Buds showing great and started on day 10-11 of 12/12. I’m happy with the progress so far but I could dial the feed back a little bit and I’ll be adding in more light for a better footprint during week 4 of flower

Growing Fast Finally. Almost Ready to cut few clones for friends! One friends lend me his growlush 600w Veg Led Light. 2.7umol 247 watt use. Cruising Nicely!💪

She only grew 8cm this week. The stretch is slowing down a lot now. She's doing well. Nothing else to the report as I'm just letting her do her own thing. Still loving her Sativa-like leaves!! 😍 They are as thin as a blade! For nutrients I'm using 15g of 20-20-20 powder mixed with 10L of water. Also added 4ml/L of both Cannazym and Terpinator. This brings it to around 1600ppm including ~300ppm for my clean water. Timelapse Sequence: *** Blue Dream *** Auto Jack Pineapple Express CBD Compassion *** BLue Dream *** Auto Jack Pineapple Express CBD Compassion

unstoppable :p Day 29: on the video, the 2 on the right side are the Ayahuasca Purps, the other ones are Peyote critical. getting real bushy, need to defoliate soon day 32: they got their first feeding, I only use a minimal amount of blooming nutrients. day 33: plucked some leaves , cuz there was no airflow at all, also installed a new ventilator. day 36: had to pluck some leaves again

So 5 weeks into flower. All well no issues. Happy lady's starting pk and boost today. Make them fatten up. They smell amazing and are starting to get lots of tricomes. Not bad for a 1st on a low budget.. Iv found out that if my temps drop a little at nyt. Does not really affect this stain of og. Which I was very worried about.. Happy growing peeps..

Day 36 I guess I can call it bloom. Nice strong pistils shooting all over. She is the tallest so far making me raise my lights a little more. Day 38 Now Californian Snow is the tallest :) Ztrawberry stopped at a perfect height, it looks like she's gonna develop into a beautiful lady. Fat white pistils all over 😻 Day 39 Happy girl got 2500ml cm bg bb bh 6.3ph ~1EC She is perfect, symmetrical, stopped stretching at about 50cm, flowers are mostly leveled, branches are strong, leaves point up unless I water. I think she's also turning purple. Beaut 😻 Day 42 I think I saw some burnt tips but she still looks super happy and healthy. The most vigorous plant I've had.

Week 7 begins for Divine storm. Both ladies are looking good and healthy, bud sites continue to bulk up and frost up. Switched out big bud coco for overdrive as we approach the end of the grow. Thanks for checking in, tune in next week! 👽🌳🔥

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.

SUNDAY 4/21: I fed them about 1/3 gallon each today. Switched to Beastie Bloomz and increased terpinator. I inspected them for nanners and found none today. Will take some photos tomorrow- MONDAY: Too busy with life to spend much time in the garden today. TUESDAY: I rearranged and took some photos today. WEDNESDAY: I took some photos and a video. I watered all but one of the C4 hybrids today. Only the best one still needs water..tomorrow- THURSDAY: I watered with about 1/3 gallon and included some terpinator, calimagic, and beastie bloomz. I did a bunch of training on them to get some separation and better light penetration into the lower flowers FRIDAY: I did some more training on them today and I made some improvements to my fresh air a/c intake in the tent that dropped the temp a couple of degrees, and the new dehumidifier is keeping the RH right where I want it..45-50%.👌 This allows the evap cooler to be more effective at cooling as well...above 50% RH and it's basically just a fan..

