The Grow Awards 2026 🏆
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This week went by quick but they grew a lot! I didn't do anything different than last week but just increase their water intake from 1L to 1.5L and then followed my same nutrient regiment. I use the Fish Poop then the next day I just water. Then I use the Real Growers Soil Recharge and then I just water the next day. Then I use the MaxiGrow and then I just water the next day. Then I use the Stash Blend and then I use just water the next day. You can pH (using soil) between 5.5 and 6.5 so I always pH my Nutrient Solutions at 6.2 and use my pH'd water which is a 6.8 (7.0 for soil) but I pH my H20 after adding my Nutrient Solutions. I use my H2O that's always 65 degrees! I find it's better and easier to have a bucket with pH'd water ready to go at all times. It makes it easier when watering and feeding your plants especially if you have a few to care of!
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@LAShugars
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So excited to see how FastBuds Photos do
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📆 Semana 2 – Floración Comienza la floración activa. Se aprecia el estiramiento controlado y la aparición clara de pistilos. La planta mantiene un verde sano y una estructura abierta y equilibrada. Se inicia la aplicación de Sticky Finger, apoyando el arranque floral sin generar estrés. Raíz y parte aérea responden de forma estable. Semana de transición bien encarrilada. Seguimos creciendo fuerte 💪!
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Hello my friends! Almost weekend, are you ready for it ? I can't wait, the work drained me soooo much this week! Good that this little Titan gives me so much joy and satisfaction every time im back home! Back to us! Today is friday and marks the last day of her 10th week. Today is kinda important, is exactly 77 days since the plant showed up from the soil. RQS is saying that normally this plant is ready to harvest in about 70 to 75 days. Mine is already 77 and is not ready yet. As you can see from the picutres and clips especially the last ones of this week...you can see that her trichomes are not quite ready yet. The trichomes look like they are 85%/90% ready right now, as I am writing this post. The pictures and clips are also from this morning, is all fresh material. Most of the trichomes are cloudy but you can still see that few of them are not ready yet, also there is no amber colour at all. All of this it must mean that the plant can go couple days more. This week and the previous one I was reading and checking online about this plant and her previous grows. I understood that the plant in reality takes a little longer to get FULLY ripe and ready. A little over 80 to 85 days. I will let her run for another week more or less, today is day 77. For peace of mind I am checking the trichomes every 2 days to don't miss it or be late. It would be a shame to cut it down right now. Why? I can see the buds getting bigger and bigger everyday! She's getting thicker literally in front of my eyes, especially in this late phase of flowering. I can see the buds increasing in size day by day. I am sooooo happy! Dope! So harvest probably next week! WATERING This week I've started the FLUSH cycle. The plant got 6 L of plain water adjusted to 6.3 pH and splitted in 3 watering sessions by 2L each. In all 3 waterings the drained water was around 1 liter. NUTRIENTS No nutrients this week, same story next week. Just plain water till harvest, the water will be adjusted to the correct pH. No more no less. The harvest should fall exactly on the day that marks 2 weeks of no nutrients. So actually with this we are really spot on! Perfect I would say. LIGHTNING The light is always 100%, 24/7. The only update here is that at the beginning of this week I lowered the light about 10 centimeters for this last days of flowering. Is an experiment...anyway my light is only 70 watts in the end. So I am not too worried about it, probably I should lower it couple of week ago to give that extra boost to the plant. But it is what it is, now is too late ahahahah. Anyways talking about the light...before I've got 25 centimeters between the led lamp and the plant, now is about 15 centimeters of distance. TRAININGS NO MORE training techniques were applied to the plant. At the beginning of this week I REMOVED all the LST that was trapping and keeping her strapped to the pot. I wanted the plant to BE FREE during the last two weeks of her life. Like a little treat and mercy for this beautiful prisoner ahhahaha. Removing the LST I allowed the plant to lift up a little bit more her branches. In this way the buds sites went up and closer to the led lamp, closer about 10/20%. Maybe is not much but in the end everything counts on the scale. We will see the results. The height of the plant didn't change in this last weeks, it reached 48 cm and stayed there. Actually after I released her from the LST last week, it gained 2 cm. So now at the end of her life the plant is 50 cm tall. The smell is strong and pungent, refreshing somehow. Very pleasant, I love it. OVERALL Everything is going well, just a little bit late on the schedule. The patience is the key for good and big buds! I CAN SEE THE FINISH LINE, WE ARE ALMOST THERE. See you next week for the final update! Stay safe y'all!
