I would absolutely love to see what journal those studies came from, as that is an incorrect statement.Before you tell how the effect of THC used to be different I just want to say that people can't even tell if they have taken LSD or not. There are controlled studies done with experienced users who couldn't tell the difference of a placebo (non active) or a full dose of LSD.
Yea, maybe look at the data before you try to be scientific and mask hypothesis as theories.I would absolutely love to see what journal those studies came from, as that is an incorrect statement.
That is one of the greatest obstacles for doing double blind LSD research, or any psychedelic research for that matter. Every participant knows exactly who got the real thing and who got the placebo, so it's impossible to obtain objective information on the effects of psychedelics from the participants.
Sure you can. I thought for months after my first trip that I had a dud and nothing happened, despite ...you know... the windows turning pink and wobbly. I even have a written note being convinced of it 6 weeks after.if you have ever had real experience with LSD, you cannot mistake it for a placebo.
Your point is valid. Up to a point. But I've already pointed that outSure you can. I thought for months after my first trip that I had a dud and nothing happened, despite ...you know... the windows turning pink and wobbly. I even have a written note being convinced of it 6 weeks after.
My point is that even a simple binary question (have you taken LSD) can't be answered reliably. And then to go the stretch and say that a different drug effect 30 years later is because the drug changed and not because the subject changed is difficult in my mind.
We can now discuss the data extensively (eg is looking at the mean useful when discussing subset analysis), look at other studies etc. but that's beside my point.
I was a little confused too. I understand the notion but trying to be objective is not particularly useful in this caseI'm a little confused when you say "the windows turned pink and wobbly" – an observation that appears fully cognisant – yet try to quantify this by saying you weren't sure "anything happened". I mean, you just told us something happened.
Anyone who has taken anything more than a _micro_ dose of real LSD knows there is absolutely no mistaking it's effects.As always, the detail is in the nuance . . .
We don't know who was given a placebo and claimed to have ingested LSD, but I would surmise that if you have ever had real experience with LSD, you cannot mistake it for a placebo. Unless you thought you'd been given a micro-dose.
If you have never taken LSD, I would suggest you would be much more inclined to think you had been given a dose – the "placebo effect" – because you wouldn't be knowing what to expect, and you would have a fair assumption (and good odds) you had taken LSD.
The devil is in the detail.
Yes, and with green light. Green photons are absorbed by interacting chl-b molecules which are only present in PSII. You may know the sub-canopy spec largely devoid of blue and red. Here, GL drives PSII and FRL PSI, since FRL is more prelavent the PSII enlarges to increase its light-harvesting capacity to arrive at a balanced photosystem stoichiometry.Far Red has a synergistic relationship with red light.
No, you are not familiar with the EEE because you just confirmed a multitude of errors.I’m familiar with the Emerson effect. The problem is that the Emerson effect doesn’t take place under low light conditions. As you mentioned it is a cooling system (regarding electron excitation) to reduce the effects of photo-inhibition, which typically only occur under high ppfd/high temperature conditions.
I'd love to see Teknik develop some nice 690-710nm diodes, they may be able to drive PSI without excessive stretching, plus have a higher absorbance. I'd put my money on it.If all LEDs were equal, then 680nm red would be the clear winner, followed by 700nm red (PSII photosynthesises at twice the rate of PSI).
First, to base all your assumptions onto the chlorophyll-absorption peaks when dissolved in diethylether isolated in a flask is wrong. Yes this can tell us something about the strength of absorption BUT IN VIVO alters this, due to the spatial arrangement and various proximity of these porphyrinrings, sometimes enabling a shared orbital of the Pi-electrons and altered excitation states. So we have dimeric, trimeric or quattrimeric chlorophylls (plus some accsessory pigments) completing the absorption over a much broader range, and esp. when sampled over a much higher case incident (due to the Detour-effect) to almost homogenous uniformity within PAR, as evidenced by the McCree curve. In other words photoautotrophs just use mainly the rather narrow chlorophyll chromophore as a base building block to harvest quite dynamically and plastically over a huge bandwidth. That is why the photosystems have each +100 such molecules arranged like a funnel with the charge separating trap in its mid (or end).I also think the research being done still has flaws, as most of the studies I’m reading about regarding spectrum quality, effects of far-red light and so on.. are using inferior spectrums as their “control”.
For example, as taken from a referenced study from Dr. Bugbee, they were comparing the effects of background FR light to white light. The white light used as their control looked like this…
View attachment 5352879
As well as this one, from Bruce Bugbee’s study…
View attachment 5352884
I hate to keep calling these studies out, but much like the Nichia Hortisolis paper, the effects of far red were compared to a photosynthetically inferior control spectrum, one which didn’t effectively cover the red end of Chlorophyll-a and had a heavily Blue weighted spectrum. It’s not surprising that photosystem I would react to far-red when it wasn’t properly being excited in the first place. Again the second study was done at lower flux conditions (<400ppfd).
