Week 10 Flower — The Beauty Before the Finish This week marks a very special chapter in the Eternity Grow Cup. As we approach harvest, the garden is simply glowing with beauty. Every corner, every canopy, every branch tells a story — and this week, I’ve taken the time to slow down and capture that story as best I can through the lens of my camera. All the photos you’ll see in this update were taken with care and intention. I use my Sony camera in full manual focus mode, and I don’t just snap and go — I spend time with each plant, each angle, waiting for that perfect moment when everything aligns. These are not just photos to document — they’re my attempt to reflect the feeling of the room, the energy of the grow, and the soul of each plant. Just like with the videos, I don’t shoot randomly and decide later. I record what matters, and what I record, I use. It keeps me focused, organized, and deeply connected to the process — and I believe it helps me tell the story more clearly, whether through stills or moving pictures. All five Runtz phenos are finishing beautifully. Each one expressing unique traits, but all carrying the same stunning quality — dense, clean, colorful, resin-rich flowers that fill the room with pride. This garden is finishing spotless, and I couldn’t be happier. This week’s YouTube episode will reflect that beauty. If you’re seeing this here on GrowDiaries, I highly recommend checking it out in full 4K once it’s live — there are moments that simply can’t be translated in photos alone, even though I try my best. But for those who love the details, the full spread of pictures is right here, as always. t this point in flower, the girls are not eating — they’re just drinking clean water with nothing but System Clean in the reservoir, at a rate of 0.25 ml per liter. This is part of a gentle, prolonged flush phase I like to implement, giving the plants a chance to metabolize and fade naturally. The goal is to promote clean, vibrant flowers that finish with optimal expression, without rushing the process. No forced flush, just time and care. Lighting-wise, the spectrum has been tuned with precision — we’re currently running 40% on the whites, with reds and UVs at 100% to drive trichome development, resin production, and color expression in these final days. The plants are loving it — they’re soaking in the deeper wavelengths that signal the end of their life cycle and responding with a final push of energy. And yes — we’ve been running 11 hours of light and 13 hours of darkness from the very start of flower. It’s not the usual 12/12, and it comes with its pros and cons. On the upside, it helps speed up ripening slightly, encourages more compact flower formation, and mimics the natural seasonal decline in daylight. On the flip side, it slightly reduces the overall DLI (daily light integral), so you need to ensure your PPFD and spectrum are dialed in just right to avoid sacrificing yield. For me, the trade-off is worth it — the plants are expressing themselves beautifully, finishing strong, and packing on the final magic. Now it’s your turn — I’d love to hear from you. Which phenotype is standing out the most to you in this garden? Which one is catching your eye with its colors, its fade, its structure, or just that vibe that speaks to your soul? Is it the frost? The density? The posture? Each of these girls has her own personality, and I know many of you have been following closely — so drop a comment, let me know: which one is your favorite? Which one would you take home? This run has officially earned the Dog Doctor Official Wax-Sealed Stamp of Approval. These genetics are beautiful — expressive, vibrant, clean. It’s been a joy to grow them, and an even greater joy to share this journey with all of you. Of course, we still have the final word coming after harvest, drying, and curing — that’s when the full picture reveals itself. But until then, based on everything we’ve seen and lived in this grow… this is the real deal. To everyone following the journey — thank you. To the sponsors, the community, the silent observers, the passionate growers, the haters, the lovers — I see you all, and I appreciate every bit of energy you send. This cup has been about more than just growing. It’s been about sharing. Connecting. Creating something beautiful together. And we’re almost there. Next stop: harvest? provably yes lets see ! Growers love always 🌿❤️ DD Genetics - Runtz https://www.zamnesia.com/6000-zamnesia-seeds-runtz-feminized.html Nutrients - Plagron https://plagron.com/en/hobby - Aptus Holland https://aptus-holland.com/ Controls - Trol Master https://www.trolmaster.eu/ LED - https://www.futureofgrow.com/en LED - https://www.thinkgrowled.com Soil - https://www.promixgardening.com/en Germination - Cannakan https://cannakan.com/?srsltid=AfmBOopXr-inLXajXu3QFgKXCXXos4F1oEvScjMKIB5MR5dk8-GJ-F49 DOGDOCTOR 15% off Smoking Papers - https://ziggioriginal.com/ Terpene saver - https://grovebags.com/ As always thank you all for stopping by, for the love and for it all , this journey of mine wold just not be the same without you guys, the love and support is very much appreciloved and i fell honored with you all in my life With true love comes happiness Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so As always, this is shared for educational purposes, aiming to spread understanding and appreciation for this plant. The journey with nature is one of discovery, creativity, and respect. Let’s celebrate it responsibly and continue to learn and grow together! Growers Love To you All 💚 #EternityGrowCup #RuntzHunt #GrowersLove #CannabisCommunity #AptusHolland #ProMixSoil #TrolMaster #Zamnesia #Plagron #ZiggiPapers #Grovebags

Hey folks. Into week 6. Not much happening. Just letting the girls settle back in after the windstorm have em a good whipping. Just standard watering when needed and some lst here and there.