⏳🌳The Endless GREEN Garden🌳⏳ ____________________________________________________________________________________ 🌳 18.3 ... 🌳 19.3... 🌳 20.3... 🌳 21.3... 🌳 22.3 ❗❗❗ We have come to the end of this cycle with these beauties. Today I have collected everything, removed the leaves for sunbathing and put aside the sugary leaves. 501 grams total, excluding the 181 of the bowl in which they barely fit. I emptied 7 jars. I am quite satisfied, considering that they grew in a 120x120 box with a 150w led lamp, which proved to be exceptional! Viparspectra P1500. a real beauty, as soon as I can I take another one, certainly from the XS series! bestial, and it doesn't even cost that much. today day 1 of drying in a wedryer .... it is not a little stuff, but there was just right. the final review of this trip soon, yeah! ____________________________________________________________________________________ 📜👀 A look at the details of what I'm growing 👀📜 ✌️Dos-si-Dos 33✌️ 🌞🚜 Barney's Farm 🚜🌞 📋 Details 📋 ⚧ Gender ▪️ Feminised ➰ Genes ▪️ 60% Indica / 40% Sativa 🎄 Genetics ▪️ Dos Si Dos x Gelato #33 🚜Harvest ▪️ 800 g/m² 🌷Flowering ▪️ 60 - 65 days ✨THC ▪️28.0% ✅CBD ▪️ N/D 🏡Room Type ▪️ Indoor 🌄Room Type ▪️ Outdoor 🕋Room Type ▪️ Greenhouse 🎂Release Year ▪️ 2019 ________________________________________________________________________________ 👀📷🥇 Follow the best photos on instagram 🥇📷👀 https://www.instagram.com/dreamit420/ 🔻🔻🔻Leave a comment with your opinions if you pass by here🔻🔻🔻 🤟🤗💚Thanks and Enjoy growth 💚🤗🤟

9/27/2018 Been a rainy damp week,cooler nights, no moulds as of yesterday and will update photos shortly if weather permits. Speak of the Devil, this am #2 has two spots of mould,cut ✂️ out,and trashed. All others no mould, #4 is covered with sand it keeps getting blown over!.#2 fading, #1 still Growing nice green very little fade just lower leaves lots of new pistils,#3 all hairs gone brown, and smells like Real old school Skunk!👍not much bud but still have couple weeks of flowering to fatten up and taste of Skunk getting me excited😁 10/02/2018 Week 7, day 5. Rainy days still very little mould just #3 so far. #1 looking fantastic.#2 pistils brownish,#3 pistils all brownish red dont see any New pistils but branches drooping from their weight #4 is still popping New flowers but lots brown all over, hope 2 weeks to finish! But cold is coming soon. #1 no signs of slowing down putting out lots of fresh flowers! Does not mind the cooler weather. Last bit of molasses to super charge microbes in the soil. Hope she comes in at 8-10 weeks👍 53-70 days flowering.

