Die vorliegende Arbeit beinhaltet verschiedene Aspekte der Embryogenese des Pfeilschwanzkrebses Limulus polyphemus (Chelicerata, Xiphosura), darunter die frühe Neurogenese, die Axogenese, eine Analyse der "Kopf"segmentierung bei Cheliceraten und anderen Arthropoden, sowie das Expressionsmuster des Homöoboxgens Distal-less insbesondere in neuronalen Zusammenhängen. Darüber hinaus wurde eine neue Embryonalstadieneinteilung geleistet. Markierungen mit Phalloidin sowie weiterer neurospezifischer Marker ergaben, daß die frühe Neurogenese bei Limulus polyphemus durch die Immigration von Zellclustern erfolgt. Die Zellen nehmen eine flaschenförmige Gestalt annehmen, bevor sie sich aus dem ventralen Neuroektoderm lösen. Die Anzahl der Zellen pro Zellcluster steigt mit fortschreitender Entwicklung. Die Zellcluster konzentrieren sich in in Zentrum jedes Hemisegmentes, und in ihrem dorsalen Bereich beginnt die rasch voranschreitende Axogenese. Die Untersuchung der "Kopf"segmentierung mittels alpha-Tubulin-Markierungen bei Limulus polyphemus, Triops cancriformis (Crustacea) und Lepisma saccharina (Hexapoda) ergab sowohl bei der Entwicklung des circumoesophagealen Neuropilringes und der Innervierung der dazugehörigen Anhangspaare als auch hinsichtlich des Verlaufs des Stomatogastrischen Nervensystems beachtliche Übereinstimmungen, die entgegen der klassischen Auffassung den Schluß zulassen, daß das Deutocerebrum der Cheliceraten keineswegs reduziert wurde oder mit dem Tritocerebrum verschmolzen ist, sondern die Chelicere innerviert. Somit wäre das Chelicerenneuromer homolog zum Deutocerebrum der Crustacea und Hexapoda (1. Antenne). Der Vergleich des Expressionsmuster des Homöoboxgens Distal-less bei Limulus und Lepisma saccharina ergab neben den typischen Expressionen in auswachsenden Extremitäten- und andern Anhangsknospen bei beiden Vertretern Expressionen in neuronalen Zusammenhängen (im Lobus opticus, Ganglien bei Limulus oder in das ZNS umgebende Zellen bei Lepisma), an den verschiedensten Positionen späterer Sinnesorgane wie Mechano- oder Chemorezeptoren. Doppelmarkierungen mit Synorf-1 deuten darauf hin, daß es sich bei den Dll-positiven Zellen zum größten Anteil um Glia-Zellen handelt. / The following study contains different aspects of the embryology of the horseshoe crab Limulus polyphemus (Chelicerata, Xiphosura) with the main focus on early neurogenesis, axogenesis and the "head"segmentation in chelicerates and other arthropods. The expression pattern of the homeobox gene Distal-less was examined with main focus on neuronal correlations. In addition, a new staging was provided. Phalloidin stainings and other markers showed that the early neurogenesis in Limulus polyphemus happens via immigration of cell clusters. Cellclusters in the prosoma contain cells that become bottle shaped before they immigrate from the ventral neuroectoderm. The number of these cells increases during further development, and the cells concentrate in the middle of each hemisegment. Axogenesis starts at the dorsal edge of these concentrated cellclusters and progresses quite fast building the typical ladder like CNS of arthropods. The investigation of the "head"segmentation using alpha-tubulin stainings in Limulus polyphemus, Triops cancriformis (Crustacea), and Lepisma saccharina (Hexapoda) showed remarkable similarities in the development of the circumesophageal neuropil ring, the related appendages, and the course of the stomatogastric nerves. These results lead to the thesis that the deutocerebrum of chelicerates is neither completely reduced nor totally merged into the tritocerebrum but innervates the chelicerae which contradicts the classical view. According to these results the neuromer of the chelicerae would be homologous to the deutocerebrum of Crustaceans and Hexapods (first antennae). The expression pattern of the homeobox gene Distal-less was examined and compared in Limulus polyphemus and Lepisma saccharina. Beside the typical expression pattern in the developing appendages a participation of the gene in development of the nervous system was observed. Dll positve cells were found in or at least in direct contact with the CNS (optical lobe, ganglia in Limulus or surrounding the entire CNS including the brain of Lepisma), at different positions of later mechano- and chemoreceptors (lateral spines, bristles, flabellum, Johnstons organ etc.). Double stainings using Dll and Synorf-1 showed that at least most of these Dll-postive cells are most likely glia cells.

The relationship between initial intracellular pH (pHi) and associated cell volume change was investigated by simultaneous measurement of pHi and cell volume with fluorescence imaging in polarized fungiform taste receptor cells (TRCs) loaded with BCECF in vitro. Ammonium pulses caused a brief, reversible alkalinization in pHi and induced cell swelling. Sodium-acetate pulses reversible decreased TRC pHi and induced cell shrinkage. Removal weak acids and return to Control Ringer's solution (CR) causedTRC pHi and volume to overshoot baseline levels before fully recovering. Replacing CR with zero-sodium solution resulted in irreversible acidification of TRC pHi and induced cell swelling. Addition of sodium allowed reversal of TRC pHi and volume and return to baseline levels. Treating TRCs with cytoskeleton inhibitors, phalloidin and cytochalasin, before acidic stimulation did not affect TRC pHi, but did result in an altered TRC volume change. I conclude that a decrease in TRC pHi induces cell shrinkage via the actin cytoskeleton. Cell shrinkage as a result of a change in pHi activates NHE1 to restore TRC pHi and volume.