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@Dunk_Junk
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She grew another 17cm this week! 145cm tall!!!!!!!!! She is totally out of headroom now, her top cola is through the lights and getting close to the roof of the tent 😅 Fastbuds do say it can reach 1.4M... 😁 It's accurate, she is a MONSTER of a plant. This week I have done a quick video showing the result of my experiment a few weeks ago where I FIMed a couple of side branches. Take a look 😃 Nothing else to the report as I'm just letting her do her own thing. 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
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Diesmal ein KRUMME GURKEN STECKLINGS-Run Bestellt schon Mitte November, mit Termin wunsch am/zum 7.1.2026. Es hat nicht einmal 24 Stunden gedauert, da waren die 3 bei mir. Temperaturen waren zu der Zeit konstant unter 0 Grad (draußen) Fit und vital ging es direkt in die 15 Liter End-Töpfe.. Alle drei haben den Versand und das eintopfen gut überstanden...
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@farahweed
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I used overdrive fertilizer again this week. My God, girls get more beautiful like this. The last weeks make me very happy.😍🌷💐💥⚘️👽👽🎍 From now on, I will be very careful because the more I improve the conditions, the better results I get Especially the temperature difference between night and day. humidity Box ambient temperature 👊👊💧♠️
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Yellow butterfly came to see me the other day; that was nice. Starting to show signs of stress on the odd leaf, localized isolated blips, blemishes, who said growing up was going to be easy! Smaller leaves have less surface area for stomata to occupy, so the stomata are packed more densely to maintain adequate gas exchange. Smaller leaves might have higher stomatal density to compensate for their smaller size, potentially maximizing carbon uptake and minimizing water loss. Environmental conditions like light intensity and water availability can influence stomatal density, and these factors can affect leaf size as well. Leaf development involves cell division and expansion, and stomatal differentiation is sensitive to these processes. In essence, the smaller leaf size can lead to a higher stomatal density due to the constraints of available space and the need to optimize gas exchange for photosynthesis and transpiration. In the long term, UV-B radiation can lead to more complex changes in stomatal morphology, including effects on both stomatal density and size, potentially impacting carbon sequestration and water use. In essence, UV-B can be a double-edged sword for stomata: It can induce stomatal closure and potentially reduce stomatal size, but it may also trigger an increase in stomatal density as a compensatory mechanism. It is generally more efficient for gas exchange to have smaller leaves with a higher stomatal density, rather than large leaves with lower stomatal density. This is because smaller stomata can facilitate faster gas exchange due to shorter diffusion pathways, even though they may have the same total pore area as fewer, larger stomata. Leaf size tends to decrease in colder climates to reduce heat loss, while larger leaves are more common in warmer, humid environments. Plants in arid regions often develop smaller leaves with a thicker cuticle and/or hairs to minimize water loss through transpiration. Conversely, plants in wet environments may have larger leaves and drip tips to facilitate water runoff. Leaf size and shape can vary based on light availability. For example, leaves in shaded areas may be larger and thinner to maximize light absorption. Leaf mass per area (LMA) can be higher in stressful environments with limited nutrients, indicating a greater investment in structural components for protection and critical resource conservation. Wind speed, humidity, and soil conditions can also influence leaf morphology, leading to variations in leaf shape, size, and surface characteristics. Small leaves: Reduce water loss in arid or cold climates. Environmental conditions significantly affect gene expression in plants. Plants are sessile organisms, meaning they cannot move to escape unfavorable conditions, so they rely on gene expression to adapt to their surroundings. Environmental factors like light, temperature, water, and nutrient availability can trigger changes in gene expression, allowing plants to respond to and survive in diverse environments. Depending on the environment a young seedling encounters, the developmental program following seed germination could be skotomorphogenesis in the dark or photomorphogenesis in the light. Light signals are interpreted by a repertoire of photoreceptors followed by sophisticated gene expression networks, eventually resulting in developmental changes. The expression and functions of photoreceptors and key signaling molecules are highly coordinated and regulated at multiple levels of the central dogma in molecular biology. Light activates gene expression through the actions of positive transcriptional regulators and the relaxation of chromatin by histone acetylation. Small regulatory RNAs help attenuate the expression of light-responsive genes. Alternative splicing, protein phosphorylation/dephosphorylation, the formation of diverse transcriptional complexes, and selective protein degradation all contribute to proteome diversity and change the functions of individual proteins. Photomorphogenesis, the light-driven developmental changes in plants, significantly impacts gene expression. It involves a cascade of events where