The Grow Awards 2026 🏆
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July 20: smoke arrived this morning to go with our heat wave. Awesome. Extra watering, misting air, and wetting the sides of the grow bags with hose water to keep things cooler and hydrated. So far so good in the heat. Did foliar spray of Extreme Blend and potassium silicate. Also note that for all my grows I use apple cider vinegar for pH adjustment and a Dr Bronners liquid soap as a wetting agent (surfactant). Euphoria is doing great, but to ensure that it finishes early enough for this latitude (53N) where the UV light gets very weak after mid-August, I’m starting the force flowering tonight. Already starting to flower but I want a strong flower set and as much flower growth under strong sunlight as possible. Force flowering schedule is 2-3 weeks of in dark garage at 9 pm followed by 730 nm far red light and then back out at 7 am. The light initiates dark mode 2 h faster so it’s like having a 26 h day. Good trick use as a bloom booster, also moves up the finish 2-4 weeks. So, 10+2 is 12 h dark and 14 h daylight. Might sound bogus but it works. July 21: first night of force flowering caused a big stretch. Notably stretched after darkness in hot garage overnight. Hot outside overnight too but was much hotter inside garage and recorded here as 24 C. Seems okay and high overnight temperature might be ideal at this early flowering stage. Warm overnight temperatures continue for a few more days. July 22: record hot overnight low forecast for tonight of 24 C and feels like 27 C with humidity. Wow, that is really incredible for here and 13 C above historic average. July 26: six days into flowering and she is doing fine. 👍👍
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@Targona
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Targona: 36 days since my little girl sprouted from seeds🌱 Fifth week of growth of my Apple Fritter Automatic 🍎🍏🍎 Nutrients: I use Advanced Hydroponics Of Holland nutrients - three basic components, still according to the table for growth and flowering, I only change the dosage according to the plant phase 💓 - - Dutch fertilizer Formula 1 Grow - supplies the plant with substances necessary for the perfect development of roots, stem and leaves; intended for the growth phase 🌾 - Dutch fertilizer Formula 2 Bloom - contains a large amount of nutrients necessary for rapid growth and fruit development, supplies the plant with energy; intended for the flowering phase 🌸🌿 - Dutch fertilizer Formula 3 Micro - increases oxygen intake, improves plant immunity, ensures better absorption of nutrients; intended for the growth and flowering phase 🌴 --------------------------------------------------- -------------------------------------------------- ------ Plagron Power Roots - Root Stimulator Plagron Roots is a biological root stimulator that supports the formation of the root system. I use it until the fifth week of growth 🍃🍃 - I fertilize for the last time in the fifth week of plant growth - this week I fertilize for the last time. -------------------------------------------------- -------------------------------------------------- -------- BioBizz Calmag - The special Calmag supplement was designed for professional and hobby growers who need to supply their plants with calcium and magnesium in organic quality for a long time or immediately. The 100% organic 💩💩 and certified BioBizz Calmag product is made of calcium carbonate and magnesium sulfate supplemented with humic acid. -------------------------------------------------- -------------------------------------------------- -------- BioBizz Bio pH - is an organic pH regulator. An aqueous solution of citric acid, which occurs naturally in citrus fruits 🍋🍋 ---------------------------------------------------------------- ------------------------------------------------- During the flowering period, I add stimulants: - JUNGLE X Environ is a highly effective complex preparation for stimulating flower formation. 🌸🏵️ - Bud Candy - carbohydrates for my girls 🍭🍭🍭 General: Apple Fritter Automatic 🍎🍏🍎 - The girl is beautiful. I have to keep an eye on her 😁. She has grown to a considerable height - for an Indica dominant she is really very tall, she has outgrown all her sisters by a large chunk. She is strong and so far responds well to nutrients, the stem and branches are thick and the leaves are still beautifully green, strong and large Training: This week I did LST on the adult young branches by attaching them to the edges of the flowerpot with string, just like the others. There was no need to defoliate, the girl is not leafy at all, so at this time I only occasionally cut off a leaf that is blocking and shading 💚🌞🌞 Light: Mars Hydro TS1000 The plants respond effectively and the light is technically very well managed - I try to have 25 cm between the light and the plants, so I regularly move it up 💡💡💡 Thanks for the likes :) See you soon 😍😍
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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.
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Aquí han pasado al interior, comienza la floración, día 26/08.
