to that of wild-type mice, abolishing the slight reduction of baseline neurogenesis at this age. The described age-dependent susceptibility of adult neurogenesis to PD-like dopaminergic degeneration and its responsiveness to physical activity might have implications for the understanding of the pathophysiology and treatment of non-motor symptoms in PD

The LabTogo-Project

A joint project between West African Science Service Center on Climate Change and Adapted Land Use (WASCAL), the University of Lomé and the German Biomass Research Center (Deutsches Biomasseforschungszentrum; DBFZ) was initiated in 2020. The project aims at evaluating alternative and regenerative energy sources for rural areas and creating the basis for successful implementation. In three different work packages, therefore, biomass potentials should be quantified, technologies should be examined with regard to their suitability and - in the case of biogas application - a research structure, pilot biogas laboratory, should be created that is necessary to enable the sustainable implementation of technologies

Common variants in breast cancer risk loci predispose to distinct tumor subtypes.

BACKGROUND: Genome-wide association studies (GWAS) have identified multiple common breast cancer susceptibility variants. Many of these variants have differential associations by estrogen receptor (ER) status, but how these variants relate with other tumor features and intrinsic molecular subtypes is unclear. METHODS: Among 106,571 invasive breast cancer cases and 95,762 controls of European ancestry with data on 173 breast cancer variants identified in previous GWAS, we used novel two-stage polytomous logistic regression models to evaluate variants in relation to multiple tumor features (ER, progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and grade) adjusting for each other, and to intrinsic-like subtypes. RESULTS: Eighty-five of 173 variants were associated with at least one tumor feature (false discovery rate < 5%), most commonly ER and grade, followed by PR and HER2. Models for intrinsic-like subtypes found nearly all of these variants (83 of 85) associated at p < 0.05 with risk for at least one luminal-like subtype, and approximately half (41 of 85) of the variants were associated with risk of at least one non-luminal subtype, including 32 variants associated with triple-negative (TN) disease. Ten variants were associated with risk of all subtypes in different magnitude. Five variants were associated with risk of luminal A-like and TN subtypes in opposite directions. CONCLUSION: This report demonstrates a high level of complexity in the etiology heterogeneity of breast cancer susceptibility variants and can inform investigations of subtype-specific risk prediction

The German National Registry of Primary Immunodeficiencies (2012-2017)

Introduction: The German PID-NET registry was founded in 2009, serving as the first national registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the European Society for Immunodeficiencies (ESID) registry. The primary purpose of the registry is to gather data on the epidemiology, diagnostic delay, diagnosis, and treatment of PIDs. Methods: Clinical and laboratory data was collected from 2,453 patients from 36 German PID centres in an online registry. Data was analysed with the software Stata® and Excel. Results: The minimum prevalence of PID in Germany is 2.72 per 100,000 inhabitants. Among patients aged 1–25, there was a clear predominance of males. The median age of living patients ranged between 7 and 40 years, depending on the respective PID. Predominantly antibody disorders were the most prevalent group with 57% of all 2,453 PID patients (including 728 CVID patients). A gene defect was identified in 36% of patients. Familial cases were observed in 21% of patients. The age of onset for presenting symptoms ranged from birth to late adulthood (range 0–88 years). Presenting symptoms comprised infections (74%) and immune dysregulation (22%). Ninety-three patients were diagnosed without prior clinical symptoms. Regarding the general and clinical diagnostic delay, no PID had undergone a slight decrease within the last decade. However, both, SCID and hyper IgE- syndrome showed a substantial improvement in shortening the time between onset of symptoms and genetic diagnosis. Regarding treatment, 49% of all patients received immunoglobulin G (IgG) substitution (70%—subcutaneous; 29%—intravenous; 1%—unknown). Three-hundred patients underwent at least one hematopoietic stem cell transplantation (HSCT). Five patients had gene therapy. Conclusion: The German PID-NET registry is a precious tool for physicians, researchers, the pharmaceutical industry, politicians, and ultimately the patients, for whom the outcomes will eventually lead to a more timely diagnosis and better treatment