Riecht maximal sexy! Main Bud hinten rechts ist ein Monstrum!

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Week 3 for the solo is officially complete. She's been growing with no trouble. Root development has been excellent. As you can see, I decided to mainline. Seeing as she's in a solo cup, I'm not too worried about stunting. I'm horrible at measuring the water intake, but the cup needs to be watered daily. It's as lite as a feather everyday.

Day 78: watering 2 gal of ph water a few amber trichomes on some buds extended night cycle to 20/4 Day 82: trimmed off most fan leafs hung up to dry have a humidifier to keep it 50-60% and the temp will be 50-70°F smells super good again. Day 88: put into jars havent trimmed yet about 12 to 15 grams in each jar and there 12 jars so im guessing about 4 oz total after trimming Finished trimming finally have been curing for 8 days dank smell more and more everyday. Ended up with a dry weight of: 4.39 Oz Smoked 1 test joint and tasted alot like a dryer sheet. 31.45 grams of trim I will make into wax

Hey guys :-) . I did not do radical LST again this week :-) I will now make radical topping this week :-) The only reason is that they are otherwise too high for me, because I only have about 40 days in the flower tent 😂. Don't be shocked next week 😅 it will look fatal 😂👍. Typ: Sour Diesel (Zamnesia) ☝️ Genetik: Diesel x Northern Lights 👍 Vega Lampe: 2 x Todogrow Led Quantum Board 100 W 💡 Flower lampe: 2 x Todogrow Led Cxb 3590 COB 3500 K 220 W 💡 ☝️ Erde: Canna Terra Professional + ☝️ Dünger: Canna Termittel Vegra Vega, Canna Terra Flores, Rizotonic, Cannazym, CANNA Boost, Pk 13/14, Canna Cal/Mag, Canna Ph - Grow, Canna Ph - Flores ☝️ 🌱 Wasser: Osmosewasser mit normalem Wasser gemischt (24 Stunden abgestanden, dass das Chlor verdunstet) auf 0,2 EG. Fügen Sie Cal/Mag zu 0.4 Ec Ph mit Organic Ph - zu 6.0 💦 💧

GENERAL COMMENT. So the RQS STRESS KILLER AUTO is down. Now we have the NL to manoeuvre and try to keep her alive for the final flush. RQS NORTHERN LIGHTS AUTO COMMENT. Many but slim colas emerged, showing extreme spotting and deficiencies, but gained weight since last week and started turning purple, first time that happens. So now the final flush started and hope, afraid taste could be off, because of the problems i ran in with her, probably a good strain to considere light feeding, the smell is very gentle, a good strain to do stealth. 10-14 day to go! Yield could be amazing but will be common because of the locks, nothing out of the curve in my opinion, something to retry and correct to deal with this strain. Not turned on or off by her just feeling neutral and glad she made it. Trichomes wise she is just ready, mostly cloudy, she will finish with some amber will do a nice sleeping aid. Trim job will be a pain on this one because i will clean all the small affected spotted leaves.

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.

acho que ainda consegui produzir uns tricomas com as correções da água, mas como o estágio da floração já estava bem avançado, as folhas começaram a descolorir muito cedo, tive que colher 3 plantas precocemente, as outras 3 menos vou tentar seguir mais 2 semanas, não estão mostrando tricomas Ambar ainda!

