Day 59, she continues the very healthy flowering 🙌 size 65 cm👏🏻👏🏻 temperature 24º C ☀️, humidity 60% 💧 watering 750 ml alternating one day with nutrients and another without nutrients with osmotized water 💦💦 Session 45 min. of binaural sounds for growth and healing 🎼 and music 😉👍

Rainy weather is clearing up . Lots of sunshine this week. Can’t wait to see the progress week 6

Gracias al equipo de Fast Buds 420 por la donación de las semillas y poder inscribirme en el concurso del año. Creada a partir de la genética de la Girl Scout Cookies y la Gorilla Glue #4, seleccionadas a mano y en combinación con nuestra famosa Gorilla Cookies Auto, esta variedad lleva todos los mejores atributos de sus padres al más alto nivel. Este híbrido maravillosamente equilibrado prospera en el interior y en el exterior, y en todo tipo de climas, a la vez que es superresistente a los bichos y las plagas. Es una productora masiva que ofrece a los cultivadores de todos los niveles rendimientos de hasta 650 g/m² de cogollos de primera calidad que no decepcionan en absoluto. Siendo una de las versiones más potentes de esta genética, la Gorilla Cookies FF (Fastflowering) presume de un enorme porcentaje de 29 % de THC que se traduce en montones de resina y terps sabrosos que hacen las mejores extracciones. Es la elección perfecta para los cultivadores de hachís que buscan cepas de gran potencia que produzcan sabores y aromas excepcionales. Consigue aquí tus semillas 😁🌻🚀: https://2fast4buds.com/es/seeds/gorilla-cookies-fast-flowering 📆 Semana 7 de floración: La planta mas grande y con mas resina de todas las que tengo, esta aceptando muy bien los nutrientes. Los cogollos comienzan a formarse y continúa cargandose de resina.

2022-11-13 The Plant looks happy and Green, she gets Daily aSolution packed with beneficals and nutes like listed small Flowers appear website for for my Fertilisers: https://greenbuzzliquids.com/en/shop/ Code: mrs_larimar Breeder Info: 👉Black Sugar is an indica dominant hybrid of Black Domina, L. A. OG and Critical. It has kept the medicinal properties of L. A OG, a good flowering rate on the Black Domina lineage, and the compact size of the classic Critical strain. With its small growth, the strain produces large yields of up to 600gr/m2 on bushy branches. The buds are very dense and stinky. Black Sugar has a high THC level. The variety has a fruity citrus aroma. Dense smoke gives the effect of relaxation and body buzz. Good for Smoking before going to bed. It can become one of your favorite Seedsman strain Genetics Black Domina x L.A OG x Critical Harvest 450 - 500 g/m² Flowering 50 - 55 days THC 20.0% CBD 1.0%

Last week, fed the plant the plant with a dose of Top Bud, just at the begginning of this week, and then, i will be flushing until she is done...so last photos with nutrients, next days she should be yellowing :) Hairs were like 50% orange at the beggining of the week, but some buds need to develope more so i think the timming will be fine im trying to flush for 1 to 2 weeks, until she is done, with like 90-100% of brown hairs Good vibez GD !!!

Gorilla Glue #1 - Harvest Comment - I Am Very Satisfied With What I Got, I got 3 ounce 7 grams - I Uses Advance Nutrients PH perfect In veg then I switch to the iguana juice organic juice for the flowering stage. I notice a much more slower growth when I switch to organic nutrients.00

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

Day 136. Girl is in flower mode, stretching and in video looks amazing, photos don't show real beauty .... Still no feed, but think to top dress her this Saturday before holidays ... And to clear bottoms a bit too. I don't want to overconcentrate her because of bud rot. Happy Growing !

It’s been a real pleasure to watch them grow☮️💨..

