Week 4: look at het flapping her wings. A tremendous growth spurt in the last two weeks. I managed to identify and treat some humidity and over-watering issues and think I got her dialed in right now. But, this is what I love about this grow journey, improvement comes being consistent in learning and adapting. Once again great genetics from Humboldt Seeds and the stability of Just Cannabis soil certainly helps lessen the impact of my noob mistakes and, we back in flight mode. Topped up with couple liters of PH water only. No nutrients at this point just PH water and living soil. A few changes this week; moved her to a more comfortable space. Dropped the light gradually throughout the week and settled at 40cm. Temp slightly lower lately but I managed to keep humidity idling between 65/75. Added an extra fan to the grow air to improve ventilation. Will be focusing more on extraction and dehumidifiers as from next week.

o Compost tea in week 3 -earthworm casting -steer manure / compost -DynaMyco -Bokashi juice -PK BOSTOER o Major Defoliation o Foliat Stapy tap water PH 8.50 o increase the amount of bloom booster

[ Information ] For all information on this grow, including strain and grow room details, please see Week 1 of Veg. [ Updates ] Day 10 - Topped at the end of Day 9. Foliar sprayed with neem at lights on today. C02 has been increased to 800 ppm average, humidity lowered to 70%. Light power has been increased, now running at 35%. Amazing growth, finally removed all the rogue sunflowers as I didn't notice any significant gains having them. They're getting thirsty today but I'm going to give them another day, possibly 2, before I feed again. I'd like one last heavy wet/dry period for root stretch and then I'll go heavy with some organic nitrogen into flip. I can't use the same net as previous harvests because of the new room design so I'll have to create a new frame to start building the final even canopy. I'm fairly happy with how both groups of plants are growing into an even canopy within their expected timelines. Day 12 - Light intensity increased to 40%. Fed today, 1.05ec (6.8ph) with 10-15% runoff. No signs of light bleaching or stress, their leaves are almost always praying upwards. They could use a lollipopping, but with how quick they're growing I'll most likely wait until a couple days before flip to clean them up now.

This week with this girl has been awesome she has really started to take off now that her soil is rite! She grew over 5" in the last week and that's what I chose to take for my clones. 2 to be exact and hopefully will have better results with this go around. Took me 2 clones off this mom plant so now she has been topped twice. Hopefully with the lessons from personalsmoke will end up with a couple clones of puffinz. They look sad at the moment but I havnt seen what normaly happens to clones 24 hours later. I give momma about 330 ml of de-clorinated 6.8 ph water every 2 or 3 days when the hydrometer goes around 3. She is in living soil so for now will just sit how we are and just straight water to make her happy! Thanks everyone for the love All sent back 10 fold love

----- WEEK 9 ----- ----- Day 57 ----- Easy day of watching. Just 1 pic today so far. not much reason to go downstairs to take a pic yet. Glookies is turning Purple on sugar and fan leaves now. Harvest is very soon. I'd wager within 7 days now just going to depend on the High I get off tester nugs. ***Update*** I destroyed the trellis and took em out for some pics and vids. Trichs = Tropicana is ready Tuesday, Wedding Cake probably Friday or within that weekend. ----- Day 58 ----- Last couple days. Fed about 30ml of Cal/Mag and 30ml of Molasses. Wanted to just keep the photosynthesis process and the plant in general alive for reveg. Was getting a bit too yellow for my liking. Harvest soon. ----- Day 59 ----- Harvested Tropicanna Glookies today Deleted this week by accident trying to make it a harvest week, so remade it. Will add harvest week once plants are dry and tester has been smoked to give proper info Put some more photos in. Basically the tent is 4 feet wide and the ruler is 12 inches long from bottom of duct tape Really loving the colors of this plant. ------ Day 60 ----- Fed only the Wedding Cake - 5-10ml of Calimagic and 20ml of molasses (NO Liter level marked or PPM or PH, i could cut today its done but im just maturing the trichs) Tropicanna Glookies is a friggin BEAUTIFUL strain. Moved the Wedding Cake in the tent so largest nugs are furthest away from light and dropped light from 1000w to 600w to save electricity Chop on Wedding Cake happens at mostly amber trichs. Prob 5-6 days max for that i'll know when I check trichs tonight and update with photo. ----- Day 61 ----- Wedding Cake is about 5% amber... so prob 6 days or so. Slow day today. ----- Day 62 ----- Feeding is today, going to just use some CaliMagic and Molasses again. Trichs aren't golden yet, so not chop time ... 8-9 weeks is what it is supposed to take, but it's got at least another 5-8+ days until 30-40% amber trichs for Indica couch-lock effect to shine in the Wedding Cake. Tropicanna could still be going right now, but I did not want more than 5-10% amber gold trichs to prevent a couch-lock effect. This has worked very well. On day 64 I will post a smoke report and full harvest/trim details as Saturday/Sunday is trimming. Will have dry weight results of Tropicanna (per plant, and as a whole). Tropicanna being sent to lab for full analysis will post results when they arrive (Usually 2-3 weeks after sending sample via mail) ------ Day 63 ------ Nothing to talk about today, slow day. almost done. *Update* 1 pic, i think it explains everything.

