A catastrophe happened, The 4 Eleven Roses died from what i expect, veing shadowed by the other bigger plants as i found the corpse of the plants very stretched, like they were searching light (i don't know how to mark this on this platform) . On the bright side there are 8 female examples, 4 g13 and 4 santa bilbo full of hell flowering. There is a bit of plague, but thats also a negligence i caused by reusing soil from the outdoors. Why i highlight this? because, as the plant are near mid flowering, the use of foliar sprays will not longer be a viable option and i must stick with the basics. Kind regards homies.!

The plant has recover won't be the biggest but that is fine with me as it's for RSO/CBD oil

Alaskan Purple auto is doing good. She had a solution change. I also trimmed out the bottom of the plant today. While doing some selective defoliation in the canopy. She is doing good under the Medic Grow Mini Sun-2. She is stretching now, and should start developing her colas soon. Thank you Seedsman, and Medic Grow. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

😁🍀👨‍🌾🏻👍✌️💚

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.

She was topped 1 time and LST From week 3 till week 10 then Stopped LST when the limbs would stay on there own

Started the week with a big mid flower feed with NFTG. Also tried to defoliate some leaves blocking some light. She is growing tall for sure. 3 ft tall. Her buds are forming real well ! love this plant. Day 57- NFTG mid flower feed/ Mammoth P/Recharge @ 6.5 Ph Day 58-59 No watering Day 60- Recharge/Cal-Mag/Mammoth P/ Bloom Khaos Feed @6.5ph Day 61- No water

Week 3 (06/02 - 12/02) During this week I will try to apply the LST to the plants. On the inkbird, I will switch the fan with the extractor. The heating/cooling system parameters will be: 23.5°C (+0.5°/-3°C). The extractor will be on 5 hours in the morning, 5 hours in the afternoon. I will continue to feed the plants with tap water and only 2ml/l of Bio-grow. I will increase the light up to 75% with a distance of 30cm from the top of the plants. 06/02 D15: - 07/02 D16: first LST, bent down the pants directly to the soil. Watered the plants with tap water (0,5l each) 08/02 D17: I increased the inkbird cooling parameter to +1°C because the temperature inside the tent starts to increase faster. The plants seem to have responded well to first training 09/02 D18: watering day. I added 2ml of Bio-grow to 1.5l of tap water. 10/02 D19: - 11/02 D20: today I applied a second LST bending because the plants started to grow strait. After the training I sprayed the pants with tap water. 12/02 D21: watering day, I added 3ml of Bio-grow to 1.5l of tap water

Today is the day my big bud seeds come out of the soil, they have all started to take root in 25 liters of soil without any problems

She's looking very happy and healthy,let's see how this wonderful lady performs,looks like she's not gonna be very productive but always quality over quantity. Hope you guys enjoy. This lady has started the 4 week since planted on August 26th but also it's the start of her 1st week of flower,let's get the job done! 🔝💎💚✌️

I’m actually Super happy they sprouted on the 1st it just makes keeping track of what day your on so much smoother l think, but I think one was having a hard time getting the shell Off so I helped just I tiny bit!

2/12: I moved the Platonium, both Sucrose Overdose, and the last Muscadine Wine into the dark. The Velvet Sugah Bref, GG4, and Berry Bomb are the last plants from this diary, and they are just getting water and Liquidsoil. They are all in the closet now and getting blasted with extremely cold winter air and intense UVB for their last week. 2/13: I harvested the Platonium, both Sucrose Overdose, and the last Muscadine Wine tonight. Sexy sexy bitches...ooh la la! Not embarrassed to say that I got major wood while giving them a bath...😜

Still seedlings. Two weeks ago these were seeds floating around in cups.