It’s these “subtleties” that make me question the conclusions that some have come to (including Bruce) about the overall efficacy of Red heavy spectrums and Far-Red wavelengths. I think we certainly need as many is those usable nanometers as the plants can take. The question I have is in what ratio/proportions/flux densities will give the best results?
I’m not sure I’ve put forward any theories other than questioning the total yield/cannabinoid efficacy of supplemental FR light in the presence of a “broader” spectrum of white light.No, you are not familiar with the EEE because you just confirmed a multitude of errors. Also the last review you posted doesn't support your theories at all (I just read it).
I’m not sure where you’re getting this? I’ve looked at a multitude of absorption and action spectrums of Chlorophylls/accessory pigments (with different methods of measuring) and compare them to known photosynthetic quantum yield charts, to try to gain a comprehensive understanding of how spectrum effects plants. This is such a dynamic process, that the only assumption I typically make is that sunlight is a known benchmark for plant performance, and to make my comparisons accordingly.First, to base all your assumptions onto the chlorophyll-absorption peaks when dissolved in diethylether isolated in a flask is wrong.
Again, I don’t know what theory I’ve put forward other than questioning the efficacy of added FR to a better balanced broad spectrum white light. My point in mentioning the spectrums used in the Bugbee studies, was that there was inadequate coverage of the photosystems action spectra to draw conclusions that would relate to real world conditions (sunlight/broad spectrum white light/high ppfd). I can expand more on this idea if you’d like.The cited Bugbee control specs were often in use in either science, or, e.g. cloning. The RB actually has a super ontight SPD directly set to these native chlorophyll max peaks (high absorbance). It's rather that Bugbee's FR SPDs don't target these, so your argument is contradictory to your own "theory". In reality the FR photosynthetic effect has its max at ~730nm.
Sorry, reading this back myself after finishing; its a pretty long and rambly thing, i dont blame anyone for not getting my point, its almost the definition of tldr...I’m not sure I’ve put forward any theories other than questioning the total yield/cannabinoid efficacy of supplemental FR light in the presence of a “broader” spectrum of white light.
What I should have said, is “I’m fairly familiar with the general concept of the Emerson Enhancement Effect”…
ie- The Emerson effect is the increase in the rate of photosynthesis after chloroplasts are exposed to light of wavelength 680 nm (deep red spectrum) and more than 680 nm (far red spectrum). When simultaneously exposed to light of both wavelengths, the rate of photosynthesis is far higher than the sum of the red light and far red light photosynthesis rates.
And my statement you quoted was indeed in error. I conflated the general mechanism of the EEE and FR role in photoprotection, assuming they only happened in tandem. Upon further reading, it does appear that FR light can ehnhance photosynthesis in certain species below the saturation of the photosynthetic apparatus (low ppfds), like @Rocket Soul mentioned previously. But it also appears that at higher light saturations (up to a limit) Far-Red light can actively reduce non-photochemical quenching by keeping Photosystem 1 in an exited state, helping keep PS I & II in a balanced state of electron donation, like you had mentioned regarding FR light and photoprotection. I confused the 2 mechanisms, sorry.
I’m not sure where you’re getting this? I’ve looked at a multitude of absorption and action spectrums of Chlorophylls/accessory pigments (with different methods of measuring) and compare them to known photosynthetic quantum yield charts, to try to gain a comprehensive understanding of how spectrum effects plants. This is such a dynamic process, that the only assumption I typically make is that sunlight is a known benchmark for plant performance, and to make my comparisons accordingly.
Again, I don’t know what theory I’ve put forward other than questioning the efficacy of added FR to a better balanced broad spectrum white light. My point in mentioning the spectrums used in the Bugbee studies, was that there was inadequate coverage of the photosystems action spectra to draw conclusions that would relate to real world conditions (sunlight/broad spectrum white light/high ppfd). I can expand more on this idea if you’d like.
I agree with you that plants have evolved to utilize most of the sunlight spectrum, and that (overly simplified) a photon is a photon.
Obviously spectral quality/flux will effect the balance/efficiency of both PS I & II and all the accessory pigments, as well as photomorphology.
But keeping in mind that we as cannabis growers are typically looking for the highest yielding dry weight of flower, as well as the highest cannabinoid content, what is the best spectral balance/flux levels to achieve those goals? I’m pretty sure that question has yet to be answered.
