Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
J Exp Biol ; 204(Pt 16): 2795-801, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11683435

ABSTRACT

Although many aspects of firefly bioluminescence are understood, the mechanism by which adult fireflies produce light as discrete rapid flashes is not. Here we examine the most postulated theory, that flashing is controlled by gating oxygen access to the light-emitting cells (photocytes). According to this theory, the dark state represents repression of bioluminescence by limiting oxygen, which is required for bioluminescence; relief from this repression by transiently allowing oxygen access to the photocytes allows the flash. We show that normobaric hyperoxia releases the repression of light emission in the dark state of both spontaneously flashing and non-flashing fireflies, causing continual glowing, and we measure the kinetics of this process. Secondly, we determine the length of the barriers to oxygen diffusion to the photocytes in the aqueous and gas phases. Thirdly, we provide constraints upon the distance between any gas-phase gating structure(s) and the photocytes. We conclude from these data that the flash of the adult firefly is controlled by gating of oxygen to the photocytes, and demonstrate that this control mechanism is likely to act by modulating the levels of fluid in the tracheoles supplying photocytes, providing a variable barrier to oxygen diffusion.


Subject(s)
Coleoptera/physiology , Luminescent Measurements , Oxygen/physiology , Periodicity , Adenosine Monophosphate/metabolism , Adenosine Triphosphate/metabolism , Animals , Coleoptera/anatomy & histology , Diffusion , Electric Stimulation , Firefly Luciferin/metabolism , Kinetics , Luciferases/metabolism , Oxygen/administration & dosage
2.
Phys Med Biol ; 43(7): 1851-5, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9703047

ABSTRACT

We have designed and constructed RF coil assemblies and the appropriate instrumentation for combining proton NMR imaging with LODESR imaging. This has enabled us to collect sequential images from the same sample using both methods. The coil assembly consists of a crossed ellipse coil for LODESR and proton NMR signal detection and a saddle coil for excitation of the ESR resonance. Images have been collected of phantoms containing copper sulphate and Tempol solutions. NMR images were collected (4.3 min) and within 30 s LODESR data collection started (collection time 2.5 min). Only the Tempol solutions are visible in the LODESR images.


Subject(s)
Electron Spin Resonance Spectroscopy/methods , Magnetic Resonance Spectroscopy/methods , Animals , Biophysical Phenomena , Biophysics , Copper Sulfate , Cyclic N-Oxides , Electron Spin Resonance Spectroscopy/instrumentation , Free Radicals/metabolism , Magnetic Resonance Spectroscopy/instrumentation , Phantoms, Imaging , Protons , Radio Waves , Spin Labels
SELECTION OF CITATIONS
SEARCH DETAIL
...