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@SamDo
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Hello,, fin de semaine 6.🤟 Les plantes ont très bien récupérées de leur défoliation de la semaine dernière. Le feuillage est redevenu bien dense. Je les passe en floraison aujourd’hui. J’ai donc fait une défoliation pour laisser pénétrer un maximum de lumière. En espérant que cela leurs soit profitable. 🤞 Voilà pour cette fin de semaine... Happy grow...😎
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@Mr_BFL
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N 80 P 113 K 224 Ca 50 Mg 95 S 100 Fe 1,2 👌
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They're really starting to bush out, I think I'm liking the topping of all tops on the whole plant 1 time. Makes it easy to train as well. We'll see how they compare in harvest amount to my LST long veg plants.
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@QoverQ
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Hey guys :) The girls got topped once now, they still recovering from the light burn i did, Trying to ‚LST‘ 😄 Started giving nutes in a Half dosage at week 3 !
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6/13/2023 Week 10- Day 1 of Flower (Day 131 overall) (Day 70 of Flower) Auto Pilot Day 6.. Checked the Trichomes and the bud density and both are looking good.. Definitely needs a little more time for the Trichomes to be where I like, so based on my check I think we are still looking right around the end of the competition 22June to be done and ready for harvest. I do like that the fade is coming in the leaves nicely, so my chart I think is dropping off the Nitrogen exactly like it is supposed to. 6/14/2023 Week 10- Day 2 of Flower (Day 132 overall) Auto Pilot Day 7.. Decided I would take some contrasting pics today with my light up to 100 and my light all the way on Dim. I hope you enjoy the pics. 6/15/2023 Week 10- Day 3 of Flower (Day 133 overall) Auto Pilot Day 8.. Decided to take a look at the Trichome's today and Check to see where they are at and honestly if I might ho ahead and start my flush tomorrow and harvest on Sunday. 6/16/2023 Week 10- Day 4 of Flower (Day 134 overall) (Day 74 of Flower) Today I pulled an Armageddon however instead of darkness they are going to get 48 hours of light. The reason why they are going to get light instead of dark is when I was taking out the netting a lot of the buds were so heavy they fell over and exposed some areas I really want to get some light to... so 48 hours of light at 40% while I watch what should be a beautiful final fade as the plant eats up the last Nutes. If anything goes wrong I can abort take the photos and cut so will pay really close attention to how it is looking over the next 48 hours. Added 30 Gallons of PH only Water. Reduced Lighting to 40% removed program time off. 48 hours of light. 6/17/2023 Week 10- Day 5 of Flower (Day 135 overall) (Day 75 of Flower) I had someone tell me that a few growers had done as I did and Gone Armageddon on the plants. Filling it with PH only and said the plants did not respond well and they were taken out of the comp at the very end because they felt like the pictures just wouldn't come out right. Even though I did go Armageddon, The PPM is at 353PPM with the residue of what was left in the buckets after draining as well as what I am getting from the TAP so I think they are doing good but I am checking them every few hours to see how they seem to be doing and I think they are doing good still and are on track. I also started prepping the area for the pics tomorrow T-24 Hours until Chop 6/18/2023 Week 10- Day 6 of Flower (Day 136 overall) (Day 76 of Flower) (Harvest Day) What a day.. what a day.. what a day.. as I was setting up and trying to figure out how I was going to get my pics #3 stems started breaking, it fell over and other stems broke.. So no really stunning competition photo for her, she had such a nice purple fade.. #2 stayed up in the Tent so that is the one I had to go with to submit for the contest. I wet trimmed them as they went into the tent and they took up three rows hanging in tent. I also decided I wanted to try some so I put a little in the freeze dryer for a 48 hour smoke test.. I will weigh it and add that to my total weight for the plants when it is all done.
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We’re in the home stretch. I’ll start flushing #3 at the end of this week. #1 will get one or two more weeks of feeding before I start it’s flush #2 is about two weeks behind #1.
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Nothing different this week. Plants are still changing fast and looking healthy. Will probably top dress this coming week.
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OMG OMG OMG finding hard to put on words all i am felling with this one, she was a delight to grow and without trying yet her medicine she wen strait to my top 3, i mean super strong Mama, strong to everything pests you name it, amazing structure her terpene profile is taking me back to the 90s with her almost like gasoline smell mixed with limes and pines OMG cant wait to try out this one much but much respect to DutchPassion on this creation of them she is so so so , like glue that you cant touch without getting it everywhere <3 <3 haded the last 3 weeks and harvest time-lapse i fell like this one could have gone more than the 71 days in flower that she did, but there is no time for that in this run but i will run her again thats for sure and a must for me. Guys trust me on this one , she is a must , a real must in any garden <3 <3 <3 Thank you so much Dutch Passion for this blessing of an opportunity and for everything you guys do for the community much respect and appreciation <3<3<3 Everyone best of luck for the contest this was an amazing and fun one <3 <3 <3 As always thank you all for stoping by for the love and for it all, i truly appreciate and enjoy the ride so much more with you guys around <3 <3 <3 you guys make me fell super blessed <3 <3 <3 #aptus #aptusplanttech #aptusgang #aptusfamily #aptustrueplantscience #inbalancewithnature #trueplantscience #growerslove #dogdoctoofficial With true love comes happiness <3 <3 <3 Always believe in your self and always do things expecting nothing in return and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so <3 <3 <3 More info and updates @ https://growdiaries.com/grower/dogdoctor https://instagram.com/dogdoctorofficial https://youtube.com/channel/UCR7ta4DKLFMg2xxTMr2cpIg <3 <3 <3 Growers love to you all <3 <3 <3 I will post more photos from her dry trimmed bud report smoke etc asap <3 <3 <3 and need to clean space on my iPad so that i can upload the rest of them photos and videos , my apologies <3 <3 Done hehehe waiting on this beauties to dry now <3 <3 <3
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The final Week, before harvest! She has some massive towering buds! 2.5 gallons of water is lasting this plant 5-6 days before drying out, and ready for more.. She was harvested instead of being watered!
