3D TIME-LAPSE RESISTIVITY MONITORING OF WATER INFILTRATION INTO A MODEL LEVEE BY MEANS OF A HIGH-SPEED RESISTIVITY MEASUREMENT TOOL

2016 ◽  
Author(s):  
Hiroshi Kisanuki ◽  
Tomio Inazaki ◽  
Sugio Imamura
Author(s):  
W.F. Marshall ◽  
K. Oegema ◽  
J. Nunnari ◽  
A.F. Straight ◽  
D.A. Agard ◽  
...  

The ability to image cells in three dimensions has brought about a revolution in biological microscopy, enabling many questions to be asked which would be inaccessible without this capability. There are currently two major methods of three dimensional microscopy: laser-scanning confocal microscopy and widefield-deconvolution microscopy. The method of widefield-deconvolution uses a cooled CCD to acquire images from a standard widefield microscope, and then computationally removes out of focus blur. Using such a scheme, it is easy to acquire time-lapse 3D images of living cells without killing them, and to do so for multiple wavelengths (using computer-controlled filter wheels). Thus, it is now not only feasible, but routine, to perform five dimensional microscopy (three spatial dimensions, plus time, plus wavelength).Widefield-deconvolution has several advantages over confocal microscopy. The two main advantages are high speed of acquisition (because there is no scanning, a single optical section is acquired at a time by using a cooled CCD camera) and the use of low excitation light levels Excitation intensity can be much lower than in a confocal microscope for three reasons: 1) longer exposures can be taken since the entire 512x512 image plane is acquired in parallel, so that dwell time is not an issue, 2) the higher quantum efficiently of a CCD detect over those typically used in confocal microscopy (although this is expected to change due to advances in confocal detector technology), and 3) because no pinhole is used to reject light, a much larger fraction of the emitted light is collected. Thus we can typically acquire images with thousands of photons per pixel using a mercury lamp, instead of a laser, for illumination. The use of low excitation light is critical for living samples, and also reduces bleaching. The high speed of widefield microscopy is also essential for time-lapse 3D microscopy, since one must acquire images quickly enough to resolve interesting events.


Author(s):  
Mark Kimball

Abstract This article presents a novel tool designed to allow circuit node measurements in a radio frequency (RF) integrated circuit. The discussion covers RF circuit problems; provides details on the Radio Probe design, which achieves an input impedance of 50Kohms and an overall attenuation factor of 0 dB; and describes signal to noise issues in the output signal, along with their improvement techniques. This cost-effective solution incorporates features that make it well suited to the task of differential measurement of circuit nodes within an RF IC. The Radio Probe concept offers a number of advantages compared to active probes. It is a single frequency measurement tool, so it complements, rather than replaces, active probes.


2021 ◽  
Vol 11 (7) ◽  
pp. 3122
Author(s):  
Srujana Neelam ◽  
Audrey Lee ◽  
Michael A. Lane ◽  
Ceasar Udave ◽  
Howard G. Levine ◽  
...  

Since opportunities for spaceflight experiments are scarce, ground-based microgravity simulation devices (MSDs) offer accessible and economical alternatives for gravitational biology studies. Among the MSDs, the random positioning machine (RPM) provides simulated microgravity conditions on the ground by randomizing rotating biological samples in two axes to distribute the Earth’s gravity vector in all directions over time. Real-time microscopy and image acquisition during microgravity simulation are of particular interest to enable the study of how basic cell functions, such as division, migration, and proliferation, progress under altered gravity conditions. However, these capabilities have been difficult to implement due to the constantly moving frames of the RPM as well as mechanical noise. Therefore, we developed an image acquisition module that can be mounted on an RPM to capture live images over time while the specimen is in the simulated microgravity (SMG) environment. This module integrates a digital microscope with a magnification range of 20× to 700×, a high-speed data transmission adaptor for the wireless streaming of time-lapse images, and a backlight illuminator to view the sample under brightfield and darkfield modes. With this module, we successfully demonstrated the real-time imaging of human cells cultured on an RPM in brightfield, lasting up to 80 h, and also visualized them in green fluorescent channel. This module was successful in monitoring cell morphology and in quantifying the rate of cell division, cell migration, and wound healing in SMG. It can be easily modified to study the response of other biological specimens to SMG.


First Break ◽  
2017 ◽  
Vol 35 (8) ◽  
Author(s):  
Atsushi Suzaki ◽  
Shohei Minato ◽  
Ranajit Ghose ◽  
Chisato Konishi ◽  
Naoki Sakai

Author(s):  
Simone Di Prima ◽  
Thierry Winiarski ◽  
Rafael Angulo-Jaramillo ◽  
Ryan D. Stewart ◽  
Mirko Castellini ◽  
...  

<p>Preferential flow is more the rule than the exception, in particular during water infiltration experiments. In this study, we demonstrate the potential of GPR monitoring to detect preferential flows during water infiltration. We monitored time-lapse ground penetrating radar (GPR) surveys in the vicinity of single-ring infiltration experiments and created a three-dimensional (3D) representation of infiltrated water below the devices. For that purpose, radargrams were constructed from GPR transects conducted over two grids (1 m × 1 m) before and after the infiltration tests. The obtained signal was represented in 3D and a threshold was chosen to part the domain into wetted and non-wetted zones, allowing the determination of the infiltration bulb. That methodology was used to detect the infiltration below the devices and clearly pointed at nonuniform flows in correspondence with the heterogeneous soil structures. The protocol presented in this study represents a practical and valuable tool for detecting preferential flows at the scale of a single ring infiltration experiment.</p>


Sign in / Sign up

Export Citation Format

Share Document