Everything about this grow was amazing! She was a late shooter meaning she was quite small up to the flower stage then after defol she went crazy and sprouted so many sites and buds were huge, frosty and dense! Best of all was the smells during! Like candyland had landed in my nostrils! Honestly no regrets with this one! I have the buds curing in a 3L jar with 62% Boveda packs! Shall add a smoke and ash report once the buds have fully cured! I’ve added a few photos since cute! This bud is fantastic tastes and smells like fruits and yummyness literally all the way through and it’s so strong! Has pineapple cube kinda flavour too! Loved growing her!

This girl is still going strong I’m trying to figure out if I could breed this plant or is it to late I’d be sad if I couldn’t she definitely is a small beauty would love to get more seeds I do have pollen stored

Flowering day 58 since the time was changed to 12/12 h. Hey everyone 😁. We have reached the end of bloom 👍. The trichomes are now 80% milky and 20% amber ☺️. I have again today freshly made all the water and added canna flush. Now the last few stoves in the vicinity will be used for the next few days The day after tomorrow I will turn off the lights so that the plants get 48 hours of darkness before trimming begins 👍. I turned the watering cycle down so that you only get 2 minutes of water every 5 hours :-). I'm so happy to be trimming this Pehno again 😍. He is and remains one of my favorites 👍. As always, there will be an interim update of the harvest Ernte before the last update. Until then, I wish you all a lot of fun with this update. Stay healthy and let it grow.🍀 You can buy this Strain at : www.Zamnesia.com ☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼 Strain Gelato clone from mother (Zamnesia ) ☝️ Genetics: Wedding Cake x Gelato x Gelato 33 👍 Vega lamp: 2 x Todogrow LED CXB3590 COB 55 W 1 x Sanlight S2W 62 W 💡 Flower lamp : 2 x Todogrow LED CXB3590 COB 55 W 1 x Sanlight S2W 62 W 💡 ☝️ Grow Aero System : Growtool 0.8 ☝️ Fertilizer: Canna Aqua Vega A + B , Canna Aqua Flores A + B , Rizotonic, Cannazym, CANNA Boost, Pk 13/14, Canna Cal / Mag, Canna Ph - Grow, Canna Ph-Bloom ☝️🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EG. Add Cal / Mag to 0.4 Ec Ph with ph- to 5.2 - 5.8 💦 💧

Es ist die letzte Woche bevor ich sie in die Blüte schicke

Buenass, las Frisian Dew creo ya están para cosechar, tienen casi todos los pelos naranjas, y las flores se caen del peso, asique el lunes que viene seguro las cosecho, ayer ya las regué solo con agua, a la única que le puse agua con fertilizante es a la The Ultimate de la izquierda que esa tiene toda la pinta de que puede engordar un poco mas, detecte de forma temprana una plaga de arañas rojas, aparecieron por la baja humedad y las altas temperaturas, asique estuve cortando varias hojas que vi afectadas, y ya me encargue de bajar la temperatura (bajando el calefactor) y subir la humedad (riego en mayor cantidad), cuando revegete usaré algún producto orgánico como jabón potásico y aceite de neem para mantenerlas a raya, y si puedo incorporar mariquitas mejor (el tema es conseguirlas jeje). A la The Ultimate de la derecha solo le puse agua con un producto anti estrés, si veo que está bien en la semana capaz le mando un poco de fertilizante, pero con respecto a antes está bastante mejor, al final era un problema de PH, un amigo trajo su medidor de PH y el agua con la que riego tiene un PH de 9, asique voy a comenzar a comprar vinagre para reducir el PH del agua, pero se la bancaron bastante bien todo este tiempo, el suelo vivo ayuda bastante a regular el PH... saludos :) (Adición: la semana 19 se me subió recién cuando agregué la semana 20, se me había bugueado jeje)

Muy buenas gente Aquí otra semana más con esta planta y la verdad que viene super bien con muchas ramas, buena estructura y cargándose de resina. Está siendo regada semanalmente con hype company, bioestimulantes orgánicos. Con una temperatura entre 24/25 encendido con todo al 100% Y apagado entre 16/18 Humedad entre 40/45 Veremos cómo sigue la próxima semana.

