scholarly journals Historiography of Arabic influences on Mozarabic: theory and history (711–1492)

2021 ◽  
Vol 1 (3) ◽  
pp. 83-91
Author(s):  
Софья Хосуева
Keyword(s):  
Language Contact ◽  
Three Dimensions ◽  
Research Centers ◽  
Research Papers

The present research focuses on the historiographic aspect of Arabic influence on Mozarabic between 711 and 1492. Among the goals of the present research, we cannot but mention: 1) consideration of the most explored issues in Mozarabic studies; 2) identification of the research centers and names related to Mozarabic studies; 3) systematization of contents of the most significant works and research papers on the above-mentioned topic; 4) review of the language contacts that have taken place during the selected period as reflected in the accessible literature. The studies of this topic are far from being numerous while the trace of medieval Arab Spain remains visible by now in a variety of forms that make the chosen topic relevant. Regarding the outcomes of the work, it has been shown that the problem under analysis is not among the most researched ones; geographically it is mostly connected with Spain; the suggested works of scholars have some noticeable drawbacks and, lastly, the sphere of language contact being applied to the issue is underdeveloped and can be viewed via or on the level of three dimensions: 1) phonetical; 2) lexical and 3) graphical.

scholarly journals Introducing and testing an advanced quantitative methodological approach for the evaluation of research centers: a case study on sustainability science

2019 ◽  
Vol 29 (2) ◽  
pp. 135-149 ◽  
Author(s):  
Omar Kassab ◽  
Rüdiger Mutz ◽  
Hans-Dieter Daniel
Keyword(s):  
Sustainability Science ◽  
Research Evaluation ◽  
Methodological Approach ◽  
Research Performance ◽  
Three Dimensions ◽  
Research Center ◽  
Research Centers ◽  
Evaluation Approach ◽  
Ex Post ◽  
Global University

Abstract With the growing complexity of societal and scientific problems, research centers have emerged to facilitate the conduct of research beyond disciplinary and institutional boundaries. While they have become firmly established in the global university landscape, research centers raise some critical questions for research evaluation. Existing evaluation approaches designed to assess universities, departments, projects, or individual researchers fail to capture some of the core characteristics of research centers and their participants, including the diversity of the involved researchers, at what point in time they join and leave the research center, or the intensity of their participation. In addressing these aspects, this article introduces an advanced approach for the ex post evaluation of research centers. It builds on a quasi-experimental within-group design, bibliometric analyses, and multilevel statistics to assess average and individual causal effects of research center affiliation on participants along three dimensions of research performance. The evaluation approach is tested with archival data from a center in the field of sustainability science. Against a widely held belief, we find that participation in research centers entails no disadvantages for researchers as far as their research performance is concerned. However, individual trajectories varied strongly.

Special Issue on J-GRID (Japan Initiative for Global Research Network on Infectious Disease)

2014 ◽  
Vol 9 (5) ◽  
pp. 765-767
Author(s):  
Sumio Shinoda
Keyword(s):  
Infectious Diseases ◽  
Phase Ii ◽  
Collaborative Research ◽  
Research Network ◽  
World Health ◽  
Research Centers ◽  
Health Statistics ◽  
Special Issue ◽  
Research Papers ◽  
Set Up

