Yoo it’s kofi cultivates it’s week 3 veg the growth has been explosive from week 2 to week 3 Thanks for following along with my journey. Keep on growing

This week flushing the wedding cake i thought that was the problem was an excess of nutrients, but instead the water was quite clean, around 1100ppm at the first drain, after several flushes water is now on 600ppm.. It seems that the others are starting to have the same deficiency that hit wedding # 2 .. now I'm treating them with 0.5ml of cal-mag adding it to the other nutrients for once a week (except wedding # 2) I will wait for the soil to dry out, to give her only clean water since the final harvest is not long. ⚠️ UPDATE DAY 45 ⚠️ Yesterday flush for dos si dos and today flush for (wedding cake 1) they are having a nutrient lockout too..😪 The (wedding cake 1) is clearly healthier than her sister (wedding cake 2) by looking at her color, but unfortunately she had excessive PPM / EC too.. So i did the same procedure by using only tap water, but this time added only 0,5ml of cal-mag. Water was at 6.5 ph until I got a better runoff, it went from 5.7 to 6.0 PH and from 1800 to 700-600ppm 😬 I have never thought of overdoing nutrients so much.. I will certainly learn a lot from these mistakes 🙌🏻

So far, I can't comment on the effects and taste of the girl, because I was just weighing a wet product. The smell is strongly aromatic, the girl smelled the whole apartment. I no longer gave the girl nutrients, only clean water, and she remained in the dark for the last two days. I will dry the buds for about 10 days before I dry in the jars and update here. 😉 Update: The taste is sweet, delicate, does not scratch at all, the effect comes after a while. She's great. 😍

empieza a ter un olor muyy fuerte a gelato 33 con toques a vainilla sin duda sera una planta brutal, resina muy gorda , esta empezando a joder un poco algun gusano por eso y no parece demasiado resistente a los homgos con esos cogollos tan gordos y prietos

👉Alrighty Then👈 So we are at DAY 28 with the Sugar Larry 👈 And she's doing fantastic 👍 Updated today DAY 32 , all is well so far 😀 decided to showcase pheno #2 , definitely has different traits then #1 very interesting 😀 thoe both are killing it 👈 Except for some slight watering , ive been doing some defolation as well as some LST manipulation to pull branches to the side 👌 👉I had to Top her during the middle of week 👍 she gonna be a tall girl with long legs 😛 👉WeeklyRoundup Video is finally posted 😕 😒 😪 😢 Happy Growing 👉Soil Provided by ProMix.ca 👉Nutrients Provided by Agrogardens 👉Lighting Provided by MarsHydro.ca Thanks my friends for the great support over the years 🙏 Happy Growing

This girl flowers and branches are very heavy Despite not being sugar coated Flowers She is still in development and will become much more heavy . I think that we are looking at probably three more weeks of development to start to check on flower Maturity maybe more but despite being treated Brutally she is a survivor with so much Height she is ideal for our Canadian outside summer. Thank you for reading I continue to update have a happy grow

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.

It’s week 9 and you can definitely see the flowers now. The seeds were all 60-70 day to flower and they all started at week 8-9! Awesome

Inicia segunda semana de floración, las plantas se recuperaron muy bien después de la defoliacion que se realizó antes de entrar a floración. Ya se ven los primeros pistilos en las 3 plantas.

The Apple Cup hermied this week along with the Baker's Dozen. Fortunately Tropicanna Poison is flowering so fast that it seems to be unbothered by the hermies next to it. The hermied plants will be stunted as more energy will be focused on developing pollen/seeds. Also I'll have to chop them down early before any seeds begin to solidify within the buds. It's ideal to immediately remove any hermies as soon as pollen sacs are spotted. Unfortunately I only have my small closet space so I decided to leave them and observe the growth of hermies.

Growing fast liking the #3 for far #1 is the slowest growing Top plants heads on 7/18/2 Seedlings was transplant on 7/21/25 into the 5 gal Put in my 4x4 to continue veg

This week I have separated the plants into 2 tent, to allow for wider canopy per plant. Day 5 - LST and defoliation needed

