@article{BeckenbachScheidweiler2016,
  author    = {Beckenbach, Isabel and Scheidweiler, Robert},
  title     = {Perfect ƒ-Matchings and ƒ-Factors in Hypergraphs - A Combinatorial Approach},
  series = {Discrete Mathematics},
  volume    = {240},
  journal   = {Discrete Mathematics},
  number    = {10},
  publisher = {Elsevier},
  address   = {Amsterdam},
  issn      = {2192-7782},
  doi       = {10.1016/j.disc.2017.05.005},
  pages     = {2499 -- 2506},
  year      = {2016},
  abstract  = {We prove characterizations of the existence of perfect ƒ-matchings in uniform mengerian and perfect hypergraphs. Moreover, we investigate the ƒ-factor problem in balanced hypergraphs. For uniform balanced hypergraphs we prove two existence theorems with purely combinatorial arguments, whereas for non-uniform balanced hypergraphs we show that the ƒ-factor problem is NP-hard.},
  language  = {en}
}
@article{BeckBuchleitnerFerreinetal.2014,
  author    = {Beck, Daniel and Buchleitner, Martin and Ferrein, Alexander and Niem{\"u}ller, Tim and Steinbauer, Gerald},
  title     = {Mostly Harmless \& AllemaniACs - mixed innovations},
  pages     = {1 -- 8},
  year      = {2014},
  language  = {en}
}
@article{BechtSchollmayerMonakhovaetal.2021,
  author    = {Becht, Alexander and Schollmayer, Curd and Monakhova, Yulia and Holzgrabe, Ulrike},
  title     = {Tracing the origin of paracetamol tablets by near-infrared, mid-infrared, and nuclear magnetic resonance spectroscopy using principal component analysis and linear discriminant analysis},
  series = {Analytical and Bioanalytical Chemistry},
  volume    = {413},
  journal   = {Analytical and Bioanalytical Chemistry},
  publisher = {Springer Nature},
  issn      = {1618-2650},
  doi       = {10.1007/s00216-021-03249-z},
  pages     = {3107 -- 3118},
  year      = {2021},
  abstract  = {Most drugs are no longer produced in their own countries by the pharmaceutical companies, but by contract manufacturers or at manufacturing sites in countries that can produce more cheaply. This not only makes it difficult to trace them back but also leaves room for criminal organizations to fake them unnoticed. For these reasons, it is becoming increasingly difficult to determine the exact origin of drugs. The goal of this work was to investigate how exactly this is possible by using different spectroscopic methods like nuclear magnetic resonance and near- and mid-infrared spectroscopy in combination with multivariate data analysis. As an example, 56 out of 64 different paracetamol preparations, collected from 19 countries around the world, were chosen to investigate whether it is possible to determine the pharmaceutical company, manufacturing site, or country of origin. By means of suitable pre-processing of the spectra and the different information contained in each method, principal component analysis was able to evaluate manufacturing relationships between individual companies and to differentiate between production sites or formulations. Linear discriminant analysis showed different results depending on the spectral method and purpose. For all spectroscopic methods, it was found that the classification of the preparations to their manufacturer achieves better results than the classification to their pharmaceutical company. The best results were obtained with nuclear magnetic resonance and near-infrared data, with 94.6\%/99.6\% and 98.7/100\% of the spectra of the preparations correctly assigned to their pharmaceutical company or manufacturer.},
  language  = {en}
}
@article{BechstedtHaasHackeretal.1985,
  author    = {Bechstedt, U. and Haas, H. and Hacker, U. and Hardt, Arno and Henn, K. and Martin, S. and Wimmer, J.},
  title     = {Magnets for the German Spallation Source SNQ},
  series = {IEEE transactions on nuclear science. Vol. 32, iss. 5},
  journal   = {IEEE transactions on nuclear science. Vol. 32, iss. 5},
