Week 6 day 1 video Week 6 day 4 video I’m still pushing very hard with carbs every watering, humic acid, soluble n, soluble pk, microbial mass, b+, fishshit. Already tried testers for lowers. Very potent hits harder than a pen. Feels like 30-40% baked for 1-3h per j, different phenos. Not harsh just testers dried for 0:01:15, checked seeds and developing for 2-3 weeks

Getting a growth spurt on switched to flower mode on the 600w led, installed the extractor and carbon filter as it's getting to smell a little fruity even at this stage. Lite feed in this early stage with the listed nutes, seem to be responding well. 17/10 Defoliated today and made a CBD smoothie from the lower canopy with almonds, apple, lemon and lime, the leaves were very fresh, it was pretty nice. Looking forward to the next defoliation, there are many health beenefits using all of the cannabis plant so i'm making the most of her as the grow progresses. https://www.medicaljane.com/category/cannabis-classroom/consuming-cannabis/juicing/#introduction-to-juicing-cannabis

Absolut ungewohnt das Zelt mit so abgemargerten Pflanzen zu sehen 🤣🤣🤣 Die Ladys von draußen sind endlich nach innen gezogen für den restlichen Blüte Schub. Sehen wie Crackys aus im vergleich zu den den davor drin waren 🤣🤣

This is week 3 going into 4. Not any proplems apart from neededing a ppfd reader. Anyone recommend any good ones.

From this point on, the plants of my two active diaries will be together in the grow with a 12x12 photo period. So I'll put the same photos in both diaries.

Well week 12 and week 2 of flower started yesterday 8/22. Other than the clones everything is looking good. But to be fair I haven't really done much with them. They're like a bastard step child, I only kept em around out of moral obligation. Lol. J/k...sort of. Nah, just some weird bumps on a couple leaves and from what I can tell it's a copper and or zinc thing so I'm gonna get some Proactive, lol. So the mothers have definitely stretched, lol. Bruce has been shorter than Sky the whole time but whatever. That's pretty much it. Happy growing everyone ✌️🍀✌️ UPDATE: 8/24 AND WE HAVE BUD STARTING ON THE CLONES!!!!!!! UPDATE: 8/25 Just uploading a few pics. Happy growing ✌️🍀😎

So I am halfway through my first harvest and I'm starting to feel like I may have been impatient! Would appreciate any advice or constructive criticism from any experienced growers out there! Do you think I harvest the rest of my plant now or leave it a while? Any tips/hints on the best way to maximize bud density? Thanks in advance

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.

Week 10, first day of flower set both light up now runing a total of 730 wats, for now will turn both light up over time and will add a extra co2 bag @growerchoice @SHOGUN COCO A 4ml/L 160ml @SHOGUN COCO B 4ml/L. 160ml @SHOGUN ACTIVE BOOST 2ml/L. 40ml @SHOGUN CAL MAG 1ml/L 20ml @SHOGUN ZENZYM 2.5ml/L. 100ml

Sep 1: there might be a bit of lower leaf damage on WP1 after the 2 C night here two nights ago. Otherwise everything seems fine and the buds are progressing. Sep 2: removed some yellowing fan leaves that had been damaged by cold temps. Sep 3: WP1 has finally stopped getting taller and is starting to flower. Good thing too cuz the days get short pretty fast now and it will be iffy as to whether this plant will finish in time. Sep 6: Well, I spoke too soon as WP1 is still getting taller, and it grew 4 inches in 3 days. This far north, it should be flowering not vegging by early September. Oh well. Lots of insect life on WP1 (ladybugs, spider, flys, few ants even) and a few aphids so it seems to be in a balance and the plant is fine. WP2 in the city was force flowered a while ago and is progressing nicely. These are in small 5-gallon pots in an attempt to limit their size and to encourage flowering.

10/17/2022 start of week 3. Plants still look healthy. Been LST the Strawberry Gushers and Newberry for a few days and some of the lower branches are catching up. Trying to keep the canopy as uniform as possible. The Strawberry Gushers appears to be in preflower already, which is a bit concerning. Was hoping to get at least another week out of her. Orange Bubblegum is still the smallest of the three, but she continues to grow at a steady pace. I think someone pulled a fast one on me with my cover crop. I have what looks like blades of grass growing, with only a few small clovers showing up so far. Guess that is what I get for shopping on Amazon. Also, increased my DLI to 500. Not much more to report at this time. On 10/19/2022 I watered 1 liter per pot with the Rootwise and ThermX again. This amount every 2 to 3 days seems to be sufficient for their current size. The pots are wet on the bottom, but no run off. Also, removed just a few of the lowest leaves and fan leaves blocking the lower branches. The LST is allowing the lower branches to catch up. 10/21/2022 watered both the Strawberry Gushers and Newberry with about 1.5 liters each. They are both really growing fast now. The Orange Bubblegum is beginning to speed up, it's just seems like a shorter plant with shorter node spacing. I just misted the surface of the Newberry since the pot was heavier than the other two. Still doing some minor LST on the main trunk and some selective deformation and leaf tucking of leaves blocking bud sites. 10/23/2022 was a big day for the Strawberry Gushers. Top dressed with Gnarly Barley, BuildASoil Craft Blend, and BuildASoil BuildFlower, then watered 2 liters. Plant is starting to stretch so I wanted to make sure she has access to the nutrients she needs. The Newberry and Orange Bubblegum just got 1 liter like usual. Plan to top dress them as well once they get a little bigger. Avg. VPD: .8 PPFD: 500 DLI: 32