In the developed countries including Japan, malignant tumor (cancer), heart disease and cerebral apoplexy are major causes of death, but infectious diseases still responsible for high mortality in the developing countries, especially for children less than 5 years of age. World Health Statistics published byWHO indicates a high percentage of mortality from infectious diseases such as HIV/AIDS, diarrhea, measles, malaria and pneumonia in children of South and Southeast Asian and African countries (World Health Statistics 2014,World Health Organization). Many of these infectious diseases have the potential for borderless transmission and invasion to Japan. Given this situation, Japan’s Ministry of Education, Culture, Sports, Science and Technology (MEXT) introduced Phase I of a program “Founding Research Centers for Emerging and Reemerging Infectious Diseases,” running from fiscal 2005 to 2009 and involving 8 Japanese universities and 2 Japanese research centers. The program was established to: 1) Create of a domestic research structure to promote the accumulation of fundamental knowledge about infectious diseases, 2) Set up 13 overseas research collaboration centers in 8 countries at high risk of emerging and reemerging infections, Japanese researchers are stationed at these centers, where they conduct research in partnership with overseas instructors, 3) Develop a network among domestic and overseas research centers, 4) Develop human resources. The program, supervised by MEXT, and managed by the RIKEN Center of the Research Network for Infectious Diseases (Riken CRNID). Dr. Yoshiyuki Nagai, Program Director (PD), heads CRNID and is organizing the program. Phase II of the program was set up as the Japan Initiative for the Global Research Network on Infectious Diseases (J-GRID) and was established for fiscal 2010-2014. Participating universities, institutes and countries in J-GRID are as follows: Hokkaido University : Zambia Tohoku University : Philippines The University of Tokyo : China Tokyo Medical and Dental University : Ghana Osaka University : Thailand Kobe University : Indonesia Okayama University : India Nagasaki University : Vietnam Kenya (Associate*) Niigata University : Myanmar (Associate*) National Center for Global Health and Medicine : Vietnam National Institute of Animal Health : Thailand *Two associate members were involved in 2011. Each university and institute set up its collaborative research center in a country and conducts research on infectious diseases, especially typical regional diseases. The program’s outcome of each collaborative center is announced by the publication of various research papers or outreach programs, such as open lectures for citizens, and so on. The Asian-African Research Forum (AARF) on Infectious Disease organized by J-GRID is dedicated to reporting and discussing the research results of the collaborative research centers. Details and activities of J-GRID can be seen at http://www.crnid.riken.jp/jgrid/. The Figs. 1 and 2 show examples of the home page indicating the countries and the collaborative research institutes involved. J-GRID publishes the magazine entitled “Monthly CRNID,” which is available by mail upon request to “https://krs.bz/crnid/m?f=2&m=1110&t=8cdk&v=076691d2.” This publication contains various topical information on infectious diseases, such as research papers, newly announced news from WHO, overseas trip news, domestic infections, new drug developments, explanations, events, etc. Phase II will terminate on March 2015 (the end of FY 2014), and Phase III will begin in April 2015 at the start of the new FY. This special issue on J-GRID is being edited on the occasion of the final year of Phase II. The outlines of J-GRID and those of all the collaborative research centers are reviewed by Dr. Nagai, PD of CRNID, and the representatives of each respective collaborative center in this issue. Finally, I extend my sincere thanks to all authors and reviewers involved in this special issue.

scholarly journals Accuracy of Ultrasound Measurements by Novices: Pixels or Voxels

2011 ◽  
Vol 5 (3) ◽  
pp. 303-309 ◽  
Author(s):  
Tho Quynh Nguyen ◽  
Melanie Flores
Keyword(s):  
Three Dimensional ◽  
3D Ultrasound ◽  
Three Dimensions ◽  
Two Dimensional ◽  
3D Image ◽  
Volume Data ◽  
Research Papers ◽  
The World ◽  
Ultrasound Measurements ◽  
2D Ultrasound

ABSTRACT During the last two decades three-dimensional (3D) ultrasound has become increasingly popular around the world. There have been a great number of research papers studying its feasibility as well as reliability and accuracy. Compared to two-dimensional (2D), 3D ultrasound produces better visualization with minimal probe manipulation. The sonographer performing 2D ultrasound has to mentally assemble crosssectional images of a structure and/or object into a 3D image. In cases with uncertain anatomic orientation less experienced examiners may experience difficulties in envisioning three dimensions of the visualized structure, lesion or organ. Patients and parents are often faced with similar problems. A number of studies have shown that novice operators can efficiently store and interpret the volume data by 3D ultrasound, which may have many positive implications in the practice.

