Not the biggest week for growth it was rainy first half of the week but getting nice sunshine at the end. Was able to clean up the bottoms and grab a few clones. Watered with boogie brew again at end of the week.

IVE MADE MORE VIDEOS BUT THEY JUST DON'T SEEM TO UPLOAD AND IT'S FAR TO SLOW TO DO IT FROM HOME 6/27 Made last week a five day week to get back on track. It's still overcast and rainy. It's not raining a lot bit it's consistent. Despite the weather the plants are doing phenomenal. I'll update later. It's 1pm. It's been raining consistently since 11. Just a sprinkle but it's steady. I'm going to begun uploading the weeks weather on my diary. I may start a new diary for the plants I light depped as they are flowering pretty good. Rain stopped and it's just overcast for now. I looked at some videos and did a comparison of videos one week ago and videos today and HOLY SHIT! WHAT A DIFFERENCE. Especially the light depped 10th planet. Well everything but that was the most significant difference. I'm astonished at the health and growth despite the crummy weather. Continued to rain. Just got harder. Plants are taking it but it's flooding underneath the pallets a little but it will be fine. The light dep however has me concerned. The 10th planet is looking spectacular. The bigger purple punch I'd looking good too. The smaller one though looks to have a pollen sack coming off one of the branches. Considering its not on the otherside I assume it's not just a swollen calyx. I don't mind chucking it especially if that means I don't hurt my other girls so I want to make sure. I sent videos to a few other growers and I'll add a question on here. Those three plants have been isolated from the rest for a few days due to rain. I have the suspect isolated alone until I can confirm. It sucks cause the light Depp was going good and the6ve all got little flowers. 6/28 Well that fucking sucks. ALL THREE plants I tried to light depp hermed on me. I could see male flowers. Luckily I had been keeping a really good eye on them and it was preflowers mostly. At least I caught it. One or two stamines on each plant. Would've been really easy to miss. Only one had STARTED to elongate into a stem so I think I caught it early enough. Plus since all this rain they've been kept in a different location then my big girls. Glad I did that now. Boy the roots looked good on those plants. I just grabbed the stalk and lifted and it came right out of the pot. I held it there admiring it for a minute. This sucks. At least the real plants are doing good. As far as I know. No male preflowers that's for sure. I've got some feedback from other growers and the videos are a little blurry but I had found a light leak and I'm certain these plants hermed. I know I could've tried to save them but I didn't want to risk it. I compared what I was seeing with Google photos and other websites. Aside from the larger ball with its stem, there were also several little bumps besides developed calyxes that were weaving into little buds. Trust me that I wouldn't cut down my plants if I wasn't 110% sure. I might've been able to "save them" but to me it's just not worth the risk. 6/29 I was second guessing myself pretty hard last night due to some responses I got on my light dep and messages I got from other growets. Made my anxiety horrible but I looked on several video's I'd taken again and I know what I saw. I felt better after that. This was after I researched and waited THREE days until I saw the ball on the stem and the groupings of small nubs under a fresh yellow flower. These plants were flowering good and it sucks to lose them. One MAY have been ok but one was a runt and had all the characteristics of a true hermaphrodite. They were only in 3's and I couldn't risk my harvest for an experiment. Still sucks. Oh well. Sun is starting to come out. Plants seem to be doing fantastic. I have one spot on a leaf that looks like a pillar munched on a leaf so I'll probably get the bt out soon as I have a dry day that I can apply it. I'll have to check the weather. I need to start a nute regiment but the plants aren't telling me they need anything yet. 6/30 I fucked up dates or dodnt do it yesterday or it didnt save right so I'm leaving this blank today is the 1st. 7/1 I have still only watered s couple times and I haven't had to feed. This week I'm going to start nutes. I had some external ersonal situations that have kept me from my plants. I'm hoping to get back on track. I noticed some pillar damage so I'll need to dig out the BT. This morning I saw this giant ground hog by my cage. Hated too but had to get rid of him. Of course some of the blowback landed on the leaves of one of my plants. I tried to clean it as best I could. Better than that fat bastard eating everything in one night. I broke a branch either falling around it or bulling through when I was pissed or I LST it the wrong way and the wind broke it against the tomato cage. Nice big branch too on top. I tried to fix it with duct tape but we'll see. The plants need me to spend sometime with them. I need to clean them up. Apply bt and give them their first feeding. I'll update as I go. They don't seem nutrient deficient by any means but I don't think it would hurt to start the nutes. 7/2 Bags were lighter today and if it wasn't going to rain tonight and tomorrow I'd he watering. Plants look great so soil isn't depleted yet I guess. They're growing rather rapidly. The branch I broke didnt make it. Had an idea it wouldn't but I had to try. I waited on the BT on account of the rain. I may go back over and change my mind and water with silica or a mild nute solution or maybe apply the BT. Depends what time I get back. I have some work I need to do over there. There's a few that I need to clean up the bottoms on. Pest damage is minor and limited to one or two plants and a leaf or two only. 7/3 More rain. It was supposed to rain this morning too but it didn't. We got .33in yesterday and through last night so I thought that was ok. Looking back on my previous diaries I'm doing things significantly different than before. I had used a lot more nutes earlier on. This morning I mixed two gallons of 2tsp of big bloom and fed it to the 9 plants in smart pots leaving the container plants as they have much more water in them. Looking back at other diaries I previously had, WPM and septoria by this time not to mention a shit ton of other pests I was fighting by this time. Since I poisoned where the cagexwas multiple times and sprayed the cage before it was moved I luckily don't have that problem yet knock on wood. I'm planning to apply BT tonight to deal with the moth larvae if there are any. I'm looking at plants around this area and im seeimg SOME septoria and pm on raspberry bushes and burdock so it is around. I made sure my cage is not by any other vegetation this year and is sitting on asphalt with the bags on raised pallets. Good thing I did or I guarantee they'd be flooded by now. I've been seeing multiple complaints from maine growers online (AND THEY HAVE HEALTHY PLANTS!) saying this is the worst year ever. Maybe they need a dose of fusarium oxysporum to keep them humble. This is maine. If you don't like the weather just wait five minutes. Meanwhile I'll be doing my sun dance hoping for sun. "Hard to grow cannabis with no sunlight" said another grower on my forum.

