OldCoolSativa
Well-known member
Punto rojo often has a beautiful peppery, spicey aroma.
How can the level' of myrcene and ocimene be influenced, very interesting that the same clone had such different levels. do you have any idea's of what factors could have contributed to this? awesome information about 2.5 - 1 ratio with BCP and Humulene, thanks for information.The Orissa gold from landracemafia had a fasciated phenotype with a bunch of ocimene and carolyohene. Profile is near identical to piff s2 clone.
View attachment 18899718
View attachment 18899719
View attachment 18899720
The ratio of myrcene and ocimene can be influenced in ocimene favor. Keeping myrcene under .5 is desirable to avoid couch lock phenotypes. For example the first piff s2 test score from piffcoast had .09 ocimene and .9 myrcene but a sample this year same clone had .4 myrcene .25 ocimene .15 beta carolyohene. The cbga production also increased dramatically.
So myrcene and ocimene share a common synthase family G.How can the level' of myrcene and ocimene be influenced, very interesting that the same clone had such different levels. do you have any idea's of what factors could have contributed to this? awesome information about 2.5 - 1 ratio with BCP and Humulene, thanks for information.
Soil type, latitude, how far above sea level.How can the level' of myrcene and ocimene be influenced, very interesting that the same clone had such different levels. do you have any idea's of what factors could have contributed to this? awesome information about 2.5 - 1 ratio with BCP and Humulene, thanks for information.
Looking at things now i think the stress induced of actually cutting and cloning the plant increased the Menthyl Jasmonate hormones, and the clones should have naturally lower gibberellin levels than mother resulting in decreased myrcene levels slightly because myrcene is more related to fibre type trichomes as opposed to flower or drug type, while redirecting more myrcene into synthesis of ocimene because of the stress of being cut and cloned. the mother between myrcene and ocimene had .99% and the clone had .65%, it would be helpful to find out how much myrcene in needed % wise in the production of ocimene, IMO based on ocimene's description its a blend of myrcene, limonene, and pinene.So myrcene and ocimene share a common synthase family G.
all ocimene starts off as myrcene so if the transcription rate of that myrcene to ocimene is increased the ratio tips in ocimene favor..
this could be induced with different red spectrum daylight hours night temps but the big one in nature is pests.
Ocimene is a defense against aphids it mimics the alarm pheromone aphids make. Trick them into turning around.
Methyl jasmonate is the phytohormone which is injected when aphids are sensed so foliar application can artificially induced terpene production without the bugs.
In this specific case I'm not sure how these gains were made but I'd say led color spectrum and high Temps are at play. If anyone knows the grower like to know the set up
Interesting, I wonder if a combination of priming agents would work better than just using one or the other.Have you ever done any reading on the usage of melatonin as a foliar/soil drench? One of it's key claims to fame is in resetting hormone levels after stress. If you want to experiment with it, an easy route is to take a 10mg/1mL solution and to add 0.25mL to a gallon. The one, I use, has a little sodium benzoate in it, as a preservative. Once it is diluted, I couldn't imagine it amounting to much at all and have never seen a problem. Anyways, it works really well for priming seeds too, and saw an article showing that it helped partially with genetic decay, in old seed stock. Something I have never seen any other treatment being able to boast. You can use it once a week. However, if your goal were to see if reset hormones caused a commensurate change in growth habit, as per your hypothesis. You might not want to use it more than once or twice. As it tends to encourage secondary growth a lot. So that would change it's growth habit in yet another way. Defeating it's purpose, in this case.
I found that it definitely seems possible to overdo it with combining different agents.Interesting, I wonder if a combination of priming agents would work better than just using one or the other.
heres a list of common primming agent and their ratios for 1 gallon of solution. I added in alfalfa extract because seaweed extract has to high levels of cytokinin's to auxins and alfalfa has the opposite levels so it balances out. and cut original seaweed extract in half with addition of alfalfa. I have not tried melatonin before, but it could be useful using after cloning for sure.