11/22 Day 31 from flip. Today is the first day that I took a tape measure from the lights to the topmost part of the canopy and I haven’t seen a change. I’ll check again tomorrow but I’m really hoping the stretch is finally done. I still have about 10 inches of space between the lights and canopy so I think I’ll be ok with that. I took the chance to do what is hopefully a near final defoliation of a few leaves and some smaller sucker branches that won’t amount to much. Everything still looks super healthy, no red anywhere on any stems and no discoloration on the leaves. Everything is spot on. Light adjusted to 840 PAR / 36.3 DLI. 11/25 Day 34 from flip. I made some adjustments to my nute mix to be more firmly at 1.3 EC, which means I’ve added some additional nutes into the mix. I also tested runoff EC and discovered things were spiking a bit more than I’d like. So I mixed up a few batches of my new mix and I’ve been feeding every few hours to flush things out a little bit. I’ve brought it down from 1.9 to 1.5 so far after this. I may finally need to break down and set up some timers to feed multiple times throughout the day. Obviously once a day is not getting done right now. 11/26 Day 35 from flip. I finally got the timer hooked up to my pump to begin automatic watering. For now, I have it set to water at noon for a minute when the lights come on, a 2 minute pause to let that settle, and then 30 seconds more to make sure both are fully saturated. The second fertigation event will be at 6:00 for 45 seconds, and then right before lights off another 45 seconds. I’ll have to keep an eye on it to see if I need to adjust any more for now. I haven’t adjusted the lights since last time, but the latest reading is 885 PAR / 38.2 DLI at the highest point of the canopy. It’ll stay there for now.

reach for the sky!! Holy cow these ladies are going off. watch the time-lapse the end of week 3 and the stretch begins. the dark devils are showing the auto gene well they are stretching as well but not like the red poisons wow. going to le the dark devils dry out a little i think that strain does not like to much water. the red poisons are drinking like crazy. so already starting to flower at the end of week three. going to hold off on any flowering supplements for now to see if they are still eating the food that's in the mix still. cruising along see Ya next week.

📆 Week 1, 6-12 May 2024 6 May - 3rd sprout appeared. Waiting for main root to appear before transferring. 8 May - Main root appeared on the 1st sprout, transferred to its permanent home (see pictures). 9-12 May - Observed and watched the seedling grow. 📑 Transferred seedling into permanent Deep Water Culture, 2 gallon system. I’ve always had the best response when the main tap root appears prior to this process, it helps to ensure success. This plant seems to be getting off to a slower start, but steady. All seeds germinated, sprouted and became seedlings. I’ll be finding homes for the other 2 as my grows are limited by space and number. Another reason I like to only germinate a single seed at a time and primarily why it needs be viable. “One good seed is all you need”. 🍶 8 May initial nutrient solution started 🍽️ 8 May initial feeding schedule started 💧 Using reverse osmosis water with EC/TDS at 0 🐉 Nutrient solution EC 1.0 at 72 degrees F 🔆 Light power at 50%, DLI 12-15 canopy coverage at 18hrs 😤 Using PYPABL, Air Pump, 400GPH That is it for this week. Thanks for the look, read and stopping by.

4cm vertical growth this week. Flowering stretch finished now. She is ~1m wide........

Seguimos en fase de Vega con alguna que otra plaga... pero de momento todo bajo control, pasaremos a foliar con delta 9 para ver los resultados. Pasaremos a flora con el nuevo equipo Led para intentar reducir el calor de los focos y ahorro energético. Iremos informando farmers buenos Humos!🍁

Sunday, May 29, 2022 Plant #3 is stretching away by a foot over Plant #2. Both Plants looking well but displaying different leaf behaviour (particularly of the upper growth). When well watered, in full sun, Plant # 2 has perky, praying leaves that go down somewhat at night. In the same conditions, Plant #3 has droopy leaves that get even more tucked in at night. It was only from feeling the strong turgidity of the Plant #3 leaves when under good water and comparing them to Plant #2 that I accepted that it was ok and that's just how it wears its' clothes. The red and white pistils are filling out from top to bottom on all stems on Plant #2. Even though it's not as tall as its' neighbour, the six main stems on plant #2 seem proportional to, hopefully, support nice thick colas. Plant #3 is furring out much slower and though I am happy for the height, I am concerned the stems aren't thick enough to support much weight.

