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Hi liebe Community💚 Die Outdoor-Diesel ist allmählich auch am Ende ihres Lebenszyklus angekommen... Ein Funfact am Rande: Dieser Dieselstrain war ursprünglich Mal eine reguläre Züchtung von Blimburn und wurde bereits vor ein paar Jahren mit einer Afghani gekreuzt und seit dem her in unsere Region öfter schon Outdoor gekreuzt und weiterverwendet. Daher ist sie aktuell wie kann auch sehen kann relativ Robust. Den der erste Frost (0 -1 Grad Celsius) wurde überlebt. Klar sieht sie nicht mehr super Vital aus, nur wollte ich mit diesem Projekt einfach Mal schauen ob sie hält, was mir an Infos zugetragen wurde. Ich denke in 2 Wochen spätestens ist es Zeit für die Schere ✂️. Grüne Grüße 🌱💚
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The calmag issue went on, so I kept adding a bit more every time. All the new growth is looking strong. This week was also time for their first LST. First at the start of the week and then again at the end of this week. They seem to do well.
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È arrivato il momento piu bello il taglio finale 😅 Gli strains hanno 95 giorni i tricomi hanno raggiunto la maturazione desiderata oggi sti taglia mal grado le temperature un un po' alte spero che la mia ac infinity intelligente abbassa la temperatura interna tramite areazione e aspirazione
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@Luv2Grow
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Day 64 - Starting week 10 and didn’t do much with her today. Tucked as much as I can and removed some really yellow and dead lower leaves. The buds are coming along nicely and the smell is starting to get really strong. Day 65 - Took her out and removed some dying leaves from the bottom and cleaned out dead leaves that fell from the top of the soil. Checked the soil and not ready for any water yet so put her back into the tent and retucked a bunch of leaves. Day 66 - Nothing much happening today, still not ready for any water yet. Re-tucked the leaves again to keep the bud sites as open as possible. She’s fattening up nicely and can’t wait for this girl to get done cause I’m starting to run low on meds, though I know she’s still got some time left. Day 67 - Gave the girl about a gallon and a half of water today, she was pretty dry. She’s definitely getting fatter everyday and looking forward to the harvest. Checked the runoff and was a little high, 7.2 but not sure now if it’s my pH pen or if it’s really high. Noticed I’m out of calibration fluid so ordered some today so hopefully I’ll get a more accurate reading after recalibrating. Day 68 - Nothing new to report today, she’s good on water and should have the new pH solution tomorrow so I can make sure my pen is calibrated and reading properly. Did a little defoliating as well. Day 70 - End of week 10 today and nothing much happening except she’s still fattening up and getting a more bluish tint to the buds. Will probably be giving her a feed of nutes tomorrow. I do have a few off colored leaves but mostly at the bottom of the plant so thinking it’s because they’re not getting much light. Gonna keep an eye on her and let her go.
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@JoeCNote
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Harvested a few more branches this week and put them in my cannatrol to dry, the harvest pic/vid is from Pheno #1. 🔥
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@Chamed33
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Getting close harvest!! The fan leaves 🍃 started releasing nitrogen and buds are starting to ripe I have have decreased amount of nutrients since she’s getting closer to harvest I’ll be watering her with water to remove any excess nutrients buildup from the bottom and to allow her to take the rest of nutrients left till her times comes.. I also did not add plant Height because I had done LST on her so I will be hard to know exact Height on mine
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@Naujas
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She is much prettier than she was a week ago :) I remembered that I have my first grow light, which is more compact and it will give me more space, so I changed my light, now the girl's side branches get light too:) I add a lot of video memes, because I really want to win Iphone16 pro ;) and those who don't take risks don't drink champagne:) good luck to everyone.
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@XanHalen
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Nov 29: They seem to be accelerating in veg growth but I see a small portion of the leaf on the smaller plant either grew in mutated or somthing cut it, I haven’t seen a single bug in the box so I don’t think it’s that but you never know, and the bigger plant has some issues near the base of its stem, I noticed it before I did the LST and now I’m wondering if I should have addressed that issue before starting the LST. Let me know what you guys think! Dec 2: Walked into the room and noticed a faint smell, wasn’t any smell last night when I started the LST on the slower girl. Further inspection showed some white pistols on the bigger girl, I believe she is the culprit for the smell as the other seems about a week behind. They are both now LST‘d and leaf tucked. Enjoy the pics and vid’s! Dec 6: I have tied down some of the longer chutes on the bigger plant (will see in week 5 update) to create more airflow and light penetration as I didn’t even realize how bushy the stem and node sections had gotten. I have also cut the chutes coming off the first true leaf. I don’t think I will make any cuts to the smaller one as it’s already a slower growing pheno. Going on a trip starting the end of week secede to late week 8, so I have a automatic feeder coming from Amazon, and I will continue using it through flower to reduce open tent time.