Last days in veg—she’s doing very well and I’m really hyped for the bloom phase. Thanks to the topping and consistent LST, she didn’t just form a canopy—it’s more like a full-on “sea” of tops. Everything is spread out wide and super even, with tons of strong growth points all sitting on the same level. The main stem is thick as hell, and the four mains built from topping are insanely solid—each one feels like its own plant. Structure is dialed in perfectly, light penetration is on point, and she handled every bit of training like a champ. She’s more than ready for the flip

Starting week 8 droped day and night temps to 70 day 68 67 night started bring out colors in both strains! Runts is insane orange color solid fat nugs with the pie is purple and frosted almost to a white color. The smell of both strains is out of this world keeping the temps consistant is the key to having high terpiene content. Just the slightest touch makes both these girls so loud of fruit and cake batter or cookies from the runtz, too the overpowering lemon or manderin orange from the pie. Starting to get real close on the beauties gana push them to their limits!!!

Welcome to week 6. Day 36: Took off a few fan leaves today and gave water only. Day 37: Height 28cm Day 39: Fertigated with an extra strong mix, I'm going to up the nutes now until I find her maximal tolerance, she is starving. Day 40: Still starving. I'm keeping her constantly topped up with quite high strength nutes but it's not enough. I think 200ml may have been an overly generous estimation of her root space volume. Day 41: I knew this would be a challenge but it is proving more difficult than I expected. I hope the effort is worth it! At least so far I have learned more about autoflower flowering triggers with this grow. Day 42: in trying to get enough food in to her I have nute shocked. Need to somehow flush and hope for the best. I may have dealt her a fatal blow. Alright so to end up this week I have flushed the ever loving crap out of this lady. I've burned her with too much nutes, I didn't think it was possible but I went really over the top. So I have used a combination of a straw and 2l of PH corrected water and a lot of time and patience to repeatedly saturate and then upend and allow to drip out (with the aid of blowing bubbles in there with the straw). Eventually the run off stopped being dark brown. Then much later it became clear. I do not know if I can save this plant now I have really hurt her she looks in BAAAAD shape. Let us see what happens over the next week. I have adjusted the timer such that the main tent is now getting 20/4 upped from 18/6. After monitoring DLI at 18/6 for a week I am unhappy with the overall level but because of the varying heights of the plants I am limited in what I can do in adjusting the light height. Some areas were only getting 20 DLI. So I have rearranged to have the taller plants on the edges and the lowest in the middle and doing it this way all plants are getting between 35 and 50 DLI at 20/4 - although one or two cola tips here and there are getting 55. Will monitor for a week.

Look out for my next grown fast budz gorilla cookies and a other crack at blueberryz

Week 7 begins for LSD and Green Crack. These girls are sticky, getting frosty and slowly bulking up. They look happy and will hopefully start filling out over the last 2 weeks. Thanks for stopping by growfessors tune in next week for another episode of growfessor theatre! 👽🌳💚

In the beginning of this week ( Monday in the late afternoon) I started seeing some burnt tips. Not really a big deal if you give less nutrients in the future, but i don't like it. Thats why i decided to flush my plants and check the run-off. PH levels where decent but the EC was to high. Not a suprise because I forced them a bit last week by giving some more nutrients. So right now my PH and EC for the kushes are arround PH 5.8-6 with 1.3-1.5 EC and for my shamans PH 6.3-6.4 with ec 1.5-1.6 After my flush, I gave all the plants some Canna RHIZOTONIC ( root stimulator). I advice everyone to give root stimulator after stressing the plant out with like flushing. In this grow i always weight my pots, therefor i always know when to perfectly feed them. They dronk 9 to 10 liters of water/feeding in like 96hours(4 full days) which is insane because it wasn't that sunny/hot (evaporation) and they are not trees being in the open ground. and maybe the most importent thing is that normaly your roots will stress a bit because of overwatering(flushing) and will go into a shutdown or having a hard time for a period as a result that your pots will stay heavy(full of water) for some days. In my case, this didn't happen at all. Wednesday I sprayed all the leafs with Canna Cure for some nice leaf nutrients,getting rid of minor trips and to prevent other unwanted renters. Friday I started feeding them again with nutrients, like 2-3 liters each plant and today I gave them water 2-3 liters each plant with only Enzymen in it. It was a crazy thirsty week for them with an average of 1.6-1.7 liters a day😅 Sadly one lower branch got damaged and had to get rid of it but I didn't mind that much since these buds where far behind other buds in developement. I placed one bud under the microscope for fun and saw insane amounts of thc on it haha, and that for just week 5 of flowering for a outside grow. Made a picture of it, just take a look at it. - Critical kushes started getting into preflower, finnally!! but still, only 6 weeks left before it gets to cold outside. - Did some LST again because the criticalkushes are still stretching. They might still stretch for another 1 to 2 weeks, its getting out of hand haha. - Shamans and the critical kushes get different feeding schedules, Should had done that waaaaay earliyer but I didn't care about it until now. - Forgot to supercrop my plants LOL, for the shamans it is to late, don't want to stress them out in their stage, but i did in on the kushes, since they are only 1 week in flowering, still growing a bit, it would't harm them that much. No need for steering them around, already done that. Just doing it to stress them out a bit so they will send more nutrients to the branches for bigger yield. Have to keep remind myself that this is just an outside fun grow but I just can't help myself buying stuff and wanting to do more/better. Hope you guys enjoyed watching and reading.

