I was very shocked on how fast it grewand how much it produced very great strain a must for you Indica lovers very strong I went to about 80% red hairs perfect smoke a lot of cannabinoids and a lot of leftover sugar leaves great for lovers of bubble hash

The plant is drinking over 3 gallons of water every day. I’ve lowered the PPM’s to 600. Everything seems to be ok now. I will try to change the reservoir water every 5 days from now on. She started to smell amazing! Very lemony 🍋 P.S. Lowerd the TDS to 550 PPM on day 46. Also just realized that I stressed my plan with to much light. I moved the light at 13” and dimmed to 95% ... I will continue to dim it 2% every day...

F29 beginning of 4th week of flowering SD3 - initially sweet orange then engine grease SD2 - initially sharp vaseline then engine grease mixed with kerosine.I personally like SD2 more. Even with the stunted growth. SD3 is getting yellow from the bottom and i dont know what to do. I had thrips so i sprinkled diatomaceus earth on top of the soil and rubbed some on the fan leaves and stems. Sorry for the reddish pics

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9.7.2k24✅ 💚 Flowering 🌸👌 Nutri: Plagron Alga Bloom = 4 ml/l Plagron PK 13-14 = 1,5 ml/l Plagron Sugar Royal = 1 ml/l 🌹🌹🌹 Fan adjusted and large leaves torn off 🌿 13.7.2k24 + Biobizz Alg-a-Mic = 4 ml/l

This week i flush the roots with tap water ( PPM : 310 , PH : 7.5) after i add water with 0.7 grow powder and 0.1g of Booster PK+ to reach 720PPM and adjust PH to 5.8 ---------------------------------------------------- -Daytime temperature: 27°C -Night temperature: 23°C -Humidity: 45-65% -Lamp: Mars Hydro FC3000. intensity 80% at 40cm from the top leaves -Room: Mars Hydro 100x100x180cm -Extractor: Mars hydro 402 CFM Max. power 2/10 -Substrate : 70% coco, 25% perlite, 5% vermiculite. My instagram : https://www.instagram.com/p/CuMhQ_BsjRP/?utm_source=ig_web_copy_link&igshid=MzRlODBiNWFlZA==

Topped Fendi 2, 3 & 4 this week. Also defoliated the oldest leaves that were toasted. Also set up an indoor garden in my living room with some storage shelves and moved these lil ladies in there.

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.

End of Week 15 (8th week of flower) Still cruising, everything has been running very smoothly and the smell is just undoubtedly off the charts. The ladies are showing off some colour and are fading naturally bringing out hues of orange and purple. I also noticed that the leaves and buds closest to the lights are showing significantly more colour that the ones that are further away. The colas are also getting heavy and there are some side colas that are hanging and needed to be reinforced to keep them upright. (This is a good thing obviously) I know I said I would start the flush (not giving any more nutrients/top-ups) but I decided to give them a small dose of Boom Bloom just to give the ladies that final boost. I boosted them in the middle of the week and the flush has begun after that. Only water from now until harvest. Pest Report: None Smell Report: HEAVEN

A really good plant. Gave a okay yield. 60g dry all covered in resin! Smells really funky little citrus but also very 🧀

Procede tutto egregiamente. Son riuscito a coprire la rete quasi per intero. La punta di alcune foglie si stanno ingiallendo, ma non è importante visto che siamo quasi vicino al raccolto. Inizio della seconda settimana senza nutriente per pulire le piante. Spera che la prossima settimana sia di raccolto. Saluti (A)narchici 🖤❤️ Doctor Cannas

Hellow growers. Not quite sure whats going on but im now under the impression this isnt an auto as labelled. Lights have been on an 18/6 schedule but now i have set them to 12/12. I should be seeing pistils by now if it was an auto lol. I aint mad if it aint but i have veged a monster. Her stem has lots of girth her canopy is nice and even. Defoliated 22/11 Yay positive they are not automatic. So correcting info.

Defoliated fan leave, week 2... WC1 Has the strongest smell WC2 is taller with greater internodal spacing

Die Ladys haben sich hervorragend entwickelt 😄. Die Lichtintensität wurde von 25 % auf 50 % erhöht, mit einem Abstand von etwa 60 cm zur Krone 👑. 💡PPFD ca. 500 Happy Growing 🙏👋

Day 85. Began flushing. 1 more week to go

She stretched much because no space, hope to adjust her when I will chop the first Wedding cake. Removed just some big fan leaves

Info: Unfortunately, I had to find out that my account is used for fake pages in social media. I am only active here on growdiaries. I am not on facebook instagram twitter etc All accounts except this one are fake. Flower Day 65 since time change to 12/12 hrs. Hey everyone 😀. We arrived last week. The lady developed very well to the end 👍. I am very curious how it will be. As always, it is left in the dark for 48 hours before the harvest. The harvest update is coming next week. Until then, I wish you a lot of fun and all the best ☺️ You can buy this Strain at : https://www.exoticseed.eu/ Type: Herz Og ☝️🏼 Genetics: Larry OG X Kosher Kush Indica 60 % / Sativa 40 % 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Fertilizer: Green House Powder Feeding ☝️🏼🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.5 - 5.8 .