2/1/2024- Pre-Germination Activities Day 1 I have 21 weeks until final photo is do.. I took 3 seeds out of cold storage and will let them get to room temp for the next 48 hours before I go with Glass of water for germination. I have 3 beans because I will start from the very beginning helping ensure I present the best Pheno. This is going to be a fun one.. I am a few days away from being able to clear my tent out for this run.. I have a breeding run in right now and the Seeds are a few days away from being mature enough for me to take down the girls. Once I get them down I will need to get my tent cleaned up and turned over right away. This is going to be close, I will have to time them to the water and into the tray at the right time.. because I will need to get lighting on them right away.. I have my 2X2 and my light ready incase I need to hold them in the cloning machine if the others are not done in the next few days.. Glad I have options that can stretch me out for a week or 2 to give me a little more time. 2/2/2024- Pre-Germination Activities Day 2 I checked on my breeding run to see how close the seeds are and if the tent is ready for me to clear and clean but alas I am still going to need a few days. I setup the emergency 2X2 and that should give me 2-3 weeks. The plan is to still wait one more day to allow the beans to warm up to room temp and then drop them in Water sometime tomorrow. Form my Emergency 2X2 I have the following: 4" inline fan and carbon filter Fan VS-2000 light 2/3/2024- Germination Activities Day 0 - Dropped the Beans in.. Today is 0 day.. Go.. Go .. Go.. 2/4/2024- Germination Activities Day 0-1 - Checked in on them this morning and no tap roots yet.. covered them back up and back in to the closet they went. I setup the Root Riots and the Seed tray for them. I Ensured my water that I was soaking the root riots in was PHed to 5.8 and I used RO water. Afternoon Update: Checked on my Breeders and they are done. I started to harvest them, I took down the one I had reversed with STS and I took down the Black African Magic- All but one bud, I wanted to get some pics of that one today. I was only able to get 2lbs into the Cannatrol because I had to be very careful to keep the bud from the plant that was treated with the STS separated from the other seeded bud that was pollenated from the plant I reversed. Cannatrol could have held an additional 2oz of wet but not today. Ideally I need 1 more Cannatrol so I can take an entire Tent, but will figure that out. I put an additional 1.5lbs into the freezer to wait it's turn into the Cannatrol, I would have left it on the plant and taken it in 4 days when the dry cycle gets done but wasn't sure how much 2.2 lbs was equivalent to chopped and wet trimmed. 2/5/2024- Germination Activities Day 0-2 - Checked in on them this morning and 2 of them have very small tap roots out.. one still doesn't going to give them some more time. I will check in on them this evening and see if they are more open if so I will transfer the ones that are ready to their medium and seed tray. 2/6/2024- Planting Day TRUE Germination Day 0- Checked in on them this morning and all 3 of them have tap roots out. I broke the bottom of the tap root for #1 which was the biggest.. pretty sad.. I hope she survives.. I tried to be careful it just snapped off when I was trying to get it in the root riot right. Other than that all three are now in their in-between home in the 2X2 while if finish clearing and cleaning out their forever homes. 2/7/2024- Germination Day 1- Checked in on them and no surprise no sprouts yet. Sprayed the dome to moist it and light spray to the tops of the Root Riots. 2/8/2024- Germination Day 2- #3 is popped and it looks like #2 will be popped by this evening.. I got my second Cannatrol today so now I can take down the rest of the tent and get it into the dry/cure. 2/9/2024- Germination Day 3- #2 is popped as well.. so I have #2 and #3 up and still waiting to see on #1 but that might be a loss since I accidently broke off some of the Tap root when transplanting. 2/10/2024- Germination Day 4- #1 has Popped... We have ignition on all 3.. YAY!! I finished clean up and install of RDWC system, this time was unique the back left buckets 3 inch pipe wasn't seated correctly so I had to clean up about 12 gallons of water all of the floor. I also had two leaks coming from one of the Waterfall return junctions, this is why I do a full pressure test before I put anything in. I will continue to monitor it through tomorrow to ensure that I am good to go and then I will finish setting up the baskets and prepping the water to be ready for the ladies planting day!!! 2/11/2024- Germination Day 5- #1 Of course is going to be my trouble plant.. No matter what If she lives through planting in the system and making it, I think I might not cull her at all regardless, she has been such a problem, makes me wonder if she will be super worth it towards the end.. We will see as we go through this grow, but #1 has a piece of the shell on the leaves, Other than that I set up a new thing I have been doing since last grow converting my Baskets into Sure plants so I can see exactly where the water is when I plant them and ensure I have the water up high enough that they are able to access it and grow but not too high were they are drowning. 2/12/2024- Germination Day 6- Everything seems to be going good.. will just keep them moist and let the roots grow for a few more days before I transplant to forever home. 2/13/2024 - Germination Day 7- Just keeping them Moist. 2/14/2024 - Germination Day 8 - Planting day.. they are now in the system.. :-)I had to fill the water to the bottom of the basket where I could see water on the bottom rocks and just coming up where I had created my whole/ sure plant. 2/15/2024 - Germination Day 9- Top fed just a little to keep them moist and encourage root growth towards the water. I ensured the PH is right at 5.98-6.02 range. 2/16/2024 - Germination Day 10- Top fed just a little to keep them moist and encourage root growth towards the water.

