This dataset is affiliated with the publication https://doi.org/10.1007/s00348-022-03455-0. All of the data provided is necessary to reproduce the results with the aforementioned publication. The data in this repository is for the wake of a wind turbine at high Reynolds numbers. The data is mainly used for reproducing the statistics (deficit and variance profiles) and the phase averaged results.
Kiefer, Janik; Brunner, Claudia E.; Hansen, Martin O. L.; Hultmark, Marcus
Abstract:
This data set contains data of a NACA 0021 airfoil as it undergoes upward ramp-type pitching motions at high Reynolds numbers and low Mach numbers. The parametric study covers a wide range of chord Reynolds numbers, reduced frequencies and pitching geometries characterized by varying mean angle and angle amplitude. The data were acquired in the High Reynolds number Test Facility at Princeton University, which is a closed-loop wind tunnel that can be pressurized up to 23 MPa and allowed for variation of the chord Reynolds number over a range of 5.0 × 10^5 ≤ Re_c ≤ 5.5 × 10^6. Data were acquired using 32 pressure taps along the surface of the airfoil. The data are the phase-averaged results of 150 individual half-cycles for any given test case.
This is the raw experimental dataset and the corresponding code to reproduce plots from the paper "Shear-induced migration of confined flexible fibers".
Brunner, Claudia E.; Kiefer, Janik; Hansen, Martin O. L.; Hultmark, Marcus
Abstract:
Reynolds number effects on the aerodynamics of the moderately thick NACA 0021 airfoil were experimentally studied by means of surface-pressure measurements. The use of a high-pressure wind tunnel allowed for variation of the chord Reynolds number over a range of 5.0 × 10^5 ≤ Re_c ≤ 7.9 × 10^6. The angle of attack was incrementally increased and decreased over a range of 0° ≤ alpha ≤ 40°, spanning both the attached and stalled regime at all Reynolds numbers. As such, attached and separated conditions, as well as the static stall and reattachment processes were studied. A fundamental change in the flow behaviour was observed around Re_c= 2.0 × 10^6. As the Reynolds number was increased beyond this value, the stall type gradually shifted from trailing-edge stall to leading-edge stall. The stall angle and the maximum lift coefficient increased with Reynolds number. Once the flow was separated, the separation point moved upstream and the suction peak decreased in magnitude with increasing Reynolds number. Two distinct types of hysteresis in reattachment were observed.
The data provided in this DataSpace consists of sample training data to be used for Fluorescence Reconstruction Microscopy (FRM) testing. We provide a subset of the keratinocyte (10x magnification) dataset used in our paper, in which interested parties may find more complete information about our data collection methods. Matched pairs of phase contrast and fluorescent images are given. The nuclei were stained using Hoechst 33342 and imaged using a standard DAPI filter set.
The data provided in this DataSpace consists of sample training data to be used for Fluorescence Reconstruction Microscopy (FRM) testing. We provide a subset of the MDCK (20x magnification) dataset used in our paper, in which interested parties may find more complete information about our data collection methods. Matched pairs of DIC and fluorescent images are given. The cells stably expressed E-cadherin:RFP which enabled imaging of junctional fluorescence, while the nuclei were stained using Hoechst 33342 and imaged using a standard DAPI filter set.
We provide all the test data and corresponding predictions for our paper, “Practical Fluorescence Reconstruction Microscopy for High-Content Imaging”. Please refer to the Methods section in this paper for experimental details. For each experimental condition, we provide the input transmitted-light images (either phase contrast or DIC), the ground truth fluorescence images, and the output predicted fluorescence images which should reconstruct the ground truth fluorescence images.
This is the dataset for the plots presented in the article "CO2-leakage-driven diffusiophoresis causes spontaneous accumulation of charged materials in channel flow."
Force-driven parallel shear flow in a spatially periodic domain is shown to be linearly unstable
with respect to both the Reynolds number and the domain aspect ratio. This finding is confirmed
by computer simulations, and a simple expression is derived to determine stable flow conditions.
Periodic extensions of Couette and Poiseuille flows are unstable at Reynolds numbers two orders
of magnitude smaller than their aperiodic equivalents because the periodic boundaries impose
fundamentally different constraints. This instability has important implications for designing computational models of nonlinear dynamic processes with periodicity.
Ant colonies regulate activity in response to changing conditions without using centralized control. Harvester ant colonies forage in the desert for seeds, and their regulation of foraging manages a tradeoff between spending and obtaining water. Foragers lose water while outside in the dry air, but the colony obtains water by metabolizing the fats in the seeds they eat. Previous work shows that the rate at which an outgoing forager leaves the nest depends on its recent experience of brief antennal contact with returning foragers that carry a seed. We examine how this process can yield foraging rates that are robust to uncertainty and responsive to temperature and humidity across minutes to hour-long timescales. To explore possible mechanisms, we develop a low-dimensional analytical model with a small number of parameters that captures observed foraging behavior. The model uses excitability dynamics to represent response to interactions inside the nest and a random delay distribution to represent foraging time outside the nest. We show how feedback of outgoing foragers returning to the nest stabilizes the incoming and outgoing foraging rates to a common value determined by the ``volatility’’ of available foragers. The model exhibits a critical volatility above which there is sustained foraging at a constant rate and below which there is cessation of foraging. To explain how the foraging rates of colonies adjust to temperature and humidity, we propose a mechanism that relies on foragers modifying their volatility after they leave the nest and get exposed to the environment. Our study highlights the importance of feedback in the regulation of foraging activity and points to modulation of volatility as a key to explaining differences in foraging activity in response to conditions and across colonies. Our results present opportunities for generalization to other contexts and systems with excitability and feedback across multiple timescales.
