Flowering goes good, also found the possible reason of slowy grow of one of the plants.

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.

Loved the smoke small yeilds ive only grown a few yeild worthy autos but all have been terpy and packs a punch

This is the first week and I am already so so so excited to grow this strain from such reputable breeder! At first I wasn't going to write a journal but since this is going to be a Mainline + Scrog style of grow I believe its worth to keep an online journal for others to use as reference hopefully. Week 1: Germination was nice and quick, 15h on water cup, less than 24h on paper towel and the tap root was already shooting out far, after 2 days I planted on soil (Promix HP) and use tap water on a spray bottle to maintain soil damp and humidity high. The morning after going on soil seedling sprouted and started to grow nicely. Seedling was under a Sunblaster 45w CFL lamp. Stay Lit folks! Follow my Instagram for daily stories @GirlGoneWeed

Hello!! Too bad I only found this site now and didn't take too many photos during the first month. About the plant, it was the smallest of my plants at first, but then it grew very weel and now is the biggest of my girls. She entered in flowering a week later than expected, but beacuse of that she could grow more than the others. I've done only some LST and the plant just loved it, now i have like 11-12 main stems. Today I also have done some lollipopping but very cautiously because it was my first time doing it, and I didn't want to mess up.

The two northern lights auto are dry. Together 45g before drytrim. Not too bad, concidering the cloudy, wet weather..

09 October 2018 - Day 106 Flush run well, Buds have increased and thickened up nicely. Day 107 - No more burn and buds are growing. Day 108 - Conditions are good. Day 109 - Noticed heavy and healthy root growth. Last day before trim Day 110 - Trimmed and Harvested. ** Tent was required ** Day 111 - Colour and smell has become stronger Day 112 - Still drying

Surprisingly slow growth, but the colour on most of them looks healthy. Plant #4 might be a goner, it had problems getting out of the seed and nearly died the other day. It's likely just going to be a very weak plant. Keeping my fingers crossed though. Update #1: After getting some helpful advice from Mark at Dinafem Seeds, I transplanted the three largest ones into 7 gal smart pots and placed them outside where they will stay. The remaining two will likely head outside either tonight or tomorrow depending on the weather (these are the smallest two, #2 and #4). Update #2: As of June 2 (Day 13), all plants have been transplanted into 7 gal smart pots and will remain outside.

This week went pretty well for my sour diesel auto. She Finally stopped growing vertically at about 48 inches to the top of the highest cola. We did have a serious heatwave and high humidity I been dealing with as well, but so far so good. The only thing I changed this week with nutrients is I raised my ec value to 1.6, at the advice of another grower, and the sour diesel took it like the piglet that she is. I am still on an 18/6 light cycle,which I plan to stay with the entire grow, and still feeding Maxibloom, calmag, and koolbloom. I am seeing some bright orange colored spots on the top leaves, but I am hoping it is just a little light bleaching. I have no experience with this as I have NEVER grown anything indoors before other than vegetable seedlings. I just wanted to say thank you to this community for all the advice, tips and encouragement along the way, very much appreciated all, and Blaze On!

Day 43 - Commence the flowering! Flower sights are becoming clear now, with lots of pistils appearing along the top of branches. Watered with 1.5L with a run off of 120ml(8%). Day 44 - Watered with 1.6L today. Run off of 200ml(12.5%). Day 45 - She's getting thirstier again. Watered with 1.6L with run off of only 65ml (4%). Can really see the height gain by the day... Hoping the tent will be tall enough. Day 46 - Watered with 1.8L today with run off of 100ml(5.5%). Had a few warmer days outside causing more water evaporation. Will move to 2L soon if run off stays low. Day 47 - Watered with 2L with run off of 260ml (13%). Flower sites really starting to stretch out now. Day 48 - Watered with 2L run off of 260ml(13%). Will continue to water with 2L and only note when changes are required. 2L seems to be the sweet spot for this week. Day 49 - That brings us to the end of Week 7 and the first week of flower. Bud sites are now really established - I'll be increasing nutrients to 1.5ml/L for Advanced Nutrients and 0.75ml/L on CalMag. Total growth of 12cm this week compared to the usual 7cm over the last couple of weeks. An extra 5cm of growth can be attributed to pre-flower stretching.