Growth hormone (GH) was upregulated in the zebrafish inner ear following sound exposure in a previous study. To identify the specific role of GH in hair cell regeneration and the possible cellular mechanisms of this regeneration, groups of zebrafish were divided into baseline (no sound exposure, no injection), buffer-injected and GH-injected groups. Buffer- and GH-injected fish were exposed to a 150 Hz tone at a source level of 179 dB re 1 μPa root mean squared (RMS) for 36 h. Phalloidin-staining was used to assess the effects of GH on hair cell bundle density; BrdU-labeling was used to assess the effects of GH on cellular proliferation; TUNEL-labeling was used to assess the effects of GH on apoptosis in the zebrafish inner ear following acoustic trauma. The time-course of hair cell bundle density, cell proliferation, and apoptosis was established by combining data for baseline fishes and sound-exposed fishes at post-sound exposure day 1 (psed1), psed2, and psed3. GH-injected fish exhibited greater densities of hair cells than bufferinjected controls. In addition, GH-injected fish had higher levels of cell proliferation and lower levels of apoptosis than buffer-injected controls. This suggests that GH may play an important role in zebrafish inner ear hair cell regeneration by stimulating cellular proliferation and inhibiting cellular apoptosis.

Nemertodermatida is a group of microscopic marine worm-like animals that live as part of the marine meiofauna in sandy or muddy sediments; one species lives commensally in a holothurian. These benthic worms were thought to disperse passively with ocean currents, resulting in little speciation and thus wide or even cosmopolitan distributions. Individuals occur in low abundance and have few light microscopically available characters, which altogether may explain why only eight species had been described between the discovery of the taxon in 1930 and this thesis. We used molecular methods to address the diversity and phylogeny of this group for the first time. In a study of two nominal species with samples from all around the world, a high degree of cryptic speciation was discovered and several new species described. Diagnoses were based on molecular data complemented by morphological characters, where available. Given the patchy geographical record it can be assumed that the majority of the biodiversity of Nemertodermatida is yet to be described. A phylogenetic study including all but three known species revealed a deep divergence between the two families of Nemertodermatida but non-monophyly of the taxon was rejected by an Approximately Unbiased test. Confocal laser scanning microscopic studies of several species show that the pattern of the body-wall musculature and the nervous system are specific for different genera. The muscular system of all species consists of a basic orthogonal grid with specific diagonal musculature and specialized muscles associated with body openings. The mouth appears to be transient feature in Nemertodermatida, developing only after hatching and being reduced again in mature worms. The nervous system is highly variable with very different ground patterns between the genera, such as an epidermal net, a centralized neuropile or a commissural brain. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4. Manuscript.</p>

This thesis presents a comprehensive phylogenetic and taxonomic study of an acoel subgroup, the Childiidae. Members of this taxon are characterized by well-developed male copulatory organs with conical/cylindrical stylets. The phylogenetic analyses, by means of total evidence approach, based on three molecular markers (18S and 28S rRNA genes and Histone H3) and 50 morphological characters reaffirm the non-monophyly of the Childiidae sensu Dörjes, 1968 (Actinoposthiidae and Childia+Paraphanostoma). The total evidence phylogeny strongly support the Childia+Paraphanostoma clade separate from other former members of the Childiidae, which are now placed in Actinoposthiidae. The monophyly of Childia+Paraphanostoma is well corroborated by several morphological characters. A new taxon Childia is defined, in accordance with the PhyloCode, comprising all former Paraphanostoma species and a member of the monotypic genus C. groenlandica. A new diagnosis for the current members of Childia is provided. Several structures, shown to hold promising phylogenetic signals for unraveling acoel relationships, such as musculature pattern, sperm and male copulatory organs, are investigated, using a combination of traditional and modern techniques (ultrastructure, immunocytochemistry and confocal microscopy), with main focus on Childia and its closest relatives. New characters are described and their phylogenetic significance assessed. Morphological characters relating to body-wall musculature, statocyst muscles, male copulatory organ musculature and ultrastructure, and sperm cytoplasmic granules are shown to carry important phylogenetic signals at lower taxonomic levels, while most of the characters related to sperm ultrastructure are useful at higher taxonomic levels within the Acoela. The data obtained undermine the phylogenetic use of the seminal bursa in Childia. In addition to this, it is shown that most of the classical morphological characters used in acoel taxonomy, obtained using traditional histological methods, may be misleading in identifying monophyletic entities within the Acoela. The most corroborated synapomorphies, identified in this thesis, are used in determining the taxonomic placement of a new viviparous acoel, Childia vivipara, into the taxon Childia.

(EN) This work has been focused on the development and optimization of analytical methodology, using high performance liquid chromatography with diode array detection (HPLC-DAD) and high performance liquid chromatography with diode array and tandem mass spectrometric detection (HPLC-DAD-MS/MS) for the determination of amatoxins (α- and β-amanitin) and phalotoxins (phallacidin and phalloidin) in the crude extract from cap of Amanita phalloides with the option to later use for clinical purposes. In order to guarantee the reliability of the analytical results the influence of various parameters on the quality of the separation and the determination of toxins was studied. The developed HPLC-DAD method achieves good linearity in the concentrations range 1 - 100 µg/ml, with correlation coefficients higher than 0,997. Limits of detection (LOD) and quantitation (LOQ) were calculated for all the studied toxins with following values: for α-amanitin 0,90 µg/ml (LOD); 2,99 µg/ml (LOQ), β-amanitin 1,07 µg/ml (LOD); 3,56 µg/ml (LOQ), phallacidin 2,17 µg/ml (LOD); 7,26 µg/ml (LOQ) and phalloidin 0,79 µg/ml (LOD); 2,64 µg/ml (LOQ). Key words: Amanita phalloides,-amanitin,-amanitin, phallacidin, phalloidin, solid-liquid extraction, HPLC-DAD, HPLC-DAD-MS/MS .