07.11 New flower week is here, for now all going good, still cant wait to see final product and how big and tick buds can be, but ride is joyfull and exciding. Watering 1.3 l all 3 with nutrients and cal-mag, ph 6.2-6.5( i got ph meter without calibration fluid) but how much time i did mesuring i know how big ph is after i get water from tap [7.5-7.9(did mesuring 120 times minimum, before nutrients, after nutrients and after i add down if i need)] and yea, dont see much differnts on plants in few days without ph meter, but he is here in case, better check up,air flow is good , humidity good(above light zone 45-55%, down by plants 55-65%) and temp day 25°-27°,night 18°-24°. I adjust pots every day 2 times minimum so every side get some correct light in all parts( maybe silly but i think its not anything bad to keep every side in some parts of day better lighted). Wish me best for tomorrow i will need it, and them also in rest of the grow proces🍀💪🏻🍀🤞🏻🙏🏻 08.11 Today they was out to get some neem spray and see bit of light till weather is not bad, and to not spray in tent, better photos then last time i guess, they look happy and healty, today no watering i saw that soil is not dry 09.11 Today's subject..watering 1.3l pro plant with nutrients and cal mag, ph 6.2- 6.4. How i see its good, going good and wish them best till end and more, weekend is here 10.11 Watering 1.3 l pro plant with cal mag and nutrients, ph 6-2-6.5 I saw some gold colors on end of the leafs I think i forgot put down light intensity after spraying them with good amount of neem oil, i got some time to do it, and normal i am busy so, why not i guess Hope its not some problems with plants, looks like burned a little not like sick and dry, and only top of leafs Wish them bless and the best 🙏🏻🍀😋 11.11 Watering 1.4 l with nutrients and cal mag, ph 6.2-6.5 Plants looking good , still on big one bit of yellow color on leafs, hope it will go soon, this 9 weeks was gone fast ,but this part like clock was stoped i wish till end good situation with them, good run, and all what they need🙏🏻🍀💚 12.11 I decide to try give them one day water with cal mag,ph 6.2, 1l to each of them,try to flash a little bit in hope that will help better recovery from damage, next time when i spray neem i will leave outside a bit dry and try to keep light intensity lower, bit of adjusting fen and vent, still recovering from burning down from light.. nervously waiting end😊😋😁💚🍀🙏🏻 13.11 Waterin 1.4l pro plant with cal mag and nutrients, ph 6.2-6.5 Smallest one chaching up with 2 bigger , realy happy how she turn tabels and cant wait to see how she will look on the end, plant are happy, good health with no problems, only that few of yelowing leafs that almost all had recoverd,like i said, realy happy with what i saw , now they have bit stronger smell(can feal it when i get in apartment, even if i put vent out i can taste it but ok, thats how should be, need to smell a little) And from other stuff, today was first time snowing ❄️ Soo hard winter is in front of us, till then girls would be dryed and cured probably not 100% but enoguh to go outside, take a walk on cold and smoke one Ladys stay hard till end and good 🍀🙏🏻💚❄️ P.S night temperature when lights are off is 15-17°[problem is with opened window becuse of vent,dont know what total resault of that would be(maybe i should let lights on night so i can have better temperature in tent, aka switch ciclus of light to be dark weil i work)] thoughts ?

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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.

Welcome growfessors to Growfessor theatre! We have 10 plants in the 4x8, under the brightest lights in SacVegas! Day 1, week 1 of flowering, flip mode!! 5 Mandarin dreams, 2 Green Crack, 2 LSD and 1 Divine storm round out the grow lineup. Lights are two custom built Samsung strip lights, LM561's, each one powered by HLG-480-48A driver's. Thanks for stopping by, tune in next week for another episode of growfessor theatre! 👽🌳💚

lots of cloudiness and a hint of amber starting to show in the trics, overall banging growth on the blue dreams. I mislabeled one (the purple AF one) so thats unknown strain. lol I won't have someone help germinate next time. lol other than that. looks like a great run. ill be doing multiverse beans run next. going to make a seed to harvest video for the Haptic Nation Growmies YouTube channel too.

