Questa settimana ho deciso di montare una lampada di supporto a LED per poter far arrivare a tutte le piante abbastanza luce, le piante continuano a crescere e i fiori sembra che stiano maturando per bene spero di raccogliere almeno 4/5 piante entro 2/3 settimane,perché alcune sono molto indietro rispetto ad altre.

Welcome to LSD-25 Grow by PoshGrow! 🍀 Week #1 2020 November 4th. - 11th. General Info: When planted: 2020 October 28th. Week: 1 Days: 1 - 7 Last Update Day: 2020 November 6th. Plants: 6 LSD-25 girls by @FastBuds. Equipment: Tent: MarsHydro 1mx1mx2m Lights: HLG 260w V2 Rspec QB Kit & Spider Farmer SF-2000. Exhaust: 4" 322 CFM fan + Viper Carbon Filter. Intake: 4" 100 CFM Inline Fan. Oscillating Fan:             Upper: 4" Ram Fan.             Lower: 9" Voxon Box Fan. Humidifier: Taotronics TT-AH001. Dehumidifier: Pavlit MD750. Soil: NPK soil 40% Compost, 50% Peat Moss, 10% Agroperlite. Pot: 5 gallon Fabric Pot x 6pcs. Nutriens: GHE Trio & Botanicare CalMag Plus. PH Correcton: Chemoform pH-Minus Granulat. PH Pen: Cheap Chinese one, I callibrate it every time I use it. Digital microscope: cheap Chinese USB X4, 1600X. Comment: Hey and welcome back to PoshGrow series! Germination week went perfect, all girls doing great. 6 plants from 5 seeds lol 😆😍 Check germination week for twins info😉 Twins look healthy and growing as fast as other girls, one is abit smaller, but I think the reason for this is 2 times transplanting, its not recommended to transplant autos, but I had no choice if I wated to save both twins. For this week ill be watering pH corrected water till the middle of the week, then they will get first feeding. Going to use nutes every other watering. Also ordered Spider Farmer sf-2000 to support these girls in flowering stage. Happy growing and stay tuned! ✌️

Buenas a tod@s... Seguramente ya estamos en la ante última semana... Están espectaculares todos los frutos, tanto de esta variedad como las otras, muy muy pretos como rocas, delicioso aroma y muy grandes, han crecido una exageración en una semana, se nota que comieron bien, no hay queja de mi parte hacia este cultivo, este riego con nutrientes será el último, el próximo ya es de limpieza de raíces y lo de más ya sabemos...😉 En el próximo cultivo se vienen cosas nuevas... Mientras tanto... A disfrutar está última etapa... Siempre se disfruta haciendo esto q nos gusta, con dedicación, esfuerzo y trabajando duro siempre... A seguir creciendo 🧠😎🙌🏻. Buenos humos para tod@s nos vemos la semana q viene... 😎💀🇦🇷🤝🏻🇪🇦

Solo cup challenge continues to press along. Not much change, plants are in veg, growing and healthy. Still a few weeks before the flowers start so I hope to get a bit of size going before it does. Having fun and really like looking at the other entries in this contest. Check out WildeWeed, Butterstotch and BeanswithPork, silky, larimar, fireman

Day 78 plants are now going to grow outdoor. Clones coming along nicely. This week I'm giving the mothers a chance to get used to outdoor grow. Day 84, mother enjoying the sun, got 91 clones from the first 3 batches.

Clones adventure. Mom's recovering. Spoiler: it was a very bad idea to put the clones into such large plastic pots and flood the propagator with too much water. Yes, the environment was fine, but there was no airflow through the coco, so the cuts rotted and I had to re-transplant the clones again after cleaning off the damaged parts. Meanwhile, the mom is happy and recovering very fast.

I'm struggling with maintaining a regular humidity level The new light is working out great! The plants are growing at much different rates. If they were all as good as the best plant I'd be happier It's gonna be interesting to see how things finish! ___________________________________________________________________ So I made an attempt to save them/balance them. I fed them with just ph'd water to give them some time and incase they needed to chill a bit The runoff wasnt over 6.5 so I dont think they are locked up. I'll be back to feeding them again, but the difference in each plant has me concerned!

✌️🎃 Thank you for checking my cultivation. 🌱✨ They’re looking very well.

Cette semaine à était très riche en engrais naturelle et en eau !!!! *Fumier de vache pour les différents apport qu'ajoute cet engrais au fil du temps , *Marc de café , *Purin d'ortie , *Peau de banane *Cendre de bois Arrosage tous les jours en petites quantités pour aider à assimiler tous les apports donné Et voilà que c'est demoiselle ont pris un coup de speed pour la poussée , obligé de continuer le palissage encore à ce stade... Ça grandit , ça grandit !! Nous sommes fin Juillet , je suis dans l'attente que les jours réduisent pour le passage en floraison naturel grasse à la nuit... Je ne sais pas si je dois procéder à une grosse défoliation pour les feuilles du dessous sur le principe d'un "Lollipopping" , qu'en dites vous ?? Des avis ? Des questions ? Des choses à dire ? C'est toujours intéressant de discuter sur les différents mode de culture !!