* *********** Week 11 - June 20 to 26, 2020 - Days 71 to 77 from germination *********** * These girls have been continuing their growth this week and looking better all the time. GSC2 still slow though and will not have much yield. Her leaves have turned very dark this week due to lockouts I suspect. Her hairs are still very white and coming out pointy looking for pollen and swelling. GSC is still swelling and her buds are bigger at the end of the week. Purple colours also coming out in her. The big girl has done well being squished in the corner as I had to put the two in one tent this week. The frost in GSC has been coming out for the last two weeks and is really getting sticky this week. The pH is still crazy high for the girls but they are pushing through this issue and finishing up. These are very resilient plants and I am impressed with her vigour!! Still giving them feedings in the 3.0 pH range to help as her runoff is still coming in at mid 7’s......for both girls. GSC has been feed hard because her leaves have a nice pale colour, unlike GSC2, so keep her going and swelling. They were given a heavy watering of 8L each on day 71 to find out where the medium is. They were 7.9pH when started and last runoff was roughly 7.1pH......should have gone further to bring down more but stopped there so I didn’t flush out all of the feed since they have a couple fo weeks left. The hairs on GSC are turning more of a tan colour rather than snow white. I suspect she they have roughly this week plus another yet before thinking about harvest.......I see them going to 84 days roughly, 12 weeks. GSC bud sites are getting pointy this week. Added bamboo steaks to GSC to tie the long branches to and support her weight. GSC2 less so and are still looking more round as she continues to fill in her buds. GSC stems have been turning purple more and more this week. Suspect it is a combination of pH and stresses with temps. GSC2 was tied more this week as well to let more light in closer to the main stem. This paid off as well as she is stacking the lower points more. She, GSC2, has also paid a bit of a price over the last week because she was kept in the flower tent with other more mature girls. The environment in that tent was striving for 76 degrees and 51% humidity but GSC2 wants 82 degrees and 65% humidity........didn’t have much choice😢 Fast Buds has rocked this strain and dialled her in after the generations of breeding!! She is very frosty for an auto and had she been given the correct watering, she would be considered an easy grow In my opinion! The two girls are growing very different but that is grower related to transplant and not genetics. Awesome job Fast Buds......the girls are keeping me smiling......and scratching my head at the same time👍👍👍👍 Little more detail....... June 20/20 - Day 71 - 6L low ph flush of plain water @ 4.0 to bring down pH..........3L each girl. - Followed with a low pH feeding of 4L watering with Rezin, Liquid Wt, CalMag, B52 @ 2ml, Piranha @ 1ml, Voodoo @ 0.5ml/L, = 1170ppm and pH 4.4 - GSC1 tops are getting lots of purple in the bud. - GSC1 is filling in nicely and top leaves are starting to fade yellow. - GSC2 is dark😞 June 21/20 - Day 72 - continuing flush with 12L of plain water pH to 3.3 to bring down pH. - 6L given to each girl. - added bamboo stakes to pull GSC1 apart and open up the middle bud sites to more light. - GSC1 is 38" tall and 36" across now😀👍 - GSC2 is 20" tall and 24" wide👍 June 22/20 - Day 73 - 2L each watering with Rezin @ 1ml - hairs are turning more red and more white to tan now. - GSC1 is closer.....getting to home stretch soon. June 23/20 - Day 74 - 5L - Massive @ 3ml/L, Rezin & L.Weight & B52 @ 2ml/L, Vitathrive & Dual Fuel @ 1ml/L = 1110ppm - GSC 3L, GSC2 - 2L - they are getting close to the end so getting the last bits of everything into them😀 - noticing GSC1 top cola may start to bleach out a bit. - GSC2 feels like she has stalled. June 24/20 - Day 75 - watering 3L each with Massive & Terpinator @ 3ml/L, Rezin & Vita & L.Wt @ 2ml/L, Dual Fuel @ 1.5ml/L, CalMag @ 1ml/L = 1385ppm and pH to 3.9...crazy! - moved the two girls together today as the other two are going into darkness now, they are done. June 25/20 - Day 76 - Dry out day - GSC is doing well with her buds filling in now and firming up. Top leaves are drying more. - GSC2 is dark.....F......plain water and not much more we can do. June 26/20 - Day 77 - 7L watering with Rezin and Sensyzime @ 2ml = 75ppm and pH at 4.0 - 4L given to GSC and 3L given to GSC2. - Staying with RO water now.......tap water appears to have been an issue. - too bad the ph was such an issue.....GSC would be a monster😞 - run off numbers in pots: GSC 7.6pH and 780ppm GSC2 7.6pH and 1850ppm (she has stalled) Awesome strain Fast Buds.......will be running her again!!!!!!

08/11/25 - Chunkadelic 1.5L 5ml per L microben terra actus😋