March 17, Day 76: As written I collected the last three plants. At the moment I got a partial of 224 grams from the first three plants and I think of doubling with the last three. Among the latter is the plant with the largest bud which obviously becomes my favorite. This time I managed to take photographs of the plants before cutting them. With these last three plants I got the most productive plant, the one with the largest bud and the one with the longest bud 😉 For a final report on this strain: The Gorilla by RQS is an excellent strain for anyone who loves a high THC content and I particularly recommend it to growers who pass for the first time from photoiperiods to autoflowering. You will grow very large and very productive plants very similar to photoperiodic ones. This strain branches out a lot and must be defoliated and de-branched. You can grow it well with the SCROG technique, but if like me you have no space problems you can also use the Sea Of Green technique. In conclusion I want to thank all the growers who have followed this my first diary to which I have a happy growth! A big thanks also to GrowDiaries and to the whole team for having created the best social network dedicated to the world of growers 👏💪😉 March 24 Final Report: Hi growers, with this last post I'm going to close my first diary. First I have to say that I am very satisfied with the total harvest, from the last three plants I got 369 grams which added to the 224 of the previous harvest make a total of 593 grams. I started this diary with 8 Gorillas and 2 Cheese. 6 Gorillas completed their cycle in the same time frame, the 2 remaining gorillas showed a photoperiodic genetic predominance, one of them is in an advanced flowering phase while the last one after three months still shows only a few pistils. I'll probably kill her, and move on by putting new seeds in the soil. Unfortunately, where I live is illegal to grow marijuana, otherwise I would have simply moved outdoors, but I can't and must be ruthless. Regarding the two cheeses there is not much left at the end of their cycle and I started to give only water to one of the two plants. Good and happy growth to all! 😜

Declared by the breeder for another 2 weeks. Let's see, plants began to drink much less. The leaves started to burn. In general, everything is fine. Meals according to the table removed heaven.

It's been a really nice week for weather, but also very dry. When did pick up a few times and I had to readjust my canopy again to get a tighter so I didn't hit the top of my plants. It's doing a really good job keeping the crud off but it does have a few spots where it's leaking so I might tape those up just to keep my plants dry. We just hit 13 hours of light in my area, and buds slowly transitioning into more rapid growth they are smelling pretty stinky from far away already. Water twice this week About 6 gallons each time and one with compost tea.

18 september 2022 flowering: week 8 -now 2 weeks of water only -the 10 heavy top heads need assistance -I used wires to keep them up -Harvested the smaller-lower-more mature branches -- 154g wet -felt like it would speed up maturation of main heads -also fun having less mature weed

Week 1

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.

Been flushing for days now. I put 20L per day through her. . These pics are Day 132, She will be chopped tomorrow. I don't expect much weight TBH, the flowers are quite light and airy. Trichomes are milky/amber so it is time. . Upon doing more research on this strain and after speaking to somebody about bud shape/density brought me back to my thinking months back. After a very long (for an auto) veg period I suspected the genetics of this plant were not very strong with the Ruderalis genes. But I dismissed that because why would a seedbank put out a 'sub standard' product?............ I think I would have had better results with her if the lights were on 20/4, I may even grow all my autos from now on 20/4 just in case the Ruderalis genetics are not prominent enough. . You live and learn, but don't forget: Knowledge is power 😋 . Harvest to follow............

started some little low stress training with some rubber bands and some aluminum rods I have laying around. Plant is growing greatly not seeing any signs of pre flower but I'm happy for that bigger plant more smoke "I guess".. but she showed sex already. Still feeding pat poo and bat poo tea, Plant looks green and healthy better than her sister seed i planted on the outdoors who has already started showing pre flower and Mutated from the shift from indoor germination to outdoor extrem heat .... .

