stardustsailor
Well-Known Member
For 660 light just read/study for Phytochromes...
Neither at veg ,neither at bloom...
(I think Knna,also had mentioned that exact , same thing...)
While others ,seem to get along just fine...
As,for the rest you are right ,more or less ...
But...
1)-You are referring to really actinic green light from an actinic led (525 nm....)
Not much of this band in white leds...
Mainly peak power ,for 500-599 nm ,is at yellows (560-590 ) ..
2 ) - Some Shade Avoidance Syndrome,is needed as I 've just explained,above ...
If not ,yield is diminished...( Say....Sativas vs Indicas,concerning yields,relative to species leaf structure & area / total number of leaves )...
3) -Oh , without "cloudy days ", light antagonism & with 12 hours (at flowering ) of continuous illumination..
Plus the close distance between leaf canopy- and light source ...
Yes,plenty of photo-receptors reach and pass their saturation point.
(" All other "....It's kind of absolute ,isn't it ? ...
And I strongly trust that, nothin' in the whole Universe is absolute...
Except for some researches for green light,maybe...)
4) You should study ,also,what researches from N@S@ ,say about green light and plants grown in controlled enviroments...
In real life,testing has shown that some strains do not tolerate ,not even one led at 660 nm......Thus, the parameter R:FR, which is the ratio of the photon flux density in the 655-665 nm waveband, to that in the 725-735 nm waveband, has become the standard way of characterising daylight for photomorphogenic purposes.
http://biology.mcgill.ca/Phytotron/LightWkshp1994/2.1 Smith/Smith text.htm
High R:FR Ratios (Meaning a lot of 655-665 nm red light )
Fluorescent tubes and high pressure sodium vapor lamps are popular PAR sources in CE, and both provide R:FR ratios several times higher than sunlight. Due to the spectral properties of Pr and Pfr, changes in R:FR above ca. 1.5 do not cause a proportional change in the phytochrome photoequilibrium (Smith and Holmes 1977). Therefore, the R:FR-based neighbor detection mechanism is likely to be distorted or disabled when canopies are grown under extremely high R:FR ratios. Some experimental evidence for this idea has been provided by studies with amaranth, in which CuSO[SUB]4[/SUB] filters were used to increase the R:FR ratio of the light received by the canopies and reduce stem elongation. These studies have shown that very high R:FR ratios result in decreased (rather than increased) canopy net productivity. It is not clear whether this decrease is caused by (1) the elimination of an active sink of assimilates (i.e. the growing internodes), a change in the pattern of light penetration through the canopy (see below), or a combination of the two. In any case, these results appear to directly contradict the notion that canopy growth at high densities is limited by the diversion of photosynthate to "shade-avoidance" responses. Of course, the use of artificially high R:FR ratios may be a convenient way to obtain short-statured plants in CE, which may be desirable for many crops grown for horticultural or ornamental purposes (McMahon and Kelly 1990, Rajapakse and Kelly 1992).
Another predictable consequence of the use of extremely high R:FR ratios in CE is the elimination of phototropic responses triggered through phytochrome. Since these responses may play a role in the dynamics of gap-filling by the canopy, it is suggested that the increase in light interception over time (and therefore canopy growth) will be slowed under very high R:FR. Of course, the extent of this retardation would depend upon (1) the quantitative importance of phototropic responses in gap-filling by the shoot population, and (2), the extent to which phytochrome and B-absorbing photoreceptors play redundant roles in controlling phototropic responses in canopies.
Finally, very high R:FR, which disable the phytochrome-mediated mechanism of neighbor detection, will almost certainly result in increased size structuring in dense plant populations. From a plant grower stand-point the establishment of a strong size hierarchy in the population might have two negative consequences: reduced total yield at high densities and reduced yield uniformity.
http://biology.mcgill.ca/Phytotron/LightWkshp1994/2.3 Ballare/Ballare Text.htm
Neither at veg ,neither at bloom...
(I think Knna,also had mentioned that exact , same thing...)
While others ,seem to get along just fine...
(Anyway,even in natural sunlight ,this band of red,has pretty diminished r.power ..)
