RTIL-system: a Real-Time Interactive L-system for 3D interactions with virtual plants

2011 ◽  
Vol 16 (2) ◽  
pp. 151-160 ◽  
Author(s):  
Ludovic Hamon ◽  
Emmanuelle Richard ◽  
Paul Richard ◽  
Rachid Boumaza ◽  
Jean-Louis Ferrier
Keyword(s):  
Real Time ◽  
System A ◽  
L System

scholarly journals A Highly Selective Turn-On Fluorescent Probe for the Detection of Zinc

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3825
Author(s):  
Ling-Yi Shen ◽  
Xiao-Li Chen ◽  
Xian-Jiong Yang ◽  
Hong Xu ◽  
Ya-Li Huang ◽  
...  
Keyword(s):  
High Selectivity ◽  
Fluorescence Probe ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Turn On ◽  
Imine Nitrogen ◽  
System A ◽  
Plot Analysis ◽  
L System

A novel turn-on fluorescence probe L has been designed that exhibits high selectivity and sensitivity with a detection limit of 9.53 × 10−8 mol/L for the quantification of Zn2+. 1H-NMR spectroscopy and single crystal X-ray diffraction analysis revealed the unsymmetrical nature of the structure of the Schiff base probe L. An emission titration experiment in the presence of different molar fractions of Zn2+ was used to perform a Job’s plot analysis. The results showed that the stoichiometric ratio of the complex formed by L and Zn2+ was 1:1. Moreover, the molecular structure of the mononuclear Cu complex reveals one ligand L coordinates with one Cu atom in the asymmetric unit. On adding CuCl2 to the ZnCl2/L system, a Cu-Zn complex was formed and a strong quenching behavior was observed, which inferred that the Cu2+ displaced Zn2+ to coordinate with the imine nitrogen atoms and hydroxyl oxygen atoms of probe L.

The FL-system: a functional L-system for procedural geometric modeling

2005 ◽  
Vol 21 (5) ◽  
pp. 329-339 ◽  
Author(s):  
Jean-Eudes Marvie ◽  
Julien Perret ◽  
Kadi Bouatouch
Keyword(s):  
Geometric Modeling ◽  
System A ◽  
L System

scholarly journals A STUDY OF THE T SYSTEM IN RAT HEART

1970 ◽  
Vol 44 (1) ◽  
pp. 1-19 ◽  
Author(s):  
W. G. Forssmann ◽  
L. Girardier
Keyword(s):  
Rat Heart ◽  
Photometric Method ◽  
Ventricular Muscle ◽  
Transverse Tubular System ◽  
System A ◽  
L System ◽  
Line Region ◽  
Specific Granules ◽  
Sizable Proportion ◽  
T System

The technique of extracellular space tracing with horseradish peroxidase is adapted for labeling the transverse tubular system (T system) in rat heart. In rat ventricular muscle the T system shows extensive branching and remarkable tortuosity. The T system can only be defined operationally, since it does not display specific morphological features throughout its entire structure. Owing to branching of the T system, a sizable proportion of the apposition between the T system and L system (or closed system) occurs at the level of longitudinal branches of the T system and is not restricted to the Z line region. The regions of apposition between the T system and L system are analyzed in rat ventricular muscle and skeletal muscle (diaphragm) and compared with the intercellular tight junctions (nexuses) of heart muscle by the use of a photometric method. The over-all thickness of the nexus is significantly smaller than that of T-L junctions in both cardiac and skeletal muscles. The thickness of the membranes of the T and L systems are not significantly different in the two muscles, but the gap between both membranes is larger in the heart. In atrial muscle the following two types of cells are found: (a) those cells with a well-developed T system in which the tubular diameter is quite uniform and the orientation predominantly longitudinal and, (b) cells with no T system, but with a well-developed L system. Atrial cells possessing a T system are richly provided with specific granules and show little micropinocytotic activity, whereas cells devoid of T system show intense micropinocytotic activity and few specific granules. The possible functional implications of these findings are discussed.

Automatically Recording of Machining Tasks and Status

2013 ◽  
Vol 718-720 ◽  
pp. 1290-1294
Author(s):  
Zu Wen Lin ◽  
Bin Yao ◽  
Ming Jun Peng ◽  
Yong Zhuo ◽  
Dong Sheng Zhang ◽  
...  
Keyword(s):  
Data Acquisition ◽  
Real Time ◽  
Basic Data ◽  
Component Technology ◽  
Cnc System ◽  
System A ◽  
Com Component ◽  
Mes System

Record machining tasks and machine status automatically based on one development kit for CNC system. A custom control is developed based on COM component technology to view recorded machining tasks and machine status on the CNC screen real-time. The function of data acquisition implemented by this article, can not only provide the basic data for the MES system, but also facilitate the operators to view the machining tasks and machine status.

scholarly journals An on-chip imaging droplet-sorting system: a real-time shape recognition method to screen target cells in droplets with single cell resolution

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Mathias Girault ◽  
Hyonchol Kim ◽  
Hisayuki Arakawa ◽  
Kenji Matsuura ◽  
Masao Odaka ◽  
...  
Keyword(s):  
Single Cell ◽  
Real Time ◽  
Shape Recognition ◽  
Target Cells ◽  
Recognition Method ◽  
System A ◽  
Time Shape ◽  
Droplet Sorting ◽  
On Chip ◽  
Sorting System

scholarly journals Species identification of Anguilla japonica by real-time PCR based on a sequence detection system: a practical application to eggs and larvae

2009 ◽  
Vol 66 (9) ◽  
pp. 1915-1918 ◽  
Author(s):  
Yuki Minegishi ◽  
Tatsuki Yoshinaga ◽  
Jun Aoyama ◽  
Katsumi Tsukamoto
Keyword(s):  
Real Time ◽  
Species Identification ◽  
Developmental Stages ◽  
Detection System ◽  
Anguilla Japonica ◽  
Sequence Detection ◽  
Target Region ◽  
System A ◽  
Sequence Variations ◽  
Eggs And Larvae

Abstract Minegishi, Y., Yoshinaga, T., Aoyama, J., and Tsukamoto, K. 2009. Species identification of Anguilla japonica by real-time PCR based on a sequence detection system: a practical application to eggs and larvae. – ICES Journal of Marine Science, 66: 1915–1918. To develop a practical method for identifying Japanese eel Anguilla japonica eggs and larvae to species by a sequence detection system using a real-time polymerase chain reaction (PCR), we examined (i) the sensitivity of the system using samples at various developmental stages, and (ii) influences of intra- and interspecific DNA sequence variations in the PCR target region. PCR amplifications with extracted DNA solution at 7.0 ng µl−1 or lower were efficient at distinguishing A. japonica from other anguillids. A single egg at the gastrula or later developmental stages could also be identified. Two sequence variations in the PCR target region were observed in 2 out of 35 A. japonica collected from three localities, and from four year classes at a single locality. These mutations, however, did not affect the result of species identification achieved by A. japonica-specific PCR primers and probe. The accuracy of this PCR-based method of species identification will help in field surveys of the species.

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