Week 19 november - 25 november 23 november - D1 flowering I watered it a little too much. as it is colder I will start giving 1.5L of water instead of 2L

Greetings fellow growers 🖖 and welcome to my first grow ever. This adventure actually started several months ago when I decided to stop buying flower from dispensaries and just grow my own bud. How hard can it be!? This is actually my second seed of this strain. The first bean sadly died due to over watering (sorry girl, RIP). I was literally watering the cube to the point where water was dripping from the bottom, then heavily sprayed the humidity dome and tray with the vents completely closed. Everyday. Multiple times. I never let the dome or try dry out. So after about 8 days of not sprouting, there was a funky smell of rot. So that was that. Later I learned that rockwool retains a lot of water and can easily drown seeds. So a wet/dry cycle is best for rockwool germination. So even after hours of researching and digging through forums and tutorial videos, I was still under prepared for this journey. Did not consider how delicate the germination phase is. Oh well. Lesson learned. Reset and try again! I hope everyone is safe and stoned during this corona crisis. Just like everyone else in the world, I want this pandemic to be over with. But in the meantime, let's grow some weed! 🖖 [START OF WEEK 01] Day 01 - Monday - 08/03/20 - Total Days: 001 ----------------------------------- - [0830]: Light Schedule: 24Hrs/0 --- Soaked cube in 5.5 PH water for 10 min. Did not shake water out. --- NO NUTES! Only PH'd down to control the PH levels. --- Did not use the default hole (way too deep). --- Flipped cube upside down and made a shallow hole for the seed (less than 0.25" deep). --- Placed seed in and pinched hole close. No additional water added. --- Sprayed the tray and dome with straight water (5.5 PH). --- Vents are cracked opened a for ventilation (about 1/4 opened each). --- Distance between the light and tray was 53" --- AC was set to 80 °F --- Exhaust fan was set to 86 °F --- Room average temp was at 85 °F --- Dome humidity was at 85-99% when sprayed. --- Allowing to completely dry before respraying. - [2200]: Dome and tray were completely dry! Sprayed only tray and dome with more water. Day 02 - Tuesday - 08/04/20 - Total Days: 002 ----------------------------------- - [0845]: Sprayed dome and tray in the morning. Everything was dry. --- Hoping for the best! - [2130]: Everything was dry again, so sprayed dome and tray at night along with a light spray on the cube. Day 03 - Wednesday - 08/05/20 - Total Days: 003 ----------------------------------- - [0830]: Everything was dry again. Resprayed dome and tray. Slightly sprayed cube. - [2125]: Hooo damn!! She popped! Am little stub is visible! Resprayed dome and tray again. --- Still going 24/0 for lights. - [+0033]: Just checked up on her and I swear she grew a bit taller! Getting excited! Day 04 - Thursday - 08/06/20 - Total Days: 004 ----------------------------------- - [0845]: Wow! Went from a little stub to fully sprouted overnight! Everything was pretty dry again so resprayed dome and tray. - [2200]: Tap root is visible! Over 1" long too! Just resprayed dome and tray again. -- Going to prep for hydroton transplant tomorrow! Day 05 - Friday - 08/07/20 - Total Days: 005 ----------------------------------- - [0930]: She keeps growing! -- Added a bit of CalMag to the spray bottle (8 drops to 650ml of distilled water). Resprayed dome and tray. Water was at a 5.4 PH with 141 PPM. - [1045]: Prepped the bubble bucket with 4.5gal of water. Water is high enough to reach about 0.25" above the bottom of the net pot. --- Added 3 drops of Superthrive --- Added 3.5ml of CaliMagic --- Added 2ml Hydroguard --- Then PH'd down to 5.6 --- Solution Strengh: 120 PPM --- Water chiller is set to 20 °C - [1100]: Transplant time! --- Filled the net basket 1/3 with hydroton. When placed in the bucket, air bubbles are not visible, but are slightly below the surface (slight digging will reveal the water/bubbles below). --- Removed plastic on rockwool cube and placed in basket, then filled around and covered with hydroton. Making sure to block any light from passing through the net pot and into the nutrient solution. --- Covered with a half-bottle dome sprayed with the CalMag water from earlier. --- Hoping for the best! - [1300]: Raised Bucket 5" higher. Now light distance is 48" to top of bucket. - [1820]: Lowered tent exhaust temp to 76 °F --- Lowered AC to 75 °F --- Raised bucket even higher so light distance is 30" to top of bucket. - [2300]: Looking good! --- Sprayed dome and surrounding hydroton with more CalMag water. --- Attached timer to light! So new 18 Hrs On/6 Hrs Off light schedule. --- Lights On: [1600] (4pm) --- Lights Off: [+1000] (10am the next day) --- Decided to go with lights on during the evening/night and off during the later mornings/afternoon (the hottest part of the day) to see if temps can be controlled better. --- Please survive girl! Day 06 - Saturday - 08/08/20 - Total Days: 006 ----------------------------------- - [0800]: Everything was dry. Resprayed hydroton and dome. - [2000]: Here first night cycle seemed to go well! Get'n taller! --- Dry again. Removed the dome. --- PH went up to 6.5 so PH'd down to 5.7 --- Ran the top feed drip ring for a bout a minute to wet the hydroton and rockwool with the nutient solution. ---Too scared to leave the top feed on 24hrs (I don't want over water her and cause dampening-off). Will let dry before re-watering. - [2100]: After closer inspection, I think she's looking a bit yellow. --- Decided to add a bit of grow nutes to the bubbler solution. --- Added 2ml of Sensi Grow A --- Added 2ml of Sensi Grow B --- Solution strength after adding more nutes: 176 PPM --- PH went up to 6 --- I hope that the extra chelating properties of the 'PH Perfect' solution is enough of a buffer for proper nutrient uptake. Day 07 - Sunday - 08/09/20 - Total Days: 007 ----------------------------------- - [0800]: Water dropped a bit (mostly due to evaporation) so solution strength was at 190. --- Checked PH again. Was still at 6, so PH'd down to 5.4 --- Ran the top feed for a minute to wet the hydroton a bit. - [0915]: Since she's looking perky but still a bit yellow. So decided to up the nutrient concentration even more before lights out. --- Added 2ml more of Sensi Grow A --- Added 2ml more of Sensi Grow B --- Solution strength after adding more nutes: 199 PPM --- PH went up to 5.8 - [1700]: Checked nutrients. --- PH: 5.9 --- Solution strength: 202 PPM --- Added 4ml of Voodoo Juice --- Added 4ml of B-52 --- PH after adding more nutes: 5.9 --- Solution strength after adding more nutes: 238 PPM - [2130]: Decided to make a new foliar spray to address the continued yellowing. --- Started with 500ml of distilled water. --- Added 3 drops of CaliMagic --- Added 3 drops of Sensi Grow A --- Added 3 drops of Sensi Grow B --- Added 3 drops of B-52 --- Added 1 drop of Superthrive --- Solution strength: 164 PPM --- PH was at 5.9 and did not adjust. --- Gave her one spray. --- Also sprayed the surrounding hydroton. [END OF WEEK 01]

