It harvest time for this lady, my second Jack Herer from Fastbuds. Grown under just 100w from seed to week 10, & On Her final week I’ve managed to put her in my other tent under a 300w led & instead of 48hrs of darkness I left her in 48hrs of light before I harvested. Seed to harvest in 81 days.

Update folgt …

Looking great so far. Removing more fan leaves every other day or whenever i find the time to check the garden.

Mein 1.er grow mit meinem neuen Upgrade 🤩 Kannst kaum erwarten bis alles aufgebaut ist. Nach monatelanger Recherche habe ich mich nun für eine neue Box mit neuem Licht entschieden und einiges mehr. Meine "babies" warten auch schon auf ihr neues Zuhause 🌞🌅🌻

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6/30 I messed up and put 8 days last week so I'll have tp do a six day week to get back on schedule. Pounded rain last night I guess. Very intense but very brief. As you can see in the video the plants are found great. A few have revegged so I'll need to defoliate the middle. I could make a TON of clones but it's pretty late for that. I might clone a couple outstanding plants to keep the genetics. Still seeing some pillar damage. Might do bt tonight. I'll keep this updated. 7/1 Super hot yesterday. Reached 90°. We are getting SOME rain today and thunder showers day after tomorrow. Bags still had some heft and everything looked good. I went back aroundcand found about half were at the point of needing water. He'll, they probably all did. My watering can is 2 gallons not 1.5 as advertised. So that means I used 5 gallons on the garden (not watering the 50) focusing the more water on the lightest bags. That tenth planet I'm seeing more septoria like leaves. This makes enough for me to be fairly positive ill need to treat it. I have plant doctor but I think copper works better. I also see more pillar damage so I've gotta apply something. I also need to lst more and I keep to clean put the interior of the plants so they don't get pm. EDIT: IT WAS 80° and no rain at 6:30. Humidity close to 100% bit plants look AMAZING! I'm hoping this may be my best year yet! I won't grow a bigger plant than tjat blue cheese in the 50 but so far everything is looking good. I may add some nutes to the pink kush in the 50 due to tje slightly less green color. I assume it's just because the other soil is all New amd this was a mix. I defoliated lightly to prevent pm but I have more to do. I just wanted to get a video of the girls looking good. 7/2 82° at 9am. Glad I decided to water even thoughvi watered yesterday. I need to up my volume. Thirty degree temp swings don't help much either. I said I used 4 gals but I used 5. I had one phed already. I'm hoping this will be one of my best years. IT looks like it! I won't have that MONSTER blue cheese in the 50. It was the smallest plant anyway and shows the difference between using NEW soil and mixing old soil WITH new soil. It's a much lighter green. Still need to apply bt and do a little more defoliation. EDIT: IT'S 90° WITH LIKE 100% RH. PLANTS LOOK A LITTLE HEAT STRESSED BUT OTHERWISE PRETTY DAMN GOOD. EVEN MY FATHER MENTIONED (KNOCK ON WOOD) "THAT I DONT HAVE ANY SHOT ON THEM THIS YEAR." LOL. I UPLOADED A VIDEO TO SHARE. HOPE YOU GUYS ARE HAVING AS MUCH FUN AS I AM! 7/3 83° at 9:40a.m. I need to increase my watering volume so I don't need to water every day. I used 5 gallons to water everything but the 50. I think I'm underwatering. However it was supposed to be severe thunder storms with torrential rain, high winds and hail. I'll gratefully take this hot sunny day instead. However in the future I think I'm not goingvto add in the predicted rainfall in my schedule. Unless it's a torrential down pour obviously. Everything g is still looking good and I've still got some work to do. EDIT: ITS 5PM AND NO "GOLF BALL SIZED HAIL. WE GOT A BRIEF RATHER INTENSE SHOWER. AT LEAST THE GIRLS GOT SOME WATER. IM GERY GRATEFUL THAT WE DIDNT GET THE STORM AND HAIL THAT WAS EXPECTED. 7/4 Didn't even get a chance to inspect the plants this morning as the wife had a medical emergency. My father called me (as I was about 5 mins away in route) telling me my plants were drooping and one was "really bad." I figured that since i had watered consistently the past few days and it was only 70 not 90 that they would be OK until noon. Boy was I wrong. I've upped my watering volume. I watered EVERYTHING with at least a gallon. I may have only given the tens 3/4s. Everything was back up by the time I left but the one on the end. I had forgotten flat I hadn't watered that one and needed to mix another gallon to water that plant. Thats why that plant looks worse on the video. I think my watering is going to need to increase to more than a gallon but it's a good start. I'll keep this updated. 7/5 Had to leave early again but I'll be back before noon. The wind is still whipping! I DID go around the cage and lifted every pot to make sure they were heavy. Even with the heavy wind the bags still were heavy. I really need to get some shit done this weekend. Last day of this week. Still haven't applied bt or done the pruning that needs to be done. I'll update as I go. EDIT: MY INTUITION WENT OFF AND I DODNT WATER TODAY SINCE I HAD JUST INCREASED VOLUME. THESE ARE MONSTERS THOUGH. I WENT OVER AT LIKE 1PM AND FIVE WERE DOWN. SOME SEEMED FINE. THE WIND IS REALLY STRONG THOUGH. CAUGHT ME TOTALLY BY SURPRISE. IM NOT EVEN TOTALLY SURE HOW MUCH I WATERED I WAS GOING SO FAST. IT WAS EITHER 17 OR 20 GALLONS. I KNOW THAT TJE PROBLEM PLANTS ALL GOT TWO GALLONS AS WELL AS SOME OF THE OTHERS. EVERUTHING IS BACK UP AND LOOKING GOOD THOUGH! IM REALLY CONSIDERING LIGHT DEPPING THE 10S. I DONT WANT A REPEAT OF THAT PLANT WITH ALL CALYXES LAST YEAR.