  issn      = {1558-1578 (E-Journal); 0018-9499 (Print)},
  pages     = {3631 -- 3633},
  year      = {1985},
  language  = {en}
}
@article{BayonValeroGarciaBartualetal.2016,
  author    = {Bayon, Arnau and Valero, Daniel and Garcia-Bartual, Rafael and Vall{\´e}s-Mor{\´a}n, Francisco Jos{\´e} and L{\´o}pez-Jim{\´e}nez, P. Amparo},
  title     = {Performance assessment of OpenFOAM and FLOW-3D in the numerical modeling of a low Reynolds number hydraulic jump},
  series = {Environmental Modelling \& Software},
  volume    = {80},
  journal   = {Environmental Modelling \& Software},
  publisher = {Elsevier},
  address   = {Amsterdam},
  isbn      = {1364-8152},
  doi       = {10.1016/j.envsoft.2016.02.018},
  pages     = {322 -- 335},
  year      = {2016},
  abstract  = {A comparative performance analysis of the CFD platforms OpenFOAM and FLOW-3D is presented, focusing on a 3D swirling turbulent flow: a steady hydraulic jump at low Reynolds number. Turbulence is treated using RANS approach RNG k-ε. A Volume Of Fluid (VOF) method is used to track the air-water interface, consequently aeration is modeled using an Eulerian-Eulerian approach. Structured meshes of cubic elements are used to discretize the channel geometry. The numerical model accuracy is assessed comparing representative hydraulic jump variables (sequent depth ratio, roller length, mean velocity profiles, velocity decay or free surface profile) to experimental data. The model results are also compared to previous studies to broaden the result validation. Both codes reproduced the phenomenon under study concurring with experimental data, although special care must be taken when swirling flows occur. Both models can be used to reproduce the hydraulic performance of energy dissipation structures at low Reynolds numbers.},
  language  = {en}
}
@article{BayerTemizArtmannDigeletal.2020,
  author    = {Bayer, Robin and Temiz Artmann, Ayseg{\"u}l and Digel, Ilya and Falkenstein, Julia and Artmann, Gerhard and Creutz, Till and Hescheler, J{\"u}rgen},
  title     = {Mechano-pharmacological testing of L-Type Ca²⁺ channel modulators via human vascular celldrum model},
  series = {Cellular Physiology and Biochemistry},
  volume    = {54},
  journal   = {Cellular Physiology and Biochemistry},
  publisher = {Cell Physiol Biochem Press},
  address   = {D{\"u}sseldorf},
  issn      = {1421-9778},
  doi       = {10.33594/000000225},
  pages     = {371 -- 383},
  year      = {2020},
  abstract  = {Background/Aims: This study aimed to establish a precise and well-defined working model, assessing pharmaceutical effects on vascular smooth muscle cell monolayer in-vitro. It describes various analysis techniques to determine the most suitable to measure the biomechanical impact of vasoactive agents by using CellDrum technology. Methods: The so-called CellDrum technology was applied to analyse the biomechanical properties of confluent human aorta muscle cells (haSMC) in monolayer. The cell generated tensions deviations in the range of a few N/m² are evaluated by the CellDrum technology. This study focuses on the dilative and contractive effects of L-type Ca²⁺ channel agonists and antagonists, respectively. We analyzed the effects of Bay K8644, nifedipine and verapamil. Three different measurement modes were developed and applied to determine the most appropriate analysis technique for the study purpose. These three operation modes are called, particular time mode" (PTM), "long term mode" (LTM) and "real-time mode" (RTM). Results: It was possible to quantify the biomechanical response of haSMCs to the addition of vasoactive agents using CellDrum technology. Due to the supplementation of 100nM Bay K8644, the tension increased approximately 10.6\% from initial tension maximum, whereas, the treatment with nifedipine and verapamil caused a significant decrease in cellular tension: 10nM nifedipine decreased the