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

4/1/2023 Week 7- Day 1 of Veg (Day 59 overall) Water Change Day!!! Water was really low it was just above the hump in the Res cutting it close to not having enough water in the system to keep it going. They drank a lot making it close going the full 14 days. I am still going with the previous grows and adding 36 Gallons but even looking at the root I think the SILICA is working and the roots are further along at this point than in previous grows. This next two weeks will watch how much they drink and how low my Res starts getting, and will make a decision on changing the water weekly from here on out or still keep on the plan of every other week until Week 4 of Flower. Added 36 Gallons Mammoth SILICA= .5Mil/Gal = 18Mil CALMAG= .5Mil/Gal = 18Mil Root Drip= 1Mil/Gal = 36Mil FloraMicro = 5.4Mil/Gal = 194Mil FloraGrow = 4.2Mil/Gal = 151Mil FloraBloom = 4.6Mil/Gal = 166Mil ORCA = .5Mil/Gal =18Mil PPM= 536 PH=5.84 PPFD=500 Tent Temp= 76.5 Water Temp= 71.4 Humidity= 58% 4/2/2023 Week 7- Day 2 of Veg (Day 60 overall) Not much today, PH was at 5.81, I brought that back up to 5.90. I took care of some badly needed defoliation in each of the back sides .. I was able to see some really good clone material to use on the lower backside of each of the plants. I will be taking two clones from each to breed over the next few weeks depending on when I am going to flip them. 4/3/2023 Week 7- Day 3 of Veg (Day 61 overall) A little FIMing, A little Topping, and a Little bit of defoliation. Might have to take my clones during the week this week, I am trying to wait until Saturday to hit week 8 but again they are getting all over the place and I need to trim some of the sides and lower areas. 4/4/2023 Week 7- Day 4 of Veg (Day 62 overall) I decided to take my clones and clean up the lower half of the plants. I took 2 clones from each plant to go into the cloning machine. 4/5/2023 Week 7- Day 5 of Veg (Day 63 overall) Water Temp is sitting at 73. Right in my ideal range for my setup. Ideal range 70-74 My Temp Tent is my ideal zone75.6 Ideal for this grow 70-78 The lights are still waiting the switch to flower to get maxed out... The Humidity is coming in right at 60% I love it.. I took so much off yesterday I figure it was a good day to let them rest. 4/6/2023 Week 7- Day 6 of Veg (Day 64 overall) I needed to Defoliate some and I topped a little. The plants might force me to flip them soon. Next Wed is the 10 week mark half way through the 20 weeks. The net is Bingo... Which means that If/when the plants hit the net I will have to flip them. The Net is set to the max height that I can let them get based on the Breeders Stretch report 75%. 4/7/2023 Week 7- Day 7 of Veg (Day 65 overall) #3 is 22 inches Tall, #2 is 19 Inches Tall. Net is set at 24 inches. Net is also set as my Bingo point, if they hit the net then I have to flip no matter what to account for the Breeders recommended 75% Stretch allowance. I think I am going to have to flip right at the 10 week mark of the Competition which is Wed 12 Apr. I topped a little, I de-foliated a lot to start getting it ready for the anticipated Flip.