Día 83 (08/04) Riego 1,25 Litro H20 + Wholly Base 2,5 ml/l + Solid Green 1,5 ml/l + Big Bloom 1 ml/l de Gen1:11 TDS 1000 PPMs - pH 6,2 Día 84 (09/04) Velocidad de crucero ON... Las plantas se acercan a su fecha de cosecha teorica (49 días en floracion = 13/04/2024) Muestran ligeros signos de senescencia, pero siguen creciendo las flores, el consumo de agua no baja... 😍💥 Día 85 (10/04) Riego 0,5 Litro H20 sin nutrientes. TDS 225 PPMs - pH 6,6 Día 86 (11/04) Riego 1,25 Litro H20 + Wholly Base 2,5 ml/l + Solid Green 1,5 ml/l + Big Bloom 1 ml/l de Gen1:11 TDS 1000 PPMs - pH 6,2 Día 87 (12/04) Empezamos a revisar el color de los tricomas y se encuentran en su mayoría trasparentes con alguno turbio. Va a necesitar unos días más para madurar Día 88 (13/04) Riego 0,5 Litro H20 sin nutrientes. TDS 225 PPMs - pH 6,6 Se abre la ventana de la cosecha! 😍 Justo hoy cumplen 7 semanas (49 días) en floración Día 89 (14/04) Riego 1,25 Litro H20 + Wholly Base 2,5 ml/l + Solid Green 1,5 ml/l + Big Bloom 1 ml/l de Gen1:11 TDS 1000 PPMs - pH 6,2 💦Nutrients by Gen1:11 - www.genoneeleven.com 🌱Substrate PRO-MIX HP BACILLUS + MYCORRHIZAE - www.pthorticulture.com/en/products/pro-mix-hp-biostimulant-plus-mycorrhizae

🌟 Welcome to the TrolMaster Chronicles: Seed to Harvest Adventure! 1st run🌟 Hey, Grow Fam! It’s DogDoctor here, and I’m thrilled to kick off this exciting new series with you. Today marks the beginning of our journey through the TrolMaster sponsorship, and we’re diving right into the heart of the action with germination and unboxing. 🌱✨ We’re starting strong with the Germination Station by @thecannakan, a game-changer for this process. I’ll be showing you all the details as we delve deep into every aspect of our grow adventure. Here’s today’s lineup for the germination extravaganza: 1️⃣ Mandarin Squeeze - Terpyz Mutant Genetics. 🌈 One seed germinated. 2️⃣ Punch Pie RQS and Tyson 2.0 Genetics. 🍰 One seed germinated. 3️⃣ RS11 by Kannabia Seeds. 🚀 One seed germinated. 4️⃣ Green Papaya by Super Sativa Seed Club. 🍍 Tester unreleased seed, one germinated. 5️⃣ Gorilla Mellon by Fast Buds. 🍉 Two seeds, one germinated (the first one didn’t make it). 6️⃣ Tropical Smoothies - Tried all seeds from the pack, but unfortunately, none germinated. 🌴 We’re also using the complete organic mineral line from @aptusholland, which includes top-notch nutrients to ensure our plants get the best start possible. 🌿✨ Plus, we’ve got the new ProMix Mycorrhizae soil, which will help create a thriving root environment. 🌱 Throughout this journey, I’ll be breaking down every step, sharing tips, and keeping it real with both the successes and challenges. I’m excited to share this adventure with you, and there’s so much more to come! For more in-depth coverage and exclusive content, make sure to check out my YouTube channel and subscribe—where you’ll find full video breakdowns, detailed insights, and more. 🌟🎥 Follow me on Instagram for additional exclusive updates and behind-the-scenes peeks that you won’t find anywhere else! 📸✨ Your support means the world to me, and I can’t wait to have you along for every step of this amazing journey. Let’s grow together and make some magic happen! #TrolMasterChronicles #SeedToHarvest #GrowDiaries #GrowJourney #TrolMaster #TheCannakan #GrowLife #PlantAdventure #HighFrequency #PositiveVibes #GrowWithMe #SubscribeNow #ExclusiveContent #AptusHolland #ProMixMycorrhizae P.S. 🌟💚 I want to take a moment to express just how honored and grateful I am to be the first TrolMaster Maverick. This opportunity is a dream come true, and I’m beyond excited to embark on this journey with all of you. Being a part of this incredible community and pushing the boundaries of indoor horticulture with TrolMaster and ThinkGrowLED is a privilege I don’t take lightly. 🙌 A massive shoutout and thank you to the entire TrolMaster and ThinkGrow team for believing in me and supporting this adventure. Your trust and support mean the world to me, and I promise to give it my all to make this journey as amazing as possible. 🌟🙏 Thank you, Grow Fam, for being here from the start. Your encouragement and enthusiasm fuel my passion and make every step of this journey worth it. Here’s to making magic happen together and to many more incredible milestones ahead. Let’s grow, learn, and shine! 🌱✨ With all my heart,Growers Love and thank you. 💚 #FirstMaverick #TrolMasterFamily #ThinkGrowLED #GratefulHeart #GrowTogether #MakingMagic Lets Play a game , FB Gorilla Melon Jump in to the future, can you guess the week ? Let me know in the comments before we get there , this is just for fun Lets Grow 💚💚💚 Growers Love everyone 💚💚💚

Such an amazing flower, really great especially a phenomenal hash producer yall will be super satisfied with this one!! She’s a shorty but Make sure you top 4 to 6 times or even more to have all them gooey bud producing heads , Dirtyblonde is absolutely an amazing plant!!