Early harvest because mold

Bit of a difficult start to these girls seeing as this is my first grow and all, but they’re still growing and overall looking pretty healthy, good colour, springy, but I’m suspecting nute deficiency maybe but I’ve upped the food so we’ll see how we do! Now, when to start topping 🤔... Puff, puff, pass ✌️

Just showing y’all how beautiful this strain is. Even tho the buds didn’t turn out purple I’m hoping the pheno on my other girl is a purple type

2/1/2024- Pre-Germination Activities Day 1 I have 21 weeks until final photo is do.. I took 3 seeds out of cold storage and will let them get to room temp for the next 48 hours before I go with Glass of water for germination. I have 3 beans because I will start from the very beginning helping ensure I present the best Pheno. This is going to be a fun one.. I am a few days away from being able to clear my tent out for this run.. I have a breeding run in right now and the Seeds are a few days away from being mature enough for me to take down the girls. Once I get them down I will need to get my tent cleaned up and turned over right away. This is going to be close, I will have to time them to the water and into the tray at the right time.. because I will need to get lighting on them right away.. I have my 2X2 and my light ready incase I need to hold them in the cloning machine if the others are not done in the next few days.. Glad I have options that can stretch me out for a week or 2 to give me a little more time. 2/2/2024- Pre-Germination Activities Day 2 I checked on my breeding run to see how close the seeds are and if the tent is ready for me to clear and clean but alas I am still going to need a few days. I setup the emergency 2X2 and that should give me 2-3 weeks. The plan is to still wait one more day to allow the beans to warm up to room temp and then drop them in Water sometime tomorrow. Form my Emergency 2X2 I have the following: 4" inline fan and carbon filter Fan VS-2000 light 2/3/2024- Germination Activities Day 0 - Dropped the Beans in.. Today is 0 day.. Go.. Go .. Go.. 2/4/2024- Germination Activities Day 0-1 - Checked in on them this morning and no tap roots yet.. covered them back up and back in to the closet they went. I setup the Root Riots and the Seed tray for them. I Ensured my water that I was soaking the root riots in was PHed to 5.8 and I used RO water. Afternoon Update: Checked on my Breeders and they are done. I started to harvest them, I took down the one I had reversed with STS and I took down the Black African Magic- All but one bud, I wanted to get some pics of that one today. I was only able to get 2lbs into the Cannatrol because I had to be very careful to keep the bud from the plant that was treated with the STS separated from the other seeded bud that was pollenated from the plant I reversed. Cannatrol could have held an additional 2oz of wet but not today. Ideally I need 1 more Cannatrol so I can take an entire Tent, but will figure that out. I put an additional 1.5lbs into the freezer to wait it's turn into the Cannatrol, I would have left it on the plant and taken it in 4 days when the dry cycle gets done but wasn't sure how much 2.2 lbs was equivalent to chopped and wet trimmed. 2/5/2024- Germination Activities Day 0-2 - Checked in on them this morning and 2 of them have very small tap roots out.. one still doesn't going to give them some more time. I will check in on them this evening and see if they are more open if so I will transfer the ones that are ready to their medium and seed tray. 2/6/2024- Planting Day TRUE Germination Day 0- Checked in on them this morning and all 3 of them have tap roots out. I broke the bottom of the tap root for #1 which was the biggest.. pretty sad.. I hope she survives.. I tried to be careful it just snapped off when I was trying to get it in the root riot right. Other than that all three are now in their in-between home in the 2X2 while if finish clearing and cleaning out their forever homes. 2/7/2024- Germination Day 1- Checked in on them and no surprise no sprouts yet. Sprayed the dome to moist it and light spray to the tops of the Root Riots. 2/8/2024- Germination Day 2- #3 is popped and it looks like #2 will be popped by this evening.. I got my second Cannatrol today so now I can take down the rest of the tent and get it into the dry/cure. 2/9/2024- Germination Day 3- #2 is popped as well.. so I have #2 and #3 up and still waiting to see on #1 but that might be a loss since I accidently broke off some of the Tap root when transplanting. 2/10/2024- Germination Day 4- #1 has Popped... We have ignition on all 3.. YAY!! I finished clean up and install of RDWC system, this time was unique the back left buckets 3 inch pipe wasn't seated correctly so I had to clean up about 12 gallons of water all of the floor. I also had two leaks coming from one of the Waterfall return junctions, this is why I do a full pressure test before I put anything in. I will continue to monitor it through tomorrow to ensure that I am good to go and then I will finish setting up the baskets and prepping the water to be ready for the ladies planting day!!! 2/11/2024- Germination Day 5- #1 Of course is going to be my trouble plant.. No matter what If she lives through planting in the system and making it, I think I might not cull her at all regardless, she has been such a problem, makes me wonder if she will be super worth it towards the end.. We will see as we go through this grow, but #1 has a piece of the shell on the leaves, Other than that I set up a new thing I have been doing since last grow converting my Baskets into Sure plants so I can see exactly where the water is when I plant them and ensure I have the water up high enough that they are able to access it and grow but not too high were they are drowning. 2/12/2024- Germination Day 6- Everything seems to be going good.. will just keep them moist and let the roots grow for a few more days before I transplant to forever home. 2/13/2024 - Germination Day 7- Just keeping them Moist. 2/14/2024 - Germination Day 8 - Planting day.. they are now in the system.. :-)I had to fill the water to the bottom of the basket where I could see water on the bottom rocks and just coming up where I had created my whole/ sure plant. 2/15/2024 - Germination Day 9- Top fed just a little to keep them moist and encourage root growth towards the water. I ensured the PH is right at 5.98-6.02 range. 2/16/2024 - Germination Day 10- Top fed just a little to keep them moist and encourage root growth towards the water.