Im defenetely finding that goin into 25L instead of 15 Liters is worth it plant size but the 15h of light instead of 20+ really makes a difference with bud development.

week two flower everything looks healthy :D today i defoliated them i watered them with 1.5l every 48h the light i use was set to 80% and it hangs 80cm away from the tops

All 6 chopped after 48 hours dark. The old rainwater brought some wicked Col ours out and there’s plenty of buds bleeding purple. Loved these and they’ve been nice and straightforward. I did give them a bit of a hard time with under and over feeding but there still looks a decent amount of really dense bud there. Will add some better pics and weights when it’s ready. Now hanging at 55F and 65RH not the temps and humidity in the video 😂. Happy New Year 💚

Lots of bud sites with nice buds forming , some trichomes are now on the plant , it's eating the feed really fast and looking healthy

Harvest soon 🙂

The cbd rich has made big buds, the stems have difficulty supporting their weight. He still needs a few days of rinsing for harvest. The smell is fruity and a little herbal The juanita have impressive senescence colors, one has become purple with red-yellow gradients on the large leaves. The other 2 also have intense orange and yellow colors, they are starting to be rinsed enough for harvest. The smell is still fruity and exotic but but it seems like it's starting to smell a bit like lemon as the reggae seeds description says. I could have cut the gourmands underneath but I never thought of doing that. The trichomes in the buds are still clear and milky, not as easy to see in the photo as with the magnifying glass directly. I watch every day to harvest at the perfect time. Opening the box means staying 15 minutes watching them every evening 😄🌈 27/03 update

Day 79 since seed touched soil. Found some bud rot on other strains yesterday, so made early chop for #2 and #3. Both needed time, #2 needed like 3 more weeks, would be huge ;))) Day 112 since seed touched soil. last one is done. Ganja Farmer 2024 project is over. Happy Growing !!!

Dam everytime I grow autos it's great low maintainance, great cold ability , quick growing and fastbuds never seems to disappoint .This will be my 6th auto flower by the company and they go above and beyond to get you what you need .. This makes me excited for my next I door run ... She's gonna stack up ..

12/28 - Day 43 / Day 15 Flower - Feed Day Pots were mostly dry on this day. It has been about a week since I last fed them. I've only had two small waterings since last feed, about a half gallon of water for each of my 5 gallons and about 8oz of water for my bonsais. My plants are drying out within about 48 hours of each small watering. For today's feeding I decided to pull Grow Big out of the solution and focus exclusively on bloom nutes. My solution consisted of: - 1 gallon distilled water - 4ml CalMag - 2 tsp of FF Big Bloom (2/3 dose) - 1 tsp of FF Tiger Bloom (1/2 dose) - pH: 6.7 - TDS: 582 - EC: 1.2 The pH of my solution was down around 5.3 when first mixed so I pH'd up with baking soda to get to a final pH of 6.7. I gave each of my 5 gallons about a half gallon of the fertigated water each which wasn't enough to produce runoff. I gave them each about another 1/4 gallon distilled water to generate enough runoff to test. I tested the runoff of my Z52 which gave me readings of: - pH: 6.4 -TDS: 1620 -EC: 3.3 I gave about 12oz of fertigated water to each of my bonsais. My ZB2 runoff posted readings of: - pH: 6.8 - TDS: 718 - EC: 1.5 **************************************************** 12/30 - Day 45 / Day 17 Flower Pots were close to dry so gave each of the girls a light watering. Gave about 1/4 gallon of de-chlorinated, pH'd water to each of the 5 gallons and 6oz to the bonsais. Everything looking good aside from the fact that my girls are getting too tall for my tent. I've ratcheted my lights up as far as they'll go but the tops are now starting to get within 12". May need to take action to lower the canopy. **************************************************** 1/1 - Day 47 / Day 19 Flower Happy New Year! Pots were getting pretty dry again so provided another light watering with no nutes. **************************************************** 1/2 - Day 48 / Day 20 Flower I am officially concerned with the the distance between the tops and my lights. After reading a few forums to see what other growers have done in my situation, the consensus feedback is to do some supercropping. I ended up supercropping both of the main stems on my 5 gallon pots. I counted three nodes from the top, massaged the stem a little bit where I planned to bend and and then bent each branch to almost 90 degrees. Luckily, the stems didn't snap or show any signs of breakage. Had to remove the shelf in what should be a second compartment of my tent and attempted to do a little LST to widen my plants and lower their canopy.

Video was taken 2 days ago right before a feed, today they are all praying to the lights and look good.