Día 73 (12/08) Riego 500 ml H2O pH 6,55 Todas las plantas muestras las preflores hembras! (excepto LemonPaya) Día 74 (13/08) Riego 250 ml H2O pH 6,55 . Están muy bien hidratadas Pequeños ajustes de LST Día 75 (14/08) Hoy día de lluvias torrenciales Riego 250 ml H2O pH 6,55 Día 76 (15/08) Detecto mosca blanca en varias plantas. Aplico Spruzit a 10 ml/l ahora que aún no estamos en floración Riego 500 ml H2O pH 6,55 Día 77 (16/08) Riego 500 ml H2O pH 6,55 La mosca blanca ha desaparecido completamente Día 78 (17/08) No riego. Mañana a primera hora aplico Top Dress y riego profundo Va a empezar la floración! Día 79 (18/08) Alimentemos el suelo con Top Dress! 💥 Aplicamos 4 g/L sustrato de Tasty Flowers TD by Lurpe Solutions. Total = 84 gramos / maceta Riego con 1 Litro H2O pH 6,5 con 25 ml/L de Humus de Lombriz Liquido Aplicación foliar Kelp hidrolizado de Lurpe Solutions a 0,25 ml/l 💦Nutrients by Lurpe Solutions - www.lurpenaturalsolutions.com 🌱Substrate PRO-MIX HP BACILLUS + MYCORRHIZAE - www.pthorticulture.com/en/products/pro-mix-hp-biostimulant-plus-mycorrhizae

Welcome to week 5 of flower for this lovely project! The ladies should start to put on some serious weight over the coming weeks as I've noticed most plants are done their stretch now (except macmelonz). We got lots of crazy smells coming from these plants some are harder to tell then others but some are extremely pleasing smelling already. Banana Smoothie is really putting off that banana cream smell accompanied by berries as an undertone. Creamy Cereal Crunch smells like Fruit loops and milk , its very unique and very pleasing if your into cereal anyways haha. Over all excited to see what this week will bring! Huge shout out to @MarsHydroLED for making such cool lights and tents that really make growing a breeze. Huge shout out to all my followers and people who stop into the diary alike , keep on inspiring to grow! -The Projexx Day#29F Ladies are starting to display some bulking up. Day#30F Pictures N/A. Plants seem to be stretching a bit more but concentrating on bulking up flowers. Some really nice smells coming out. Day#31F Macmelonz is still stretching along but stacking hard and the rest are starting to put on noticeable weight. Day#32F Ladies are grooving along nicely, going to look to trim up some of the middle allow for more air flow to the plants. Day#33F Banana Smoothie #1 and #4 are really starting to put out Banana Cream aromas its quite intense now. Day#34F The canopy deff needs a light defoliation. Going to defoliate slowly but surely over the coming weeks. Day#35F Pictures N/A. Ladies are really thirsty going to be upping the water next feed. Flowers are bulking like crazy! Recap: Things have gone really well this week, everyone's bulking like crazy and macmelonz who stretching out is still stacking like crazy. Lots of interesting and exciting aromas from the plants, I hope they taste as good as they smell! Over all very pleased with the performance of the plants its going to be exciting to watch them grow over the coming weeks!

Man you should pray for this pheno ....its unreal and easier than your your high school prom date!