All round a very good plant to grow , one of them stretched but I lollypopped and topped it late into flower due to outgrowing my tent and she took it well, producing absolutely top quality buds covered in milky thricomes and glistening all over the nuggs. Absolutely frosted. The smell at this point was around 7.8 smelling strong of orange and citrus , the main cola nice and dense, with lots of other colas branching off. Easy strain to grow to this point although I did have a calcium deficiency but it was fairly rectified.

Did some defoliation and lst this week. Spread out the branches a little better because they were too close together. I lollipopped them a couple days ago. Theyre growing very wide, bushy and fast. Budlets will form any day now. Giving her one last shot of sugar royal. Only one of them isnt getting it because she looked quite packed with nitrogen. Dont want the same like my last grow to happen this time. :)

Week 12 The buds are slowly fattening up. Dutch Passion issued a warning on their website that certain strains like this one can cause them to produce male flowers when exposed to too much stress. So I only do careful rounds of minimum defoliation in order to hopefully prevent this from happening.

Cleaned the crown out and lifted the canopy gonna give them another week then flipping 🤙

on essaye de palier aux carences

5/14- Future #1 buds are continuing to fatten up. Some of the top bud leaves look like they might be getting some light damage but will continue to monitor in case I need to dial it back a bit. Otherwise, continue to feed balanced pH water and limited nutes.

🍓🍌🚗 Red Strawberry Banana Auto by Sweet Seed 🍓🍌🚗 🍌8.8 🍌9.8 🍌10.8 🍌11.8 🍌12.8 🍌13.8 It resumes with the updates yeeeeah !!!! I have developed 18 branches at the moment, and I will stop here, now I wait for it to come into bloom, very ready to give my best. yeah !!! Super Big Up for the Sweet Seeds sponsor who continuously produces these wonders 🤘🤘🦄🦄🦄🔥 🍌14.8 __________________________________________ ❓ Are you new to the world of the cultivation and don't know where to safely buy your seeds? 😮From SweetSeeds you can find award-winning, sweet, fast, fragrant, beautiful, and delicious genetics !!! ✅http: //bit.ly/SweetSeeds_ __________________________________________ 👀 Are you looking for a good lamp to start with? 👀 🌞Viparspectra has something more than the others, take a look at their site. ⏩ Use "GDVIP" for an extra discount or "ViparDreamIT" for an extra 5 %% discount 👀 Search for it on Amazon ✅Amazon US: https://amzn.to/30xSTVq ✅Amazon Canada: https://amzn.to/38udUVe ✅Viparspectra UE: bit.ly/ViparspectraUE 👀 Watch my ViparSpectra XS1000 unboxing on YouTube, leave a like and write to the channel 🦄 ✅http://bit.ly/UnboxingViparSpectraDreamIT ______________________________________________ 📷🥇 Follow the best photos on Instagram 🥇📷 https://www.instagram.com/dreamit420/ 🔻🔻Leave a comment with your opinion if you pass by here🔻🔻 🤟🦄💚 Thank you and enjoy the growth 💚🦄🤟

my dry and cure style is this: 4 days of hanging upside down to get water activity lower to around 0.6 in 50% humidity and 26 C temp (i know its a little high but we are in a hot summer right now and i cant get it lower even with air conditioner) and then after 4 days of drying i remove leaves and stalks, trim buds and move them to jar for the rest of their life :D . and in the first 4 days of curing i open the jar door and let hem get some fresh air in the jar for about 5 minutes and close the jar door again, after 4 days of curing like that buds are smokable but they will get better as they getting cured about 1 month. buds are one of the hardest as fucking rocks type of buds! very dense , compact , sticky , smelly , amazing at every aspect growing stage was 56 days and flowering stage was 75 days total (harvested tops at day 64th) the total weight of dry buds was : (plant #1 & #3 top buds 56 G + lower buds 22 G ) 78 G + (plant #2 top buds 47 G + lower buds 18 G ) 55 G + (plant #4 top buds 120 G + lower buds 67 G ) 187 G = 367 G

They have been in sleep for more than 5 days . The space is a bit tight for all of.the plants but soon enough they will be transfered in another enviorment and we have to wait for them to expand and start to bloom .