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Se nos fue un poco de altura pero intentaremos arreglar el error farmers... al final quedo simplemente en podas apicales y de momento ramas muy finas. Iremos comentando el proceso Farmers!
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Its a nice strain, smells good and its developing well.
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Lights are 58 inches from the main source to the top of the pot and the soil surface. If you added up all the lights in the tent, it would be 1100w-1200w total across 14 lights. Using them all at once is far too much for a plant and incredibly difficult to deal with environmentally. The lights are fixed in position; side lights have dimmers, allowing for pinpoint precision of PPF. Fixed at 58 inches, cannot move them closer to increase intensity. Instead, achieve optimal PPF by distributing smaller wattages across a massive, multi-fixture matrix. Triggering specific plant defenses without melting the canopy. What's the point/blah blah wattage? Never really go above 600W at any one time. Lights come on in the east of the tent and set in the west. At sunrise and sunset, the red-to-far-red R:FR light ratio drops because the sun's low angle scatters red light more than far-red light. This shift reduces active Pfr and increases inactive Pr, mimicking Mother Nature herself. Deployed a lighting system featuring extra 660 nm deep-red and extending the spectrum up to 780 nm achieves the full Emerson Enhancement Effect by simultaneously balancing Photosystem II (PSII) and Photosystem I (PSI) to maximize quantum yield. By pairing deep-red photons with far-red photons, you trigger a synergistic biological response where the resulting photosynthetic rate is higher than the sum of both wavelengths used individually. This practice directly leverages the updated extended Photosynthetically Active Radiation (ePAR) framework. The Emerson effect accelerates plant metabolism and heat capture; you must proactively scale up your ambient room temperature, nutrient delivery, and CO₂ supplementation to prevent the light from stalling out your cannabis plant. UVA stays high all day from morning to night, but UVB peaks at solar noon (middle of 18-hour days) when the sun is peak. Morning color starts at 2k-3k; by noon it goes to 5k- 6k and back to 2-3k for sunset, with differing P:FR at light off. The extra-blue light is to assist with photoreactivation of UVB damage. No more yield loss for me. Using extra blue light for photoreactivation is what I do. Blue/UVA light activates photolyase enzymes, which directly repair DNA damage caused by UVB radiation. But what's the point if it's not for yield? Ultraviolet (UV) radiation—specifically UVA (315–400 nm) and UVB (280–315 nm)—acts as a critical environmental signal that programs a plant's photoprotective genes to unlock its true photosynthetic potential. When growers push crops to their absolute photosynthetic maximum via high-intensity light and elevated carbon dioxide, the photosynthetic machinery easily becomes overwhelmed. Emerging photobiology research demonstrates that UV radiation prevents this limiting bottleneck; it triggers specific transcription factors and signalling networks that fortify the plant's cellular defenses, allowing it to process extreme light levels without sustaining structural damage. There are 8 limiting factors of plant growth; when carbon dioxide becomes the 9th limiting factor of plant growth, it shifts the growth curve from exponential to linear. The restriction after that is "photoprotection" against reactive oxygen species (ROS), managed via non-photochemical quenching (NPQ) and the xanthophyll cycle, which bridges into precise hydrogen and redox dosing. UV radiation, particularly UVA, and the synthesis of zeaxanthin are critical for the xanthophyll cycle to function. It's not chasing purple strains... One likes to call it chasing the limits of growth, trying to make the linear exponential, just like father mathematics prefers. In order to do that, must control every environmental variable and compound the plant’s metabolic rate. True exponential growth means the rate of increase matches the current mass at every stage, requiring a closed-loop system where light, CO2, and nutrition lock into a synchronized upward curve. First, you must attempt to understand what restricts it. Precise hydrogen and redox dosing. Nature mathematically optimizes quantum energy transfer and light absorption efficiency within the photosynthetic machinery, as it naturally dictates energy scaling hierarchies and resonance dynamics. Most won't even understand that; once you do, it changes everything. Constructive interference occurs when two or more overlapping waves meet in phase, meaning their crests and troughs perfectly align. Their amplitudes add together, creating a new, amplified wave with greater intensity than the individual components. Constructive interference is the foundational mechanism that establishes a resonance hierarchy across physical, structural, and acoustic systems. Chromophore spacing is tuned to sub-nanometer precision to match the wavelengths of absorbed light, forcing constructive