**Encontrarás la traducción a español al final de la descripción** From/Desde: 19/04/19 || To/Hasta: 25/04/19 From day/Desde día: 57 || To day/Hasta día: 63 You can find the Gorillas Diary here (Texts are the same this week): ** Podéis encontrar el diario de las Gorilla aquí (Los textos son iguales esta semana):** https://growdiaries.com/diaries/25675-makingmoney-with-gorilla-mm-vs-gorilla -----IMAGES & VIDEOS----- 1 - Before defoliation 2 - Defoliation 3 - After defoliation -----WEEK SUMMARY----- (Following text was translated with tools and reviewed, sorry for mistakes, misspellings or nosense things) As you can see I've done a defoliation this week. Yes, I have really gone over the top, I have removed many more leaves than I had, and the tails of the plants has not come to join at all due to the failed defoliation. Being the first defoliation I do, I did not really know what I was doing and I went crazy. Now that it has been several weeks since I made this defoliation, I realize that I should not have removed the leaves from the nodes of the tails, because they have stopped growing and have not joined with their superior parts. Anyway, the plants are beautiful today and although they could be much better I feel very happy with them. I know I've made 2 fatal mistakes in this grow - The first has been the massive defoliation badly done, defoliation yes, but with head ... do not follow my example. - The second failure that I see today, is that I did not leave enough growth time (18/6) after having made the last pruning and that has made the tails have been a length much less than what would have been desired, I think that 2 more weeks of growth would have been perfect. -----WATERING CALENDAR----- 20/04/19 - 1,250 ml with Sensizym, Silica, Rhino Sk, Bud Ignitor, Big Bud, Bud Candy & Bud Factor-x @ PH6.4 & 1.2 E.C. 23/04/19 - 1,250 ml with All week nutrients - (Silica, Sensizym & Bud Ignitor) @ PH6.5 & 1.5 E.C. *****ESPAÑOL***** -----IMÁGENES Y VÍDEOS----- 1 - Antes de la defoliación 2 - Defoliación 3 - Después de la defoliación -----SUMARIO SEMANAL----- Como podéis ver esta semana he hecho una defoliación. Si, efectivamente me he pasado de listo, he quitado muchas más hojas de las que debía y las colas de las plantas no ha llegado a unirse del todo debido a la fallida defoliación. Al ser la primera defoliación que realizo, no sabía muy bien que hacía y me lancé a lo loco. Ahora que han pasado varias semanas desde que realicé esta defoliación, me doy cuenta de que no debí de haber quitado las hojas de los nodos de las colas, pues estos han dejado de crecer y no se han unido con sus partes superioras. De todas maneras, las plantas están preciosas a día de hoy y aunque podrían estar mucho mejor me doy con un canto en los dientes. Se que he cometido 2 errores gordos en este cultivo - El primero ha sido la defoliación masiva mal realizada, defoliación si, pero con cabeza.... no sigáis mi ejemplo. - El segundo fallo que yo veo a día de hoy, es que no dejé suficiente tiempo de crecimiento (18/6) después de haber realizado las últimas podas y eso ha hecho que las colas hayan quedado de una longitud muy inferior a la que hubiera deseado, creo que 2 semanas más de crecimiento hubiera sido perfecto. -----CALENDARIO DE RIEGO----- 20/04/19 - 1.250 ml con Sensizym, Silica, Rhino Sk, Bud Ignitor, Big Bud, Bud Candy y Bud Factor-x @ PH6.4 & 1,2 E.C. 23/04/19 - 1.250 ml con todos los nutrientes semanales - (Silica, Sensizym y Bud Ignitor) @ PH6,5 & 1,5 E.C.