These are clones that I managed to take from my summer garden that became a disaster due to a heat wave that we had breaking 100 year records. I expect everything to be 48” in height at maturity.

I would definitely recommend the White Widow Max Auto to a beginner grower! I hope it tastes as good as it looks.

This was my first time growing a photoperiod and I decided to put her outside along with some autoflowers this past summer. I started Purple Shot Photoperiod Fem. from Exotic Seeds in a one liter air pot and moved her into a 5 gallon phat sack on day 14 when she was 2.5 inches tall.🌱🌱🌱 By the start of week three she was 6.5 inches tall and looking quite happy in her new five gallon home. A short while later she was moved outside to adjust to her new environment.☀️☀️☀️☀️ By day 35 she was 16.5 inches tall and developing a nice bushy structure. She started to flower towards the end of week 10 By week thirteen it was evident this girl was going to be making some nice tight lil nuggets 😁 By week fourteen I could hardly take my eyes off of her as she started to show her fall colors. I harvested her on day 130 18wk 4d She was 43" tall and looking pretty as can be. Her nuggets are not large but they are hard as rocks and sticky as fuck. The original plan was to turn all the outside plants into hash but I like this one too much just the way she is 😋 After a nine day dry and month and a half to cure the dry weight for this girl was 78.50g / 2.80 oz ✌️😎💨

Long flowering due to minor reveg. Bouncing back well and should show true colors by next week

Was another easy week - lots of healthy growth. Simply watered when dry, did some daily LST and leaf tucking. The green crack is definitely the fastest growing out of all the plants, and the one runt LSD25 is a bit smaller but still chugging along.

First time growing! Let’s see how this goes

Did more tie downs, she's very resilient. Planning to flip to flower end of this week. debating when to remove root protection, before or after flower. Love being able to interact with plants on a daily.. got a 5×5 in flower and that tent is just in auto mode lol.. Happy growing