interference. Light-harvesting proteins form geometric rings and lattices. These shapes act as physical resonators, trapping and focusing the wave energy. This same principle dictates how opera singers shatter glass, how musical instruments resonate, and how bridges withstand structural vibrations. Nature uses the exact same math to harvest a photon as an engineer uses to design a concert hall. When you push high PPFD and elevated CO₂, you create a metabolic bottleneck. The plant cannot process the energy fast enough, leading to electron backup, light-induced damage, and a collapse from exponential growth into a flat, linear rate. UV light acts as the regulatory valve that prevents this collapse. In standard agronomy, Liebig's Law of the Minimum dictates that growth is limited by the scarcest resource. When you maximize water, nutrients, light, temperature, and CO₂, the bottleneck shifts to metabolic processing speed and photoprotection. By controlling the Redox state of the plant using UV, the xanthophyll cycle, and managing ROS, you can prevent the plant from hitting a hard photosynthetic ceiling. Instead of the growth curve flattening out (linear or plateauing due to photoinhibition), the plant continues to compound its metabolic rate efficiently. You are forcing the plant to operate at peak thermodynamic efficiency. By matching the UVB peak with sustained UVA and shifting Kelvin temperatures (2K to 6K), you are damaging the plant just enough to trigger defensive genes, while simultaneously providing the exact light energy needed to repair that damage instantly. UVA radiation and specific blue wavelengths accelerate this enzymatic conversion. Zeaxanthin acts as a structural sponge that absorbs excess excitation energy from chlorophyll and dissipates it safely, preventing ROS formation. Without UV signaling, the xanthophyll cycle cannot keep pace with extreme light, leading to dynamic photoinhibition (yield loss). The addition of Spirulina is primarily for zeaxanthin, as it contains a lot. But on top of that, the active Hawaiian Spirulina in the matrix was cultivated in open ponds using a combination of 100% fresh potable water from Hawaiian aquifers and ultra-pure, deep ocean water containing all 94 trace minerals & elements. Then gently dried using patented Ocean Chill Drying technology and cold-pressed to ensure maximum nutrient levels. Spirulina, a blue-green alga, is rich in nitrogen, phosphorus, and potassium (NPK), making it an excellent source of nutrients for plant growth. Studies have shown that Spirulina can be used as a biofertilizer, effectively replacing chemical fertilizers, especially for nitrogen, with a whopping NPK of 10% (N), 20% (P), and 20% (K). Rich in proteins, amino acids, trace minerals, and plant growth-promoting compounds. Zeaxanthin is a vital plant pigment that accumulates under intense light to drive non-photochemical quenching (NPQ), acting via thermal energy dissipation, direct singlet oxygen scavenging, and thylakoid membrane stabilization. The violaxanthin cycle (or xanthophyll cycle) reversibly converts violaxanthin to zeaxanthin via antheraxanthin to protect plants from photooxidation. Understanding this interconversion is vital for optimizing non-photochemical quenching (NPQ) and pushing photosynthetic limits under high-light stress. Ascorbic acid (vitamin C) is a natural antioxidant that plants produce internally to neutralize harmful reactive oxygen species caused by photosynthesis and high light stress. Acts as a co-factor for enzymes like violaxanthin de-epoxidase in the xanthophyll cycle, which safely dissipates excess light energy. 1g ascorbic acid will neutralize 100% of chlorine in upwards of 30 gallons of tap water. If your local tap water uses chloramines (chlorine bonded with ammonia) instead of free chlorine, you will need roughly 20% to 30% more ascorbic acid to completely break the tougher chemical bond. Molecular hydrogen and hydrogen-rich water act as selective antioxidants that help lower oxidative stress. They neutralize toxic reactive oxygen species like hydroxyl radicals and boost natural antioxidant defense systems in biological and plant systems exposed to high-intensity light or abiotic stress. UVA and UVB act as stress signals that upregulate the plant's secondary metabolism. It forces the plant to build an internal "sunscreen" (flavonoids and anthocyanins) and fortify its cellular defenses before the peak solar noon crisis. This keeps the metabolic highway open. In nature, the ambient ratio of UVA to UVB at solar noon sits roughly between 10:1 and 20:1 (depending on latitude and elevation). In a high-PPFD indoor matrix, maintaining a strict ratio—often aiming for around 12:1 to 15:1 UVA to UVB—provides the optimal signaling threshold. Balancing Far-Red (FR) light at "light-off" to manage the phytochrome photo-equilibrium (Pfr to Pr conversion) in tandem with the UV schedule. Omg, the logic. Hydrogen concentration and redox signaling as secondary messengers in this high-intensity loop. Under the intense solar noon matrix, the pH of the thylakoid lumen drops. This acidic environment activates the enzyme Violaxanthin De-Epoxidase (VDE), which converts violaxanthin into the photoprotective