She’s a little shorter than the rest only by a couple of inches! I’ve opened her up by defoliating the bigger fan leaves and letting light get to the lower bud sites allowing better quality buds (non airy/popcorns) humidity hit between 50 and 56% and that’s perfect! Will lower in the last 2 weeks to 40% and hold during flush! Thanks for stopping by!

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.

On the first day of week 4 I did FIM on the plant at 6 node. Not sure if I overdid it and accidentally top her instead of FIM but we will see how it progresses Up to this point the plant has been growing very strong and healthy almost as fast as Autos I have grow before. Day 22 the plant doesn't seem stressed out at all and in fact is pumping New Growth right away I thought it was going to be sad for a day or two but no way the genetics are very strong the plant is very vigorous . Day 24 I did some minor defoliation to allow the light to penetrate everywhere in the plant. Also looks like the fim was a failed and end up topping instead I will continue to update thank you for reading and have a happy grow.

All 3 plants are adapting very well to LST, the shape its growing into have been allowing the light to reach further into the lower growth nodes and branches. I like to start bending the branches close to the main stem as early as week 3 of VEG. Now these 3 Northern Lights Auto seeds are from Sun West Genetics, they were all germinated, planted, trained, fed the same way they have been on the same controlled environment since day 1, the 3 are totally different, I know each plant is unique in its own way, but I find strange that 1 plant is taller and stronger than the other 2, the smaller one is growing weak leaves with signs of mutation, all 3 plants show signs of Magnesium deficiency, these 3 plants are sharing a grow tent with a Haze Auto from Seedsman, all 4 plants are under the same diet, the Haze have no signs of deficiencies or mutations, I guess that shows what good genetics look like. For the Magnesium deficiency I have mixed my own Epson salts into water and applied as a foliar spray, internet said the spray should be used every other week, wait 2 weeks to see results. Signs of Nutes burn, I decided to stop feeding for this coming week. The 3 NL leaves are looking unhappy, kind of clawing under, they look lifeless, I have ruled off a few potential problems such as: Wind Burn Under Watering Water PH Light Burn, just moved the QB higher to 17 inches from the highest canopy today. If any of you fellow growers have advice for the leaves, please let me know. Stay Lit folks 👩‍🌾🏻

This week has been fun still no problems with the grow no deficiencies this has been a easy grow like always for me.i need to do a defoliation on the plants today sometime

The plants have grown very fast this week, easily doubling in size. I moved them closer to the light to 90 cm from 110cm. Watering as needed and I am keeping the soil surface moist with light watering twice a day. I have fed the plants twice this week. First with a half dosage humic + fulvic acids, microbial inoculant and Seagro. The second feeding was half dose Seagrow and Biobizz BioGrow with some CalMag and Silicon. I am preparing a compost tea with some added kelp meal, insect frass and worm castings for the next feeding before I start LST.