Update week 2 veg👽

7/4 SUN was poking out a little bit. Plants loved that little feeding and seen to he noticeable larger this morning. I'm considering starting the nutes. At least the organic ones as well as upping the water intake I've been scared to water with all this rain and my experience last time. I plan on applying BT this afternoon and doing some work on the bottoms of the plants. I also saw a chipmunk in my cage so I have some spots in my fence that need to be patched. I know I can't compare this year to orher years as these are seeds and all the other years were clones. I CAN say for certain that my plants are healthiest they've been out of any of my journals. Previous plants were much larger but I was fighting numerous fungal, pathogens and pests at the sane time. Ear wigs would've lollipopped most buddies by now but I've seen no sign of them. I'm going to apply more poison where they were and add some rat traps inside the cage for the chipmunks. Once I fix the cage I think I'll be good. UPDATE: Went back over and fixed the holes on my cage from high winds. I found an old wire trap or cage and just cut sections and ziptied them to the existing wire and to the structure thus covering any open holes. I'll need to put lathes aroubdvtge outside because if a rodent REALLY wanted in they could get in. My belt had been wearing thin but I use shit until it breaks (yesterday the heal came off my shoe lol) so I was working hard sweating my nuts off and my belt gives out totally. At least ive got the major stuff done. I took a few videos too. I'm imagining it was this little bit of sun that gave these plants that boost of growth but I'm wondering if the added nutes had anything to do with it. Bags weren't light and I could feel moisture in the soil so I didn't water. I'll check again tomorrow morning. Since I didn't see many plants or even leaves for that matter with damage I decided to hold off ob the BT and the plant doctor. Only time will tell if that was the right decision. 7/5 Plants look fantastic. I see a few more holes in leaves sporadically amd I'm hoping it's pillars. I've seen lots of lightning bugs on my camera though and grasshoppers are abundant. Not one growth shoot has been chewed (knock on wood) which is what the earwigs had always done. I watched a video from last year and by nowcthey had lollipopped all lower leaves. It may not be the best weather growing season wise but despite the rh consistently in the 90's I still don't have pm or fungal pathogens. Need to get the BT out. Didn't water as we've had all that rain. I'll water either tonight or tomorrow morning. Sunny high in the 90s low is 66. Tomorrow looks good too. UPDATE WENT BACK OVER AROUND FIVE. IT WAS 88 DEGREES SO I WANTED TO CHECK THE GROW BAGS. THE POTS ARE FINE. IT WAS HUMID AS HELL. ONE PLANT WAS SLIGHTLY DROOPY BUT VERY LIGHT AND DRY. I FOUND TWO OTHERS THAT SEEMED LIGHTER THAN THE REST BUT HADNT DROOPED. I MIXED TWO GALLONS OF WATER WITH 1TSP KANGOROOTS AMD PHED IT CLOSE TO 6. I FED THE 3 PLANTS THAT WERE SUPER DRY LIKE A HALF GALLON AND SPRED THE REST OVER THE OTHER EIGHT PLANTS. THEY WERENT DROOPING BUT THEY WERE VERY DRY. I PLAN ON A FULL WATER TOMORROW. I WOULDVE DONE IT TODAY IF THE TEMPS WERENT SO HIGH. ITS RAINED A MONTH STRAIGHT SO I HAVENT HAD TO WATER. I MADE A COUPLE VIDEOS BUT I'LL HAVE TO UPLOAD TOMORROW. 