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@MOTB666
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Been pretty busy lately but these girls just keep at it. I did go several days with out topping them off this last week, probably only had a gallon left of water in thier buckets when I switched to transition. Only problems is a little bit of light burn and maybe a little bit of pest damage on one of them.
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@Paul_on
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Can't upload video or photo ,keeps telling me video didn't upload try again 😕
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Esta semana, poca cosa a añadir, tan solo que continuamos como la semana pasada. Riegos alternos entre abono y agua, según tabla de fertilización de JUJU Royal by BioBizz. Hemos aumentado la potencia de extracción para evitar olores.
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Day 30: Let grow, no water no feed. Thick stalks, RapidStart making a HUGE difference. Baby + Speed looking good for a baby. Big + Speed taking LST well. Tent Temp: 77º RH: 53º PPFD: 700 VPD: .67 kPa Day 31: Both + Speeds looking really good. Excited to see how they stretch in the coming weeks. Fed 4ml FloraMicro, 4ml FloraGro, 6ml FloraBloom, 2ml CALiMAGic, 1ml RapidStart, 2.5ml ArmorSi, 1ml Floralicious Plus, 1ml Liquid KoolBloom and 5ml FloraNectar. Solution Temp 70º PH: 5.8 PPM: 950 Tent Temp: 77º RH: 52% PPFD: 750 VPD: .66kPa Day 32: Same as yesterday. Good. Tent Temp: 77º RH: 51% PPFD: 800 VPD: .67kPa Day 33: Let grow, no water no feed. Tent Temp: 77º RH: 52% PPFD: 750 VPD: .67kPa Day 34: Both + Speeds doing well. May perform some slight defoliation on the larger + Speed in the next few days. Leaf tucking for now. Removed small bud sights and lower fan leaves from smaller + Speed. Watered .5gl RO water PH: 6.1 Tent Temp: 75º RH: 55% PPFD: 750-800 VPD: .58 kPa Day 35: Looking healthy and happy. Starting to get a slight skunky smell in the tent. Tent Temp: 75º RH: 55% PPFD: 750-800 VPD: .58 kPa Day 36: Ready for feed again. Cutting out FloraMicro on this feed, Cosmo and + Speed(s) showing slight signs of nitrogen toxicity. Fed 4ml FloraGro, 6ml FloraBloom, 2mg CALiMAGic, 1ml Floralicious Plus, 2.5ml Armor Si, 1ml RapidStart, 1ml Liquid KoolBloom and 10ml FloraNectar PH: 6.1 Solution Temp: 71º PPM: 925 Tent Temp: 76º RH: 52% PPFD: 750-800 VPD: .67 kPa
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So it must be that she prefers to be defoliated the training seemed hard on her for me. She wilted really hard through the weekend. I even reduced her light hours way back and separated them. Now they're back together again. I find that shes also a heavy drinker. I'm super excited shes definetly flowering now! And rather large for the container size. Hope you enjoy & check back next week to see just how fast she grows! And remember its 4:20 somewhere!!!!!!
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Day 58 - As you can see, buds are looking full but still looking like they want to go a bit longer, checking the trichomes frequently and seeing a lot of cloudy.. think i saw the first few ambers too. Any how, we shall keep going. Flush time soon. Day 62 - Looking good, smelling better.. really fruity and sweet. Seems ripe too. Feeds lowered and a little flush. Buds are rock hard, very dense and sticky. Looking forward to harvesting. She will be ready by day 63, but I'll see weather or not ill let her go longer. Stay tuned. Day 64 - trichomes ready, little flush and shes ready for the chop. Beautiful smelling strain and easy to grow. Very hard dense gassy and sweet buds. Once dry and cure, will be back with a little update.