Just topped it couldnt wait for it to get to 5-6 nodes. Was getting big looking healthy and at 4. So I topped it at the 3rd node the 4th was big enought to use as a cutting got 5 all together gave them to my dad he likes gardening not smoking. And there is a picture of all the plants in my tent the royal gorilla. Two mango sapphire in the darker pots. A chocolate haze is the more mature of the lighter pots. The seedling is a white widow that's going outside probably not the late June early July.

Starting out great in the begining of week 3 we had a little accident in week 2 were her pot fell over an she got a little roughed up but she came back nice an strong can deffinetly tell she stalled out for a day or 2 tho other then that she's been growing great seems to be loving this fold 6 led from medic grow Ending week 3 the Tropicana Cookies is doing pretty good now she's not doing as good as the other auto but seeing how we had a little accident with her she's doing pretty good deff loving the cronk nutrients

Continued training and caring for the life in the soil... I'm trying to think of it as growing soil more then growing plants

Week 2 veg. Starting some LST this week. Pretty new to this so hopefully all goes well!

week two flower everything looks healthy :D today i defoliated them i watered them with 1.5l every 48h the light i use was set to 80% and it hangs 80cm away from the tops

Week 5 At the beginning of the week I set up and tested auto-pot system for 2 plants using the same reservoir of feed water. All connections work fine with no leaks, the floats are free moving and work as intended, I have air pumping into the reservoir and all connections are good there as well. I used black tubing for the feed lines and placed towels over he reservoirs to block out light from the water in the system. After all checks were made, I placed the plants in the pots and turned the system on. At the end of the week I had 3 new nodes of growth since the last topping, so I topped for the third time (4 cuts this week on the 4 set from last week and also removed the lowest). I now have 8 colas set. Feed this week was 400ppm total before add-ins. I used 360ppm Veg concentrate mix (recipe week 2) and 40ppm Bloom concentrate mix (recipe above). However, I also added 1ml/gal of CaliMagic (General Hydroponics 1-0-0) to all feeds and ph balance this week was for 6.3. Next week will consist of training the colas to go where I want them to. I plan to train 6 to the outer ring and 2 to the inner ring. Once I have enough new growth I will set the tomato rings and possibly start wire training. Feed will increase in total ppm and bloom mix and I plan to reduce ph to the 5.8 range slowly, so about 6.1 this week and 5.9 next before flip on week 9.

Day 81 - Rock machine & Doctors Choice #1 getting cut down today! I am so glad I decided to let them go another 2 weeks because buds on both plants got much thicker the last 2 weeks. DC#1 has a strong fruity smell & has purple hues all over the bud & the Rock machine is caked in crystals and has more of a gassy smell! Can’t wait to see how they smoke, stay tuned for the harvest update & make sure to go check out Doctors Choice for some 🔥 genetics! Thanks for following & happy growing friends!🙏🏼✌️🏼🌱

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.

27 weeks in and she decides to reveg, I never could of expected that Lamb’s Breath would be harvested before Monday’s Blue, and Blue is looking so delicious and the smell, dam… the only thing I am loving is the thickness of the bud and it’s still growing, talk about good news.

1x topping and still waiting for a new place.. a new place for my fast-flowering Forbidden Mochi flower Pre-fertilized with cow manure and chicken manure, a large pile of shells and old used substrate on a former compost pile. I'm still waiting for it to warm up. At the end of the week, I will do a radical topping cut of the entire flower, it will go outside in a week. Spraying Biobizz Fishmix 1ml/l

10/29/20-Day 23 #1) 4.5” tall, nice looking 4th set of leaves. #2) 5.75” tall. All new growth, including lower axillary buds, is yellowing. Green tint toward tips, brown/copper spots on 3rd set of leaves. #2 is taller because is lacks chlorophyll and is stretching to get more light. 10/31/20-Day 25 - watered 300ml each 11/2/20-Day 27 started LST on #1.

