4,489 research outputs found

    Replica-symmetry breaking in dynamical glasses

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    Systems of globally coupled logistic maps (GCLM) can display complex collective behaviour characterized by the formation of synchronous clusters. In the dynamical clustering regime, such systems possess a large number of coexisting attractors and might be viewed as dynamical glasses. Glass properties of GCLM in the thermodynamical limit of large system sizes NN are investigated. Replicas, representing orbits that start from various initial conditions, are introduced and distributions of their overlaps are numerically determined. We show that for fixed-field ensembles of initial conditions, as used in previous numerical studies, all attractors of the system become identical in the thermodynamical limit up to variations of order 1/N1/\sqrt{N} because the initial value of the coupling field is characterized by vanishing fluctuations, and thus replica symmetry is recovered for NN\to \infty . In contrast to this, when random-field ensembles of initial conditions are chosen, replica symmetry remains broken in the thermodynamical limit.Comment: 19 pages, 18 figure

    Development and field assessment of a quantitative PCR for the detection and enumeration of the noxious bloom-former Anabaena planktonica

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    Anabaena planktonica is a harmful, bloom-forming freshwater cyanobacterium, which has arrived recently in New Zealand. In the short time since its incursion (<10 yr), A. planktonica has spread rapidly throughout lakes in the North Island. To date, the identification and enumeration of A. planktonica has been undertaken using light microscopy. There is an urgent demand for a highly sensitive and specific quantitative detection method that can be combined with a high sample processing capability in order to increase sampling frequency. In this study, we sequenced 36 cyanobacterial 16S rRNA genes (partial), complete intergenic transcribed spacers (ITS), and 23S rRNA genes (partial) of fresh-water cyanobacteria found in New Zealand. The sequences were used to develop an A. Planktonica specific TaqMan QPCR assay targeting the long ITS1-L and the 5´ terminus of the 23S rRNA gene. The QPCR method was linear (R2 = 0.999) over seven orders of magnitude with a lower end sensitivity of approximately five A. planktonica cells in the presence of exogenous DNA. The quantitative PCR (QPCR) method was used to assess the spatial distribution and seasonal population dynamics of A. planktonica from the Lower Karori Reservoir (Wellington, New Zealand) over a five-month period. The QPCR results were compared directly to microscopic cell counts and found to correlate significantly (95% confidence level) under both bloom and non-bloom conditions. The current QPCR assay will be an invaluable tool for routine monitoring programs and in research investigating environmental factors that regulate the population dynamics and the blooming of A. planktonica

    Kesulitan Mahasiswa Ppg Pendidikan Fisika Fkip Unsyiah dalam Melaksanakan Program Pengalaman Lapangan di Banda Aceh

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    This research aimed to determine the difficulties of PPG students of Physics education FKIP Unsyiah in implemented teaching experience program in Banda Aceh. This research is a descriptive research type using a qualitative approach. The subject of this research were PPG student of physics education FKIP Unsyiah who implemented the teaching experience program in Banda Aceh in the academic year 2016/2017 which amounted to 15 students. Data collection in this research used questionnaire technique and data analysis technique used percentage test. Based on the data analysis result, it is found that the difficulties of PPG students of physics education FKIP Unsyiah in conducting lesson opening activities were low, the difficulties in mastering the learning material were low, the difficulties in implementing educational learning strategies were low, the difficulties in applying the scientific approach were very low, the dificulities in resourcing utilization and instructional media were low, the difficulties in involving students in learning were very low, and the difficulties in closing lessons activities were very low. Overall the difficulty level of PPG students of physics education FKIP Unsyiah in implemented the teaching experience program (PPL) were low with percentage of difficulty was 36,8%, which showed that PPG students of physics education FKIP Unsyiah have no difficulties in implementing teaching experience program (PPL) in Banda Aceh

    No evidence for a culturable bacterial tetrodotoxin producer in Pleurobranchaea maculata (Gastropoda: Pleurobranchidae) and Stylochoplana sp. (Platyhelminthes: Polycladida)

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    Tetrodotoxin (TTX) is a potent neurotoxin found in the tissues of many taxonomically diverse organisms. Its origin has been the topic of much debate, with suggestions including endogenous production, acquisition through diet, and symbiotic bacterial synthesis. Bacterial production of TTX has been reported in isolates from marine biota, but at lower than expected concentrations. In this study, 102 strains were isolated from Pleurobranchaea maculata (Opisthobranchia) and Stylochoplana sp. (Platyhelminthes). Tetrodotoxin production was tested utilizing a recently developed sensitive method to detect the C9 base of TTX via liquid chromatography—mass spectrometry. Bacterial strains were characterized by sequencing a region of the 16S ribosomal RNA gene. To account for the possibility that TTX is produced by a consortium of bacteria, a series of experiments using marine broth spiked with various P. maculata tissues were undertaken. Sixteen unique strains from P. maculata and one from Stylochoplana sp. were isolated, representing eight different genera; Pseudomonadales, Actinomycetales, Oceanospirillales, Thiotrichales, Rhodobacterales, Sphingomonadales, Bacillales, and Vibrionales. Molecular fingerprinting of bacterial communities from broth experiments showed little change over the first four days. No C9 base or TTX was detected in isolates or broth experiments (past day 0), suggesting a culturable microbial source of TTX in P. maculata and Stylochoplana sp. is unlikely
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