Start week 9 , Bio Bloom 4 ml/L + Sensi Cal-Mag Xtra 2 ml/L + CarboLoad 2 ml/L + Top Max 4 ml/L + Overdrive 2 ml/L (Ph 6.7).

Just waiting. The pineapple chunk is quite fat. The critical seems more hardy. It resisted the light burn and recovered slightly better.

I think the situation is very good. Im exciteed to see lst result Day 20, lst show good results. She drink so fast now. Day 21, going for week 4, what you think about she?

all together: welcome small plant😂😂 it's a bit hot but the temperatures will drop soil : plagron light mix fertilizer: advanced nutrient PH: 5,8- 6,5 I added a small timelapse of the birth

The tops are getting pretty close to the light and I can't raise it much more... hygrometer is reading about 31 degrees 5cm from the light so I think it should be ok. Nutrients are the same as last week, not much has changed except the buds are getting fatter :) Letss goooo

Started on Growdiaries at week 7 of flower. Back at the start there were four plants. Two were feminized and the other two turned out male. Unfortunate because those were the two Scooby Snacks. Actually the showcase plant. Playing the odds didn't work out for me this time. :) Two remaining plants started off at large size difference. Liberty Haze was almost twice the height of the Super Skunk. Used LST early and topping late in veg to control the canopy. Overall I got them to a pretty close height. The combination of the lolipopping and SOG produced some monster buds. Of course genetics helped but they were much larger than previous grows. The tent and the environment stayed nice and consistent throughout the grow. No unexpected incidents other then the two male Scooby Snacks. Used an updated Heavy 16 feeding schedule which seem to make the girls pretty happy. They both have been chopped and are hanging for 7 days-ish. I will take some pictures and give a taste review then. Sorry the pictures and video are so poor.

Chopped her on day 83 from sprout. Discovered some Bananas on Christmas, the plant looked due anyway so no worries, wanted to chop her anyway, guess I was right with the timing and the plant showed me it is done and did a last attempt to pollinate itself, normal behavior in my opinion, also the Bananas were blanks, didn't see any pollen. Overall great strain, will use this strain to test the limits of the prototype of my new hydro system. No mold or anything, vigorous growth, easy to train, stems did bend and not snap but are stiff enough to hold their weight. Buds are very dense, some might think the buds are a little small but there are a lot of them, good sizes in my opinion, perfect little ready to take with you buds. Even the buds are the bottom are dense, I had lights at the bottom but even inside the canopy with little light they are dense! Plant turned purple wherever there was intense light on it, visible on the short clip I took of a top branch where below the bud where there is shadow from the bud above is the branch is green and a little lower where light reaches it turned purple. This purpeling in my opinion is a great and normal feature in plants overall, probably do not expect a purple plant unless you go with intense lightning and high CO2 values to handle it. 9/10 because it hermed at the very end, didn't hurt the result because the plant was done but it would be nice if it wouldn't do it to maybe let it go some more and trade THC for more CBN and even more yield, total yield is good as it is but more is always better :) Whoever reads this at the very bottom... I hope this diary helps you out for your next grow. I hope this diary also shows that fertilizer brands are more marketing than anything, my fertilizer costs me ~ 1/5 compared to Canna, Plagron etc. etc. and it works great. Yara is used for example by Demecan a medical Cannabis producers, if they use it why not you? This is no advertisement for Yara, use Haifa or whatever just maybe don't buy overpriced fertilizer with big marketing and rather put that saved money in good quality genetic seeds. If you've got any tips, ideas, questions or whatever please leave a comment :) Update: added some pictures of roots after I harvested my other plant for obvious reasons, had to saw of the Net Cup because I did not manage to remove it, to many roots. Update: dried weight is 320g total, smoked a little besides that so maybe 330? didn't count how much so I didn't add that to the total, but it was a little more. Tastes like Wrigley's Spearmint gum! Will definitely grow this one again, so far my #1 from what I've grown, just dense, frosty and good tasting, can't really complain. 🙏 In case anyone from Mephisto reads this, make this a permanently available Strain 🙏