7/6 Another super hot day. I hefted the pots and they still had some weight but I could tell they were dry. This rain has messed up my watering schedule. Well it made it so I didn't NEED to water. These are big plants now. I need to get a schedule to stick too. They're going to probably need a gallon a piece at least. I'm still nervous watering. Right now I'm just reading the plants. I added .5tsp kelp me/you to 1 gallon of water to help with heat stress. I fed an additional two gallons to the garden this morning including the two container plants in the back. They were dry on top too but I know they have water deeper down. Next watering I'll be more consistent and try to give them there 10%. It's great having the bags elevated. I can finally see when I start getting run off. I could even measure the ph of it instead of relying on that meter. Ill check the ph when I go back over. Still a few 🐛 holes but they are few and far between. I really don't want to spray for such a small problem but if I cant find them at night that's what I'll do. UPDATE: Another 90 degree day. I went back over and gave the garden a gallon of water as they were dry and it didn't rain. Tried to use a soil ph meter to check ph. First couple were 6.4, 6.5 then I got 7.3 and I accidently dropped it. Then I got somethings that were high eights and even one 9! Obviously the Meter shit the bed. I'll lower the ph of the water slightly when I fully water tomorrow and I'm going to measure the runoff. 7/8 I must've messed up the journal again as the dates are off. GAVE PLANTS A FULL WATERING. Each girl got a gallon. I couldn't upload my videos this morning as I had to break up a fight. 3 on 1. Didn't give me a chance to put the videos up. I'll take some stills then I can upload them. I took stills and they all uploaded but didn't fucking save. I'm nit going to keep trying to upload if it's not going to. Noticed a few more holes in leaves and one skeletinized leaf so I need to either spray the bt or something more versatile. I'm putting more poison around the cage and de between the bags. I'll go check things out tonight. Sick of writing a book and uploading to just hace them disappear 7/9 Did a quick video today. Noticed the bags were fairly light despite the plants being soaked amd the pallets wet. I was pressed for time. I gave two gallons to the entire garden. I hope that will hold them over until tomorrow. I'll need to up how much water I give them. Going with a gallon and a half next time. I see more pillar spots and a moth took off when I shook the plants this morning. So I'm gonna have too apply the BT. I figure if I go over before dark tonight I might be able to see aju nocturnal insects around. Luckily my dad feeds the birds and they are always there. I think they help with pests. UPDATE IT WAS A LITTLE COOLER TODAY BUT MICH MORE HUMID. I WENT AROUND SIX TO MAKE SURE THE GIRLS WERE OK WITH WATER AND TO GIVE THEM A TREATMENT OF BT. I WENT THROUGH THE GARDEN ANDCGOUND THREE LEQVES TO DEFOLIATE AND LITERALLY A COUPLE LEAVES ON TWO PLANTS WITH PILLAR HILESM WHEN I ARRIVED TWO BIRDS FLEW OUT. A HORNET CAME IN WHILE I WAS THERE. THIS DO LESS APPROACH SEEMS TO BE REALLY WORKING. I DODNT SEE NEARLT ENOUGH DAMAGE TO WARRANT SPRAY8NG MY EXTREMELY HEALTHY GIROS WITH ANYTHING. ILL KEEP AN EYE ON THEM AND CLEAN THEM UP A BIT. I DO NEED TO INSTALL THE VERY8CAL TRELLIS FOR SUPPORT. THEYRE PRETTY HEALTHY THOUGH. ONE PLANT IS ABOUT AS WIDE AS IT IS TALL. STILL......PLANTS ARE EXPLODING AND ITS GETTING TIGHT IN THERE. I NEED TO GET THE TRELLIS UP THOUGH. 7/10 I went over and was planning to water. Plants were wet and it's raining. Top of the medium was moist but the bags were light. ONE bag was super light but seeing that we are having showers all day and an additional half inch of rain coming tonight so I didn't water them. Especially since they looked great. Decided to to spray BT yet as the damage is so small and i think the birds have been taking care of the pillars for me. Now I'm wondering if I should've gave that ONE plant a little bit of water but it will be find. Did a video. I'm being careful not to over water. Last year this is when all my buddies were devoured by earwigs. And no senescence like the years before. I think it was hust those earwigs. I haven't lost shot for leaves. Even the stalks are bright green and look amazing.