light signals, perceived by photoreceptors, trigger changes in gene expression patterns, ultimately leading to the development of a plant in response to its light environment. Genes are expressed, not dictated! While having the potential to encode proteins, genes are not automatically and constantly active. Instead, their expression (the process of turning them into proteins) is carefully regulated by the cell, responding to internal and external signals. This means that genes can be "turned on" or "turned off," and the level of expression can be adjusted, depending on the cell's needs and the surrounding environment. In plants, genes are not simply "on" or "off" but rather their expression is carefully regulated based on various factors, including the cell type, developmental stage, and environmental conditions. This means that while all cells in a plant contain the same genetic information (the same genes), different cells will express different subsets of those genes at different times. This regulation is crucial for the proper functioning and development of the plant. When a green plant is exposed to red light, much of the red light is absorbed, but some is also reflected back. The reflected red light, along with any blue light reflected from other parts of the plant, can be perceived by our eyes as purple. Carotenoids absorb light in blue-green region of the visible spectrum, complementing chlorophyll's absorption in the red region. They safeguard the photosynthetic machinery from excessive light by activating singlet oxygen, an oxidant formed during photosynthesis. Carotenoids also quench triplet chlorophyll, which can negatively affect photosynthesis, and scavenge reactive oxygen species (ROS) that can damage cellular proteins. Additionally, carotenoid derivatives signal plant development and responses to environmental cues. They serve as precursors for the biosynthesis of phytohormones such as abscisic acid () and strigolactones (SLs). These pigments are responsible for the orange, red, and yellow hues of fruits and vegetables, while acting as free scavengers to protect plants during photosynthesis. Singlet oxygen (¹O₂) is an electronically excited state of molecular oxygen (O₂). Singlet oxygen is produced as a byproduct during photosynthesis, primarily within the photosystem II (PSII) reaction center and light-harvesting antenna complex. This occurs when excess energy from excited chlorophyll molecules is transferred to molecular oxygen. While singlet oxygen can cause oxidative damage, plants have mechanisms to manage its production and mitigate its harmful effects. Singlet oxygen (¹O₂) is considered a reactive oxygen species (ROS). It's a form of oxygen with higher energy and reactivity compared to the more common triplet oxygen found in its ground state. Singlet oxygen is generated both in biological systems, such as during photosynthesis in plants, and in cellular processes, and through chemical and photochemical reactions. While singlet oxygen is a ROS, it's important to note that it differs from other ROS like superoxide (O₂⁻), hydrogen peroxide (H₂O₂), and hydroxyl radicals (OH) in its formation, reactivity, and specific biological roles. Non-photochemical quenching (NPQ) protects plants from damage caused by reactive oxygen species (ROS) by dissipating excess light energy as heat. This process reduces the overexcitation of photosynthetic pigments, which can lead to the production of ROS, thus mitigating the potential for photodamage. Zeaxanthin, a carotenoid pigment, plays a crucial role in photoprotection in plants by both enhancing non-photochemical quenching (NPQ) and scavenging reactive oxygen species (ROS). In high-light conditions, zeaxanthin is synthesized from violaxanthin through the xanthophyll cycle, and this zeaxanthin then facilitates heat dissipation of excess light energy (NPQ) and quenches harmful ROS. The Issue of Singlet Oxygen!! ROS Formation: Blue light, with its higher energy photons, can promote the formation of reactive oxygen species (ROS), including singlet oxygen, within the plant. Potential Damage: High levels of ROS can damage cellular components, including proteins, lipids, and DNA, potentially impacting plant health and productivity. Balancing Act: A balanced spectrum of light, including both blue and red light, is crucial for mitigating the harmful effects of excessive blue light and promoting optimal plant growth and stress tolerance. The Importance of Red Light: Red light (especially far-red) can help to mitigate the negative effects of excessive blue light by: Balancing the Photoreceptor Response: Red light can influence the activity of photoreceptors like phytochrome, which are involved in regulating plant responses to different light wavelengths. Enhancing Antioxidant Production: Red and blue light can stimulate the production of antioxidants, which help to neutralize ROS and protect the plant from oxidative damage. Optimizing Photosynthesis: Red light is efficiently used in photosynthesis, and its combination with blue light can lead to increased photosynthetic efficiency and biomass production. In controlled environments like greenhouses and vertical farms, optimizing the ratio of blue and red light is a key strategy for promoting healthy plant growth and yield. Understanding the interplay between blue light signaling, ROS production, and antioxidant defense mechanisms can inform breeding programs and biotechnological interventions aimed at improving plant stress resistance. In summary, while blue light is essential for plant development and photosynthesis, it's crucial to balance it with other light wavelengths, particularly red light, to prevent excessive