Light experimental LST throughout the week. Started getting signs of root rot on 7/3/2023. The res had started to smell like a pond, and the roots were browning heavily. Added 35mL of 3% H2O2 to the reservoir, followed by a double dose (~16mL) of Hydroguard

ола washing machine пересажены в горшки на пмж и включены в систему. ppm 590. ph 5.9. полив: через час после включения света(7.00) помпа включается на 30минут и через 12часов ещё на 30минут

Always good seeds from RoyalQueen Seeds.. The pineapple kush was clones. Unfortunately something happened and it didnt got finished. Other than that, some different strains i have beeen growing over the years :)0

Chop Day Today....66 days and I feel the runts and Mac could have gone longer but the godfather is crossings 30% ambs and the stash is almost empty!

Looking very good, this ladies are breaking the shield within 48hs since planted as I was expecting, let's see how my beautiful queens develop on this "little run" on a 2x4! Growing with a tsl2000 by mars hydro! 👨‍🌾💯✌️ Stay tuned guys.

Gracias al equipo de Kannabia Seed, Marshydro, XpertNutrients y Trolmaster sin ellos esto no sería posible. 💐🍁 Moby Dick 🐋: Criada a partir de dos parentales icónicos, como es el cruce de White Widow y una Haze pura G13, este choque de titanes provoca un híbrido que golpea a las puertas de las sativas más fuertes disponibles en el mercado. Estamos ante una criatura impresionante en todos los sentidos, con ejemplares que florecen en solo 9-10 semanas en interior y arrojan un peso en lonja de 550 gr./m² Al igual que su padre Haze, nuestra Moby Dick ofrece agradables notas cítricas, pero con efluvios de vainilla y eucalipto, una mezcla de aromas que genera una combinación intrigante, que puede llenar cualquier habitación con una fragancia inolvidable. El sabor es muy parecido a su olor, con toques de limón agrio que harán que tu lengua cosquillee al inhalar, convirtiéndose lentamente en un humo dulce y terroso, con pinceladas de madera e incienso que se adhieren al interior de la boca al exhalar. 💡TS-3000 + TS-1000: se usaran dos de las lámparas de la serie TS de Marshydro, para cubrir todas las necesidades de las plantas durante el ciclo de cultivo, uso las dos lámparas en floracion para llegar a toda la carpa de 1.50 x 1.50 x 1.80. https://marshydro.eu/products/mars-hydro-ts-3000-led-grow-light/ 🏠 : Marshydro 1.50 x 1.50 x 1.80, carpa 100% estanca con ventanas laterales para llegar a todos los lugares durante el grow https://marshydro.eu/products/diy-150x150x200cm-grow-tent-kit 🌬️💨 Marshydro 6inch + filtro carbon para evitar olores indeseables. https://marshydro.eu/products/ifresh-smart-6inch-filter-kits/ 💻 Trolmaster Tent-X TCS-1 como controlador de luz, optimiza tu cultivo con la última tecnología del mercado, desde donde puedes controlar todos los parametros. https://www.trolmaster.com/Products/Details/TCS-1 🍣🍦🌴 Xpert Nutrients es una empresa especializada en la producción y comercialización de fertilizantes líquidos y tierras, que garantizan excelentes cosechas y un crecimiento activo para sus plantas durante todas las fases de cultivo. Consigue aqui tus Nutrientes: https://xpertnutrients.com/es/shop/ 📆 Semana 4: Aparecieron un monton de erizos esta semana, el temporal ha hecho algo de mella en la carpa al bajar las temperaturas aunque todo sigue correcto. Continuamos con las dosis de nutrientes recomendadas por el fabricante.

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16/07 gave her the chop after 8 days flush and 2 days darkness. Aiming for at least 10 days drying time. My scales couldn't read her wet weight without being cut up, which in not doing yet.

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.

seems ok. at least 10 days left. Next watering wil be the last with nutes D65: 1L of tap water per plant D67: 1L of tap water per plant D69: 0.5L of tap water per plant D70: choping time!! ------------------ Energy: 20 kWh ------------------ Water: 7.5 L ------------------ Nutrients Root juice: 0 mL Bio Grow: 0 mL Bio Bloom: 0 mL Top Max: 0 mL Bio Heaven: 0 mL Alg A Mic: 0 mL Acti Vera: 0 mL GS: 0 mL ------------------ TOTAL: 122€ excluding 4th plant that was choped at D33, 135€ including it (seed, soil, nutrients and water) ------------------ Seeds: 24€ (6€ per seed) ------------------ Soil: 20L biobizz lightmix - 4€ (10€/50L) Dynomyco inoculant - 1.5€ (35€/340g) ------------------ Energy: 236 Kwh - 59€ (0.25€/kWh) - Light: 160 Kwh - 40€ (0.25€/kWh) - Others (fans and exhaust fan): 43kWh - 11€ - Heater: 33 Kwh - 8€ (0.25€/kWh) ------------------ Water: 110L - less than 0.6€ (5€/m3) ------------------ Nutrients: 46€ Root juice: 56 mL - 2.7€ (11.95€/0.25L) Bio Grow: 191 mL - 2.3€ (5.95€/0.5L) Bio Bloom: 196 mL - 2.3€ (5.99€/0.5L) Top Max: 157 mL - 4.4€ (13.95€/0.5L) Bio Heaven: 287 mL - 17.8€ (30.95€/0.5L) Alg A Mic: 196 mL - 4.7€ (11.95€/0.5L) Acti Vera: 287 mL - 6.9€ (11.95€/0.5L) GS: 24 mL - 5.3€ (21.95€/0.1L) ------------------