We come a long way to her final week She is just drinking water now, in 5 days I will harvest. She looks very good. I would leave her another week but I need to harvest on next Thursday. Its been an amazing strain no issues at all. Not the biggest buds I have seen but very very nice smell and quite decent size buds. Looking forward to get final weight.

I tried trimming one plant. I left the other one untrimmed and went to dry them. We’ll see what happens :D Just a little experiment. The trimmed plant looks really funny, but at the same time it actually doesn’t look bad at all.

16/5/22: Week 3: VD15 for both. AN stands a little taller. But she comes of enzymes and TP goes on them this week, following their guidelines as far as when to give them the nutrients but I'm far of giving their recommend dose. 15.5 CM for AN GROW & 14cm for TP GROW. Both have been put into the 150x150x220 homebox and I have my 70x70x160 inside my big tent, this will allow me to keep the RH high in that tent while the photos veg and autos will be in full bloom. 17/5/22 both girls were topped above the 5th node. 18/5/22 Figuring out how VPD works. You could read for hours about this stuff and still not dial it in for years. But here's the basics. VPD 0.4-0.8 kpa for early seedling. So under or around 23c and around 50-60 RH. atm my VPD is 1.05kpa and for most of my plants the optimal range is .8-1.1 kpa. Temp is 80 F 25C and RH is 70%. To find the perfect VPD (Vapor Pressure Deficit)check out optimal ranges of VPD for growing stages, also your strain should have the optimal VPD. I don't have an infrared temp to check the LVPD (Leaf Vapor Pressure Deficit) that's a whole other ball game. Im not going to get too boged down at the moment with VPD&kpa. As I said that's in a whole other league. Im going to run a basic VPD environment though. In heavy flower my temp will defo be in the 26-28 range as I'll have the 20L dehuimifier in my 5x5x7. 22/5/22 Solid growth coming from these 2 ladies. 15+ cm growth in a week is great. Hopefully I'll get another 4-7 days of growth before they start flowering.

Hey guys Wo this week I'm hoping that the sherbert mimosa will go into full flower by next week. They have grown very fast this week, and are always hungry! The gelatocake as you can see are looking good and flowering nicely. They don't need no more work on them th sherbert mimosa have all been bent over and re tied them next week I will do a final defoliation next Wednesday. I'm on week 5 of the biobizz feed schedule. Temps are hard at the moment but keeping it at between 24°c - 28°c. Humidity is at around 55%. I will take this down once all in flower. Any questions or advice, just ask Happy growing guys 💚💜

I have harvested this planet but there was a problem one of my six inch fans stopped working so two bud stems had two small peach fuzz spot of white mould. So I chopped half the planet off with garden secateurs and disposed of straight away, and after inspecting the over half of the plant finding no evidence of mould I washed with warm water. It is now in quarantine drying in my shed. That was the reason I haven't taken pictures in case my shed gets broken into 😂 so until next time ✌️ out my fellow Growmies and all going well I should have a very small amount of weed for dry weight and smoke review

It’s the 1st week of flower I flipped the plants to 12/12 a few days ago. There is a lot going on and a lot of cool and amazing things coming in the near future. Make sure to check out my YouTube page. I bought me a DJI gimbal this week. Might be my new favorite toy. The temps are starting to break for the summer. I don’t see it being very long until winter is here and it’s time to use a heater and not an ac unit. All of the plants are healthy. The plants have all grown so well I turned down the light intensity a bit today the plants didn’t seem like they was starting to strech very much. Hopefully the lower light intensity will make them strech out just a bit

Flower next week so upped the nutes with some bloom nutes. Topped all the tallest tops which was about 15, so all the lower branches have a chance of picking up to the taller ones. Day 61 // had to clean the girls up and strip them a bit, removed about 50g of Leaves and small branches and shoots i didn’t want