The humidity is loco…the heavy rain continues. My stem is drying out…I’m not sure what is causing it All insights are welcome.

30/10/22 - Week 2 Begins 31/10/22 - Increased light height by 2 Inches to increase light output upto 75% - slight yellowing on the leaves will monitor this week - will pot up into final pots by end of the week 03/11/22 - Transplanted 2 of the 4 final seedlings into their final pots. - Lower left plant had far smaller roots compared to the top right so may well pick other seedlings 05/11/22 - All plants transplanted - lower left plant removed, weak roots and no longer growing at same speed as others, sent to the gulag. - 3 x 3 inch plants and 1 x 4 inch - went from 250ml feed each to 750ml each plant - humidity 65% heat 21C

- Week 7 - ----- Day 43 ----- Fed 1150ppm @ 6.4ph 23 Liters. Hard to get above 1200 ppm now. More molasses being used, maximum Koolbloom dry powder as well. Tropicanna Glookies is starting to turn purple. Wedding Cake is fattening up FAST More photos later this afternoon mid light cycle. *Update* Big bulk phase is 100% on right now. Wedding Cake is thicker than a tall can of beer in 4-5 nugs easily. Tropicanna Glookies is sweating out trichomes and getting super sticky while slowly turning purple Great things await for these 2 ladies over the next 20 days. *Update* 2 close up shots of some purpling on the Tropicanna Glookies. ----- Day 44 ----- Here's a video. slow easy day of nothing ----- Day 45 ----- I see a tiny bit of yellowing at edges, nothing serious. I don't have to feed every 2 days now anyways its slowed to 3. I top off the ones near turgor pressure loss levels ( I check my whole hand down side of pot for moisture now) with tap water when needed today. Tomorrow will be feeding ~1000ppm most likely due to using Diamond Nectar chelating nutrients with large amounts of blackstrap molasses when combined and left in the reservoir before use. This seems to drop the detectable ppm even though it retains a high level of nutrient content... with Cal/mag (1-0-0) and KoolBloom Powder which is like a 0-30-40 its wildly powerful. Back right Tropicanna smells like Pineapple Sour Patch Kids without the sour. Its insane. I wish I had smell o' vision for you folks right now. Wedding Cake is like sugary sweet but weed esque... earthy esque type of thing. Not the Tropicanna... Shits fruity like kool-aid. Nugs are getting humongous and its pretty fun to watch it fill in, I had a low level anxiety of it never "Filling" in... but yea it's day 45 and look at Big Bertha... nearly dwarfing my fat ass arm... wild shit. Feel like these ladies have at least another 14~ days on the lower end. Wedding Cake should finish a week after Tropicanna... Trying to grab Wedding Cake "indica" tendencies and max them by going for 40-50% amber, 60-50% cloudy trichomes with under 2% (like literally 1-3 clear per 60X magnifying pic) clear trichomes. Tropicanna only 20% ish amber until clear is only about 20% of trichome and cloudy makes up roughly 60% of total trichome finishing... ----- Day 46 ----- Easy day Fed 1050ppm @ 6.4ph 13 Liters only. I want the root zones to dry out more and quicker, less chance of mold and other root rot issues. Cutting watering/feeding in half now but will be feeding prob twice as much. Buds are fattening FAST and are turning purple. Looks like I got the purple pheno Wedding Cake. Woot. ----- Day 47 ----- Easy day Buds are gettin freaky. Really poppin out now. It's quite awesome to see. **Update** *** HEIGHT CHANGE EXPLAINED! *** Took the Tropicanna's off the pot risers I DIY'd and brought them to the floor. Gives light in between the 2 plants at the side and also helps remove any light burn on the tropicanna, as I have been noticing a very slight tinting of too much light in the central part of the tent. Plants look incredible, tiny bit of tip burn but im not too worried, I'm feeding 1000-1200 ppm at the moment. Speaking of which, fed some tap water, 500ml each, they were dry enough to warrant a turgor pressure loss top up. Feeding tomorrow. Enjoy some lights off shots. ----- Day 48 ----- Fed @ 1150ppm 6.4ph 13L Easy peasy lemon squeezy, here's a new video for you guys n gals. 14~ days to go. ----- Day 49 ----- They're getting super thirsty again. woke up dry. gave 500ml tap water each plant. Will do the same this evening. Tomorrow feeding going to go to 16 Liters instead of 13 Liters. I'm lazy and don't want to water daily. Plants look phenomenal, buds are getting massive. The Wedding Cake on the left is throwing out paintbrushes thick of pistils, it's quite insane. Gonna be a hell of a plant around day 63!!! Day 53 i'll start checkin trichomes and start posting x20-x60 shots.