biomechanical stress around 6,5\% and 50nM verapamil by 2,8\%, compared to the initial tension maximum. Additionally, all tested measurement modes provide similar results while focusing on different analysis parameters. Conclusion: The CellDrum technology allows highly sensitive biomechanical stress measurements of cultured haSMC monolayers. The mechanical stress responses evoked by the application of vasoactive calcium channel modulators were quantified functionally (N/m²). All tested operation modes resulted in equal findings, whereas each mode features operation-related data analysis.},
  language  = {en}
}
@article{BaumgartnerFidlerWethetal.2008,
  author    = {Baumgartner, Werner and Fidler, Florian and Weth, Agnes and Habbecke, Martin and Jakob, Peter and Butenweg, Christoph and B{\"o}hme, Wolfgang},
  title     = {Investigating the locomotion of the sandfish in desert sand using NMR-Imaging},
  series = {PLOS ONE},
  volume    = {3},
  journal   = {PLOS ONE},
  number    = {10},
  publisher = {Plos},
  address   = {San Francisco, California, US},
  issn      = {1932-6203},
  doi       = {10.1371/journal.pone.0003309},
  pages     = {e3309},
  year      = {2008},
  abstract  = {The sandfish (Scincus scincus) is a lizard having the remarkable ability to move through desert sand for significant distances. It is well adapted to living in loose sand by virtue of a combination of morphological and behavioural specializations. We investigated the bodyform of the sandfish using 3D-laserscanning and explored its locomotion in loose desert sand using fast nuclear magnetic resonance (NMR) imaging. The sandfish exhibits an in-plane meandering motion with a frequency of about 3 Hz and an amplitude of about half its body length accompanied by swimming-like (or trotting) movements of its limbs. No torsion of the body was observed, a movement required for a digging-behaviour. Simple calculations based on the Janssen model for granular material related to our findings on bodyform and locomotor behaviour render a local decompaction of the sand surrounding the moving sandfish very likely. Thus the sand locally behaves as a viscous fluid and not as a solid material. In this fluidised sand the sandfish is able to "swim" using its limbs.},
  language  = {en}
}
@article{BaumannTillmannAletsee1989,
  author    = {Baumann, Marcus and Tillmann, U. and Aletsee, L.},
  title     = {Distribution of Carbon Among Photosynthetic End Products in the Bloom-Forming Arctic Diatom Thalassiosira antarctica COMBER / Tillmann, U. ; Baumann, M.E.M. ; Aletsee, L.},
  series = {Polar Biology. 10 (1989), H. 3},
  journal   = {Polar Biology. 10 (1989), H. 3},
  isbn      = {0722-4060},
  pages     = {231 -- 238},
  year      = {1989},
  language  = {en}
}
@article{BaumannThomasGleitz1992,
  author    = {Baumann, Marcus and Thomas, D. and Gleitz, M.},
  title     = {Efficiency of carbon assimilation and photoacclimation in a small unicellular Chaetoceros species from the Weddel Sea (Antarctica): Influence of temperature and irridiance / Thomas, D. ; Baumann, M.E.M. ; Gleitz, M.},
  series = {Journal of Experimental Marine Biology and Ecology. 157 (1992), H. 2},
  journal   = {Journal of Experimental Marine Biology and Ecology. 157 (1992), H. 2},
  isbn      = {0022-0981},
  pages     = {195 -- 209},
  year      = {1992},
  language  = {en}
}
@article{BaumannSemenehDehairsetal.1998,
  author    = {Baumann, Marcus and Semeneh, M. and Dehairs, F. and Elskens, M.},
  title     = {Nitrogen uptake regime and phytoplankton community structure in the Southern Ocean / Semeneh, M. ; Dehairs, F. ; Elskens, M. ; Baumann, M.E.M. ; Kopczynska, E.E. ; Lancelot, C. ; Goeyens, L.},
  series = {Journal of Marine Systems. 17 (1998), H. 1-4},
  journal   = {Journal of Marine Systems. 17 (1998), H. 1-4},
  isbn      = {0924-7963},
  pages     = {159 -- 177},
  year      = {1998},
  language  = {en}
}