🌱 Ghost Train Haze — Week 4 Diary Photoperiod: 12/12 from seed Quick Recap (For New Joiners) This run follows a 12/12 from seed protocol, meaning plants are exposed to flowering photoperiod from day one. This approach typically results in: • Slower visible growth compared to veg-then-flower cycles • Earlier structural maturity • Compact, symmetrical architecture • A very honest expression of genetics Environmental conditions (temperature, relative humidity, airflow, and lighting intensity) remain identical to all other diaries in this project to allow clean comparisons across cultivars. ⸻ Week 4 Overview Both Ghost Train Haze plants are performing phenomenally. They are progressing steadily toward their 7th node, showing: • Excellent symmetry • Balanced internodal spacing • Strong apical direction • Calm, unstressed posture While growth under 12/12 is notoriously slower, this week reinforces an important lesson: slow does not mean stagnant. These plants are developing with intention and precision. ⸻ Leaf Morphology & Color One of the most striking features this week is the leaf quality: • Large, round, well-formed leaves • High surface detail and venation clarity • A lush, healthy green tone without excess darkness • No signs of deficiency, toxicity, or stress This visual expression reflects proper nutrient availability, stable root-zone conditions, and strong genetics working in harmony. ⸻ Structure & Symmetry Both plants are: • Highly symmetrical • Evenly stacked • Structurally clean and predictable This level of symmetry at Week 4 is a strong indicator of: • Stable hormonal balance • Correct light intensity for plant size • No need for corrective training at this stage ⸻ Containers & Growth Rate Observation These Ghost Train Haze plants are currently growing in plastic pots. A preliminary observation: • Growth appears slightly slower compared to plants in plastic grow bags used elsewhere in the run ⚠️ Important note: This is too early to draw conclusions. Container material, gas exchange, moisture dynamics, and root behavior need more time to show meaningful differences. This observation is logged for long-term comparison, not judgment. ⸻ Nutrition Strategy (Why They Look Like This) The plants are receiving the same locked nutritional protocol used across the project: • Balanced mineral nutrition • Root support additives • Enzymatic activity support • Controlled EC and pH Why this matters: This nutrition strategy prioritizes: • Root efficiency over forced top growth • Enzyme-driven nutrient availability • Stable uptake under 12/12 conditions The result is exactly what we see: Healthy leaves, calm growth, detailed structure, and no visual imbalance. ⸻ Studio Session Both plants were taken to the studio for a dedicated photo shoot, allowing: • Accurate visual documentation • Clear comparison week-to-week • Educational transparency for the community These visuals are part of the long-term archival value of the project. ⸻ What to Expect (and Not Expect) What to expect next: • Continued slow but consistent node development • Gradual increase in structural density • Early signs of transition in coming weeks What not to expect: • Explosive vertical growth • Stretch comparable to veg-trained plants • Immediate flower formation This is normal and correct for 12/12 from seed. ⸻ Community Note Due to YouTube community guidelines, our educational channel was taken down. While we firmly believe the content was purely educational, we respect YouTube’s decision and are actively exploring alternative platforms to continue sharing this work. 📡 Please stay tuned. 🙏 Thank you for your patience and continued support. FOR DISCOUNT CODES AND MORE JUST FOLLOW THE LINK https://website.beacons.ai/dogdoctorofficial 📲 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 Deleted by Youtube Vimeo : https://vimeo.com/dogdoctorofficial Under construction stay tuned ⸻ Explore the Gear that Powers My Grow If you’re curious about the tech I’m using, check out these links: 🔆 Lighting & Environmental Control • Future of Grow — Advanced LED lighting technology https://www.futureofgrow.com/ DISCOUNT CODE: DOG20 • Lumiflora — Under-canopy LED lighting https://lumiflorade.com/ • TrollMaster — Environmental controllers and automation gear (past collaboration) ⸻ Genetics • Zamnesia Seeds — Genetics used in this project https://www.zamnesia.com/ ⸻ 🌱 Soil, Substrates, Boosters & Root Support • Plagron — Substrates, bio mixes, and supportive products https://plagron.com/en/ ⸻ 🎒 Storage, Curing & Preservation • Grove Bags — Curing and storage solutions https://grovebags.com/ ⸻ 📸 Photography Equipment & Tools (Not sponsors, but part of my creative toolkit) • Sony A6700 • Sony full-frame macro lens + few more • Stacking photography workflow - learning • iPhone (for behind-the-scenes shots) 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. 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 💚 📸 P.S. – The Eye Behind the Lens All photos in this diary (for now — except for the ones showing the camera, which I took with an iPhone) are taken with a Sony A6700 paired with a Sony full-frame macro lens and a few more. Photography is part of the story — it’s how we share the fine textures, the glow, and the quiet details that words can’t always capture. I’ve also started experimenting with photo stacking — a technique where multiple images, each taken at a slightly different focus point, are layered together to create one perfectly sharp image from front to back. It’s not digital enhancement or AI; it’s pure photography — a way to reveal the plant’s beauty in microscopic depth, from trichome to petal. You’ll even see a few shots of "ghost me" capturing the shots — camera, lens, setup — because every grow deserves not just to be cultivated, but documented like art. FOR DISCOUNT CODES AND MORE JUST FOLLOW THE LINK https://website.beacons.ai/dogdoctorofficial NEW DISCORD - Official Server Invite Link : https://discord.gg/ksjAkA5T74

Dec 12 @1am: Her light schedule was been bumped down to 14 hrs. I have a photoperiod in the tent that needs a few days for harvest. Haze is now under the 1000W Phlizon/245W power draw lighting. Dec 12 @2:30am: New pot has been amended with approximately 65% fresh coco coir, about 20% worm castings,15% perlite and 17 tablespoons/51 teaspoons (12.75 teaspoons per gallon) in a 4 gallon pot. The pot will be thoroughly rinsed to rid salts from the old coco coir used in the pot. Dec 12 @6pm: Approximately 1" tall Dec 12: I think my dog got ahold of one of her cotyledons, unless it just disappeared. :) Dec 14 @2am: Transplanted to the newly amended pot. I watered her and the fresh coco coir mix she was transplanted into. Dec 14 @11:30pm: Her lighting went from 14 hrs to 24 with both veg and bloom lights on. (Photoperiod in tent harvested)

Queen Blue is doing well plenty of bud sites and I still think Ill have space for her daughters around the edges we shall see. She seems on schedule, this is definitely the largest plant ive ever grown, I think shes around 3-4 ft across.