Went away for seven days had a friend come by and water the garden Absolutely exploded since I’ve seen them last very pleased with all of the plants except for mystery auto number one. It is disappointing me some but hopefully the top will bring more growth. Can’t wait to see these continued to develop!!!

In the final week, highly resinous flowers that I cannot wait to sample from the 3 phenos. Had more pics and vids but the site won’t let me upload. Hope everyone has a great week! GHL

Armario posto em fase de floraçao. Rega de 4 a 4 dias com 2l de agua desmineralizasa. Deixei a lampada cair sobre elas , piqueno incidente 😣😣 Mas esta tudo bem só perdi uma folha da piquena uma da grande e algumas queimaduras 😣😣

This plant was an absolute dream to. Grow, no issues at all with health of plant, just struggled to tame her as she was a a thick strong climber 💪💪. I'm so impressed with how this turned out, I could have flushed for another 3 days to make it 12days but I needed the space. After The 2 days of dark I was recommended I can definitely say it has vastly boosted her trichomes and the smell when I opened the tent blew my head away 😍😋 Aiming for a 10-14 day hang dry, The 10-12 weeks curing in jars with humidity packs. I will update with a dry bud weight and smoke test 👌 Bud wet weight is just 500g+ Final bud dry weight is 298g. Of juicy resinous purple and orange buds 😍 smells like sherbert and hang dry smoke test revealed a candy sherbert, no banana yet but hoping like the grow it matures with cure process now. Hits eyes straight away, sandy bottom kids, giggles, munchies, fun time with Mrs, bed. Full cycle with this one very happy over here 😉😁💚 FAT BANANA AUTO FROM ROYAL QUEEN SEEDS, big thank you to the team, and the breaders. What a pheno I received. I appreciate you all

Tropicanna Banana is all done. 2 weeks in the jars to cure now. got just over 2 ounce of this plant so not too bad. should be a good daytime smoke.

Week 3 flowering begins for SLH. Added B52 to the nute mix and increased to 6L total feed. Bud sites are popping up all over her, I did a little defoliation on the lower inner most branches and a bit of LST. Looking forward to a good week! Thanks for checking out my grow. 👽🔥🌳

Chopped on day 80, hanging in 65F and 62 H. Hoping to slow this dry down to 10 days so wish me luck.

So week 9 is done and dusted and these girls are absolutely stinking , this is my first ever grow but ive smoked my fair share of bud and I must say the smell in the tent is one of the strongest ive ever smelt.... So anyway back to week 9... its been plain sailing really ive got some baby GSC autos in with the white widows so ive kept a dome on them obviously to keep the humidity up... The girls really are packing on the crystals now and I dont think we are to far away from cutting her down.. the packet said 11 weeks but im more guessing it will be around 13 weeks, either way there isn't much to report apart from she continues to be a dream to grow and ill he back for week 10's update very soon.... enjoy the pics and videos 😍 Happy growing people.... 😍😍

Muay Thai is still slowly growing. She is 65 cm tall. This week grow is slight and won’t turn her into a 3-meter sativa dominatrix. The key thing is that she won’t finish any time soon if she keeps growing. My experience is that Thai sativa can go for nearly a year. I doubt it is the case for this auto. But Muay Thai sure takes her time. The good thing about longevity is that head high seem to increase with flowering time. Muay Thai is in the sunniest spot. Bad part about this spot is that she is next to aphid and black mold nest. Neighboring plant is a hibiscus and magnolia. This is aphid season. With aphid sugar secretion, there are black mold everywhere. I think it is aspergilus niger and not that dangerous. Still, I went overboard with anti-pest microbe spray. The microbes comes in wheat flour format. And after frequent spray without the rain, white marks accumulate on leaves. Growing environment, midst of tropical winter. By European standard, mild climate but with 11 hours day light. VPD T RH % Hottest 1.88 28 50% Morning day 1.40 23 50% Night 1.21 18 41% Feeding what I am feeding my other plants. This is milk, molasses, and fish bone tea. Muay Thai would be fine without the feeding. But since I already made it for other plants and I don’t think it will overdose Muay Thai, I also fed here with these.