Day 75 - April 25, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 9:30PM * 1.77 EC * 6.19 PH * 73.94F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1206PPM CO2 (Lights On) ~645PPM CO2 (Lights Off) Day 76 - April 26, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 9:30PM * 1.77 EC * 6.14 PH * 73.58F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1206PPM CO2 (Lights On) ~645PPM CO2 (Lights Off) Day 77 - April 27, 2021 Mixed new batch of nutrients: 40-gallons (RO water) 10-gallons (tap water) 1.5 ML H2O2 (35%) 0.5 ML Mills Nutrients Vitalize 11 ML Mills Nutrients Basis A & B 1.75 EC 6.20 pH Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 7:55PM * 1.77 EC * 6.14 PH * 73.40F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1156PPM CO2 (Lights On) ~540PPM CO2 (Lights Off) Day 78 - April 28, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 8:20PM * 1.77 EC * 6.17 PH * 73.94F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1180PPM CO2 (Lights On) ~540PPM CO2 (Lights Off) Day 79 - April 29, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 8:45PM * 1.77 EC * 6.15 PH * 73.76F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1200PPM CO2 (Lights On) ~660PPM CO2 (Lights Off) Day 80 - April 30, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 9:00PM * 1.77 EC * 6.10 PH * 73.94F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1180PPM CO2 (Lights On) ~730PPM CO2 (Lights Off) Day 81 - May 01, 2021 Watering: 010:00AM-10:08AM ~0.25 gallons per pot 02:00PM-02:08PM ~0.25 gallons per pot 6:00PM-6:08PM ~0.25 gallons per pot 8:00PM-8:08PM ~0.25 gallons per pot Reservoir: * tested 9:35PM * 1.77 EC * 6.07 PH * 73.40F Lights: * Gavita LEDs On 12-hours (10:00AM - 10:00PM) ** 10:00AM Lights On (100%) * Gavita LEDs Off 12-hours (10:PM - 10:00AM) * UV Bars On 8-hours (12:00PM - 8:00PM) Air control: 70F-80F (78F AVG) (Lights On) 66F (Lights Off) 65%-75% (70% AVG) humidity (Lights On) 65%-75% RH (Lights Off) ~1170PPM CO2 (Lights On) ~540PPM CO2 (Lights Off)

The single plant of BADAZZ from RIPPER SEEDS harvested a very good amount of 67 gram of dried bud. The buds were not very big, but insanely frost and dense, she was the SECOND BEST YIELDER in the HOMEBOX tent. A VERY DANK VARIETY! She reeks of KUSH and also tastes like it when smoke a very fully, gassy aroma and taste, VERY DELICIOUS!

Day 28 flower, things are doing well, humidity and heat are stable, plucking off leafs as I go along now anything blocking bud sites. I'm on week 7 of the biobizz feed schedule full dose, these girls not showing any nute burn or stress so far either I could probably push them more. Day 33 from flip. Heat and humidity are under control. Sitting at 27°c and 40-47% humidity with lights on. And 20°c and 47% humidity lights off. Ph levels on feeds and watering is 6.5, there really loving the biobizz range and the marshydro tsl2000 combo. So today the plants are getting fatter and nice and dense. Its super sticky and stacking on trichomes. These 3 beans came from The same pack, and each one smells diffrent. Closest pheno is a really lemon citrus smell and its strong. Middle pheno is like a sherberty smell and really tickles the 👃. Pheno 3 at the back is like a lemon skunk, really pungent and its got the fattest buds so far too. Day 34 flower, Feeding molasses today in 6.5ph water, I will start the next week tomorrow and will be starting on week 8 of the bio bizz nutes schedule. Thanks for all your support so far. Keep on growing

We have arrived at the end of week 2 for the 16oz dutch bucket setup and this auto ghost og is doing my pretty well. I topped her on day 10 and started a little training on day 13. I would normally up the feed a little at this point but I have a couple plants in the system that are a week behind, so I am going to give them a few more days to catch up before increasing the dose. They are still getting 24 hour light and 24 hour irrigation. Should start to see a growth spurt by the end of next week as long as I keep them happy.

Day 1 flower