Sie haben das Umtopfen ganz gut überstanden. Eine von den dreien macht ganz gut los. Die anderen beiden haben wohl noch etwas Stress durch das Umtopfen. Alle 3 sind Samen der selben Genetik aber selbstverständlich auch verschiedene Phenotypen, sie werden auf jeden Fall unterschiedlich wachsen und aussehen. Ich finde aber No-till besser als Stecklinge und je besser der Züchter um so weniger Phenos 😉 Wir werden sehen... 😎

for the 2nd week of the euphoria I gave her 2 ml of trimix, which contain mycorrhizae, trichoderma, amino acids and microelements, all organic (is what the brand says)

8/10 Hurried morning. Today was water day and the hose fucked up. Dad got it working while I filled half the jugs needed with water and the requisite amount of plant doctor. I gave the preventative dose (which is 1/2 tsp per gallon but I upped it closer to 1 tsp per gallon) on the plants that have received the three full treatments, the 10th planet in the middle and the chemdog. The rest received their last full dose. I had watered the NATURAL mk ultra and other tenth planet yesterday so I'm waiting until tomorrow when the need water to give them their treatment. Other than the 10th planet I'm worried things are going pretty good. Tjat's probably tine too. I certainly wouldnt have even noticed it a few years ago. I only bought like half the amount of soil as last year and really tried keeping costs down. These aren't the biggest plants I've grown but I'm grateful for what I have. I'm working hard to get the most out of them I can. I'm planning to give it a few days and then feed later in the week. EDIT: I THINK I got my grow question deleted. Finally. It's strange that I didn't get ONE outdoor growers response. Doesn't matter. I figured out the best course of action. I'm lucky. Or maybe I just work hard. I defoliate twice a day. I have some pruning to do on the interior of a COUPLE plants. I've cleaned them up pretty good this year. No signs of ANY wpm which is great but suprisinging considering the rh and the rolling fog most mornings. 8/11 I gave the tenth planet in the back and the mk ultra I didn't get yesterday. The mk ultra got the preventative dose (upped from 1/2tsp to 1tsp) and the 10th planet tge full dose. I'll have to check but I think this is the last cure dose for everyone. Found a pillar INSIDE a bud on the special kush that's far ahead. Then you can see on the video a HUGE cut worm or something on the branch I pull down. Luckily I saw it. Wasn't there when I got back but it took a few bites. Looked on the camera and saw a bird swoop in and grab him. Thank the lord! It's going to be 100° today and tomorrow with heat advisory in effect. I'm going to have to treat these plants for pests/pillars some how. I might just use BT and my super alkaline water. The septoria is under control and I'm just afraid spraying anything would make things worse. I'm certainly jot going to let them eat my early flowering plant. I can't apply ANYTHING in this heat. I'll research and maybe if it gets low enough tonight I might be able to do something. I'm going to go back over and check that plant going branch by branch. That one 10th planet tgat WAS the biggest plant is severely stunted amd has some "strange" looking leaves. I wasthinking about getting it off property or just chopping and burning but I figure it's been in there long enough that the others could be infected. I think it spreads through pests if that's the case then it might be better to get rid of it. I'm not sure what I'm going to do yet. I'm going to stop and try to get some mulch today. EDIT: I found a place I can get a bale of straw and I think I'll use that to mulch. It's almost a 100°. After killing the pillar this morning and missing that cutworm I came back over to REALLY look at the special kush in later flower. I looked through every branch and every bud. I found four pillars on that plant. No REAL damage yet and extremely small. I had to pull buds apart to find them. It's like they were hiding from the heat. That was miserable hand picking them in 100° degree weather. Luckily the bird feeders are close but the bigger birds chase the smaller ones. The smaller birds have found a new food source and perch on my cage waiting. I'm leaning towards treating the flowering plant with BT-k. Seeing that tge citric acid WON'T kill fungus I'll just use OUR super alkaline water and hope for the best. Nothing will get treated during this weather. 