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Large-scale genetic census of an elusive carnivore, the European wildcat (Felis s. silvestris)
(2016)
The European wildcat, Felis silvestris silvestris, serves as a prominent target species for the reconnection of central European forest habitats. Monitoring of this species, however, appears difficult due to its elusive behaviour and the ease of confusion with domestic cats. Recently, evidence for multiple wildcat occurrences outside its known distribution has accumulated in several areas across Central Europe, questioning the validity of available distribution data for this species. Our aim was to assess the fine-scale distribution and genetic status of the wildcat in its central European distribution range. We compiled and analysed genetic samples from roadkills and hundreds of recent hair-trapping surveys and applied phylogenetic and genetic clustering methods to discriminate wild and domestic cats and identify population subdivision. 2220 individuals were confirmed as either wildcat (n = 1792) or domestic cat (n = 342), and the remaining 86 (3.9 %) were identified as hybrids between the two. Remarkably, genetic distinction of domestic cats, wildcats and their hybrids was only possible when taking into account the presence of two highly distinct genetic lineages of wildcats, with a suture zone in central Germany. 44 % of the individual wildcats where sampled outside the previously published distribution. Our analyses confirm a relatively continuous spatial presence of wildcats across large parts of the study area in contrast to previous analyses indicating a highly fragmented distribution. Our results suggest that wildcat conservation and management should take advantage of the higher than previously assumed dispersal potential of wildcats, which may use wildlife corridors very efficiently.
Unerwartete Geschäftszahlen und die daraus resultierende Notwendigkeit der Anpassung von Ergebnisprognosen zeigen sich bereits bei der Vorbereitung der Regelberichterstattung. Damit stellt sich für die Unternehmensleitung die Frage, ob sie solche Insiderinformationen adhoc publizieren muss oder ob sie die Veröffentlichung aufschieben und bis zu dem für die Regelberichterstattung vorgesehenen Termin zuwarten darf. ... Zusammenfassung Ergeben sich bei den Vorbereitungen für die Regelberichterstattung Abweichungen von den Erwartungen an die Geschäftszahlen, die im Falle ihres Bekanntwerdens erheblichen Einfluss auf den Kurs von Insiderpapieren haben können, kann sich der Vorstand des Emittenten vor die Frage gestellt sehen, ob er die Ad-hoc-Veröffentlichung dieser Insiderinformation bis zu dem Zeitpunkt aufschieben darf, der im Finanzkalender für die Regelberichterstattung vorgesehen ist. Jedenfalls dann, wenn der Termin für diese Berichterstattung unmittelbar bevorsteht, überwiegt das Interesse des Emittenten an einem solchen Aufschub regelmäßig das Interesse des Kapitalmarkts an sofortiger Veröffentlichung. Das gilt auch dann, wenn aufgrund der Geschäftszahlen Ergebnisprognosen angepasst werden müssen. Sofern nicht ausnahmsweise eine Irreführung der Öffentlichkeit zu befürchten ist oder Bedenken hinsichtlich der Gewährleistung der Vertraulichkeit der Insiderinformation bestehen, ist der Emittent daher nach § 15 Abs. 3 WpHG bis zu dem für die Regelberichterstattung angekündigten Zeitpunkt von der Pflicht zur Veröffentlichung befreit.
Poster presentation: Hyperphosphorylation of tau is a characteristic of Alzheimer's disease (AD). Our group has established a model for tau hyperphosphorylation by mutating 10 residues from Ser/Thr to Glu to simulate the negative charge of phosphorylated residues ("pseudohyperphosphorylated (PHP)-tau"). In order to analyze temporal and spatial effects of hyperphosphorylation of tau in a systemic context, we have established transgenic mouse lines that express human wild-type (wt)- or PHP-tau under the control of the CamKIIalpha-promoter that leads to a forebrain specific moderate expression in neurons, i.e. the region where also tau-pathology in AD is abundant. For the evaluation of tau-induced changes in the transgenic mice, we quantified spine densities in the neocortex and hippocampus of transgenic mice. The spine densitiy was significantly increased in PHP-tau compared to wt-tau expressing mice. It is known that AD is associated with aberrant pre- and postsynaptic sprouting. Axonal sprouting is also observed in transgenic mice expressing mutated amyloid precursor protein (APP), which suggests that Abeta plays a significant role in this process. We deduce from our results, that (pseudo)-hyperphosphorylation of tau is sufficient to induce aberrant sprouting in the absence of Abeta. Analyses whether this sprouting is induced by pre- or postsynaptic changes and if functionally active synapses are formed are in progress. It will be interesting to determine if stabilization of these newly formed synapses slows or – in contrary – accelerates the progression of the disease. Sprouting as observed in our PHP-tau expressing mice is part of neuronal differentiation. One family of enzymes that is involved in cell differentiation are mitogen-acitvated protein kinases (MAPK). Western blot analysis was performed with brain lysates from transgenic mice to check whether PHP-tau induced sprouting is associated with MAPK activation. In fact, we also observed an increased activation of the MAPK ERK1/2 evident by phosphorylation of the residues Thr202 and Tyr204. ERK1/2 is also known to phosphorylate tau at sites characteristic for AD. Our results suggest the presence of a vicious circle by which (pseudo)-hyperphosphorylated tau activates ERK1/2 which in turn phosphorylates tau.