Hi guys, What's up? Welcome back to Queen Peaky's Flower Gardens We are at work again to start a new growing journey To make these buds explode in the best way .... the touch of purple color gives the room a very sexy atmosphere😎😈😜

Bien aquí esta el día esperado la cosecha, es mi primer cultivo y considero que lo logre. En muchos medios de lectura y en especial en vídeos mencionan que no puedes esperar mucho es tu primer cultivo. En mi caso es falso y lo demuestro ya que si aprendes, investigas por cuenta y lees lo suficiente, obtendrás un alto porcentaje de que los resultados se den. Muy contento con mi plantas y sus tonos morados. Puntos a mejorar tener una carpa de cultivo y por su puesto un extractor de humedad para que baje la humedad preferiblemente a 45 grados Vendrán mejores contenidos y cosechas mas abundantes. Gracias a todos por su vistas y comentarios. Saludos y bendiciones!

Good evening and welcome back, fantastic friends of the old Weed! Sharing my growth with you is always a pleasure! These sensual -looking beauties begin to have a really nice perfume .... I think we will begin to irrigate with only water from now! see you around

What can I say, the strain is amazing, it is literary monstrous. The growth spurt from week 5 to 6 has been insane and now standing at 30cm tall. The girls have been drinking at least 4 litres a day. TD#1 is more than 2 feet wide at 30cm tall its ridiculous. I have noticed #1 is a different phenotype than #2 & #3 because of the difference in leaves sizes as #1 has smaller leaves as compared to #2 & #3. Looking forward to seeing how these girls grow out in later stages.

Day 56: These 3 girls are finishing out. Cyco nutrients did awesome for me! I found a top with some bud rot beginning to start so I lopped that off. It was not much, but I got it early (learned first hand in the Gorilla Girl grow). Humidity has been higher these days. Buds are turning slightly purple. Decent amount of sugar on the buds now. Trics are mostly cloudy, very few amber. Most pistals have withered and calyx look swollen. Smell is beginning to give a cakey-gas undertone to the up front scent of overripe cantaloupe across all 3 plants. There is a tiny bit of pine. I need a cell with a better camera :( Some more days of water and Flawless Finish then the chop.

What up Fam. These girls are growing amazing. Now that I can controll the temps a little better they've taken off with growth. Starting the flower period which we all no know what that means. The countdown is on. Over all Happy Growing.

I could have pushed the plant one week longer but im on a scedule

Happy girls. Buds swelling nicely. Got the frosties poppin off. They’re loving the fish shit. The GWK passed DG in height this week and just starting her buds. Week 5 for her.

Todo parece ir bien por estos lados, Lo importante es que las raices estan haciendo una fiesta en el sustrato!!! 😎 Hoy comienza la 4ta SEMANA! Dia 22 de cultivo, y 100% motivado por este mundo maravilloso! - Se realiza una pequeña poda en las partes bajas de las 4 plantas, por motivos de precaucion a la aparicion de algun agente perverso que pueda estropear lo avanzado. (Se aplica folear Knactive X3 ML) *El día de hoy 28/05/2020 se han regado 3 plantas en macetas de 11 litros: X2 Semillas Auto Lemon Kix= 500 ml [3mlKnactive+3ml/L ATAGrowth-C+2mLTopCrop-TopAuto] PH 6.0 / EC= X Tº=22 X1 Semilla Auto Tutankhamon= 500 ml [3mlKnactive+3ml/L ATAGrowth-C+2mLTopCrop-TopAuto] PH 6.0 / EC= X Tº=22 (Proximo riego se incorporara al parecer Flower-C de ATAMI) *El día de hoy se han regado 1 planta en macetas de 7 litros: X1 Semillas Auto Lemon Kix#3 = 350ml [3mlKnactive+3ml/L ATAGrowth-C+2mLTopCrop-TopAuto] PH 6.0 / EC= X Tº=22 *El dia de hoy 29/05/20 se realiza de manera experimental, LST nivel novato, Me gustaría sus consejos. próximamente incorporare Red SCROG de 49 espacios. *El día de hoy 01/06/2020 se han regado 3 plantas en macetas de 11 litros: X2 Semillas Auto Lemon Kix= 500 ml [1mlKnactive+3ml/L ATAGrowth-C+3mL ATAFlower-C] PH 6.2 / EC= X Tº=23 X1 Semilla Auto Tutankhamon= 500 ml [1mlKnactive+3ml/L ATAGrowth-C+3mL ATAFlower-C] PH 6.2 / EC= X Tº=23 *El día de hoy se han regado 1 planta en macetas de 7 litros: X1 Semillas Auto Lemon Kix#3 = 350 ml [1mlKnactive+3ml/L ATAGrowth-C+3mL ATAFlower-C] PH 6.2 / EC= X Tº=23 CONSEJOS ? BUENOS HUMOS!!!