White Widow – Week 3 Flower | 12-12 From Seed 🌸❄️ Cycle: 12/12 (sometimes 11/13) from seed Stage: Flowering – Week 3 Feeding: Aptus + Plagron + All-in-One Liquid ⸻ Full Flower Mode Our White Widow has fully embraced her flowering stage. This week marks her third week in flower, and she’s already showing beautiful bud formation from top to bottom. Despite her compact size, she’s filling in evenly and with excellent structure. What really stands out is the early frost. Resin glands are already visible, sparkling under the light. For such a modest-sized plant, her energy is clearly going into dense flowers and resin production, not stretch. She’s showing her true White Widow heritage, compact, resin-heavy, and vigorous. ⸻ Nutritional Strategy This week, her feeding remains consistent with the established recipe: • Aptus Regulator – 0.15 ml/L • Aptus CalMag Boost – 0.25 ml/L • Plagron Power Buds, Sugar Royal, Green Sensation – 1 ml/L each But we’ve added something new: • All-in-One Liquid 🌱 This addition is meant to give her a balanced nutrient push during this critical phase. By Week 3, plants are transitioning from bud set into flower bulking, and the All-in-One helps provide extra micronutrients and macros that might not be fully covered by the base mix. The goal is to give her everything she needs for flower development, without overloading her. We’ll be watching closely to see how she reacts, but so far, she’s thriving. ⸻ What’s Happening Now At this stage, we see: • Bud stacking beginning across multiple sites. • Resin production kicking in early, with noticeable frost. • Minimal stretch, as she stays compact and focuses on density. • Healthy leaf expression, still a deep, vibrant green. This week is often called the “foundation of flower.” The plant sets the stage now for how heavy, dense, and resinous the later weeks will be. If nutrition and environment stay on track, we can expect these bud sites to start bulking steadily over the next 2–3 weeks. ⸻ What to Expect (and What Not To) ✅ Expect: • Rapid increase in bud density. • More trichome development, the frost we see now is just the beginning. • Aroma starting to intensify as terpenes begin expressing. ❌ Don’t expect: • Major vertical growth, her stretch is over, and she’ll remain compact. • Early harvest, White Widow typically flowers for at least 8–10 weeks. ⸻ Educational Note – Why Early Frost Matters Trichome production this early is a good indicator of plant health and genetic quality. Resin glands serve as protection for the plant against heat, light, and pests, so seeing frost at Week 3 tells us she’s thriving under the current conditions and that her genetics are naturally resin-heavy. For growers, this means a higher chance of strong aroma, flavor, and potency later on. ⸻ A Quick Recap of the Journey • Germination: Not an easy start — mistakes were made, but this White Widow was the survivor. • Veg: Compact growth under 12/12 from seed, slower to show flowers, but structurally beautiful. • Flowering: Took her time to enter full flower mode, but now she’s moving fast and strong. She’s the perfect example of how patience, careful nutrition, and trust in the genetics pays off. ⸻ Shoutouts & Gratitude 🙏 🌱 Zamnesia – for the legendary White Widow genetics 💧 Aptus Holland – for reliable, precision nutrition 🌸 Plagron – for flower enhancers that push her into full bloom 💡 ThinkGrow & Future of Grow – for the light power and spectrum balance 🧠 TrolMaster – for stable and adaptive control of the grow environment And most of all — thank you to everyone following along this diary. Your time, support, and interest in this journey mean everything. This isn’t just a grow log, it’s a story we’re writing together. ⸻ 📸 This week’s gallery includes: • Close-ups of bud development and trichomes ❄️ • Studio shots highlighting her compact beauty • Room updates with environmental stability Next Week Goals & Forecast 🔮 As we move into Week 4 of flower, here’s what we’ll be watching for: • Bud Bulking – Flowers should begin to thicken, with calyxes swelling and pistils multiplying. • Resin Expansion – Expect a noticeable increase in trichome coverage, making her sparkle even more under the lights. • Aroma Kickoff – White Widow is famous for her pungent, earthy-spicy scent. We should start catching stronger whiffs this week. • Nutritional Balance Check – With All-in-One Liquid added, we’ll be observing closely for any signs of overfeeding or lockout, though so far she’s responding beautifully. • Environmental Consistency – The new AC unit is stabilizing temps and humidity — a perfect setup for flower development. Holding VPD steady will be key. ❌ What we don’t expect yet: • No real ripening signs (amber trichomes or fading leaves) — it’s still too early. • No heavy weight yet — the bulking comes between Weeks 4–7. This next stage is often described as the “early swell” phase. It’s where flowers go from just “forming” into recognizable buds with weight, density, and stickiness. 📲 Don’t forget to Subscribe and follow me on Instagram and YouTube @DogDoctorOfficial for exclusive content, real-time updates, and behind-the-scenes magic. We’ve got so much more coming, including transplanting and all the amazing techniques that go along with it. You won’t want to miss it. • GrowDiaries Journal: https://growdiaries.com/grower/dogdoctorofficial • Instagram: https://www.instagram.com/dogdoctorofficial/ • YouTube: https://www.youtube.com/@dogdoctorofficial ⸻ Explore the Gear that Powers My Grow If you’re curious about the tech I’m using, check out these links: • Genetics, gear, nutrients, and more – Zamnesia: https://www.zamnesia.com/ • Environmental control & automation – TrolMaster: https://www.trolmaster.eu/ • Advanced LED lighting – Future of Grow: https://www.futureofgrow.com/ • Root and growth nutrition – Aptus Holland: https://aptus-holland.com/ • Nutrient systems & boosters – Plagron: https://plagron.com/en/ • Soil & substrate excellence – PRO-MIX BX: https://www.pthorticulture.com/en-us/products/pro-mix-bx-mycorrhizae • Curing and storage – Grove Bags: https://grovebags.com/ ⸻ We’ve got much more coming as we move through the grow cycles. Trust me, you won’t want to miss the next steps, let’s push the boundaries of indoor horticulture together! As always, this is shared for educational purposes, aiming to spread understanding and appreciation for this plant. Let’s celebrate it responsibly and continue to learn and grow together. Friendly reminder all you see here is pure research and for educational purposes only, With true love comes happiness. Always believe in yourself, and always do things expecting nothing and with an open heart. Be a giver, and the universe will give back in ways you could never imagine. 💚 Growers love to all