High-resolution scanning electron microscopy (HRSEM) of mitochondria from various rat tissues

1988 ◽  
Vol 46 ◽  
pp. 14-15
Author(s):  
P.J. Lea ◽  
M.J. Hollenberg
Keyword(s):  
Electron Microscopy ◽  
Pigment Epithelium ◽  
Retinal Pigment ◽  
Rat Hepatocytes ◽  
Three Dimensions ◽  
Objective Lens ◽  
Rat Tissues ◽  
Thin Sections ◽  
Reconstruction Methods ◽  
Scanning Electron

Our current understanding of mitochondrial ultrastructure has been derived primarily from thin sections using transmission electron microscopy (TEM). This information has been extrapolated into three dimensions by artist's impressions (1) or serial sectioning techniques in combination with computer processing (2). The resolution of serial reconstruction methods is limited by section thickness whereas artist's impressions have obvious disadvantages.In contrast, the new techniques of HRSEM used in this study (3) offer the opportunity to view simultaneously both the internal and external structure of mitochondria directly in three dimensions and in detail.The tridimensional ultrastructure of mitochondria from rat hepatocytes, retinal (retinal pigment epithelium), renal (proximal convoluted tubule) and adrenal cortex cells were studied by HRSEM. The specimens were prepared by aldehyde-osmium fixation in combination with freeze cleavage followed by partial extraction of cytosol with a weak solution of osmium tetroxide (4). The specimens were examined with a Hitachi S-570 scanning electron microscope, resolution better than 30 nm, where the secondary electron detector is located in the column directly above the specimen inserted within the objective lens.

Inelastic Electron Scattering from Valence Electrons in Aluminum

1976 ◽  
Vol 34 ◽  
pp. 462-463
Author(s):  
P. E. Batson ◽  
C. H. Chen ◽  
J. Silcox
Keyword(s):  
Electron Scattering ◽  
Single Scattering ◽  
Three Dimensions ◽  
Inelastic Electron ◽  
Weak Beam ◽  
Scattering Spectrum ◽  
Valence Electrons ◽  
Diffraction Patterns ◽  
Electronic Scattering

We wish to report in this paper measurements of the inelastic scattering component due to the collective excitations (plasmons) and single particlehole excitations of the valence electrons in Al. Such scattering contributes to the diffuse electronic scattering seen in electron diffraction patterns and has recently been considered of significance in weak-beam images (see Gai and Howie) . A major problem in the determination of such scattering is the proper correction for multiple scattering. We outline here a procedure which we believe suitably deals with such problems and report the observed single scattering spectrum.In principle, one can use the procedure of Misell and Jones—suitably generalized to three dimensions (qx, qy and #x2206;E)--to derive single scattering profiles. However, such a computation becomes prohibitively large if applied in a brute force fashion since the quasi-elastic scattering (and associated multiple electronic scattering) extends to much larger angles than the multiple electronic scattering on its own.

Advantages of Complementary Stereo Images as Viewed with the Low-Temperature Field-Emission SEM

1992 ◽  
Vol 50 (2) ◽  
pp. 1314-1315
Author(s):  
William P. Wergin ◽  
Eric F. Erbe
Keyword(s):  
Fold Increase ◽  
Horizontal Displacement ◽  
Three Dimensions ◽  
Stereo Image ◽  
Stereo Pair ◽  
Sem Micrograph ◽  
Left And Right ◽  
The Common ◽  
The Brain ◽  
Pair Analysis

The eye-brain complex allows those of us with normal vision to perceive and evaluate our surroundings in three-dimensions (3-D). The principle factor that makes this possible is parallax - the horizontal displacement of objects that results from the independent views that the left and right eyes detect and simultaneously transmit to the brain for superimposition. The common SEM micrograph is a 2-D representation of a 3-D specimen. Depriving the brain of the 3-D view can lead to erroneous conclusions about the relative sizes, positions and convergence of structures within a specimen. In addition, Walter has suggested that the stereo image contains information equivalent to a two-fold increase in magnification over that found in a 2-D image. Because of these factors, stereo pair analysis should be routinely employed when studying specimens.Imaging complementary faces of a fractured specimen is a second method by which the topography of a specimen can be more accurately evaluated.

convergent-beam diffraction from surfaces

1987 ◽  
Vol 45 ◽  
pp. 30-33
Author(s):  
J. A. Eades ◽  
A. E. Smith ◽  
D. F. Lynch
Keyword(s):  
Reciprocal Lattice ◽  
Three Dimensional ◽  
Grazing Incidence ◽  
Three Dimensions ◽  
Plane Figure ◽  
Transmission Electron ◽  
Convergent Beam ◽  
Beam Patterns ◽  
Beam Diffraction

