Spatial behaviour in the Aquatic Warbler (Acrocephalus paludicola) during mating and breeding

Summary The range use of both sexes of the Aquatic Warbler was studied during two breeding seasons by radio-tracking. Males used home ranges of up to 8 ha. These home ranges over-lapped by up to 74 %, (mean 51 %) between individuals. During the mating period and prior to nesting, females used isolated sites of 2.8 to 6.4 ha (mean: 4.2 ha) within activity ranges of 100 to 160 ha (mean: 120 ha). Home ranges of different females overlapped by up to 20 %. However, during nest-building and incubation, the average size of home ranges in females was only 1.6 ha. Since no constant ranges were observed, we conclude that Aquatic Warblers are not territorial in the breeding season.

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Räumliches Verhalten des Seggenrohrsängers (Acrocephalus paludicola) während Partnerfindung und Bebrütung

Zusammenfassung In zwei aufeinanderfolgenden Brutzeiten wurde die Raumnutzung von Seggenrohrsängern mittels Telemetrie untersucht. Die ermittelte Größe der Streifgebiete von Männchen betrug in der gesamten Brutzeit bis zu 8 ha. In dem Streifgebiet eines einzelnen Männchens wurden bis zu elf telemetrierte Männchen festgestellt. Die Überlappungen der Streifgebiete telemetrierter Männchen betrugen durchschnittlich 51 %, maximal 74 %. Weibchen nutzten während der Paarungszeit nicht zusammenhängende inselartige Areale von insgesamt 2,8 bis 6,4 ha (Mittelwert 4,2 ha) innerhalb von Aktionsräumen von 110 bis 160 ha (Mittelwert 120 ha). Diese Areale überlappten zu 20 % mit den Aufenthaltsgebieten anderer Weibchen. Während des Brütens sank die Größe der Streifgebiete der Weibchen auf durchschnittlich 1,6 ha. Da im Beobachtungszeitraum keine konstant genutzten Aufenthaltsgebiete vorlagen, schließen wir, daß sich Seggenrohrsänger in der Brutzeit nicht territorial verhalten.

     

Histochemical investigations on sialic acid containing compounds in the CNS of teleosts (author's transl)]

By means of histochemical experiments the qualitative (microphotographs) and quantitative (cytophotometry) distribution of sialic acid containing compounds was investigated in the mesencephalon and cerebellum of Carassius carassius. 1. The perikarya of nerve cells are especially stained by means of Azur A. 2. Nerve fibres, on the other hand, showed positive reactions with colloidal ironhydroxyd (CIH). 3. In different structures of the CNS the intensity of CIH-staining is decreased up to about 55% following treatment with neuraminidase. 4. There are no differences in the reactions of 7 degrees C as compared to 20 degrees C adapted animals.     

Development and altered gravity dependent changes in glucose-6-phosphate dehydrogenase activity in the brain of the cichlid fish Oreochromis Mossambicus

Glucose-6-phosphate dehydrogenase activity was studied in the brain of the cichlid fish Oreochromis mossambicus during early ontogenetic development. In general a slight but continuous decrease in enzyme activity was found (9.5 ± 0.5 nmol substrate cleaved per mg protein and per min at developmental stage 13 {=1 day post hatch at 28°C} to a value of 7.9±0.6 in adult brain). In order to investigate the possible influence of altered gravity during early ontogenetic brain development, fish larvae were exposed to an increased acceleration of three times earth gravity (3 g) or to functional weightlessness in a fast-rotating clinostat for 7 days. A significant increase of brain G6PDH activity of approx. 15% was found after exposure to hyper gravity, whereas a significant decrease of the enzyme activity, 10%, was detected following functional weightlessness in respect to the corresponding 1 g controls.

Analyses concerning the regain of normal control enzyme activity of the larvae revealed dramatic fluctuations within the first 5 h after exposure to an increased acceleration of 3 g. Thereafter, between day 1 and day 3 after exposure, brain glucose-6-phosphate dehydrogenase decreased slowly. At day 3 after exposure no further differences of the hyper-g larvae compared to the controls were found. Only slight changes in total brain glucose-6-phosphate dehydrogenase activity occur during ontogenetic development of cichlid fish. This suggests that a more or less constant enzyme activity is important during brain development, but is reacting very sensitively to changes in the environmental factor gravity.     

Synthesis of the PPARbeta/delta-selective agonist GW501516 and C4-thiazole-substituted analogs

Sequential, position-selective, Pd-catalyzed cross-coupling reactions of 2,4-dibromo-5-hydroxymethylthiazole provided the scaffold for the synthesis of GW501516, the most potent PPARbeta/delta agonist yet described, and equally selective analogs at the thiazole-C4 position.     

Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome

Nager syndrome (MIM #154400) is the best-known preaxial acrofacial dysostosis, mainly characterized by craniofacial and preaxial limb anomalies. The craniofacial abnormalities mainly consist of downslanting palpebral fissures, malar hypoplasia, micrognathia, external ear anomalies, and cleft palate. The preaxial limb defects are characterized by radial and thumb hypoplasia or aplasia, duplication of thumbs and proximal radioulnar synostosis. Haploinsufficiency of SF3B4 (MIM *605593), which encodes SAP49, a component of the pre-mRNA spliceosomal complex, has recently been identified as the underlying cause of Nager syndrome. In our study, we performed exome sequencing in two and Sanger sequencing of SF3B4 in further ten previously unreported patients with the clinical diagnosis of Nager syndrome, including one familial case. We identified heterozygous SF3B4 mutations in seven out of twelve patients. Four of the seven mutations were shown to be de novo; in three individuals, DNA of both parents was not available. No familial mutations were discovered. Three mutations were nonsense, three were frameshift mutations and one T > C transition destroyed the translation start signal. In three of four SF3B4 negative families, EFTUD2 was analyzed, but no pathogenic variants were identified. Our results indicate that the SF3B4 gene is mutated in about half of the patients with the clinical diagnosis of Nager syndrome and further support genetic heterogeneity for this condition.     

Regulator of calcineurin 1 (RCAN1) facilitates neuronal apoptosis through caspase-3 activation

Individuals with Down syndrome (DS) will inevitably develop Alzheimer disease (AD) neuropathology sometime after middle age, which may be attributable to genes triplicated in individuals with DS. The characteristics of AD neuropathology include neuritic plaques, neurofibrillary tangles, and neuronal loss in various brain regions. The mechanism underlying neurodegeneration in AD and DS remains elusive. Regulator of calcineurin 1 (RCAN1) has been implicated in the pathogenesis of DS. Our data show that RCAN1 expression is elevated in the cortex of DS and AD patients. RCAN1 expression can be activated by the stress hormone dexamethasone. A functional glucocorticoid response element was identified in the RCAN1 isoform 1 (RCAN1-1) promoter region, which is able to mediate the up-regulation of RCAN1 expression. Here we show that overexpression of RCAN1-1 in primary neurons activates caspase-9 and caspase-3 and subsequently induces neuronal apoptosis. Furthermore, we found that the neurotoxicity of RCAN1-1 is inhibited by knock-out of caspase-3 in caspase-3(-/-) neurons. Our study provides a novel mechanism by which RCAN1 functions as a mediator of stress- and Aβ-induced neuronal death, and overexpression of RCAN1 due to an extra copy of the RCAN1 gene on chromosome 21 contributes to AD pathogenesis in DS.