🌱 Day 57 - Start of the Second-to-Last Flowering Week 🌱 Hello, Grow Friends! Today marks the start of the second-to-last flowering week—Week 9 overall, and Week 5 of flowering. 🌿 I’m getting more and more excited as my first grow nears its end. As I approach harvest, I’ve decided, based on my research, to stop feeding nutrients and stick to just pH-adjusted water for the final two weeks. 💧⚖️ Watering Routine: I’ll keep the same watering schedule—1 liter every two days, which is about 10% of the pot volume. 🌱💧 This should be enough to flush out the remaining nutrients, ensuring a clean finish for the plant. Temperature & Humidity: The temperature remains stable between 19-23°C, which I believe is ideal for this stage of the grow. 🌡️🍂 No more high temperatures to worry about! The humidity is fluctuating between 45-58%, and I’m keeping a close eye on it to stay below 60%. 💧🔍 Everything seems on track for now. 🌿 Plant Health & Growth: The plant still looks very healthy overall. 🌱💪 However, I’ve noticed that in the past three days, there haven’t been any visible changes in the size of the buds. 🤔 It could just be that I’m not seeing the growth clearly, but the only noticeable change is the daily opening of new flower calyxes. 🌸 Harvest Preparation: I’m already getting my equipment ready for drying after harvest. 🛠️ Once it’s time to cut, I’ll be hanging the plant to dry for the first 10 days. 🌿✂️ I want to make sure everything is set for a smooth drying process. Stay tuned for more updates, and as always, daily photos of the plant will be posted! 📸🌱 Day 62 - Last-Minute Decisions with Urgent Changes 🌱 Hello, my grow friends! Due to the trichome pictures I took on Day 61—which you can check out too—I’ve made an unexpected decision to harvest my plant a bit earlier than planned and make some changes. 🌿 Watering and Flushing: The last time I watered was on Day 61, using all the usual nutrients at the doses I mentioned before. But after seeing the trichome pictures, I decided to start a light flush today. I gave the plant 4 liters of plain water to begin flushing and will now only water lightly on Day 64. After that, no more water until harvest on Day 67. 🌑 Dark Period: From Day 66 to Day 67, I plan to keep the plant in darkness. I’m not entirely sure if this will make a difference, but I’m curious to try it out. ✂️ Defoliation: The plant is doing well, and I’ve done a thorough defoliation. I removed all leaves that aren’t sugar leaves or directly attached to the buds to improve air circulation and reduce the risk of mold as I approach the end of the grow. 💭 Trimming Decisions: I’m still undecided about whether to do a wet trim or a dry trim. Based on what I’ve read, especially regarding the yield from trim, I’m leaning towards dry trimming, as it might give me more usable trim material. I can feel the plant entering its final phase, and I’m getting really excited about the results and what the next few days will bring. Remember, I post a video update every day. If you have any tips or suggestions, I’d love to hear them! Until next time! 🌱

She's looking very good imo, growing nice firm buds and allready smelling real fruity and sweet. Absolutely love this lady,she will deff turn out a looker and a taster too I bet.