It is quite simple (in the transmission electron microscope) to obtain convergent-beam patterns from the surface of a bulk crystal. The beam is focussed onto the surface at near grazing incidence (figure 1) and if the surface is flat the appropriate pattern is obtained in the diffraction plane (figure 2). Such patterns are potentially valuable for the characterization of surfaces just as normal convergent-beam patterns are valuable for the characterization of crystals.There are, however, several important ways in which reflection diffraction from surfaces differs from the more familiar electron diffraction in transmission.GeometryIn reflection diffraction, because of the surface, it is not possible to describe the specimen as periodic in three dimensions, nor is it possible to associate diffraction with a conventional three-dimensional reciprocal lattice.

3-D reconstruction and analysis of mammalian mitotic spindle structure

1992 ◽  
Vol 50 (1) ◽  
pp. 578-579
Author(s):  
Kent McDonald ◽  
David Mastronarde ◽  
Rubai Ding ◽  
Eileen O'Toole ◽  
J. Richard McIntosh
Keyword(s):  
Cross Sections ◽  
Mitotic Spindle ◽  
Experimental Studies ◽  
Video Camera ◽  
Three Dimensions ◽  
Mitotic Spindles ◽  
Black And White ◽  
Reconstruction Methods ◽  
Spindle Structure ◽  
Tissue Culture Line

Mammalian spindles are generally large and may contain over a thousand microtubules (MTs). For this reason they are difficult to reconstruct in three dimensions and many researchers have chosen to study the smaller and simpler spindles of lower eukaryotes. Nevertheless, the mammalian spindle is used for many experimental studies and it would be useful to know its detailed structure.We have been using serial cross sections and computer reconstruction methods to analyze MT distributions in mitotic spindles of PtK cells, a mammalian tissue culture line. Images from EM negatives are digtized on a light box by a Dage MTI video camera containing a black and white Saticon tube. The signal is digitized by a Parallax 1280 graphics device in a MicroVax III computer. Microtubules are digitized at a magnification such that each is 10-12 pixels in diameter.

Five-Dimensional Microscopy using Widefield-Deconvolution: Practical Considerations and Biological Applications

1996 ◽  
Vol 54 ◽  
pp. 268-269
Author(s):  
W.F. Marshall ◽  
K. Oegema ◽  
J. Nunnari ◽  
A.F. Straight ◽  
D.A. Agard ◽  
...  
Keyword(s):  
Confocal Microscopy ◽  
High Speed ◽  
Laser Scanning ◽  
Ccd Camera ◽  
Image Plane ◽  
Time Lapse ◽  
Laser Scanning Confocal Microscopy ◽  
Three Dimensions ◽  
Excitation Light ◽  
Cooled Ccd

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.

The influence of confocal microscope design on imaging performance

1993 ◽  
Vol 51 ◽  
pp. 144-145
Author(s):  
C J R Sheppard
Keyword(s):  
Image Quality ◽  
Fluorescence Imaging ◽  
Confocal Microscope ◽  
Industrial Applications ◽  
Three Dimensions ◽  
Design Parameters ◽  
Weak Signals ◽  
Size And Shape ◽  
Imaging Performance ◽  
Fundamental Limitation

The confocal microscope is now widely used in both biomedical and industrial applications for imaging, in three dimensions, objects with appreciable depth. There are now a range of different microscopes on the market, which have adopted a variety of different designs. The aim of this paper is to explore the effects on imaging performance of design parameters including the method of scanning, the type of detector, and the size and shape of the confocal aperture.It is becoming apparent that there is no such thing as an ideal confocal microscope: all systems have limitations and the best compromise depends on what the microscope is used for and how it is used. The most important compromise at present is between image quality and speed of scanning, which is particularly apparent when imaging with very weak signals. If great speed is not of importance, then the fundamental limitation for fluorescence imaging is the detection of sufficient numbers of photons before the fluorochrome bleaches.

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