Cut at 9 weeks. Organic 1 gallons work great

The plant is a joy to grow smell is incredible with a very dense buds all white snow trichome coated . They seem to have like a week or more to go but I'm goin to chop all the plans in my garden at the same time so 1 and 1/2 Weeks to harvest. I will continue to update thank you for reading and have a happy grow.

Neville's Haze dont stop to grow

CRAZY NIGHT (Continued) And not only is Frontdesk girl steaming mad that NX hit it and quit it (apparently she was looking to make him breakfast and then introduce himn to the family!!!), she brought along her rather large brother! Frontdeskgirl sees the Stephanies, they see her, large brother see NX's eyes and everyone puts 2 and 2 together. Stphanie 1 was the first to smack NX accross the face, followed by S2 with a kick to the shin, more from S1, S2 with the assist, NX starts hobbling away. But no! Now Frontdesk girl has made it to the group and shes swinging at EVERYONE!!!! Luckily myself and the others in our group were safely out of arms reach and were able to witness this spectacle alongside the curious morning Montreal onlookers. The stephas start fighting back with FDG, and the brother starts to chase my brother!!! Now in most situations, my brother would get backup, bit there was just too muych going on to watch, the big dude obviously had a bum knee, and my bro had a head start and an athletic build. So, there we were, bags dumped outside the hotel, a classy fight on the sidewalk in front of us, my brother running away into the sunrise, and a whole day of events planned. I picked up my shit, my bros shit, my buddies did the same, and we noped the fuck out of there., leaving the girls to figure that shit out themselves. Never saw the Stephanies again. To this day they could still be in Montreal, who knows. My bro is still alive, and I will never know what happened to Frontdeskgirl. DIARY STUFF CHOPPED IT!!! Its huge, it stinks, and I cant wait to show you the harvest and cure photos. Im a big fan of this strain, and I hope it makes it to the FB roster!!!! Thank you Heather and the Fastbuds team for allowing me to grow and profile this wonderful genetic

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.

👹06/07/2025 Week 16 LFG!¡!👹 She's starting to come into preflower really nicely I'm surprised it took so long to stretch weeks ago I'm honestly surprised and hopeful for what's in store for the next month or so lol stay up guys I'll update as the days and weeks go on thanks again for stopping by lfg!!!

First 7 days of the Strawberry Gorilla from Fastbuds. She was germination in glass of water than move to cotton and in 2 days it had more than an inch of root so i moved to her home 12 liters pot with biobizz,coco peat and perlite for the vegitation she will have the Marshydro Ts 600 in 80 x80 grow tent.

Day 36: My plants went to flower and now i am starting to have problems with 2 plants. If anyone can inform me on how to fix these problems that would be great. I havent really changed anything during the grow yet i top feed on day 34 other than the normal. Thanks for looking and happy growing.

12/12 + 137 jours Vu qu’il y a 16 plantes mais que sur growdiaries on ne peut mettre que 8 variétés j'ai divisé en 2 diaries pour le bas de la tente 1️⃣ 🏠 90x60x90 ☀️ FC-E 4800 => puissance a 60% 🍁 Black Bomb / Philosopher Seed Amnesia Lemon / PEV Seeds Amnesia Lemon /PEV Seeds Blueberry / PEV Seeds = 17g Blueberry / 00 Seeds = 17g Wappa / Paradise Seed = 11g Dark Phoenix / Green House Seed Quick Sherbet / Exotic Seeds = 14,5 Mango Cream / Exotic Seeds Banana Frosting / Sensi Seed = 11g Hindu Kush / Sensi Seed 10,5g Mix 1 / Sweet Seed = 26,5g Mix 2 / Sweet Seed = 15g Mix 3 / Sweet Seed = 22,5g Mix 4 / Sweet Seed = 14,5g 📎 https://growdiaries.com/diaries/122084-grow-journal-by-soosan 📎https://growdiaries.com/diaries/124052-grow-journal-by-soosan 2️⃣ 🏠 30x60x50 ☀️TS1000 => 100w = 54g 🍁 Quick Sherbet - Exotic Seed = 12g Quick Sherbet - Exotic Seed = 12g Quick Sherbet - Exotic Seed = 17,5g Quick Sherbet - Exotic Seed = 12,5g 📎 https://growdiaries.com/diaries/122080-grow-journal-by-soosan

Day 8 flower Plants look like they will end up small. This was a short veg. This is a great time to train plants. _____________ Day 9Flower Plants need to be tied down to have wide arms by day 7 Day 11 flo 18.5inches tall 12inches from light 1300ppm _____________ Day 13 Aggressive defoliation and Lollipop ___________ Day 14 Secret sauce microbe blend .7/gal

Giorno 42 Un po' di caldo per le Jack 47 Xl mentre le altre piante stanno abbastanza bene. Ci vediamo settimana prossima 🖐️ ❤️

