Pleasingness vs Interestingness of Visual Stimuli with Controlled Complexity: Their Relationship to Looking Time as a Function of Exposure Time

1975 ◽  
Vol 40 (1) ◽  
pp. 3-7 ◽  
Author(s):  
Gerda Smets
Keyword(s):  
Exposure Time ◽  
Binocular Rivalry ◽  
Stimulus Pair ◽  
Significant Interaction ◽  
Visual Stimuli ◽  
The Other ◽  
Stimulus Complexity

Ss take more time to perceive interesting/displeasing stimuli than uninteresting/pleasing ones. This is consistent with the results of former experiments. However we used a different operationalization of looking time, based on binocular rivalry. Each of six stimulus pairs was presented in a stereoscope. One member of each pair was interesting but displeasing in comparison to the other member. Stimulus complexity was under control. Due to binocular rivalry Ss perceived only one pattern a time. 20 Ss were asked to indicate which pattern they actually saw by pushing two buttons. For each stimulus pair was registered how long each button was pushed during each of six successive minutes. Unlike other operationalizations this one is less dependent on S's determination of what stimulus will be looked at or for how long. It has the advantage that it is bound up more exclusively with relations of similarity and dissimilarity between stimulus elements. It allows manipulation of exposure time in a systematic and continuous way. There is no significant interaction between looking and exposure time.

Evaluation of Agreement Among Routine Methods for Determination of Fluoride in Vegetation: Interlaboratory Collaborative Study

1982 ◽  
Vol 65 (5) ◽  
pp. 1150-1154
Author(s):  
Jay S Jacobson ◽  
John J Troiano ◽  
Christina C Cosentini ◽  
John Evans
Keyword(s):  
Significant Interaction ◽  
Collaborative Study ◽  
Considerable Improvement ◽  
The Other ◽  
Mean Values ◽  
Potentiometric Analysis ◽  
Aoac Official ◽  
Vegetation Samples ◽  
Action Methods

Abstract An interlaboratory collaborative study was conducted to evaluate the performance of methods and laboratories for the measurement of fluoride in vegetation. Samples of 8 plant species containing about 5-200 ppm fluoride were distributed to 40 participants who were instructed to use their routine methods of analysis. Methods which had sufficient participants to allow the inclusion of results in statistical analyses were classified into 3 categories: (1) Willard-Winter method (similar to the AOAC official final action method); (2) semiautomated and potentiometric methods (similar to the 2 AOAC official first action methods); and (3) potentiometric analysis with prior ashing, fusion, and/or distillation (not an approved method). There was a significant interaction of methods with samples caused by 3 of the 8 samples. In the other 5 samples, the Willard-Winter and semiautomated methods gave higher mean values for fluoride content than did the 2 potentiometric methods. Despite considerable improvement in speed and simplicity of fluoride analyses during the last decade, agreement between laboratories has not improved because of the variety of methods and techniques in use, the inherent differences between methods, and, apparently, poor laboratory quality control.

CHLOROPHYLL SYNTHESIS IN SQUASH SEEDLINGS: ACTION AND INTERACTION OF RED AND FAR-RED IRRADIATION

1967 ◽  
Vol 45 (6) ◽  
pp. 929-938 ◽  
Author(s):  
Kenneth Surrey
Keyword(s):  
Energy Balance ◽  
Exposure Time ◽  
White Light ◽  
Slow Rate ◽  
Red Light ◽  
Chlorophyll Synthesis ◽  
The Other ◽  
Pigment Formation ◽  
Red Radiation

Two different rates of chlorophyll synthesis were observed in the cotyledons when squash (Cucurbita moscata) seedlings were exposed to continuous red radiation: a slow rate which lasted for about three hours and an accelerated rate that proceeded thereafter. Determination of red, far-red reversible reaction indicated that pigment formation in seedlings exposed initially to far-red was promoted by red radiation, and this promotion was repeatedly reversed by subsequent far-red treatments. On the other hand, seedlings exposed first to red radiation followed by far-red, red light cycles failed to respond according to the typical red-accelerated and far-red-inhibited photomorphogenic responses. Variations in these photoresponses were observed when the exposure time at each alternating waveband was changed, or the energy balance between red and far-red bands was changed or even when the seedlings were exposed to white light either before or after the red, far-red light treatments. The results of these experiments are reported.