The Natural Radiation Environment
The daylight spectrum. The light environment experienced by plants in nature is obviously complex, but a number of generalisations can usefully be made. Solar radiation outside the atmosphere is distributed according to Planck's radiation distribution law, with the sun behaving as a blackbody emitter with an apparent surface temperature approximating 5800[SUP]o[/SUP] K. From Wien's simplifications of Planck's radiation formulae, the wavelength of maximum quantum emission is ca 620 nm,whereas in energy terms it is ca 500 nm; radiant emission falls off sharply at lower wavelengths and more gradually at higher wavelengths. This means that about 55% of the radiation incident on the earth's surface falls within the 380-800 nm range of photochemical activity - which is fortunate, because photochemistry drives the energetic reactions of the biosphere via photosynthesis. Atmospheric components including ozone, oxygen, water vapour and carbon dioxide selectively absorb narrow wavelength bands, resulting in the typical radiation distribution of daylight at the earth's surface seen in Figure 1. This radiation distribution is remarkably constant, being affected little by clouds and other climatic conditions (Holmes and Smith, 1977a). Pathlength through the atmosphere is important, of course, and as pathlength increases with the sun's approach to the horizon at dusk (or dawn), refraction and Rayleigh scattering (inversely proportional to the fourth power of the wavelength) gives dawn/dusk radiation distributions with relatively elevated levels of blue light, and slightly increased levels of FR compared to daylight.
....
The light environment within vegetation canopies.
Ecologically, the most important fluctuations in radiation distribution occur when radiation interacts with vegetation. The photosynthetic pigments, the chlorophylls and carotenoids, absorb radiation over almost the whole of the visible spectrum (i.e. 400-700 nm). A small fraction of the "green" radiation is either transmitted or reflected, which is why leaves are green to our eyes. What is not so immediately obvious is that vegetation hardly absorbs any radiation between 700 and 800 nm. Thus, virtually all the incoming FR is either transmitted or reflected; i.e. the FR is scattered either through the leaf, or from the surface of the leaf. Since our visual systems are very insensitive to radiation beyond ca 700 nm, we fail to recognise that leaves should look far-red, rather than green! Figure 1 shows a typical daylight spectrum within a dense vegetation canopy, and demonstrates the marked depletion of red (i.e., R, 600-700 nm) and the relative enhancement of FR radiation within canopies.
http://biology.mcgill.ca/Phytotron/LightWkshp1994/2.1%20Smith/Smith%20text.htm
As one clearly can see in Figure 1 , under a dense vegetation canopy (dotted lines),more 630-640 nm red is absorbed by leaves ,rather than 660 nm...
As,for the rest you are right ,more or less ...
But...
1)-You are referring to really actinic green light from an actinic led (525 nm....)
Not much of this band in white leds...
Mainly peak power ,for 500-599 nm ,is at yellows (560-590 ) ..
2 ) - Some Shade Avoidance Syndrome,is needed as I 've just explained,above ...
If not ,yield is diminished...( Say....Sativas vs Indicas,concerning yields,relative to species leaf structure & area / total number of leaves )...
3) -Oh , without "cloudy days ", light antagonism & with 12 hours (at flowering ) of continuous illumination..
Plus the close distance between leaf canopy- and light source ...
Yes,plenty of photo-receptors reach and pass their saturation point.
(" All other "....It's kind of absolute ,isn't it ? ...
And I strongly trust that, nothin' in the whole Universe is absolute...
Except for some researches for green light,maybe...)
4) You should study ,also,what researches from N@S@ ,say about green light and plants grown in controlled enviroments...
http://biology.mcgill.ca/Phytotron/LightWkshp1994/1.3 Tikhomirov/Tikhomirov text.htmThere is a question. Is it necessary to prepare optimal light conditions for the photosynthesis of all leaves on the plant or not? What way is it determined? The correct decision on spectral composition of light depends very much on certain morphological characteristics of plants. There is a dependance upon the distribution of fruits along a stem (Tikhomirov, 1990). For example, cucumber has equal distribution of fruits(..or flowers ,before transforming into fruits...) along the stem. There every leaf supplies assimilate to its fruit. In this connection cucumber leaves at all layers must be provided with optimal light conditions. This requires a large portion of green rays in PAR (about 40%). Red rays in PAR (about 40%) provide high level of photosynthesis of upper leaves. Green rays penetrate into middle and lower leaves of plants. Blue rays have regulatory function, but its part in PAR is not very big (about 20%) (Tikhomirov, 1989).