Поливаю водой

! this is my current status, gonna upload my last veg weeks within the next week - got a bit busy around Spannabis - thank you for your understanding! 💚 Welcome to Bud Boutique Grow Diary - really appreciate all your love and support :) Dont forget to check out my other current grows! 🗓️ This Week: - Day 24: attaching once a week APTUS Foliar with Regulator & Nutrispray with the amazing CannaFogger by Petra Grow - Day 28: bud development is super beautiful and praying up, even though the plant still pretty small and compacts compared to others Thank you for still staying with me 💚 ___________________________________________ --- 🌱 Strain (Sponsor) 🌱 --- 🏷️ Big Band by Kannabia Seed Company https://www.kannabia.com/en/feminized-cannabis-seeds/big-band --- 🥗 Nutrients and Feeding (sponsored by APTUS: APTUS Ambassador) --- 🍸 APTUS: full nutrient schedule extreme -- Regulator, N-Boost, P-Boost, CaMg-Boost, K-Boost, Allin1 Liquid, Startbooster, Topbooster, Enzym+ every feeding -- Fulvic-Blast, NutriSpray as Foliar each once a week 🔗 https://aptus-holland.com/ --- ♻️ Grow Control (Sponsor) --- TROLMASTER: TENT-X + LM14 Light Adapter to dim/sunrise/sunset lights + Temp & rH Sensor all remote on App 🔗 https://www.trolmaster.eu/ --- 🚿 PetraGrow (Sponsor) --- CannaFogger Foliar Spray 🔗 https://www.petratools.com/product/petragrow-cannafogger-atomizer-new-mini-fogger --- 🏭 Grow Setup --- 💡LUMATEK Zeus Pro 600 * 🏠🌿 Indoor: Homebox 120x120x200cm (4x4) * 📐🌀 PrimaKlima exhausting Fan 1180m3/h (running on 60-80%) * 🌀 Can Light Filter 800m3/h & 1x Fanbox 1x Dyson fan for Air circulation 🔗 https://lumatek-lighting.com/zeus-600w-pro-29/ 🔗 https://primaklima.com/de/shop/ventilatoren-de/ec-ventilatoren/pk160ec-tc/ 🔗 https://canfilters.com/products/filters/ All Likes and comments are highly appreciated!!! 👨‍🌾 don't forget to check out my Instagram for daily educational content: budboutiquee - Bud Boutique

Around 11-12 weeks seed to harvest,, only had a few plants the largest yielded 72 grams the smallest around an ounce,,, just a few plants for personal medicinal use grown 100% naturally in the great british outdoors 😎

All I can say is that this thing is a beast. She likely only has a week or two left so I did one last small top dress with dry amendments as well as some ewc and super soil to top it off. Cant wait to watch this girl really fatten up. She’s already having trouble holding up the colas. 😎🍿🍻🌱

Day 66 : This lady continues fattening, faster now. Also crystal production increased. The breeder suggests 70-75 days. For now all crystals are almost milky with some cloudy. So she need 1 week for sure, maybe a bit more. That gum smell is so attractive, you want to eat it. Reduced bio grow and removed Calcium. Edit 70 : I saw the first ambers, very little. So i watered for last time with juices Next watering will be flush to reduce the juices in the soil. So if initially has 1200-1300ppm i want to reduce it to 350-500ppm. After flush continue pure water until chop chop. This is my approach for all ladies always.

This grow was fun.. I did 12/12 from seed and grew it in a 32oz McD cup.. Wow.. These are some super fat, super dank, and super citrusy colas! ETHOS FTW! Will be updating!!! 24 Hours Drying... Relative humidity in the dry area is between 68% - 72%.. I have been running the little computer fan off and on within the last 24 hours.. About 8 hours constant then off for another 8 hours then kinda blah not knowing whether I wanted it on or off the last 8 hours lol.. But hours 24-48 I'm going to leave it off and the hours 48-72 I havent got that far into the process in my head yet.. Lolol I'm sure I am WAAAY over thinking this.. But I dont want my first mold experience to be with ETHOS.. and I dont want my 3rd too dry too fast either with this strain.. The dankness is so incredible with this one.. My mind is blown by how epic ETHOS is.. If anybody knows of any other breeders that are as good as or better.. Please let me know in the comments!.. Anyways.. ZzZzZz... 72 hours of drying... Leaves are a bit crispy.. Buds are still moist a bit.. Small branches are still pretty bendy.. There was an 8 hour period that I did run the fan... The smell is a little hay like.. But this bud is so dank I'm sure the dank smell will come back.. Starting to notice that some strains smell like hay, but come back.. Some never smell like hay ever.. Idk.. Just something I've noticed.. It could just be my shitty environment tho.. Ugh.. So far so good with this one tho! Should be at least another 2 days.. But I'm shooting for a week at least.. Then into jars!!! Dried and beginning of cure... Took 5 days.. Not bad I suppose. Trimming only took about 45 minutes. It was almost difficult to WANT to trim alot of these sugar leaves because they were so incredibly covered in trichomes! But I can make a nice little bit of bubble hash with the trim so I trimmed her nice and close.. Gonna let her cure for a week or so then I'll get the weight.. I try to get them into the jars a little early.. Its easier to just burp them alot if they are too moist.. But impossible to get the up to 62% if they are too low.. I'd rather them be about 68% - 70% RH because thats technically just adding more "drying" time if you really think about it.. Then once they get to about 65% RH I slow the burping quite a bit.. Like only once or twice a week.. I've found this really helps terps and whatnot.. But anyhoo.. They have been in jars for about 24 hours.. They are already reading jar (2) 68% RH and jar (3) 64% RH.. Oh.. Let me explain the weird numbering. Lol.. My jars were already numbered.. Jar (1) is currently unavailable lol.. So jar (2) has all the nice, big, top shelf nugs and jar (3) has all the smaller, but still nice and dank as fuck nugs lol.. So excited for this! And normally I would have already started smoking what I've dried.. But since I cannot smoke, this will be perfect to actually give them plenty of time to cure nicely! So happy with ETHOS Genetics.. Fucking EPIC!!! Lol... Beginning of cure.. I tried a nug lol.. So smooth.. So fucking tasty too.. You can literally taste the citrus.. I love this strain! I can't wait to see some other ETHOS strains and see what they are about... Week one of curing.. Ive been burping daily.. Sometimes twice daily. I went ahead and put both jars into one.. Fuck it lol.. But 37 grams dried.. After 1 week of burping jars it is now reading 62% - 63%.. So now Ill stop burping daily.. Im gonna try to just go weekly.. If I can resist getting wiffs of it.. Lol.. It smells so fucking amazing