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...😈 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!👍 1/19: Looks like the FIM job didn't take on one of them..but she's got perfect symmetry. WIll probably have to just top her again next week...gonna be a tall one I think. Tonight is their first long night. It's ON!👍 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. That's it for week 4-

Week 18 Hello again everybody  I’ve to mention: Spain was awesome and Spannabis too  My buddy watered them while I was away and he made the job. Last year someone else watered my plants and killed my whole mother tent but this time everything is fine  Today is day 34. They got their tea today: 10l water pH6.5 add 150g Compost, 25g earthworm cast, 20ml Molasses and a tablespoon of bat guano. Let it bubble about 30h. Two girls (Bubblegum) got a bit stressed. One dried out a bit too much and the girl in the left corner got some brown stains on their top fan leafs. I think it’s a bit too tight for her and so I put in another ventilation for more airflow. And to keep it real, I got some light bleached buds. Maybe 5 or so, this happened to me on the OG’s and to defend myself, the distance is more 25cm from lamp to the tops. OH I LOVE MY SANLIGHT LED’s :D So, nothing more to say for now Until next time :) The Rasta

Really starting to put energy into making some delicious cookies

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.

OK so this weeks kicking off big time lots of flowering everything’s really taking off plants are really loving the nutrients super happy with this grow so far I switched bulbs at the beginning of this week to my HPS super excited about the next few weeks I’ll update soon thanks for stopping by!! Quick update its dat 31 32-ish these things are really getting big the LST worked great some of them are kind of thin in the middle but got lots of tops nice bushes the OG Kush just looks killer has a kind of open spread out look I love it it’s going to produce some big buds I can tell! It’s the end of the week I Defoliated again and tied a few more branches down one of the jacks still has a pretty low center but it’s starting to catch up all the plants seem to really be loving the feeling and are starting to really stack up the buds The next few weeks should be fun!

Week N-3. The Cookies plant is doing well. grows normally. Easy Boost Organic Nutrition works perfect. I added GHE Diamond nectar and GHE Roots this week. You can see, that I started to train plants using LST and FIM. I water the plant every day; Plants are not stressed and continue to grow normally. On the next week I plan to do: 1. Put on the air filter, as you can smell a wonderful smell right now. unfortunately not wonderful for everyone. :) 2. Place the grid for SCROG. The plant has a lot of branches, which is very pleasing. So the SCROG- MUST have. |:)

15.07.25. Day 59. Changed reservoir today. Flowers are stacking. It's a waiting game now. Can't wait. Maybe 2 to 3 more weeks.

Hey Growmies, some of you had asked to me if I prepare concentrates.......Yes I do! I don't like modern rosin extraction but instead very rarely I like to smoke some oil. The following is the recipe of cannabis oil made by ancient Mustapha's process. It needs: pharmaceutical grade ethyl alcohol (96.5% by vol.) or 95% for liquors Weed A jar with rounded bottom A lot of time This oil is 5 months aged, from 20 grams of weed I've obtained 3.5 grams of product. Trim previously dried weed (20 grams) and put into a 500 ml jar. Cover with 200 ml of alcohol and leave it partially covered with cap. Let alcohol to evaporate on itself and shake the mixture 2 times a day. The most of the solution will evaporate within 10-15 days. When the solution is evaporated by 2/3 it needs to be filtered between 90 and 120 microns. Now is the time to finish and decarboxylate the solution by heating the jar by bain-marie until the green cream sticks to glass. The jar needs to be refrigerated before you remove the cream with a spatula to transfer it into a smaller jar. Store it in a dark place and open twice in a week for few seconds. You'll obtain a petroleum green/dark amber cream (the green tone will turn into dark brown by time). If the job is well done the surface will crystallize and will shine like a mirror. This cream is insanely sticky. Smoke one drop a time. The collapse is around the corner. Tips: Best results, in terms of flavour/aroma, with single strain Let alcohol to evaporate very slowly, take away some macerated weed (after at least 48 hours infusion) and add new weed/hash pieces little by little. Act as if it were a piggy bank. The final product is a very strong shit, really narcotic.

She continues to develop nicely. Unfortunately I managed to break two more branches, from both she recovered instantly and the branches started to heal already. (Need to be a bit more careful going forwards). The quick healing I would either account to the genetics, but would also contribute it to the rizothonic from canna, as her root system is also a lot further than the plants I grew before. She already smells super strong, can bare keep the tent open for long.