Moving towards, against and away from people: the relationship between Karen Horney's interpersonal trends and the enneagram

Different theoretical approaches and interpretations offer diverse delineations and clusters of Enneagram type in terms of Horney’s interpersonal trends of moving toward, moving against and moving away from people. The present study reports the results of an empirical investigation into the relationship between Enneagram type and Horney’s interpersonal trends. A sample of 2 3 participants completed the Test of Object Relations (TOR) and 125 of these participants completed the Horney-Coolidge Tridimensional Inventory (HCTI). Two one-way, between-groups multivariate analyses of variance revealed differences between Enneagram types for each of the HCTI interpersonal trends of compliance, aggression and detachment and the TOR dimensions of separation anxiety, symbiotic merging, narcissism, egocentricity, social isolation and fear of engulfment. For each trend, an Enneagram type could be identified as a unique marker or benchmark of the trend. However, the empirical result does not offer clear support for one theoretical approach or viewpoint rather than another.PsychologyM.A. (Psychology

Development of a flow-fluorescence in situ hybridization protocol for the analysis of microbial communities in anaerobic fermentation liquor

Background: The production of bio-methane from renewable raw material is of high interest because of the increasing scarcity of fossil fuels. The process of biomethanation is based on the inter- and intraspecific metabolic activity of a highly diverse and dynamic microbial community. The community structure of the microbial biocenosis varies between different biogas reactors and the knowledge about these microbial communities is still fragmentary. However, up to now no approaches are available allowing a fast and reliable access to the microbial community structure. Hence, the aim of this study was to originate a Flow-FISH protocol, namely a combination of flow cytometry and fluorescence in situ hybridization, for the analysis of the metabolically active microorganisms in biogas reactor samples. With respect to the heterogenic texture of biogas reactor samples and to collect all cells including those of cell aggregates and biofilms the development of a preceding purification procedure was indispensable. Results: Six different purification procedures with in total 29 modifications were tested. The optimized purification procedure combines the use of the detergent sodium hexametaphosphate with ultrasonic treatment and a final filtration step. By this treatment, the detachment of microbial cells from particles as well as the disbandment of cell aggregates was obtained at minimized cell loss. A Flow-FISH protocol was developed avoiding dehydration and minimizing centrifugation steps. In the exemplary application of this protocol on pure cultures as well as biogas reactor samples high hybridization rates were achieved for commonly established domain specific oligonucleotide probes enabling the specific detection of metabolically active bacteria and archaea. Cross hybridization and autofluorescence effects could be excluded by the use of a nonsense probe and negative controls, respectively. Conclusions: The approach described in this study enables for the first time the analysis of the metabolically active fraction of the microbial communities within biogas reactors by Flow-FISH

Characterization of Bathyarchaeota genomes assembled from metagenomes of biofilms residing in mesophilic and thermophilic biogas reactors

Maus I, Rumming M, Bergmann I, et al. Characterization of Bathyarchaeota genomes assembled from metagenomes of biofilms residing in mesophilic and thermophilic biogas reactors. Biotechnology for Biofuels. 2018;11(1): 167

Forty years of carabid beetle research in Europe - from taxonomy, biology, ecology and population studies to bioindication, habitat assessment and conservation

Volume: 100Start Page: 55End Page: 14

Monitoring of methane producing microflora in full-scale biogas plants in rual area