- Potassium Nitrate (KNO3): 1 teaspoon
- Melatonin Solution (10mg/1mL): 0.25mL
- Gibberellic Acid (GA3): 1 drop (dissolved in a small amount of water)
- Hydrogen Peroxide (3% solution): 1 teaspoon
- Seaweed Extract (Liquid Concentrate): 1/2 Teaspoon
- Alfalfa Extract (Liquid Concentrate): 1/2 Teaspoon
- Epsom Salt (Magnesium Sulfate): 1/4 teaspoon
- Humic Acid Solution: 1 tablespoon (dissolved in a small amount of water)
- Aloe Vera Gel: 1/4 teaspoon
Thankyou for your input from past experience, I will look into adding melatonin to my recipe for seed germination as it has had good success for you, I am curious what you mean in this part about letting them dry after soaking? and active dry yeast i recently started using in the garden and i notice results in just a few days of sprinkling some around the base of the plants. I noticed when i used seaweed extract on my oregano plants it increased the internodal spacing and the stems seemed skinnier and looked it up and the hormone profile is 94% cytokinin's, looking at seaweed its makeup is why i think another extract like moringa, or something with similar hormone profile to cannabis would be good, even a cannabis extract could have potential. probably be best if extracts made from all parts of plant so it has varying levels of hormones.16 hr soak, followed by thorough drying to generally be the gold standard
So priming, whether hydropriming (just aerated water) or using anything from liquid yeast extract, to certain metal oxide nanoparticles to various purified PGH's, is specifically the practice of soaking a seed, so as to initiate the long chain of biochemical reactions, that culminate in germination taking place, then stopping it. So the idea is that you take seeds. Especially if they haven't been professionally cleaned, you give them a wash. I use 3% peroxide for 3 min. Mercury salts are sometimes still used and of course bleach, at I think 0.1% Rinse. Then you do your soak. Google Scholar will reveal many, many variations on the "what" and "how long?" After the soak, you rinse the seeds well. I use tap and haven't seen an issue. Then you dry them. The "how quickly" depends. Often just putting them on a paper towel and then transferring them to a new one after a few minutes and making sure to move them around a bit. So as to not allow standing water, works. Using a fine mesh strainer, with a hair drier on it's lowest setting works too, but can be tricky. I've also used the air coming out of a dehumidifier. The idea though, is that this isn't just soaking the seeds in something. It is actually triggering a cascade of biochemical reactions in the seed, but then putting it on pause.Thankyou for your input from past experience, I will look into adding melatonin to my recipe for seed germination as it has had good success for you, I am curious what you mean in this part about letting them dry after soaking? and active dry yeast i recently started using in the garden and i notice results in just a few days of sprinkling some around the base of the plants. I noticed when i used seaweed extract on my oregano plants it increased the internodal spacing and the stems seemed skinnier and looked it up and the hormone profile is 94% cytokinin's, looking at seaweed its makeup is why i think another extract like moringa, or something with similar hormone profile to cannabis would be good, even a cannabis extract could have potential. probably be best if extracts made from all parts of plant so it has varying levels of hormones.
Thankyou for the detailed explanation, i was unfamiliar with priming before your comments, if I'm an outdoor grower, how would primming seeds benefit me, in comparison to just soaking in a solution and using a paper towel method until seedlings hatch, would it be better to prim seeds, and just plant directly in soil a week or so later. and how would you store primmed seeds compared to non-primmed and i imagine they must be used sooner since there activated in a sense?but then that wouldn't agree with above comment about helping with geneti decay in old seed stock thankyou again for your time.So priming, whether hydropriming (just aerated water) or using anything from liquid yeast extract, to certain metal oxide nanoparticles to various purified PGH's, is specifically the practice of soaking a seed, so as to initiate the long chain of biochemical reactions, that culminate in germination taking place, then stopping it. So the idea is that you take seeds. Especially if they haven't been professionally cleaned, you give them a wash. I use 3% peroxide for 3 min. Mercury salts are sometimes still used and of course bleach, at I think 0.1% Rinse. Then you do your soak. Google Scholar will reveal many, many variations on the "what" and "how long?" After the soak, you rinse the seeds well. I use tap and haven't seen an issue. Then you dry them. The "how quickly" depends. Often just putting them on a paper towel and then transferring them to a new one after a few minutes and making sure to move them around a bit. So as to not allow standing water, works. Using a fine mesh strainer, with a hair drier on it's lowest setting works too, but can be tricky. I've also used the air coming out of a dehumidifier. The idea though, is that this isn't just soaking the seeds in something. It is actually triggering a cascade of biochemical reactions in the seed, but then putting it on pause.
I experimented with a FPE made from leaves. It smelled absolutely terrible. I have a strong stomach for these things too. The project blew up. So I can't comment really beyond that. Composting certainly smells better though. Anyways, I think that it is important to remember that while dissecting these various pathways can be useful, that we are still interacting with very simplistic models of complex biochemical interrelationships and that sometimes you have to design an experiment and judge a tree by it's fruit and also that the map is not the territory.
Your intuition is spot on, with the storage. What is the upper limit? Design an experiment well enough, and record enough high quality data, and you could potentially publish the answer. Its a topic on ongoing research. I would only prime something, that I planned on planting in the next 6 months. I have germinated primed seed over a year after without too ill effects though.Thankyou for the detailed explanation, i was unfamiliar with priming before your comments, if I'm an outdoor grower, how would primming seeds benefit me, in comparison to just soaking in a solution and using a paper towel method until seedlings hatch, would it be better to prim seeds, and just plant directly in soil a week or so later. and how would you store primmed seeds compared to non-primmed and i imagine they must be used sooner since there activated in a sense?but then that wouldn't agree with above comment about helping with geneti decay in old seed stock thankyou again for your time.