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Studies on ecological successions have a long tradition and have strongly contributed to the understanding of community assembly, niche theory, and ecosystem structure and functionality. Reports on ecological successions are however mostly restricted to one or two taxonomic groups, neglecting the mutual influences and dependencies between multiple taxonomic groups that are the building blocks of diverse communities. We introduce the Alpine research platform Ödenwinkel to promote observational and experimental research on the emergence of multidiversity and ecosystem complexity. We established n= 140 permanent plots along the successional gradient of the forefield of the Ödenwinkelkees glacier at the end of the Stubachtal valley in the Hohe Tauern range (Hohe Tauern National Park, Land Salzburg, Austria). In summer 2019 we completed a first full inventory of biotic and abiotic characteristics of these plots covering the diversity and composition of vascular plants, bryophytes, arthropods, and other animals, bacteria and fungi as well as some geomorphologic properties. In this paper we introduce the design of the research platform and show first results. While focusing on the diversity and composition of vascular plants along the successional gradient, we also provide data on the diversity of animals, bacteria, and fungi. The Ödenwinkel platform will be available as a long-term ecological research site where researchers from various disciplines can contribute to the accumulation of knowledge on ecological successions and on how interactions between various taxonomic groups structure ecological complexity in this Alpine environment.

Magnetic particle imaging (MPI) has been applied to various pre-clinical settings, including detection of ischemic stroke in mice. Translation of MPI to a clinical setting has been obstacled by the lack of a device with sufficient bore size and, at the same time, reasonable technical requirements. Here the authors present a human-sized MPI device with low technical requirements designed for detection of brain ischemia.

Clot formation inside a membrane oxygenator (MO) due to blood-to-foreign surface interaction represents a frequent complication during extracorporeal membrane oxygenation. Since current standard monitoring methods of coagulation status inside the MO fail to detect clot formation at an early stage, reliable sensors for early clot detection are in demand to reduce associated complications and adverse events. Bioimpedance analysis offers a monitoring concept by integrating sensor fibers into the MO. Herein, the feasibility of clot detection via bioimpedance analysis is evaluated. A custom-made test chamber with integrated titanium fibers acting as sensors was perfused with heparinized human whole blood in an in vitro test circuit until clot formation occurred. The clot detection capability of bioimpedance analysis was directly compared to the pressure difference across the test chamber (ΔP-TC), analogous to the measurement across MOs (ΔP-MO), the clinical gold standard for clot detection. We found that bioimpedance measurement increased significantly 8 min prior to a significant increase in ΔP-TC, indicating fulminant clot formation. Experiments without clot formation resulted in a lack of increase in bioimpedance or ΔP-TC. This study shows that clot detection via bioimpedance analysis under flow conditions in a blood-perfused test chamber is generally feasible, thus paving the way for further investigation.

The serine protease inhibitor neuroserpin regulates the activity of tissue-type plasminogen activator (tPA) in the nervous system. Neuroserpin expression is particularly prominent at late stages of neuronal development in most regions of the central nervous system (CNS), whereas it is restricted to regions related to learning and memory in the adult brain. The physiological expression pattern of neuroserpin, its high degree of colocalization with tPA within the CNS, together with its dysregulation in neuropsychiatric disorders, suggest a role in formation and refinement of synapses. In fact, studies in cell culture and mice point to a role for neuroserpin in dendritic branching, spine morphology, and modulation of behavior. In this study, we investigated the physiological role of neuroserpin in the regulation of synaptic density, synaptic plasticity, and behavior in neuroserpin-deficient mice. In the absence of neuroserpin, mice show a significant decrease in spine-synapse density in the CA1 region of the hippocampus, while expression of the key postsynaptic scaffold protein PSD-95 is increased in this region. Neuroserpin-deficient mice show decreased synaptic potentiation, as indicated by reduced long-term potentiation (LTP), whereas presynaptic paired-pulse facilitation (PPF) is unaffected. Consistent with altered synaptic plasticity, neuroserpin-deficient mice exhibit cognitive and sociability deficits in behavioral assays. However, although synaptic dysfunction is implicated in neuropsychiatric disorders, we do not detect alterations in expression of neuroserpin in fusiform gyrus of autism patients or in dorsolateral prefrontal cortex of schizophrenia patients. Our results identify neuroserpin as a modulator of synaptic plasticity, and point to a role for neuroserpin in learning and memory., (© 2017 Reumann et al.; Published by Cold Spring Harbor Laboratory Press.)