ROS formation and promote overall plant health. Oxidative damage in plants occurs when there's an imbalance between the production of reactive oxygen species (ROS) and the plant's ability to neutralize them, leading to cellular damage. This imbalance, known as oxidative stress, can result from various environmental stressors, affecting plant growth, development, and overall productivity. Causes of Oxidative Damage: Abiotic stresses: These include extreme temperatures (heat and cold), drought, salinity, heavy metal toxicity, and excessive light. Biotic stresses: Pathogen attacks and insect infestations can also trigger oxidative stress. Metabolic processes: Normal cellular activities, particularly in chloroplasts, mitochondria, and peroxisomes, can generate ROS as byproducts. Certain chlorophyll biosynthesis intermediates can produce singlet oxygen (1O2), a potent ROS, leading to oxidative damage. ROS can damage lipids (lipid peroxidation), proteins, carbohydrates, and nucleic acids (DNA). Oxidative stress can compromise the integrity of cell membranes, affecting their function and permeability. Oxidative damage can interfere with essential cellular functions, including photosynthesis, respiration, and signal transduction. In severe cases, oxidative stress can trigger programmed cell death (apoptosis). Oxidative damage can lead to stunted growth, reduced biomass, and lower crop yields. Plants have evolved intricate antioxidant defense systems to counteract oxidative stress. These include: Enzymes like superoxide dismutase (SOD), catalase (CAT), and various peroxidases scavenge ROS and neutralize their damaging effects. Antioxidant molecules like glutathione, ascorbic acid (vitamin C), C60 fullerene, and carotenoids directly neutralize ROS. Developing plant varieties with gene expression focused on enhanced antioxidant capacity and stress tolerance is crucial. Optimizing irrigation, fertilization, and other management practices can help minimize stress and oxidative damage. Applying antioxidant compounds or elicitors can help plants cope with oxidative stress. Introducing genes for enhanced antioxidant enzymes or stress-related proteins over generations. Phytohormones, also known as plant hormones, are a group of naturally occurring organic compounds that regulate plant growth, development, and various physiological processes. The five major classes of phytohormones are: auxins, gibberellins, cytokinins, ethylene, and abscisic acid. In addition to these, other phytohormones like brassinosteroids, jasmonates, and salicylates also play significant roles. Here's a breakdown of the key phytohormones: Auxins: Primarily involved in cell elongation, root initiation, and apical dominance. Gibberellins: Promote stem elongation, seed germination, and flowering. Cytokinins: Stimulate cell division and differentiation, and delay leaf senescence. Ethylene: Regulates fruit ripening, leaf abscission, and senescence. Abscisic acid (ABA): Plays a role in seed dormancy, stomatal closure, and stress responses. Brassinosteroids: Involved in cell elongation, division, and stress responses. Jasmonates: Regulate plant defense against pathogens and herbivores, as well as other processes. Salicylic acid: Plays a role in plant defense against pathogens. 1. Red and Far-Red Light (Phytochromes): Red light: Primarily activates the phytochrome system, converting it to its active form (Pfr), which promotes processes like stem elongation and flowering. Far-red light: Inhibits the phytochrome system by converting the active Pfr form back to the inactive Pr form. This can trigger shade avoidance responses and inhibit germination. Phytohormones: Red and far-red light regulate phytohormones like auxin and gibberellins, which are involved in stem elongation and other growth processes. 2. Blue Light (Cryptochromes and Phototropins): Blue light: Activates cryptochromes and phototropins, which are involved in various processes like stomatal opening, seedling de-etiolation, and phototropism (growth towards light). Phytohormones: Blue light affects auxin levels, influencing stem growth, and also impacts other phytohormones involved in these processes. Example: Blue light can promote vegetative growth and can interact with red light to promote flowering. 3. UV-B Light (UV-B Receptors): UV-B light: Perceived by UVR8 receptors, it can affect plant growth and development and has roles in stress responses, like UV protection. Phytohormones: UV-B light can influence phytohormones involved in stress responses, potentially affecting growth and development. 4. Other Colors: Green light: Plants are generally less sensitive to green light, as chlorophyll reflects it. Other wavelengths: While less studied, other wavelengths can also influence plant growth and development through interactions with different photoreceptors and phytohormones. Key Points: Cross-Signaling: Plants often experience a mix of light wavelengths, leading to complex interactions between different photoreceptors and phytohormones. Species Variability: The precise effects of light color on phytohormones can vary between different plant species. Hormonal Interactions: Phytohormones don't act in isolation; their interactions and interplay with other phytohormones and environmental signals are critical for plant responses. The spectral ratio of light (the composition of different colors of light) significantly influences a plant's hormonal balance. Different wavelengths of light are perceived by specific photoreceptors in plants, which in turn regulate the production and activity of various plant hormones (phytohormones). These hormones then control a wide range of developmental processes.