I cant fix the damage that was done but they are putting on a little weight and the Trichomes are starting to amber up say 15%-20% i think i can push it one more week. I will give 2 days of dark on Wednesday and chop at week 10-11 as i put them into flower on 3/20

I continued with the LST and did a defoliation.

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.

Eran 3 esquejes cherrywanna , solo pesé el nro 2, me limé pero esa fue un intermedio entre las otras: La cw 1 tenia cogos grandes y largos, el mas grande humedo pesaba 33g. La cherrywanna 3 era la del fondo, tenia mas bien pompones superiores gorditos y no mucho mas para abajo. La realidad es que puse muchas plantas para la potencia de luz q tengo, pero igual salieron muyy bien:)

This was my first cycle in tent. The Autopot System is amazing ang brings autonomy. I used fert Plantprod, calcium nitrate, magnesium sulfate and MKP. PH around 6.0 and solution fert in tank 1200 PPM . This strain is fantastic. It withstood the intense heat of the southern hemisphere's tropical climate. It was easy to prune and defoliate to control the size. The smell is of tangerine and flowers produces a lot of resin. I am very satisfied with this harvest! Thank you Sweet-seeds!!

1/14: This morning, I did a foliar application of big bloom and fulvic acid, then about 5 hours later I watered them with about a half-gallon of rainwater each and added armor si, humic acid, endoboost myco/tricho, liquid molasses, and a bunch of cal-mag. Today, I also I wired up and mounted my new samsung sun board strips (660nm/730nm) and my Solacure FlowerPower UVB fixture. I'm running the deep red/far red bud boosters a few hours per day right now, but will run them for the entire photoperiod once I start flowering them. I'll run the UVB for 4 * 15-minute sessions a day for the full flowering cycle, and if they don't protest too much I'll increase each session by 5 minutes and evaluate again. Some strains are more forgiving than others and I've got 5 different strains in this space...so really not sure much time I'll get away with exposing them to the deadly rays without damaging them too much...😈 Both "A" and "B" put on an inch overnight. Now that the soooperstunted mutant runt is acting like a normal plant, so henceforth I'll refer to her as "C." 1/15: I received one of the rapid led/growmau far red initiator pucks today. With the placement of my UVB light, I'm realizing I'll need another far red puck to have even and intense far red coverage, so I'm ordering another with Prime delivery and waiting to start flowering until I receive it. I sprayed them down really well with ph adjusted rainwater tonight to rinse off nutrient build-up from foliar applications. 1/16: I'm really excited to try flowering under 14/10. I grew photos indoors on an off for 15 years before I semi-retired. If I added up all the additional flowering time I could have done through the years if LED technology existed, I'd have had an extra truckload of bud to smoke. I did another application of Axiom Harpin a|b Proteins this evening, right before dark. I'm expecting a big growth burst this week, leading up to the flower stretch. I really need them to trigger under 14/10 within 4 or 5 days🙏 ...if not, I'll switch to 13/11 and wait a few more days🙏😟..if still no pistils are poppin, I'll go to 12/12 and chalk it up as bad luck or varietal indifference to Pr and Pfr manipulation. 1/17: I fed each of them about 3/4 gallon of full strength veg nutes. This will be the last. I'll go with half-strength veg and half-strength bloom for a week, then go with full strength bloom nutrients until I start flushing them in 6-8 weeks. 1/18: I installed the second far-red flowering initiator today and got all my timers configured for flowering: ========================================= timer#1 - power strip with qb's and red boosters 10:00am -12:00am timer#2 - (dual/independent setting) sideA- 3-way cube with uva bars 10am - 3pm 7pm - 11pm sideB- flowerpower uvb 1pm - 1:15pm 4pm - 4:15pm 7pm - 7:15pm 11pm - 11:15pm timer#3 - far red pucks 11:00pm - 12:15am timer#4 - sub-canopy tube 10am - 1pm 3pm - 6pm 8pm - 11pm ======================================== I also did some testing on the timers and sealed myself into the closet to check for any light leaks. All good.👌 1/19: Tonight is their first long night. It's ON!👍 I moved #3 into the tent with my DWC rig to veg a little longer. 1/20: I watered them today with about a half gallon each. I'm seeing calcium and magnesium deficiences here and there, so added some boomerang and heavy cal-mag-Fe along with liquid molasses, humic acid, and endoboost myco. I also foliar fed with big bloom and fulvic acid. #3 is still vegging in my SCROG tent with the #8 FFT DWC plant. She's coming along, but still not ready for prime time.. That's it for week 4-

