Week 6........... Getting frosty Edit: on day 41,I already have amber but it's still packing on weight. I don't know what to do at this point.

☘️29/12 - empieza su octava semana en Etapa de Floración. ☘️Por el momento se encuentra bien, los cogollos engordaron un poco más. ☘️La semana que viene le voy agregar Top Wash asi empiezo con su lavado de raiz. ☘️En dos o tres semanas ya la voy a podar. ☘️En estos dias seguire subiendo mas imágenes.

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]

Both phenoe are pushing on nicely. Really good growth from both phenos from 1 seed, 1 had more girt. So, there wasn't an exact even growth ratio. But no pheno was hammered in any way that affected its push through pre fower and into mid fattening. I expect another 3-4 weeks and I'll harvest. Atm there's a nice Lemon exotic smell. Really dank. Musky (earthy). And popping off fruits. Really lovely set of plants. Xpert nutrients are bringing out the best in my grows. They smell, taste and pretty much everything in that regard has improved. These are my new nutrients. As hard as I've been strain hunting. I've always used a different line of Nutrients per crop. And I'm glad to say. These are by far THE BEST nutrients I've used to enhance my crop. Feeds Are pretty much a week in week out with change (all explained with my weeks, DLI and other factors), master root/enzymes have been pult. Master Root no longer needed. Enzymes are all gone. Maintenance This wk, i applied LST bamboo sticks are have done some basic node bending to get the best out of the space in the area above and around its base. Some nodes where tied back to the sticks.. Shout out to my sponsors and all who stop by.

Día: 78 Riego: 1,5L x Pl. - Agua Día: 81 Riego: 1L x Pl. - FinalFlush 2mlxL Día: 83 Riego: 1L x Pl. - Agua

Starting 600 W Lamp

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.

# VzH 👻

What's up Growmies🤟🏽. Week # 8 is in the books🙌🏾 Hello week #9💪🏾 I went a little overboard on pictures this week, they are so happy and healthy that I got carried away. I know we are supposed to post pictures with the lights off, however it's something about the contrast it gives with the lights on that makes it look sexy to me😁. I have had to tie the stalks of both White LSD plants due to heavy sagging. I'm noticing with this strain the stalks seem to topple over even though the buds are far from fully developed. A trellis net probably would be ideal however I hate them. They are easy to put on but very difficult to take off come harvest. I use garden wire and string them as if they are puppets being controlled by the puppet master🤪. I continue my feeding schedule with the recommended "bloom" concoction using general hydroponics Flora series trio. I give them 1 liter every 3 days. I have them on a 2 to 2 cycle (feed them twice with nutes and then twice with plan water) I keep the p.h. around 6.1 to 6.6. Temps and humidity are in the perfect range I'm enjoying it while it last because spring and summer in VA makes it difficult to keep the humidity in check. All in all everything is going well for me and my ladies. I hope the same for all of you. Until next week my friends Happy Growing 🤟🏽 and may the grow goddesses bless you all with a bountiful harvest 💪🏾

È stata una settimana bellissima! Il caldo estivo italiano finalmente è arrivato con temperature alte di giorno e fresco di notte. Queste varietà sono perfette! Ogni banca dei semi di queste varietà merita il mio applauso di cuore! Alcune sono più alte di me cioè superano il metro ed ottanta centimetri di altezza! Molto diramate tutte si stanno riempiendo di infiorescenze dure, appiccicose e molto resinose con odori intensi e fruttati! Ogni varietà sta sviluppando il suo aroma in maniera impeccabile! Gli insetti e parassiti ormai non sono più un problema, la resina appiccicosa non è gradita dagli insetti! Sono cresciute molto ed in circa tre mesi verranno raccolte, adesso si riempiono fino a che possono, le infiorescenze si stanno gonfiando ed iniziano a prendere forma. Abbiamo iniziato con un po' di Atami bloombastic assieme al top max e biobloom e se continuano così tra circa 4 settimane raccoglierò alberi XXL di altissima qualità biologica con aromi speciali! Odore nauseante in giardino! Un abbraccio a tutti e complimenti ai creatori di queste varietà!

Finally made some space for her.

hi to all, brothers and masters of weed. my queens are really strong !!! I started with the flushing for these little girls who have started to turn purple .... the smell is very strong and it is really AMAZING The buds are literally covered with powerful glue that just touching them release a strong and pleasant smell .... I think I will not throw anything from the waste because every corner of the plant is covered with sparkling and powerful trichomes with which I hope to make good hashish I leave you wishing you a happy and abundant harvest for all of you see you around

Day 77 , Power at 90% and lamp distance still at 45cm. She’s getting denser every day, and the buds are looking really nice. I’ve probably got another 2–3 weeks to go, so I’ll be about two weeks late on the content, but that’s fine. The plant is coming along beautifully and should turn into some really good smoke😜👊

8/2 everything looks good 8/5 watered and took 24 clones off both of these plants. Maybe they'll go through a spurt of growth now 8/7 scrog netted plant is 37 inches the other one is 55 inches

** COST ** TO RUN - Used previous ⛺️ setup : $0.00 - Monthly electricity : $36.73 <-- other ladies sharing ⛺️ - 3 Gallon Fabric pot : $0.15 - Bonsai wire : Apx. $0.03 - Reused soil from last run : $0.00 FOR NUTRIENTS - Jadam Microbial Solution : $0.00 - Fermented Plant Juice : $0.00 APPLYING - JMS : 30ml / 1 Litter - FPJ : 30ml / 1 litter TOTAL COST : $36.91 Throughout the week, I give compost tea, and fermented plant juice once each ^^ Hope you guys have a wonderful day today ^^v *** Please Like, comment & share *** Highly appreciated -----/-----<@

To start I would like, give big thanks to Royal Queen Seeds ❤️❤️ and @James , ❤️❤️ to try their products one more time #RQSLOVER, also to @marshydrococo2 and Mars Hydro for the FC 3000 and the fan filter kit ❤️❤️ And another thanks for the GD community, for likes, comments, follows. This 2nd F1 strain run was great, Easy and beautiful, very similar with Epsilon 💚 Flower/herbal smeel 👨‍🌾🌲🌲 ⚖️ Wet yield 262g

Wedding gelato, very chunky plant and she is doing well considering the heat we experiencing recently, beautiful strain overall excited for the final outcome !

It seems that the girl is counting her last days, some of the trichomes are already showing an amber color, the buds look simply fantastic, it's a pity that I can't transfer that image with my phone - share that image with you, you need to see it live :) good luck to everyone:)

Beautiful pheno of Black cherry punch with that purple color, amazing sweet aroma just like her sisters. Fat dense nuggets, can't wait to smoke this super sweet flowers. You guys can't imagine how sweet black cherry punch is, can't believe the 5 phenos have the exact same aroma however only 2 are purple. Let's see what happens guys peace ✌️💚❤️ #probioticgardening #organic