28.10. Progress Overview • Eight days in, and the SuperBuffCherry #26 plants are showing steady recovery after the early topping on Day 4. • Growth momentum has returned — new shoots are visible at the main nodes, and side branching is beginning to expand. • The overall impression: slightly slowed by topping stress, but still on track for a healthy vegetative rhythm. ⸻ Post-Topping Recovery • The plants clearly felt the cut — minor stress signs visible (slight leaf curl and slower new growth). • However, the color remains strong, and all tops are pushing new growth tips already. • This brief recovery dip is expected after early topping and should stabilize completely within the next few days. • Once the new shoots strengthen, canopy management and gentle LST can begin. ⸻ Pest Situation • The thrips issue hasn’t disappeared entirely — still visible, but very minimal. • Continuous counter-measures are in place to keep the population suppressed. • So far, the balance seems under control, though full eradication will take consistent attention. • No major new damage spots seen — a positive sign that the preventive strategy is working. ⸻ BioTabs Performance • The BioTabs organic system continues to hold its promise: stable nutrition, no burn, no deficiency. • Even under light stress, the plants show resilience — a good indicator of strong microbial activity and root health. • The living-soil dynamic keeps everything buffered and calm, helping recovery without any liquid feed adjustments. ⸻ Notes & Outlook • Next focus: allow the plants to fully bounce back before applying any further training. • Maintain airflow and humidity control to discourage pest rebound. • If the recovery trend continues, Week 2 should close with a well-structured, evenly topped canopy ready for shaping. ⸻ 🌱 Day 8 Summary: Mild topping stress visible, but recovery underway. Thrips presence minimal and managed. The BioTabs system keeps everything stable — resilience and structure are returning fast, and the SuperBuffCherry #26 still shows solid potential moving into full Week 2. ———————————- ——————————— 01.11. Progress Overview • The vegetative phase officially comes to an end — today marks the transition into flowering. • The light cycle was switched from 18/6 to 12/12, meaning tomorrow begins Flower Day 1. • Overall, the run looks solid: strong structure, healthy color, and good vitality, with only minor pH adjustments needed. ⸻ Soil & pH Situation • Current soil pH measured at 5.7, slightly below the ideal range. • Early signs of a calcium lockout were noticed, but detected in time before major impact. • Corrective measures are underway to bring the medium back up to 6.3, the target zone for optimal nutrient uptake. • Adjustments are being made gradually to avoid disturbing the microbial activity sustained by the BioTabs system. ⸻ Pest Situation • The thrips and general pest presence are now almost completely gone. • Continuous preventive work has paid off — the situation is under firm control. • No new damage visible; foliage remains clean and healthy. • This is the most stable pest status since the start of the run — a clear sign that the reset and preventive routine were effective. ⸻ Plant Condition • Plants remain strong and compact after early topping; internodes uniform and canopy even. • Minor signs of stress linked to the low pH, but overall vigor remains high. • Once the pH correction stabilizes, calcium uptake should normalize and growth will accelerate again. ⸻ BioTabs System Performance • The BioTabs organic feeding system continues to demonstrate resilience and balance. • Even under suboptimal pH, the living-soil biology buffered the stress effectively — no burn, no deficiency spiral. • Root zone remains active, and microbial life appears to be compensating for the short-term nutrient block. ⸻ Outlook • Focus for the next few days: confirm that pH correction holds steady and monitor for the start of the stretch phase. • Expecting visible early flowering development within 3–5 days after the 12/12 switch. • The goal is now to maintain environmental stability and airflow as the plants begin vertical growth. • With pests under control and the soil balance returning, the bloom phase starts under good conditions. ⸻ 🌸 Day 12 Summary: Slight pH imbalance (5.7) addressed and under correction, calcium uptake soon to normalize. Thrips nearly eradicated — pest management finally stable. The 12/12 light cycle has begun, marking Flower Day 1 tomorrow. A clean, controlled start into bloom for SuperBuffCherry #26.

Girls doing well, clearly see all hit with hit substrate 😂 but ChemDawg is despite the hit battling n fast 😂

Water only from here 1L at a time 13/09 - Watered @ 10:43 - Health inspection 14/09 - Watered with 1l - Added extra Fan 15/09 - No water needed today. 16/09 - Watered till run down for flush 17/09 - No water today damp 18/09 - flushed 19/09 - Flushed

Info: Unfortunately, I had to find out that my account is used for fake pages in social media. I am only active here on growdiaries. I am not on facebook instagram twitter etc All accounts except this one are fake. Harvest day 71 since the time change to 12/12 hrs. Hey guys :-) Finally the time has come . The lady was harvested. After the trichomes have been checked (70% milky 30% amber) as always, it was left in complete darkness for 48 hours before it was neatly trimmed by hand. After trimming, she was put back in the drying tent on nets. There they are allowed to dry for the next 8-12 days at 62% humidity before they are put into the jar to ferment with 62% boveda packs. After about 4-6 weeks in the jar I will swap the 62% boveda pack for a 58% boveda pack where it can be ready for another 4-6 weeks to enjoy :-). As always, the remains of the leaves are used to make Ice o Lator and oil. Of course, as always, there is a final update during the fermentation process. Until then, I wish you all a lot of fun with this update. Stay healthy 🙏🏻 and let it grow 👍. You can buy this Nutrients at : https://greenbuzzliquids.com/en/shop/ With the discount code: Made_in_Germany you get a discount of 15% on all products from an order value of 100 euros. You can buy this Strain at https://www.amsterdamgenetics.com/product/super-silver-haze/ Type: Super Silver Haze ☝️🏼 Genetics: Haze x Skunk #1 x Northern Lights Type: 70% Sativa – 30% Indica 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Nutrients : Green Buzz Liquids : Organic Grow Liquid Organic Bloom Liquid Organic more PK More Roots Fast Buds Humic Acid Plus Growzyme Big Fruits Clean Fruits Cal / Mag Organic Ph - Pulver ☝️🏼🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.8 - 6.4