Growdiaries Grow 20 Welcome to my 20th grow on growdiaries, I'm doing 4 plants in this grow. This grow will consist of. #1 FFNA2410 Fastbuds test (?days flower) #2 FFNA2411 Fastbuds test (?days flower) #3 FFNA2412 Fastbuds test (?days flower) #4 Acapulco Gold MSNL (56-70days flower) This diary is focusing on: #3 FFNA2412 Fastbuds tester. I have little to no information about this strain until its been released for sale. The only information I do have is it is a fastflowering photoperiod. I have grown fadtbuds fastflowering photos before and they were 🔥 so 🤞these will also be great. Equipment on Smart plugs. 1. Light= Viparspectra Xs2000 2. Extractor= Ac infinity 4 inch 3. Oscillating fans/cameras= on 4 ext. 4. Humidifier= ram 5L/Dehumidifier= 2L 5. Feed= water pump. 6. Radiator= KW Germination. Tent settings. Extractor controller settings High temp= 23c Low temp= c Temp step=0c High Rh= 70% Low Rh= % Rh step=0% Speed max=5 Speed min=1 Smart controller settings (during lights on). Lights on=24/0 Radiator on=<c Radiator off=>c Humidifier on=<60% Humidifier off=>65% Dehumidifier on=>% Dehumidifier off=<% VPD aim=0.4-0.8 DLI aim=14-16 EC aim=0.4 PH aim=6.0 🗓️ Sun 17/12/23 #3 📋 Chose the seed and placed it in a shot glass of water at 10.40pm. 🗓️ Mon 18/12/23 #3 📋 At 7.00am tapped seed and it sunk so put it in wet paper towel. 10.00pm filled 0.6L pots with biobizz light mix and wet with 100ml water (5ml/L roots). 🗓️ Tue 19/12/23 #3 📋 7.00am tap root breaking through shell so put in soil. 5.30pm started running tent. Light 24/0 Light distance 87cm Light power=73w=30% Dli=14.5 🗓️ Wed 20/12/23 #3 📋 5.00pm looks like no soil movement, sprayed soil. 🗓️ Thur 21/12/23 #3 (Day 0) 📋 7.00am looks like movement. 7.00pm has broken ground and leaves are open. So that's the end of germination for this one. From getting the seed wet to breaking ground took 5 days. She will stay in the small pot now until the root system has developed enough to transplant. Back soon. Take it easy.

Week 8, looking great. Really putting on some size now, soon to introduce some plant bends. Stay tuned

Hi everyone! Sooo… Looks like those girls slowly are getting back🤭 Slowly increasing water volume,but nothing crazy yet. Instead of watering once a week,now i’m watering 2-3 times. Doing some topping also.height in flower room is really tight,that means i’m after in lower,bushier plants (well probably we all after that🙄) I think another week or so,and i will transplant them to final pots and can’t wait to see them flowering!

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.

Disculpen las fotos, es que las saque para consultar. Bueno primero que nada fue una semana de mucha tormanta, lluvias y humedad. lo peor que nos puede pasar en floracion. Segundo intente hacer supercroping ya que las ramas seguian superando el tejido y les llegaba luz en la noche. Y me salio desastrozo, mi primera vez. Pero los otros punteros que superaban la altura, los hizo mi compañero que sabia hacerlo (No tengo foto, luego actualizo). Y Tercero que debido a la humedad se ven en las fotos como aparecio hongos, por lo que pude observar era solo ese poco, lo cual ya fue removido vamos a ver como continuamos.

D67 removed ScrOG and repeated LST on left plant so lower buds will get more light. There is not enough space in tent to do the same with the right plant.

Hi everyone. Welcome to my🍌💜👊 week update. Hope everyone keeping well and having a great week. Daily updates and uploads so if week not over yet. Please revisit to see full week content😊 Thank you all for such amazing support 😊🤗💜 So far everything is going great. No issues at all. Both girls started preflower on Tuesday and already I can see that they started stretching nicely. Scrog net will be installed by the end of this week. Week 5 13-19 Nov. 13/11 day 36 First runoff experience for girls. Loaded both pots with approx. 2.5 ltr each in 4 stages of 500-700ml. Runoff 100-150ml from each. Runoff PH 5.9. Nutrients for this watering were same as on previous week and added only calmag. Next watering possibly Friday but with new measurements. 14/11 day 37 Both 🍌💜👊 girls started preflower on same day. Xena is catching up quick to her larger sister and possibly soon they will be sharing this growing space 50/50 15-16/11 days 38-39 Just happy and healthy days 😁 nice steady growth. 17/11 day 40 Second watering for this week. 5.5l beetwen both. Runoff Ph 6.1 19/11 day 42 Most busiest day so far. Both girls got very bushy in last few days and they stretched enough to install scrog net. Before installing net applied selective defoliation on both girls. 8-10 fan leaves from each. It's the end of this amazing week 😁 Thank you all again for such a great support 🤗✌️💚