All feeds with nutes use either a whole ratio or combination of "Veg Mix" and "Bloom Mix"concentrates DILUTED in water until a total ppm of add in is reached using a (Total Dissolved Solids)TDS Meter measured in PPM (parts per million). The "Veg Mix" concentrate will eventually be added in smaller ratios and "Bloom Mix" concentrate what will eventually replace the "Veg Mix" concentrate entirely with the ppm and ratios listed when I feed. Veg mix recipe is on week 3. Bloom Mix recipe is on week 5. Day 49 VPD is okay now - temps at 75F RH also now at 65% with ILVent at 50% = VPD of 1.04 - ppfd also same as yesterday mostly 480 to 490 around the ring with 510 and 520 in the center Took ph readings as well - 3 readings 6.43, 6.48, and 6.37 to avg 6.426 Which is good because she's starting to show signs of stress after the topping and defoliation from a couple days ago. The leaves are starting to curl at the tips and the bronze color stripping is happening again - however this time seems to be a slower progression so Im hoping that having the correct ph this time will help while she's re-routing her resources. I 'did notice also that the growth tips seem to be growing at a slower rate than before - I think she's at her limit in colas and the roots are having to find more space to spread, may even be too big for the 5 gallon pot. I have no plans to change her out just yet, but will monitor. Soil is drier today - so I will be watering tomorrow with de-chlorinated water at 6.4ph Day 50 VPD was good at 74/64 with the tent open while I feed that I left it open for a bit and took time in feeding and cleaning - after all that still good at 74F/61%RH/50%ILV ppfd was checked after water and setting back - same as yesterday as most of the newest growth is still coming from the new colas - most seem to be adjusting 1 at a time in each split but both are showing growth now on all cuts. Started feed by making new ph buffer solutions, calibrating/testing both meters. The have about a .15 variance between the two. Checked weight and made 1.5 gallons of feed. started at 228ppm added 450ppm veg and 150ppm bloom for a total of 833ppm feed/epsom salt - splashed h2o2 and ph'd to about 6.4- I fed via watering can and spray and fed the whole amount slowly since I was feeding until bottom drip and she took it all before starting to bottom drip. Afterwords I let her drain (about a quart came out) and checked ppm from runoff at 2500 (telling me she's okay but isnt eating as much as before her topping yet) ph is a mystery - I show 3 readings from top level of 6.62, 6.57, and 6.57 for an avg 6.586 but 2 separate readings from 2 meters (4 readings total) on the bottom runoff showed 5.3 and 5.6 then confirmed later. I expected a variance since the wood ash probably stuck to the top side of the soil - but I didnt expect that much of a difference. I will monitor but honestly dont know what I should do, if anything other than watch. made a video of the fan movements and runoff drip Day 51 What I am calling "stress burn" is progressing as expected. I am monitoring the ph from the top as I did before, but again, not much I can do other than over water, so I'll just watch for now and compare rate of spread until she fixes her resource pathways. It seemed to take about a week to clear up after the ash treatment last time, so I am on day 3 of 7 for now with no treatment. Looking for a spurt of new growth to show and then I'll know she's better. Adjusted the lights to accommodate a week 6 level of 500 to 600 ppfd - that means I can raise the lights to the top of the tent and increase power. So now set at 3 tick up and 37 inches from the soil or 26" from the plant top. Now her ppfd reads about 540 on both of the center colas and 500 to 510 on the surrounding ring. Adjusting lights meant I had to adjust the fans up to medium power and re-directed them to blow at the edges of the pot; made a video. VPD is steady, but still warmer than typical (only by a couple degrees nothing too much) 76F/61%RH/50%ILV for 1.15 kpa on room VPD Day 52 VPD is higher now that I have the lights to the top of my tent and the fans on the lights blowing down at the pot. I moved the IL Vent to the top sucking out with the motor and vent outside the tent now. I also opened two lower air holes with my heater set for fan on the opposite side of the tent than the vent. Currently, I am at a max of 1.2 room VPD and ranging down to 1.0 so I'll take it until it does something else. 74F/65% RH/75%ILV - I will monitor to ensure it's stable. ppfd is same as yesterday as there's little growth still. Spots are still progressing on the oldest leaves at the same rate as before - however the newest leaves are not showing signs yet, so I will continue to monitor. Day 53 ppfd was a little changed today, showing that there's growth coming back now. lowest on outer ring was 500 with most at 520 and 530 highest, center colas were tested at 540 and 560ppfd. VPD was stable as I watched it most of the day since I made changes yesterday. Temps were 74 to 76 and RH was 61% to 68%. ILV was set to 33% with the bottom heater on fan to draw in air. lockout continues on the oldest fan leaves at the last top nodes. New growth is already marked in a couple of spots. I have about 6 gallons of tap water burning off chlorine now and will use about 2 gallons to flush at 8ph. I plan to dunk this weekend with feed so this will allow time to dry out and hopefully reset the ph and lower my ppm readings at the lower part of the pot before then. Day 54 Took Control pics measured VPD and ppfd Lights are at the top of the tent and second tick from highest power level. Lights to soil is 37 inches and lights to plant is 12 inches shorter so 25 inches leaves to light. currently ranging 530 to 550 around the ring and 575/580 ppfd at center (after feed and replaced). Moving the lights (day 51) made the tent hotter so I changed my ILVent to suck out at the top and fresh air in at the bottom - I have been fighting to keep temps under 78 managed to hit 74 to 75 with the heater being set just to fan for the bottom air vents- I did also raise humidity to a setting of 65% a day before moving the lights, so Im hitting 61 to 68% between power cycles on the humidifier. Overall Tent VPD is 1.0 to 1.2 as max. Took controls for feed. Weight 16lbs 11oz. tested and calibrated 2 meters and took 4 ph readings of 6.55, 6.77, 6.53, 6.85 to avg 6.675. from top of soil (last runoff measured 5.6 and 5.3 on two meters) prepared 2 gallons of feed at 500 ppm over tap. (burned chlorine off overnight) starting ppm was 217 - added 75/25 veg/bloom ratio. ph balanced to 7.8 and 7.63 on separate meters (rinsed and retested to be sure got 7.79 and 7.63 again) I used 4 knitting needles in the soil about 3 inches from the plant center. Poured feed water over the needles until it pooled slightly on top of the soil, I then pulled the needle out a little to allow the water to drain into the holes better. I did this in 8 different spots. As soon as she started dripping water from the bottom I poured a little on the leaves and then moved the plant to another drip pan to finish pouring the rest over the top of the soil without dripping any over the sides. Took videos of the drip and waited 10 min before putting her on another clean drip pan and back in the tent. Runoff from second drip pan was measured twice at 5.8ph and 2410 ppm - and first pan 5.85 and 2670ppm (expected higher ppm since I moved perlite on the bottom with the needles) Defoliated the oldest leaves before lights out. Day 55 She mostly looks like she appreciated the clippings and ph balance from yesterday - slower progression of the lockout issue and largest new growth since topping day. So speaking of new growth, I plan to use LST in the next few days to set these colas in what will hopefully be their last bind around the ring. VPD is steady at 75F to 77F and RH is between 63 and 68%. My ILV have been set to 33% and the lower fan blowing rather than heat. top soil ph was measured with 3 readings, on a tested and calibrated meter. 6.47, 6.7, 7.12 to avg 6.763 (kinda wild in those readings so I double checked them all twice and got the same in each hole)