Day 44-4/12/21 everything is looking a lot better now!!! Day 47-7/12/21 plants are doing well a lot better now two of them are showing signs of purple!!! Day 49-9/12/21 everything is going better got some burnt leafs on a few but hopefully okay!!! Gave them a liter each today with food!!! Day 50-10/12/21 some are behind others but there’s this one plant that’s going purple I think it’s gonna be great!!!!

First photo is the plant before LST and defoliation Did some light defoliation so air can get through easily. I took out the little new buds , The little balls in the middle of the forming cola to force the plant to make buds on other stems

4/28 Day 35 I wish this plant was bigger. Could be my fault. Her transition to flower was at such an odd time(3weeks) and that’s when her last feeding was coming to an end but should I give her flower nutes early? Do half an half? Or just wait and then give flower? I waited and I shouldn’t have considering that organic inputs take time to feed your plants. Depending on what you’re using. First time trying Gaia green. I do like the ease of it but it would take some adjustments for me to utilize it best. A month between feeding is too long for my impatient ass and it gives me too long of a commitment to not fuck up. I’m also using roots organics with some other plants and I’m really liking the weekly feedings. It makes more sense than a month. What if I have a strain that’s like 10 week flower? Do I just do another dose at week 7 and 8 and then because it’s “organic you don’t need to flush” thing. Probably over thinking it but yeah here’s my plant yall 😂

She growing well, so well in fact I have started to HST the off shoot branches to keep the grow low. They are nice and green still so easy to HST and take to it well. It's getting ready to flip but waiting on my new tent...so she will just have to keep growing taking over my veg cabinet

Hey there, first time growing anything. Let's see how this works out ! So I started to germinate the seedlings 1 week prior to Video. I Haven't fed them any nutrients yet and the LED light was running only 250w. Right now everything looks healthy and is growing by the day. It even seems that one of my SBP Seedling has formed some sort of Tri-Leaf mutation. As mentioned, this is my first grow so if you feel like i'm doing anything backwards PLEASE Let me know ! Peace yo !

This is it...I'm guessing one more week and we're ready to cut. I'm very very happy with this strain. The development was always 👌 on point, veg and flower and has a amazing root ball. I'm positive the great white had an enormous contribution to it. If the water temps are very hot (> 22/23ºC) its better to run H2O2 steril system, but with regular water temps ( <21) the mycorrhiza and Bacilus are a major health contribute to the root zone and overall plant health. It keeps eating and drinking good, but with this week comes the flush. The colas ate staked of flowers, very dense, resinous and pungent smells. Definitely a strain to grow again in the future.

Day 58. Apparently the plant has a bit of excess Nitrogen, so I changed the fertilizer in the reservoir, removing CalMag I have lowered the levels and N, because CalMag has 4-0-0. Lowering the ppm to 650 (before 750). Thank you for the advice @SeedLover 😁 I also start to try the new microscope that has arrived today. :D Let's see how it progresses!

73 Day 10 Weeks to Harvest

В целом всё хорошо, за исключением некоторых нижних пожелтевших листьев

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.

Estuvimos un poco desaparecido por andar un poco desmotivado pero aquí vamos nuevamente, las nenas van bastante bien en la semana 8 la cambiamos a maceta de 3.5L y aprovechamos de darle GREAT WHITE SHARK, la técnica que usamos es de amarrar el central ya que le hicimos supper cropping y apical a nuestro central, amarramos el apical que le hicimos super cropping y le dimos fuerza a varios brazos. Para ir controlando la altura de los brazos le hicimos poda a pical a los que estaban tomando más altura y así poder ir equiparando los brazos. La verdad que no se cuantos brazos tengo que sacar y aun me quedan unas 4 semanas para poder desocupar mi armario de floración y poder pasarlas a flora, así que intentaremos hacer una muy buena estructura antes de pasarlas a floración. La defoliación la aplico cada vez que saco foto ósea semanal y trato de ir manteniendo de a 4 nudos o 6 nudos La alimentación se mantiene igual lo que si no se si lo dije pero: Rhizotonic: Lo estoy usando solo en trasplantes y cuando hago alguna poda. Cannazym: Lo estoy usando 1 vez por semana. Orca y Myco Chum: Lo estoy usando 1 vez cada 1-2 semanas Alimentación diaria: Calmag, silicia, supervit y canna coco a+b Alimento a cada una con 250-350 cc de solución, 2 horas que encienden las luces y 2 horas antes de que se apaguen. Gracias a esta receta no eh tenido tanta variedad en mi runoff y las nenas se mantienen muy sanas. Saludos

Lovely to smoke. With a great weight given the set back with nute lock. Which Is the downfall to this run. Because this happened In last 3weeks which certainly resulted in small buds. However I am totally pleased with final weight and smoke from.this girl. Xx

Flowers are forming 😎