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.

Aug 22 - plant fed yesterday a.m., then got rained-on ALL NIGHT - “week 2 Flower”, end of the week will see a Defoliation of sorts. Plant was Schwazzed re: 70% removal of Fan Leaves on day 1 of Flower. Targeting day 20 (we’re at 15) 23rd - plant grew 6cm, basically over-nite!!! Wow 25th - Microbe Tea brewing for tomorrow - Pistils are appearing… 26th - rain overnite, plant is “still”Dry-side of Medium, breakfast time; 1 gal. Posted above. - !!! Cali Crasher finally exceeded expectations and has surpassed the One Metre tall mark. Measured from the orig height, of the original soil via green wire for LST poking through the side of Fabric pot. Its a beaUtiful plant *** tested the run-off from the Feed this morning, its been a while. Run-off = < 3000ppm, so the plant was flushed till ppm dropped below 1500. Yep, it took 5 gal of pH’d water. The Last gallon (5th one) included the bloom nutes, a 2nd time, due to the Flush. That final gallon equaled 1000ppm - next week sees a Large-leaf schwazze on 31st (20days since orig schwazze). Any key, medium-sized shadow-maker gets yanked as well. Still gonna call it a 70% schwazze 28th - last day of week 2 in Flower - Nutes for Breakfast 1gal - really happy this beast climbed over the Metre-mark this week

Day 45. Plants have grown huge in last week. Tallest one about 65cm. At its closest point the light is 6 inch. The bud sites furthest away are about 18 inch. Trying g to even out the canopy with some success. Just using the string method of LST and also moving the pot around to get an even amount of strong light.

I defoliated them again last week now they go finish in 3-4 weeks max. The smell is insane at this point

Making Bhang, Bhang Chai. Making medicine. Traditional Afghani folk music. True medical strain from antiquity. Ancient cannabis bred line from north Afghanistan. End of vegetative stage. Recieving the gifts.

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I love growing its a big passion of mine , and the fact that GD exists makes everything so much better, one can interact with others and enjoy and learn from each others. Thank you all growers love and keep them green <3 <3 <3