Action inhibitrice des morphactines sur l'axe principal des Coleus

1972 ◽  
Vol 50 (6) ◽  
pp. 1237-1243
Author(s):  
Michèle-A. Dubuc-Lebreux
Keyword(s):  
Significant Interaction ◽  
Marked Reduction ◽  
Principal Axis ◽  
Factorial Analysis ◽  
The Other ◽  
Other Hand ◽  
Significant Factors

Specimens of Coleus hybridus 'Chartreuse' have been treated with two morphactins (IT 3233 and IT 3456) which were applied, either one or four times, to the apex of the plant or the soil beneath, at 25 or 50 ppm. The treated plants have shown inhibition symptoms in their growth at the principal axis. Generally the action of IT 3233 was minimal; on the other hand, IT 3456 has brought a well-marked reduction of the length of the axes. A factorial analysis of the measurements of the treated groups by IT 3456 has permitted the determination of two very significant factors: 'method of application' and 'frequency'; also it has shown a significant interaction between these factors. The two concentrations used did not produce effects that were significantly different.

COMPARISON OF METHODS FOR DRY MATTER DETERMINATION OF HIGH MOISTURE GRAIN CORN

1971 ◽  
Vol 51 (2) ◽  
pp. 405-410 ◽  
Author(s):  
G. M. JONES ◽  
R. E. LARSEN ◽  
J. I. ELLIOT
Keyword(s):  
Significant Interaction ◽  
Dry Matter ◽  
Volatile Fatty Acids ◽  
The Other ◽  
Atmospheric Moisture ◽  
High Moisture ◽  
Air Drying ◽  
Fine Grinding ◽  
Ground Corn

Comparisons were made between methods of determining the dry matter (DM) content of high moisture (HM) ground ear corn, preserved five months earlier with volatile fatty acids (VFA), and HM shelled corn at harvest. The effect of fine grinding (1 mm diameter screen) of HM shelled corn samples prior to DM determination also was examined. There were no differences in DM content of HM shelled corn between toluene distillation, oven-drying, or semi-automatic moisture testing. With HM ground ear corn, DM values obtained by toluene were greater (P < 0.01) than for the other methods. Fine grinding of the samples resulted in increased DM content (P < 0.01). However, differences between methods were apparently confounded by the presence of VFA. Air-drying HM shelled corn at 65 C for 24 hr, prior to DM determination, resulted in a 3% (P < 0.01) increase in DM content. However, there was a significant interaction (P < 0.01) with the effect of fine grinding; hence, the most accurate DM determinations were obtained when the samples were finely ground after air-drying. The least accurate sample preparation was from finely ground corn which had not previously been air dried. Moisture was apparently lost during grinding due to equilibration with atmospheric moisture.

Determination of the lattice translation across {110} APBs in GaAs

1988 ◽  
Vol 46 ◽  
pp. 600-601
Author(s):  
D.R. Rasmussen ◽  
N.-H. Cho ◽  
C.B. Carter
Keyword(s):  
Grain Boundaries ◽  
Lower Energy ◽  
Antiphase Boundary ◽  
The Other ◽  
Boundary Structure ◽  
Interface Plane ◽  
Inversion Symmetry ◽  
High Angle ◽  
Equilibrium Distance

Domains in GaAs can exist which are related to one another by the inversion symmetry, i.e., the sites of gallium and arsenic in one domain are interchanged in the other domain. The boundary between these two different domains is known as an antiphase boundary [1], In the terminology used to describe grain boundaries, the grains on either side of this boundary can be regarded as being Σ=1-related. For the {110} interface plane, in particular, there are equal numbers of GaGa and As-As anti-site bonds across the interface. The equilibrium distance between two atoms of the same kind crossing the boundary is expected to be different from the length of normal GaAs bonds in the bulk. Therefore, the relative position of each grain on either side of an APB may be translated such that the boundary can have a lower energy situation. This translation does not affect the perfect Σ=1 coincidence site relationship. Such a lattice translation is expected for all high-angle grain boundaries as a way of relaxation of the boundary structure.

Determination of the Burgers vector of a dislocation in a Fe-Mn alloy by weak-beam image in HVEM

1978 ◽  
Vol 36 (1) ◽  
pp. 330-331
Author(s):  
Y. Ishida ◽  
H. Ishida ◽  
K. Kohra ◽  
H. Ichinose
Keyword(s):  
High Order ◽  
Simulation Technique ◽  
The Other ◽  
Image Simulation ◽  
Diffraction Vector ◽  
Burgers Vector ◽  
Weak Beam ◽  
Beam Image ◽  
Edge Component

IntroductionA simple and accurate technique to determine the Burgers vector of a dislocation has become feasible with the advent of HVEM. The conventional image vanishing technique(1) using Bragg conditions with the diffraction vector perpendicular to the Burgers vector suffers from various drawbacks; The dislocation image appears even when the g.b = 0 criterion is satisfied, if the edge component of the dislocation is large. On the other hand, the image disappears for certain high order diffractions even when g.b ≠ 0. Furthermore, the determination of the magnitude of the Burgers vector is not easy with the criterion. Recent image simulation technique is free from the ambiguities but require too many parameters for the computation. The weak-beam “fringe counting” technique investigated in the present study is immune from the problems. Even the magnitude of the Burgers vector is determined from the number of the terminating thickness fringes at the exit of the dislocation in wedge shaped foil surfaces.