8/12 IT reached 105° yesterday and I had a family medical emergency. Came over this morning to several plants drooped right over despite me checking MD day and them being fine. Phone dodnt charge so I couldn't get pictures. Watered everything but the ones that got it yesterday cause they looked good and still had weight. I had to leave before the ones that were down could pick back up. The kush plants seem to tolerate this heat much better. Beside the ones in the 10s tge others are taking this hear fine. I'll update when I get back. EDIT: Went back over around 10. Another hot day. Suppised to be HOTTER than yesterday. I don't know how that's possible. both our thermometers went to 104 lately. Oh and I dont think that's beet curly top virus I think it's just great stress! I've grown this strain before and it's not the most resilient but it's other qualities make up for that. That's a loud off. I checked most buds on the plant in late flower and found a grass hopper IN the cola! No damage that I could see and I flicked him in the head which killed it. I came back to the chemdog that I didn't water drooping. I watered that and the 10th planet I didn't get this morning. The only one that hasn't got water today was the natural mk ultra and when I was there it was still heavy and looked really good so I left it. I'll have to come back around four and check things out. I'll be watering that tonight for sure. It will be hot tomorrow too then it will be better weather. I need to feed but I'm uncertain whether I should in this heat. All the kush strains I'm running are have Hindu kush as a parent and seem to be able to take the heat no problem. We don't get heat like this usually. It's different when it's 100° and 99% rh than dry heat. Edit #2 WENT BACK OVER AROUND 3:30PM EXPECTING TO WATERING THE ONE PLANT I HADNT. THE MK ULTRA THAT I LEFT NATURAL. IT LOOKED GREAT WHEN I GOT THERE AND WAS STILL HEAVY. IT LOOKED BETTER THAN NORMAL. ONE SIDE HAD A FEW LEAVES THAT WERE STARTING TO DROOP BUT ITS RIGHT WHERE THE SUN IS HITTING IT ON TH BOTTOM. ITS JUST A LITTLE HEAT STRESS. THE 10TH PLANET ARE MORE PRONE TO HEAT STRESS. I NEED TO FEED. I DEFOLIATED QUITE A FEW LEAVES TODAY. IM RUNNING OUT OF LARGE FAN LEAVES ON MY PLANT IN MID FLOWER. EVERYTHING SEEMED TO START MAKING LITTLE ROCK HARD BUDS ALMOST OVERNIGHT AND THEY ARE STARTING TO SWELL. PLANTS NEED NITROGEN I THINK. I USED LESS SOIL AND WATERED MORE. I JUST DONT WANT TO FEED DURING THIS HOT WEATHER. TOMORROWS THE LAST OF THIS HEAT WAVE AND THEN ILL BE ABLE TO GIVE THE GIRLS A GOOD FEEDING. THE SILVER LINING TO THE PATHOGEN THING IS THAT IVE BEEN MUCH MORE COGNIZANT OF LEAFING THE PLANTS AND REMOVING DEAD AND DAMAGED LEAVES. I'VE DONE A MUCH BETTER JOB WITH THAT THIS YEAR. AFTER THE HOT SPELL ILL GET IN WITH SHEARS AND PRUNE OFF LARF. IVE GOT SOME BUT I HAVE MORE I NEED TO GET. 8/13 IT was supposed to be HOTTER yesterday than the day before bit it was the same 104°. Today is supposably the end of this ridiculous heatwave. I watered everything that needed it despite having watered deeply yesterday. I put 8 1/2 gallons into the garden where it needed it most. Chemdog and the big 10th planet I got yesterday. Soil is still wet and the bags are heavy. I can't believe how well these kush plants hold up to the heat. Hopefully better Temps tomorrow so I can feed. In other news I haven't been seeing septoria leaves. Less and less everytime I go over! Keeping my fingers 🤞. 8/14 Last of the hot days. Watered the chem dog and the big 10th planet. It's supposed to rain today. The rest of the plants are heavy amd doing good. I'll update when I can write more.

Canopy filling out nicely. Still on the veg feed but flower is nearly out so just gonna too up the tanks then change to bloom nutrients in the next few days. Roots looking good.