What a fun run this was ! These Ogreberrys finished up from 81 days to 102 days with nice hints of gassy , sour purple , sweetness and glistening with frost! These ladies will cure up for a month an will be ready to test out ! So much fun , I highly recommend this strain if your looking for some oooy gooohy resiny grape smelling nugs !

Hello people, how are you doing? Week 9 is here and we are almost there to harvest those beauties. Everything is OK, no bugs, no troubles, just happy to see how the plants are growing... Thank you to follow this diary! Peace and love!

******************************************** Week 15 Start of Fade(flower week 9) ******************************************** Light cycle=12/12 Light Power=125w 52% Extractor controller settings High temp= Day 26c, Night 20c Low temp= c Temp step=0c High Rh= Day 50%, Night 55% Low Rh= % Rh step=0% Speed max=10 Speed min=2 Smart controller settings (during lights on). Lights on=9.00am Top fan on=+22.5c Top fan off=-22.0c Dehumidifier on=+50% and -26c Dehumidifier off=-50% or +26c Smart controller settings (during lights off). Lights off=9.00pm Dehumidifier on=+55% and -20c Dehumidifier off=-55% or +20c VPD aim=0.6-1.3 DLI aim=30-45 EC aim=0.2-0.5 PH aim=6.0-6.5 NPK(0/0/0) 💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧 Method= Autofeed 6 drippers. Feed=Flushing Nutes. Flawless finish=2ml/L Volume=8L Easy Ph down= 0.02ml/L ( 4 drop total) Ec=0.4 PH=6.5/6.5 Runs=16 Run times=5min (250ml each) Gap times=15min×14, 45min×2 Total runtime=80mins (4.0L each) Total flowrate= 100ml/min (50ml/min each) Auto start time=10.00am Auto stop time=4.05pm 💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧 ******************************************** ******************************************** 📅25/8/24 Sunday (day 99, day 57 flower) 📋 Sad Day, cat past away. After the drip system had ran for 75mins there was 5.5L water left only 33ml/min. Adjusted before last 5 min run. 💧 Method= automatic Feed=Flushing Nutes Volume=8.0L Easy Ph down= 0.02ml/L Ec=0.4 PH=6.5/6.5 Volume left=5L Volume used=3L (37ml/min) Volume each=3L (37ml/min) Runoff. Runoff=0.L Ec= PH=/ Extra 5 min @5.10pm Extra 5 min @6.20pm Runoff=0.L Volume left=4.5L(50ml/min) Manual=1.5L Runoff=0.2L Ec=2.2 PH=/6.2 💧 📅26/8/24 Monday (day 100, day 58 flower) 📋 📅27/8/24 Tuesday (day 101, day 59 flower) 📋 📅28/8/24 Wednesday (day 102, day 60 flower) 📋 Inspection, she is swelling and trichomes are nearly all cloudy, pistils are shrinking and mostly brown. I'd say she's about 1 week of harvest if she carries on at this rate. 📅29/8/24 Thursday (day 103, day 61 flower) 📋 messed up watering as had connected 1 pipe to the other plant to the system by mistake. 💧 Method= automatic Feed=water Volume=7L Ec=0.2 PH=6.3/6.3 (PH D=0.02ml/L) 3d Volume left=4L Volume used=3L (37ml/min) Volume each=1.5L (18ml/min) Runoff. Total runoff=0.L Ec=PH=/ Corrected system Water=manually @7.10pm 5 mins Water=manually @7.35pm 5 mins Volume left=3.4L Volume used=0.6L (60ml/min) Volume each=0.6L (60ml/min) Runoff. Extra runoff=0L Ec= PH=/ Manually watered @8.00pm Volume left=0.4L Volume used=3L Total Volume=5.0L ish Runoff. Extra runoff=0.2L Ec=3.5 PH=/6.3 💧 📅30/8/24 Friday (day 104, day 62 flower) 📋 📅31/8/24 Saturday (day 105, day 63 flower) 📋 ******************************************** Weekly roundup. 📋 I'm super impressed with this one now. She's bulked up great and looking like she's going to have a lot of solid buds with very little larf. I think she'll be harvest at the end of next week. So my next report may be the harvest report. Take it easy. Back soon. ********************************************

Love the bud structure, she’s loving life, actually had to attach her to a supporter

~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_ 12/12/21 🤘😺Week 5 of veg!! Everything is going fantastic, color looks uniform across the board now.. I think 1-2 are a little on the small size for their age but besides that everthing else is great.. everyone is getting a little feed now with every watering and we just started adding a few drops of calmag this week just to stay proactive..we hope to start flowering a week from now but their size will be the determining factor... thank you as always for dropping by friends and happy harvests everyone!! 😽💨 ~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_ 12/15/21 ...I decided to do another round of topping today on all plants, this should make 8 main branches from the 4 most have now...we'll give them at least another week of veg after topping before moving to flower 😻 ~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_

So I decided to drop a berry cookie into DWC for ol time sake. Trying to squeeze one more grow in before the summer. Anyways she's been in her basket for a week now and she seems to be digging it so far. No roots showing yet but she's young yet. New growth coming in for sure so the roots are definitely growing just a long the basket and the clay pebbles. Probably getting adequate water for now but I'm sure by next week we'll be seeing some nice beautiful white roots!

Hello my friends, ...May 30 , 2022....Day N°79.. ...Flowering day N°23... My three Feminized Watermelon Candy are fine, there are beautiful, flowers smells awesome. I feed them with the Hybrid powder and some Boster from Green House Feeding Nutrients. I gave them some CalGreen from Metrop, the best Cal-Mag of the market. They are under a MarsHydro TSW 3000 at 60% of power and at 30cm of the canopy. www.zamnesia.com www.mars-hydro.com Thank you very much for passing by. Wish you only the best with your green projects, peace. See you soon 💨💨💨

Im happy with this week results, Im only using "Veg" light from my LED, Im thinking using both lights (Veg/Blom) to see if there is any variation in growth. 2 nodes more for start topping and LST