Creciendo fuerte y adaptándose

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.

Day 10 in flower

All the photos are in the 8x8 now. just a few autos in here now FOR EVERYTHING MARS HYDRO VISIT: www.mars-hydro.com www.marshydroled.ca PROMO CODE: rocknroll VISIT THE ALIEXPRESS STORE: @marshydro_aliexpress Instagram: @marshydropenny Thanks for taking the time to read and check out my diary🤜🤛 TS3000 FEATURES: WIDEBAND SUNLIGHT FULL SPECTRUM LED GROW, Infinite close to natural sun light, suit for all plants whole stages indoor growing, rapid plant response from seed to flower, achieve maximum quality and quantity, much better than traditional HPS grow systems. HIGH REFLECTIVE & NOISE FREE-Fanless LIGHT BOARDS design will make your growing life easy and quiet, quickly heat dispersing material aluminum reducing light lost to aisles and walls, increase the light intensity up to 20%, allowing your plants receive more energy and without burning your plants for maximum headroom. 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I finally had some time to harvest everything, left her for 2 days in the dark in a vase. The smell was so intense in comparison to the painkiller. Since it rained a lot there was some bud rot but I guess that was inevitable. The honey cream still grows strong has no bud rot since the buds seem fluffy enough for a good airflow.

🌌🛸 hey hou, just putting in all pics from begging till now, cos im really low with the time,.. behind this project is biggest story of my life, not only grow story, its much more behind.. i wish nobody to get such a grow in way as i do,. actually is nothing possitive there and this project i started, cos i lost everthing what in life importnt is. with this project, once, i wanted to give back just a litle bit of that what i got,.. and it still not eneough,. some things you cant buy, you cant pay,.. and you can get back... peace and stay hard, thing about what you decide, think about twice..

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...😜

5 days before the pictures i started overdrive and dropped the floranova to 1ml

Hey now, hope everyone is having a great weekend and staying safe. Another great week for the ladies, as they are now about 3 weeks into flower, and the stretch has just finished. I am still feeding them silica, cal mag, and flower nutrients maxi bloom by GHE. I did start to add a PK booster this week pushing the EC up to 1.4. I also will be switched the light from V1 to the F1 Spectrum at the beginning of this week, and will be integrating the UV/IR bar into the light cycle later this week. I will run the UV/IR bar for approximately 30 minutes prior to lights off to get started. The tallest plants are the Sundae Driver and the Durban Nights at 42" and the Red Hot Cookies is the shortest plant at 38" however they all look happy and healthy and capable of easily giving up a half pound each. The 5X5 is really starting to fill up nicely, I am running two dehumidifiers outside of the tent and I am able to maintain around 50% RH in the tent during lights on, and around 55% RH with lights off. We did get an unexpected heat wave this weekend and it has been a struggle keeping the heat and humidity down but the flowers are just starting so no need to worry about mold or anything like that yet. As soon as this heat wave is over the temps should be good to go the rest of the way this is by far the best time of year to be flowering plants in my region. I did defoliate twice this week and I may do one or two more rounds before just letting them do their thing. Not much to do from here on out except make sure the reservoir is full and the PH is in the proper range. I hope everyone has a great weekend, Thanks for stopping by, Stay Safe and Blaze On!!! 💪 Website: https://medicgrow.com/ https://growdiaries.com/grower/medicgrowled

2nd week complete! Its growing day to day, with noticeable changes. Im waiting one more week before I switch to 12-12 and change it to the 12L container. I've been watering every 2 days, about 50 ml each time I water. One feed, one water, thats the schedule. I noticed that there are a lot of bud sites developing in the branch formation, so excited!! 👻