Week 6 Summary: First off, Happy New Year! May the new year filled with peace, love, joy and dank buds! 😄😉 Day 36-39: Despite my heavy defoliation they seem to bounce back quite quickly every time, but this is my first grow so I could be completely wrong and slowly murdering my plants... 😅 WC1 starting to frost up, the two double buds are starting to split themselves up while stretching: WIN! WC2 and WC3 really starting to show their size compared to just a week or 2 ago, really spread out now, and starting to stretch. Day 40-42: WC2 and WC3 really stretching now. WC2 almost catching up to WC1's height, and has probably spread out the most out of all plants when you compare it to a few weeks ago. Maybe defoliating is a good thing for Autos after all? I'm stoked about these. Although WC2 and WC3 are a few days behind of frost production it's definately starting to show itself by the end of week 6. Stoked for these!! These are stinking aswell, but for now the 4AM in the tent is sweetening it up! On to week7!!!

Wow what a week this has been, the plants have all undergone fair dramatic changes. A real flurry of leaf yellowing, pistil darkening/curling, and bug swelling. The smell is really coming along now, I think we're really quite close to harvest. On the assumption that pre-flowering was two weeks, this strain should be ready at the end of week seven flowering, so in the case of this diary the end of week nine (i.e. one week to go!). Pistils are about 70-80% amber, and the lower pistils on buds have started curling inward. Trichomes look to me to be something like 10% clear 80% Milky 10% White. I have smoke tested a small bud off the lower part of plant 3 today after quick-drying overnight in the airing cupboard, taking into consideration the obvious chlorophyll from the fast dry, the high was much closer to what I am expecting than the last smoke test. It came on at the normal pace, was quite effective, and lasted a good while. I am really hoping I can navigate my way through the next process, as I feel quite close now to having some home grown bud for the first time. The plants are being well watered this evening with just water, and this will be the last time that I water them until harvest. I will continue to monitor these daily, I intend to harvest at the first sign of any amber trichome. Advice and comments welcomed. P.S. Exciting news! My order from Green House Seeds arrived today for my next diaries! :)

Replantées en pot de 25 gallons, nos vers vivent dans le substrat depuis une semaine, les nutriments organiques de greenhouse ont été ajoutés à raison de 100gr par pots, le paillis recouvre le tout. Le sol vivant est prêt ! Repotted in 25gal fabric pots, the worms are in the substrate for a week, GreenHouse’s organic dry amendments are mixed into the soil, 100g into each pots, nice layer of mulch on top of it all. The living soil is ready !

Esta semana he tenido un poco de problemas con la planta debido al cambio de clima para la floración de mi planta cambio a un lugar selo exterior el clima está algo frío y con poco sol pero igual se ha desarrollado muy bien esta semana 🙏🙏🙏🙏