Die Produktion von Biogas aus landwirtschaftlichen Primärprodukten oder Reststoffen stellt einen we-sentlichen Beitrag zur Reduktion des CO2-Ausstoßes sowie zur Entwicklung einer nachhaltigen Landbewirtschaftung dar. Gegenwärtig stehen im Fokus der Forschung die Entwicklung und Optimierung von Biogasreaktoren und Betriebstechniken sowie die Optimierung der Substratbereitstellung. Über die Zusammensetzung der an der Biogasbildung beteiligten mikrobiellen Lebensgemeinschaften in landwirt-schaftlichen Biogasanlagen gibt es jedoch bis heute nur wenige Informationen. Im Rahmen dieser Studie wurde die Struktur der methanogenen Biozönose in zehn landwirtschaftlichen Biogasanlagen, welche auf Basis von Nachwachsenden Rohstoffen (NawaRo) betrieben wurden, unter-sucht. Hierzu wurde ein polyphasischer Ansatz mit verschiedenen kultivierungsunabhängigen, molekularen Verfahren gewählt. Primär wurde eine PCR-RFLP Analyse der Nukleotidsequenz der 16S rDNA sowie des mcrA Gens durchgeführt. Die Bestimmung der relativen Häufigkeit der Methan bil-denden Mikroorganismen in den Proben erfolgte mittels quantitativer real-time PCR (Q-PCR) auf Basis gruppenspezifischer Primer für das 16S rDNA Gen. Für ausgewählte Biogasreaktoren wurde ergänzend eine mikroskopische Quantifizierung mittels Fluoreszenz in situ Hybridisierung (FISH) durchgeführt. Für die FISH wurden spezifische Sonden für die Domänen Bacteria (EUB338) und Archaea (ARCH915) so-wie für die Ordnungen Methanomicrobiales (MG1200), Methanobacteriales (MB311 und MB1174) und den Familien Methanosarcinaceae (Ms821) und Methanosaetaceae (Mx825) verwendet. Die Ergebnisse der Analysen zeigten, dass in neun der zehn untersuchten Biogasanlagen die hydroge-notrophen Methanogenen, repräsentiert durch Vertreter der Ordnungen Methanomicrobiales und Methanobacteriales, vorherrschend waren. In diesen Biogasreaktoren wurde die Gattung Methanoculleus (Ordnung Methanomicrobiales) als dominierende Gattung nachgewiesen. Nennenswerte Anteile an ace-toklastischen Methanbildnern, insbesondere der Gattung Methanosaeta, konnten für sechs der untersuchten zehn Anlagen nachgewiesen werden. Jedoch wurde nur in einer Biogasanlage diese Gattung als die dominierende Gruppe von Methanbildnern nachgewiesen. Diese Ergebnisse deuten darauf hin, dass in 90 % der untersuchten Biogasanlagen die hydrogenotrophe Methanogenese der vorrangige Stoff-wechselweg für die Methanproduktion ist. In dieser Studie konnte kein Zusammenhang zwischen den jeweils zur Biogasgewinnung eingesetzten Substraten und der Struktur der Archaea-Biozönose beobachtet werden. Ebenso wenig scheinen unter-schiedliche Verweilzeiten der Substrate sowie die Raumbelastung der Reaktoren einen Einfluss auf die methanogenen Archaea zu haben. Jedoch ließ sich ein negativer Einfluss hoher Ammonium- bzw. Am-moniakkonzentrationen auf das Wachstum acetoklastischer Methanbildner, insbesondere Methanosaeta spp., in den untersuchten landwirtschaftlichen Biogasanlagen feststellen. Die aus dieser Studie gewonnenen Erkenntnisse dienen dem grundlegenden Verständnis der methanoge-nen Lebensgemeinschaft in landwirtschaftlichen Biogasanlagen, und sollen somit zur weiteren Optimierung der Biogasgewinnung beitragen.Biogas production from agricultural main products or remnants provides a substantial contribution to the reduction of CO2 emissions but also to the development of a sustainable agriculture. Currently, the re-search focuses on development and optimization of biogas reactors and reactor performance as well as optimization of substrate eligibility. However, the knowledge of the structure and dynamics of microbial communities which are involved in the biogas production is still insufficient. Within this study, the structures of methanogenic biocoenosis in ten agricultural biogas plants which are operated on basis of renewable raw materials were analyzed. Therefore a polyphasic approach with differ-ent culture independent molecular genetic techniques was chosen. First, PCR-RFLP analyses of 16S rDNA and mcrA genes were conducted. For determination of the relative abundance of methane pro-ducing microorganisms in the samples a quantitative real-time PCR (Q-PCR) on basis of 16S rDNA group-specific primers was applied. Fluorescence in situ hybridization (FISH) was carried out for direct quantification of methanogenic cells in reactor contents of six of the ten biogas plants. FISH was carried out with specific probes for the domains Bacteria (EUB338) and Archaea (ARCH915), the orders Metha-nomicrobiales (MG1200) and Methanobacteriales (MB311 and MB1174) and the families Methanosarcinaceae (Ms821) and Methanosaetaceae (Mx825). The results of the analyses showed, that in nine of the ten biogas plants the hydrogenotrophic methano-gens, represented by the orders Methanomicrobiales and Methanobacteriales, were prevalent. The genus Methanoculleus (Methanomicrobiales) was the predominating genus in these biogas plants. Acetoclastic methanogens such as organisms of the genus Methanosaeta were found only in six of the ten analyzed biogas plants. However, in one biogas plant Methanosaeta was determined as the predominant methano-genic group. These results indicate that the hydrogenotrophic methanogenesis was the major metabolic pathway for methane production in 90 % of the analyzed biogas plants. In this study, no correlation between used substrates for biogas production and the structure of Archaea biocoenosis could be observed. Also, the retention time of substrates and the organic loading rate of reac-tors seemed to have no obvious effect on the methanogenic Archaea. However, in the analyzed biogas plants a negative influence of high ammonium and ammonia concentrations, respectively, on the growth of acetoclastic methanogens in particular Methanosaeta spp. was determined. The results of this study serve the basic understanding of the methanogen community in agricultural bio-gas plants and are to contribute to further optimization of biogas production