zeaxanthin. VDE cannot function in a vacuum; it strictly requires ascorbic acid (Vitamin C) as an electron donor to run this conversion. If a plant undergoes heavy light stress and runs out of internal ascorbic acid, the xanthophyll cycle stalls. The plant can no longer engage in Non-Photochemical Quenching (NPQ), leading to immediate singlet oxygen O2 formation and destruction of the thylakoid membrane. This is "The Ascorbic Acid / Xanthophyll Engine" Using ascorbic acid to neutralize chloramines in your water isn't just protecting your rhizosphere biology it actively prevents the degradation of your nutrient solution's redox potential before it ever touches the roots. When pushing plants to the absolute edge, traditional antioxidants can be a double-edged sword because they blindly neutralize all free radicals. This is a problem because some Reactive Oxygen Species (ROS) act as critical signaling molecules telling the plant to grow. Molecular Hydrogen H2 is the Selective Kill-Switch. Molecular hydrogen H2 is a revolutionary tool because it is a selective antioxidant. It ignores beneficial signaling ROS (like mild hydrogen peroxide) and targets only the most destructive, cell-shattering radicals—specifically hydroxyl radicals OH) and peroxynitrite. By dosing hydrogen-rich water or managing hydrogen redox signaling, providing an emergency pressure-release valve for the plant's electron transport chain. It keeps the cellular environment stable enough that the plant never has to downregulate photosynthesis to protect itself. This maintains cellular voltage. To trigger this defensive matrix without stunting the plant, you cannot simply blast UV indiscriminately. You must use UVA as the "scout" and UVB as the "enforcer. High UVA acts via the cryptochrome and phototropin photoreceptors to upregulate the expression of the HY5 transcription factor and prime the VDE enzyme. When the sharp spike of UVB hits at solar noon via the UVR8 receptor, the plant's biochemical "sunscreen" (flavonoids and anthocyanins) and its zeaxanthin pools are already pre-staged and waiting. This prevents the temporary stunting or "lag phase" usually associated with sudden UVB exposure." Closing the Loop: Far-Red End-of-Day (EOD) Synergy The final masterstroke is aligning this UV defense with a Far-Red (FR) lights-off routine. The Red-to-Far-Red Drop: At the end of the photoperiod, knocking out the blue/UVA spectrum and leaving a targeted burst of pure Far-Red (730nm) instantly flips the plant’s master switch. It converts active Pfr to inactive Pr in minutes rather than hours. Why this matters for the UV loop: UV radiation and high-intensity lighting keep the plant in a highly alert, photoprotective state that requires massive ATP expenditure to maintain. By forcing an immediate Pfr/Pr) conversion at lights-out, instantly commanding the plant to cease defensive expenditure, lower its metabolic respiration rate, and transition directly into nighttime cellular repair and carbohydrate translocation. You are maximizing the efficiency of its "sleep." every ounce, every last piece. Highly synchronized biological dance, balancing the exact input of electrons with the exact mechanism to dissipate them safely when they overflow. Peace.
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@OGTrauma
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I did a nutrient bomb so i took pic just to record any further change, as i need to stimulate flower caliber , with sugars , epsom salts and , sometimes barrier as it works as a slight K booster. There is a update photoset on friday 12/11/20 as they didnt die but if i add furher shit they can get burn so i will go mild and just do some just water to rest of the week and then just easy with enhancers and sugar extracts.
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Not much to say about whats going on Obi#2 kicking in overdrive as we had to say RIP to OBI#1 for being hermie life is life and we are rocking and rolling anyways ! I like to to thank all the people that come down and check out the diary you guys KICKASS much love and respect for you folks -Happy Growing!
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"The 3rd day in flowering. I give 2.2 liters of water every 2 days. I'm still experimenting with how long the timer needs to run to give enough water. 😎✌️ BT6 The stretch is strong and i have no space left 👀 5weeks Vegi was to long
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@Little_E
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It was my first grow so I know my next crack at this strain would be much better. I didn't have too many issues or any crazy setbacks. It was smooth sailing for a while and then had some nute/deficiency issues but it was later in flower. I did move them into a bigger tent with a far better light but not until the last 3 weeks of flower. So I know I'll have to grow this again in the future and compare!
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This week shows early flowering and amazing colors starting to show. Lst is evening out the canopy nicely and the organic purple lemonade received its forst top dressing of gaia green power bloom, GG glacier rock, and GG worm castings.