* ********* Week 11 - June 20 to 26, 2020 - Days 71 to 77 from germination *********** * It is the end of flush week and she went into darkness on Wednesday night, day 75, for two days. Saturday will be harvest day and start and the dry process👍 She has certainly been going through the beautiful stage of senescence and her fade is gorgeous. The purples and yellows coming out are great......covers up the brown spots😂😂 Her buds are densing this week as we work on bring down the humidity. Running in the mid 60’s for humidity late in flower is a different experience and one that takes some getting used to. Bring down further to low 50’s has really helped to bring out her frost as well. Kept the humidity high to form big buds......now lowering to make them more sticky👍👍 I am feeling very strongly that the big part of the pH issues this run was a change in feed water. I have always used bottled RO water for all my grows, except outdoors, but this grow I switched to tap water. Dechlorinated the water with air stone and gave it 24 hours min before using. Wanted to save some money and tired of lugging bottles downstairs a couple of times a week☹️ This is worked out nicely and a lot more convenient. However, the city must be putting some crap in the water that is causing issues in my media and raises the pH after the watering. Out of the tap it is 8.4pH and 275ppm. Since ppm were not too bad in my opinion I moved forward without filtering the water.......oops🤬🤬🤬 Out of options on what is causing the issue, I switched back to RO water late last week........all the girls are happier!!!! F......missed the cause for weeks. Always learning from this plant and my own mistakes to get better every run😉👍 Also wanted to add a little more stress to girl to help push out some increased resin. I drilled a 5/16” hole into the main stem to cause her stress. I did this rather than trying to break a branch and will see how it goes this run. Sterilized a new bit in Alcohol and went for it. They went into darkness about a couple of hours later. Excited to see what happens when she comes out to get chopped😃😃 Little more detail...... June 20/20 - Day 71 - Rezin and Liquid Weight @ 2ml/L = 285ppm and 4.0ph - 8L given to get a good flush - Runoff in pots already were 7.8pH and 485ppm. - after 8L water runoff was 7.0pH and 370ppm. - she is 29” tall and 30” wide. - tricombs still mainly cloudy.....review again in couple of days. June 21/20 - Day 72 - Dry out day - buds are firming up......squeezed a couple🧐 - temps are nice outside so tent able to hold 75 degrees and 51% humidity. June 22/20 - Day 73 - Rezin @ 1ml/L = 120ppm and pH the water to 2.7!!!!!!!!! - Given 2L watering. - No runoff water and I am good with that as I want the low pH water to stay in the medium. - She will be ready soon. Thinking darkness on Wednesday and harvest on Saturday?? June 23/20 - Day 74 - 2L plain water feed - 80ppm and pH to 2.4!!!!!! - not excited about these crazy low pH numbers but doing what we can - her tops are getting really pointy now and her leaves are very yellow. - checking tricombs, I think we are done and tomorrow will be her last day so that I can take down on Saturday. June 24/20 - Day 75 - 2L plain water feed - 80ppm and pH to 3.0 - Going into darkness tonight so this was her last bit of moisture. - drilled a hole into the stem.....was going to do a couple of holes but not trying this method before I decided to leave it with one hole. - into darkness tonight So we finish up the week with her in the dark. Next update will be the harvest!! Thanks very much for taking the time to review my diary!! Sorry for running behind often on this run.........everyone has had a busy life the last couple of months in the world and its been no different here...........a huge Kudos to all the Growmie‘s that are able to keep up with their diaries on daily basis on GrowDiaries.......its a commitment😃👍👍 Mephisto has bread a very nice girl. She is big and sticky and grown very well considering the environment she has been given. Battling the high pH and still turning out as she has is awesome and much respect!!!! Great job Mephisto, can’t wait to run her again.......just so happens I have several more seeds of her😃👍

This grape is a big frosty beast. I think she has the potential to put off an easy pound if she bulks up the way I think she will. I spread the plants out a little this week so they get better light and air flow. Other than that I haven't done anything besides keep the reservoir full. Still pumping nutrients 1 minute on 20 minutes off. They are getting .5 tsp maxibloom per gallon. Not going to run any boosters this round. They dont look like they want or need it.

WELL LADIES AND GENTLEMEN!! My beautiful KOSHER KUSH #1 is already being flushed and will be chopped this weekend!! All these amazing colors are just starting to devour the plants with yellows purples and oranges inching closer and closer to harvest!! I will only be growing TOP SHELF FLOWER for my local dispensary after they reached out to me and pre ordered all of it!! I’m using some flawless finish on a couple of the feedings for flush and the other plants are still on a steady dose of flora bloom/ micro , terpinator , and cha Ching .. after a couple more feedings I’ll start flushing the rest of the girls and making sure no more nutrients is left in those pretty buds!! Till next week guys!!

Chegando o fim do ciclo.