Procedures for the Quantitative Determination of Autoprothrombin C

1962 ◽  
Vol 08 (03) ◽  
pp. 434-441 ◽  
Author(s):  
Edmond R Cole ◽  
Ewa Marciniak ◽  
Walter H Seegers
Keyword(s):  
Quantitative Determination ◽  
Plasma Sample ◽  
Quantitative Measure ◽  
The Other ◽  
Clotting Time ◽  
Bovine Plasma ◽  
Autoprothrombin C

SummaryTwo quantitative procedures for autoprothrombin C are described. In one of these purified prothrombin is used as a substrate, and the activity of autoprothrombin C can be measured even if thrombin is in the preparation. In this procedure a reaction mixture is used wherein the thrombin titer which develops in 20 minutes is proportional to the autoprothrombin C in the reaction mixture. A unit is defined as the amount which will generate 70 units of thrombin in the standardized reaction mixture. In the other method thrombin interferes with the result, because a standard bovine plasma sample is recalcified and the clotting time is noted. Autoprothrombin C shortens the clotting time, and the extent of this is a quantitative measure of autoprothrombin C activity.

Determination of Factor XIII Activity and of Factor XIII Inhibitors Using an Ammonium-Sensitive Electrode

1983 ◽  
Vol 50 (02) ◽  
pp. 563-566 ◽  
Author(s):  
P Hellstern ◽  
K Schilz ◽  
G von Blohn ◽  
E Wenzel
Keyword(s):  
Factor Xiii ◽  
Normal Subjects ◽  
The Other ◽  
Activity Measurement ◽  
Factor Xiii Deficiency ◽  
Assay Procedure ◽  
Stabilization Factor ◽  
Release Method ◽  
Sensitive Electrode

SummaryAn assay for rapid factor XIII activity measurement has been developed based on the determination of the ammonium released during fibrin stabilization. Factor XIII was activated by thrombin and calcium. Ammonium was measured by an ammonium-sensitive electrode. It was demonstrated that the assay procedure yields accurate and precise results and that factor XIII-catalyzed fibrin stabilization can be measured kinetically. The amount of ammonium released during the first 90 min of fibrin stabilization was found to be 7.8 ± 0.5 moles per mole fibrinogen, which is in agreement with the findings of other authors. In 15 normal subjects and in 15 patients suffering from diseases with suspected factor XIII deficiency there was a satisfactory correlation between the results obtained by the “ammonium-release-method”, Bohn’s method, and the immunological assay (r1 = 0.65; r2= 0.70; p<0.01). In 3 of 5 patients with paraproteinemias the values of factor XIII activity determined by the ammonium-release method were markedly lower than those estimated by the other methods. It could be shown that inhibitor mechanisms were responsible for these discrepancies.

Determination of the Number of Conserved Chromosomal Segments Between Species

Genetics ◽  
2001 ◽  
Vol 157 (3) ◽  
pp. 1387-1395 ◽  
Author(s):  
Sudhir Kumar ◽  
Sudhindra R Gadagkar ◽  
Alan Filipski ◽  
Xun Gu
Keyword(s):  
Statistical Approach ◽  
Common Ancestor ◽  
Chromosomal Rearrangements ◽  
Structural Similarity ◽  
The Other ◽  
Segment Length ◽  
Human Genomes ◽  
Genomic Divergence ◽  
Human And Mouse

AbstractGenomic divergence between species can be quantified in terms of the number of chromosomal rearrangements that have occurred in the respective genomes following their divergence from a common ancestor. These rearrangements disrupt the structural similarity between genomes, with each rearrangement producing additional, albeit shorter, conserved segments. Here we propose a simple statistical approach on the basis of the distribution of the number of markers in contiguous sets of autosomal markers (CSAMs) to estimate the number of conserved segments. CSAM identification requires information on the relative locations of orthologous markers in one genome and only the chromosome number on which each marker resides in the other genome. We propose a simple mathematical model that can account for the effect of the nonuniformity of the breakpoints and markers on the observed distribution of the number of markers in different conserved segments. Computer simulations show that the number of CSAMs increases linearly with the number of chromosomal rearrangements under a variety of conditions. Using the CSAM approach, the estimate of the number of conserved segments between human and mouse genomes is 529 ± 84, with a mean conserved segment length of 2.8 cM. This length is &lt;40% of that currently accepted for human and mouse genomes. This means that the mouse and human genomes have diverged at a rate of ∼1.15 rearrangements per million years. By contrast, mouse and rat are diverging at a rate of only ∼0.74 rearrangements per million years.

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