Planta resistente, de estructura mayormente indica, con una producción importante de resina. Planta de rápido desarrollo que tolera bien el estrés provocado por el topping, LST y frío. Altura media, con flores realmente densas y duras, tal como prefiero, avanzando en la floración dejará ver colores rojizos que deslumbrarán. Se desarrolló muy parecido a una Gelato que crecí del mismo banco. Un desarrollo fuerte y rápido para terminar brindando hermosos brotes que desprenden sabrosos aromas dulces y lucen una apariencia de dispensario innegable!. Sin duda buen trabajo de Fast Buds en estas genéticas.

Drying now. I will return later with more information and pictures

Buena planta la dichosa Hulkberry. La técnica de doblar el tallo todavía no está muy conseguida. No me gustaba el aspecto que tenían esta vez. Contra todo pronóstico, han dado más cantidad de lo que parecía a primera vista. En todo caso los resultados son superables. La planta más pesada ha dado 22 gramos, y la que menos, 6 gramos de cogollos.

Week10.. First day flush their plants and check the tricoms everyday. {Activities} (Day 64) Flush the plants with water until the ppm is equal to the water used for the flush 🚿 (Day 65) n/a (Day 66) Watered (Day 67) The tricoms ready for harvest, 70/30 milky/amber mix. (Day 68) Harvest Finish! (Finally hope you like and enjoy my diary) Thank you so much for checking out my grows. Feel free to leave a comment, push the like or give the follow.

Aug 17: Auto Overdose is a nice plant but it’s not an auto. I started this one late and only topped it once thinking it was an auto. Other growers have noticed it isn’t an auto too, so I forced it in the dark garage. Flowering has to be started by the end of July here or it won’t finish in the fall. The flowers are forming quickly and I suspect this is actually Overdose Fast. So far so good, and good genetics for a Fast plant. Aug 18: no UV light today unfortunately but it was decently sunny. Scrog net certainly seems like a good idea. This plant is asymmetrical because I broke one of the two main stems a couple weeks after topping. This changed the shape of the plant so it’s become one-sided as if I was growing it up against a wall. Lots of nice lower branches came up so she looks pretty good now.

Please tell something with me for my plants is that good grow remp? Its 18 days old is that small ?

sour 76 stopped stretching at 22, 23 and 24 inches. yeti number 4 stopped at 32 inches, while yeti 3 stretches another few inches as sour "tower" begins stacking and starting to trich up

Plants are growing good. I accidentally broke the tip off of the Norther light plant. Ahh 😱

in this past week I have defoliated the plants about 40% I have lost some leaves which have turned yellow I think the plants lack nitrogen due to the stretch the buds started to smell good. for nitrogen I add coffee grounds to keep away the pests and it is rich in nitrogen. the hardest part is fighting the humidity it’s been raining for a week 😭 humidity is the worst enemy I much prefer heat. see you soon

Unfortunately this will be the last week because the threat of the red spider has returned and I cannot afford to use other chemical remedies to eliminate it so I anticipate the harvest by a week even if looking at the trichomes I am not so far from full maturity, Too bad . !

She looks absolutely amazing! Buds are developing nicely and she has great color. I’ve done some defoliation to increase the penetration. Buds as low as 30” below the top (47” below the lights) seem to be developing quite well. I have lollipopped below this (bottom 24”). Thanks for looking.