scholarly journals Reviewing the relevance of fluorescence in biological systems

2015 ◽  
Vol 14 (9) ◽  
pp. 1538-1559 ◽  
Author(s):  
M. Gabriela Lagorio ◽  
Gabriela. B. Cordon ◽  
Analia Iriel

We review the state of the art in the research on the fluorescence emitted by plant leaves, fruits, flowers, avians, butterflies, beetles, dragonflies, millipedes, cockroaches, bees, spiders, scorpions and sea organisms and discuss its relevance in nature.

2016 ◽  
Vol 6 (1) ◽  
pp. 20150098 ◽  
Author(s):  
Markus J. Buehler ◽  
Guy M. Genin

Advances in multiscale models and computational power have enabled a broad toolset to predict how molecules, cells, tissues and organs behave and develop. A key theme in biological systems is the emergence of macroscale behaviour from collective behaviours across a range of length and timescales, and a key element of these models is therefore hierarchical simulation. However, this predictive capacity has far outstripped our ability to validate predictions experimentally, particularly when multiple hierarchical levels are involved. The state of the art represents careful integration of multiscale experiment and modelling, and yields not only validation, but also insights into deformation and relaxation mechanisms across scales. We present here a sampling of key results that highlight both challenges and opportunities for integrated multiscale experiment and modelling in biological systems.


2010 ◽  
Vol 82 (2) ◽  
pp. 493-504 ◽  
Author(s):  
Ryszard Lobinski ◽  
J. Sabine Becker ◽  
Hiroki Haraguchi ◽  
Bibundhendra Sarkar

Definitions for the terms "metallome" and "metallomics" are proposed. The state of the art of analytical techniques and methods for systematic studies of metal content, speciation, localization, and use in biological systems is briefly summarized and critically evaluated.


2020 ◽  
Author(s):  
Lukas Breitwieser ◽  
Ahmad Hesam ◽  
Jean de Montigny ◽  
Vasileios Vavourakis ◽  
Alexandros Iosif ◽  
...  

AbstractComputer simulation is an indispensable tool for studying complex biological systems. In particular, agent-based modeling is an attractive method to describe biophysical dynamics. However, two barriers limit faster progress. First, simulators do not always take full advantage of parallel and heterogeneous hardware. Second, many agent-based simulators are written with a specific research problem in mind and lack a flexible software design. Consequently, researchers have to spend an unnecessarily long time implementing their simulation and have to compromise either on model resolution or system size.We present a novel simulation platform called BioDynaMo that alleviates both of these problems researchers face in computer simulation of complex biological systems. BioDynaMo features a general-purpose and high-performance simulation engine. The engine simulates cellular elements, their interactions within a 3D physical environment, and their cell-internal genetic dynamics. Cell-internal dynamics can be described in C++ code or using system biology markup language (SBML).We demonstrate BioDynaMo’s wide range of application with three example use cases: soma clustering, neural development, and tumor spheroid growth. We validate our results with experimental data, and evaluate the performance of the simulation engine. We compare BioDynaMo’s performance with a state-of-the-art baseline, and analyze its scalability. We observe a speedup of 20–124× over the state-of-the-art baseline using one CPU core and a parallel speedup between 67× and 76× using 72 physical CPU cores with hyperthreading enabled. Combining these two results, we conclude that, on our test system, BioDynaMo is at least three orders of magnitude faster than the state-of-the-art serial baseline. These improvements make it feasible to simulate neural development with 1.24 billion agents on a single server with 1TB memory, and 12 million agents on a laptop with 16GB memory.BioDynaMo is an open-source project under the Apache 2.0 license and is available at www.biodynamo.org.Author summaryComputer simulations of biological systems are crucial to gain insights into complex processes of living organisms. However, the development of increasingly large and complex simulations is a difficult task, partly because a strong background in biology as well as computer science is required. In this paper, we introduce BioDynaMo, an agent-based simulation platform with which life scientists can create simulations that are three orders of magnitude faster than the state-of-the-art baseline. By taking advantage of the latest developments in computing hardware, we build a platform that is highly optimized. This enables the simulation of 1.24 billion agents on a single server and 12 million agents on a laptop. BioDynaMo places a lot of focus on hiding computational complexity and providing an easy-to-use interface, such that the life scientist can concentrate on biological aspects, rather than computational. BioDynaMo helps scientists to translate an idea quickly into a simulation by providing common building blocks, and a modular and extensible software design. We analyze the performance of the platform and demonstrate the capabilities with three example use cases: soma clustering, neural development, and tumor spheroid growth. The results support the view that BioDynaMo will help open up new research opportunities for large-scale biological simulations.


Author(s):  
T. A. Welton

Various authors have emphasized the spatial information resident in an electron micrograph taken with adequately coherent radiation. In view of the completion of at least one such instrument, this opportunity is taken to summarize the state of the art of processing such micrographs. We use the usual symbols for the aberration coefficients, and supplement these with £ and 6 for the transverse coherence length and the fractional energy spread respectively. He also assume a weak, biologically interesting sample, with principal interest lying in the molecular skeleton remaining after obvious hydrogen loss and other radiation damage has occurred.


2003 ◽  
Vol 48 (6) ◽  
pp. 826-829 ◽  
Author(s):  
Eric Amsel
Keyword(s):  

1968 ◽  
Vol 13 (9) ◽  
pp. 479-480
Author(s):  
LEWIS PETRINOVICH
Keyword(s):  

1984 ◽  
Vol 29 (5) ◽  
pp. 426-428
Author(s):  
Anthony R. D'Augelli

1991 ◽  
Vol 36 (2) ◽  
pp. 140-140
Author(s):  
John A. Corson
Keyword(s):  

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