A facilitative effect of red light on dark adaptation. (Proj. No. NM 001 059.28.01).

1952 ◽  
Author(s):  
Samuel C. McLaughlin
1953 ◽  
Vol 43 (6) ◽  
pp. 541 ◽  
Author(s):  
Stanley W. Smith ◽  
Forrest L. Dimmick

2004 ◽  
Vol 27 (11) ◽  
pp. 1387-1394 ◽  
Author(s):  
K. SATO-NARA ◽  
A. NAGASAKA ◽  
H. YAMASHITA ◽  
J. ISHIDA ◽  
A. ENJU ◽  
...  

1968 ◽  
Vol 51 (5) ◽  
pp. 694-700 ◽  
Author(s):  
George Wald ◽  
Edward B. Seldin

The vision of Palaemonetes is of particular interest in view of extensive studies of the responses of its chromatophore systems and eye pigments to light. The spectral sensitivity is here examined under conditions of dark adaptation and adaptation to bright colored lights. In each case the relative number of photons per one-fiftieth sec flash needed to evoke a constant peak amplitude (usually 25 or 50 µv) in the electroretinogram (ERG) was measured at various wavelengths throughout the spectrum. The sensitivity is the reciprocal of this number. In dark-adapted animals the spectral sensitivity curve consists of a broad, almost symmetrical band, maximal at about 540 mµ, with a shoulder near 390 mµ. Adaptation to bright red or blue light, left on continuously throughout the measurements, depresses the 540 mµ peak without notably changing its shape or position, implying that only one visual pigment operates in this region. Adaptation to red light, however, spares a violet-sensitive system, so that a high, narrow peak at 390 mµ now dominates the spectral sensitivity function. The 540 and 390 mµ peaks are apparently associated with different visual pigments; and these seem to be segregated in different receptor systems, since the associated ERG's have markedly different time constants. It is suggested that these two sensitivity bands may represent the red- and violet-sensitive components of an apparatus for color differentiation.


2021 ◽  
Author(s):  
Andrei Herdean

This is a simple protocol that consists of 1) 10 minutes preillumination with far red light 2) 5 minutes of illumination with actinic light 3) 5 minutes of dark adaptation with far red light qE is calculated as the differe between NPQ_Lss and NPQ_D5 qE=NPQ_Lss-NPQ_D5 qI=NPQ_D5 Protocol to be used with FluorCAM 7.0 on a PSI Open FC 800-O/1010-S. Act 2 - are the white light LED arrays ADD2 - is the far red LED array Camera is placed at ~20 cm above the measured sample. Light intensity uniformity across the 96 well plate was measured according to manufacturer instructions. !Important - protocol only works under weak far red light. Intense far red will interfere with the fluorescence measurement.


1954 ◽  
Vol 31 (2) ◽  
pp. 188-197
Author(s):  
BARBARA H. DAINTON

1. Slugs are normally active at night, but this is not a response to darkness. The onset of nocturnal activity does not necessarily coincide, either in the field or in the laboratory, with the onset of darkness. On the contrary, dark-adapted, inactive animals become active on illumination. 2. The activity which follows illumination is short-lived, adaptation being complete within an hour. 3. Dark-adaptation is slower than light-adaptation and takes between 1 and 2 hr. 4. The response occurs whether illumination is constant or intermittent and in white or red light. Once adapted to red light the slugs do not respond to illumination by white light. 5. This effect of light, in initially activating the slugs, clearly cannot account for the occasional daytime activity observed in the field, when the slugs emerge from dark resting places. 6. Once the slugs are light-adapted, the activity during the daytime remains at a very low level even under continued illumination. This low level is probably the same as occurs in the dark under similar conditions. 7. Air currents played on the body or tail of the slug increase the speed of locomotion or induce activity if the animal is at rest. 8. Air currents played on the head or tentacles results in a klinotactic response whereby the animal turns from the region of draught or moves down stream. 9. These reactions must supplement the reactions in a temperature gradient which lead the slugs at the close of activity to sheltered resting places.


1972 ◽  
Author(s):  
David J. Florip ◽  
Robert W. Bayer
Keyword(s):  

1966 ◽  
Author(s):  
Gosta Ekman ◽  
Jan Hosman ◽  
Ulf Berglund
Keyword(s):  

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