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Had a few hiccups. Plants ended up developing a nitrogen toxicity from too much worm casting. I simply did a flush on them with water PH’d to 6.3 and allowed the soil to dry out
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@rhodes68
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8/24 Week 6 Flower Reducing Grow nuets will Increase Bloom as we go. Want a lower EC with lots of runoff for tonight, been pretty high and its going up from here. Looking good what to say? Stretch has started but its very reasonable 8/25 Nuets changed to all Bloom 8ml/gal A&B and Koolbloom 1ml/gal EC at 1500 see if we can keep this until ripening 8/26 Resuming twice a day feeds 8/27 Giving a dose of Kangaroots for their early flower root building this is the last of that. Defoliated lowers removing all under growth Tent is getting pretty full ... maybe they are like goldfish... 8/28 Growing @ 1/2 - 1 inch per day still 8/29 Both her cuttings took so two clones of her upcoming 8/30 End of week six so Recharge for everyone! 2.5ml/gal one time The girls look great
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Budget development is nice plant is really healthy and sturdy clones have rooted in the vegetation room so everything is cool
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@BudXs
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Scrogging its way through the fence. Thanks fornlooking. Pistils are just starting to emerge, and im hoping inhave enough eeather for her to finish.
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@alexb420
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been feeding pretty heavily, flipping in a week or 2. hardest plants i’ve grown so far
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DAY 63 THE FINALE !!!!! Howdy all. I hope we are all well and in the green. This has been a very interesting and rewarding journey for me in so many ways on this journal. I have had the opportunity to run a seed of my own which has been a brilliant result from what I am looking at as I type this. It stayed really squat and has produced some somid hand grenade sized buds that smell of a diesel and fruit combination. I also picked up the lemon from her pollen chuckers genetics too. Should be an interesting cure I hope. I did find a couple of bud rot spots that had to be pulled out but with her density I am not shocked at all. I will be using the dehumidifier for their dry for sure. The Northern lights autos have also finished nicely too and I do think could go a little longer with a push but time is up and the next run is looming !!!!!!. She has some great sized spiked colas to enjoy my attention everytime I go in the room . Just like the other girl , she did have a couple of mould spots that had to be taken out but not too much of a loss thankfully. Her mutant sister will also be put into her dark 48hrs along with these as she is also done now. She has a lot less to harvest but looks so sweet and potent up close to the buds now. I took the Gorilla cookies out earlier in the week as they had finished perfectly. After 48hrs dark I used the bowl trimmer to help with time and get her off the stalks as I did find some mould on them too. Recent environmental changing has bought RH issues to the front again. They have given up some great smelling and solid nuggets that are now starting their drying out period in the nets. The rest of the ladies will be joining them later in the week until I can do a harvest report and my opinion of this amazing light unit from viparspectra. With new projects afoot and lots of re jigging to accommodate them , I am looking forward to the next few runs too. I hope you will join me for the fun and always welcome comments and ideas too. Be safe and well growmies
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@Naujas
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well, she is already showing signs of flowering, it's a pity that she didn't get to spend another week in vegetation :) Well, that's okay, she looks healthy and beautiful to my eyes:) which makes me happy :) good luck with the growing :)
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@Changman
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17-07-2024 We have decided to flip them this week as certain light disruptions have caused complications and we are going to avoid anymore. Let's see how they react to the nutrients and go from there
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A little confusing but i put my other to pineapple and the Hulkberry in this tent and send it into flower 2 days ago (14.3.2023) I believe the plants might have a nitrogen deficency but we are on it. All in all lookin good Now we have 2x TSL 2000 (300W) = 600W/120cm*90cm Plants: 2x Big Hulkberry (one topped early, one topped late) 2x Critical Kush (second largest plants) 2x SuperSilverHaze ( pretty small both plants) 2x Pineapple Kush (Had it rough) 1x Pinapple Kush (very small plant, 2l fabric pot..)