I’m glad my posts have at least been amusing to you. I’m not a scientist, nor do I have any higher education regarding plants, light , or really anything related to growing. I’m just a hobbyist who likes to read to gain a better understanding of cause and effect in the grow room, as well as as trying to optimize the growing space/environment.
If I make a mistake or misunderstand something, just let me know as I’m here to learn, share, and better understand how to grow the most dank of buds.
With all of that said, here is a link to a study about the effects of supplemental FR light (730nm at different flux levels) to a background of broad spectrum white light (Cree 3500k 90CRI). Basically what Bugbee should have done in their study, IMO. This study was done on Cannabis in 2022, and at least “their” results culminate just about all of the talking points I’ve been trying to make in this thread. Not saying that these results are conclusive or the end-all solution. But the results are along the lines of what I would expect based on my own personal tests, results of others from the forums, and countless hours of reading through studies and about plant physiology, and why I ask the questions that I ask. Enjoy.
For our discussion purposes, it would have been nice had the study been done using say a 3500k (80CRI) that didn’t have as much red in the spectrum. That said, it’s a very similar format to the Bugbee study, as well as others, regarding adding FR wavelengths to a control spectrum. I just think that the spectrum used in the 2022 Tennessee study, more resembles a grow spectrum than the controls used in the Bugbee studies. While true their isn’t any supplemental deep red added, I appreciate that fact just for informational purposes regarding supplemental FR to broad spectrum light. In my opinion, most of the reason that grow light manufacturers add supplemental DR (660) to their fixtures, is because they are using “Electrically Efficient” spectrums like 3500k (80CRI) or 3000k/5000k (80CRI). These spectrums lack high levels of DR/FR altogether, which is why supplemental RED/FR is likely necessary to achieve a more natural expression from the plant and increase photosynthetic efficiency.The problems i had with it was the following: it uses a base spectrum of 90cri which is already somewhat rich in far red. Second thing: it tests for something that almost no lightmaker does: adding only far red to a white spectrum. Its like far red on far red, with no red added below 680.
Spectrum will have more influence the lower the light intensity, both on yield and on morphological change. As intensity increase the influence of spectrum diminishes and intensity is more important for yield. Up to a point; when we come up towards the limit of how much light we can give to a plant before it starts getting saturated or whatever we call the process that make it hard to grow at +1000 ppfd.
These are more or less the same conclusions that I have also come to. The “best” spectrum for the plant is likely dynamic and based off things like spectral quality/distribution, flux levels, light angle, plant species, and phenotype. But, like you mentioned, once the light levels reach saturation the plant will be looking for the most efficient way to deal with any excess energy (light/heat) while reducing photoinhibition. I believe this is where where green/yellow light really deliver in terms of whole plant photosynthesis, not only deeper into the lower canopy but deeper into the leaf tissue as well.you may have different results studying one process at 400ppfd and 800ppfd even if the spectrum was kept the same, that 400ppfd would not give you half the reaction as 800ppfd
Blue/green ratios is something we never really talk about, but also an important measure. By what mechanism would this determine SAS, please link cause i really find it interesting.I’ll try to keep this short considering I’ve been writing novels just to try to share my perspective on things.
For our discussion purposes, it would have been nice had the study been done using say a 3500k (80CRI) that didn’t have as much red in the spectrum. That said, it’s a very similar format to the Bugbee study, as well as others, regarding adding FR wavelengths to a control spectrum. I just think that the spectrum used in the 2022 Tennessee study, more resembles a grow spectrum than the controls used in the Bugbee studies. While true their isn’t any supplemental deep red added, I appreciate that fact just for informational purposes regarding supplemental FR to broad spectrum light. In my opinion, most of the reason that grow light manufacturers add supplemental DR (660) to their fixtures, is because they are using “Electrically Efficient” spectrums like 3500k (80CRI) or 3000k/5000k (80CRI). These spectrums lack high levels of DR/FR altogether, which is why supplemental RED/FR is likely necessary to achieve a more natural expression from the plant and increase photosynthetic efficiency.
I had to touch up on it, but it looks like shade avoidance is primarily a function of R:FR ratios as well as total Blue/ B:G ratio. But R:FR is the main antagonist it seems.
These are more or less the same conclusions that I have also come to. The “best” spectrum for the plant is likely dynamic and based off things like spectral quality/distribution, flux levels, light angle, plant species, and phenotype. But, like you mentioned, once the light levels reach saturation the plant will be looking for the most efficient way to deal with any excess energy (light/heat) while reducing photoinhibition. I believe this is where where green/yellow light really deliver in terms of whole plant photosynthesis, not only deeper into the lower canopy but deeper into the leaf tissue as well.