Day 8: Woke up and checked on the ladies, they were bone dry. Hit em with 70 ml of AN Coco Grow diluted in my mix. Day 9: Got the new lights in today and hooked up. Girls are looking pretty good I think. Still letting em dry out a little. Gonna add a shot of Great White on next water. No nutes will be in this shot. Day 10: Still looking good. Had to stack some loose Coco around a couple as they had a good stretch going and were leaning pretty good. Also noticed a couple of brown spots on the leaves. I am led to believe after asking questions and researching, it is more than likely nute burn? No more nutes for these girls for a while. I also got a humidifier to raise humidity as it was pretty low. Day 11: These girls almost double in size every day! They would probably be a little bigger if I hadn't of tried to give em a drink of nutes earlier on! Lesson learned!! Not bad for 6 days out of the ground regardless though, I think. Got a humidifier in the tent and it stays around 50% now. Other than last night it got up to 73%. I need to get that fixed. Day 12: Nothing new to update other than they look healthy. Think I am gonna let them dry out a touch more before watering. Day 13: Gave the girls 1 cup of ph 6.0 water this morning. Thermostat battery went out and lucky my girl caught it in time. Temp got to 86° for a couple of hours. Opened the tent for an hour to get the temp back down. Humidity has been hovering around 50% for the most part. Minor fluctuations here and there. Girls are looking good for 8 days out of the earth though!! 💪 Day 14: Looking like they need another drink, dry down to around 1" deep. Gave em 2.25 cups with super diluted Coco Grow and a touch of Great White. 😳 They are doing great! 👍 Looking forward to see what week 3 has in store! Going to build a support to add my 2 CREE lights back in along with the Mars lights.

Enjoying smoking this very much. Will defo grow again

Jumped up a few feet idk yet but look like I got a winner here guys might be going in to flower idk

BIG BIG apologies to Heather from fast buds & to Growdiaries & anyone who follows. The past few months have been a massive struggle, not just with temperatures & growing weed but on a personal level. My wife has been very poorly & with covid and everything going on, it's put a massive strain on us all!! I've tries to maintain an active presence on Instagram but that's about all I've physically had time for. I've put this update together today, so far into the grow now it almost seems pointless. I lost my original Mimosa due to high temps & high RH. Moving into the attic at that time of year was a mistake. It has cost me a small fortune to keep things alive. I've had to purchase an air con unit, more fans & just more of everything to be honest. My purple punch is almost ready to harvest, any time within the next couple of days, followed shortly by Bruce Banner & Kosher cake. I wont be winning any awards for this Diary & I feel bad as I was supposed to be show casing what 420 Fast buds has to offer & I've failed...miserably. I hope you can make sense of all the pictures I've included....just a mass photo frenzy over the past few weeks. Thanks to everyone & all your comments. Wishing you all the best. One Love ❤️

At this stage and after dealing with such tall plants in such a small area it was getting more and more difficult to get around each plant. Thus making it very hard to spot any deficiencies such as mold and rot. The colas that were up close to the light were starting to show signs that they were going to get some light/heat damage as the leaves were getting fried. With all the supercropping, made some make shift crutches to help support each bend. Duct tape was also used to support each bend. The colas were starting to frosty up this week and it was very exciting to see

Everything about this strain is amazing. It grew very easily, requiring no additional nutrients and having no deficiencies. P2 (the one I harvested) was short and bushy but had some massive buds all over it. I dont think I have anything smaller than a golf ball. The test branch that broke off a few weeks ago is any indication of how it will dry, they will be very dense, almost rock hard, and caked in crystals even after a trim. P1 was a massive plant, 30 inches tall, with 15 giant cola budsites and tons of golf ball sized buds on the underside of the branches. If I had used something to support her she probably would have doubled her already massive buds. Ended up with 102g from p1 and 90 from p2. 0

BM coming along nicely, I’m just keeping up the defol and looking to get bulk bud sites I’ve got a feeling she’s about to stretch out this coming week

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.

Everyone is thriving! Things are going fairly well. Had a rough start but now everyone is living their best life! 🤩

Ha una bellissima struttura... Una su 3 sa già molto di forbidden fruit. Non molto resinose ma sono molto curioso del risultato finale

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Plodding along

So i had some some confusion going on i though it turn out to be a male since there was no white hairs so i kind of just let it go thinking of breeding it with 2 clones of NYCD was kind of busy to put up pics but to my surprice turn out to be a female so was kind of happy but mad lmao 😂🤦‍♂️AND ITS ACTUALLY DAY 19 OF FLOWERING

10/20 week 5 We have no complaints on the grow, at all. Literally nothing to address. God has been kind indeed Top dress nuets at next feed. Just maintenance, keeping the low end clear etc. Due to falling temps think the watering/feed will wait another day. Gold Leaf - Finally going vertical, two inches in two days so keeping an eye on it Green Crack - Close to topping day for her will take care of it on the top dressing Bruce Banner - finally hitting her growth as well watching Gor Glue - Just looks great not sure on topping here either GSC - Man what a turn around may regret that 3 gal pot. Cutting back on the special kanga she was getting to help the roots, seems to have worked. 10/21 Fed and top dressed - topped 10/22 GC-BB-GL all recovering from topping Plan to flip tent in a few days about the time they finish recovery Dialing back Nitrogen by switching from Fish Mix to Bio-Grow think we at the upper range of it. Had some mag spotting on the leaves of the BB think its due to the heat getting out of hand the other day (90 F for about 1/2 hour ) going to keep cal-mag in the mix just the same 10/23 After looking at the tent this morning I am seeing some small signs of Nitrogen being a tad high so ending for now the bio-grow but will continue the Bio-bloom Have to head these things off at the pass so trying Last run of kangaroots its done what its going to do by now since we aint fighting root eating critters 10/24 Fed as shown, basically its just a watering Watching leaves flipping within a day or two 10/25 Tent flipped to 12-12 10/26 Looks just great god willing and the creek dont rise we on the right path Video is on the Green Crack Diary only net is slow today Running some Big Bloom see how it does

Hello everyone week 2 of flower has passed for this Gelato auto 🍦 Spider Farmer SE7000 80% have a great day and wish you all happy growing 😎👨‍🌾🏻

Well I'll say I didn't put as much time into it as I should have but it was quite or a pretty fair grow considering it's my first time growing anything.I've learnt alot and looking forward to my second grow

I wait now its all okey if you see something text me i learn and check my youtube profile WeeDay thank you Have nice day my Friends happy new year 😜🤙

*01/24 - Week 3 Veg - Snapped a cola when adding bend clips, All clips have been removed - Uptake in nutrient feeds - Lite LST training - Lights running 18/6 - She shot up quickly in a week and 2 days - grew 6.5 inches ( 10 Inches total ) *01/27 - Mid Week 3 Veg - Uptake in nutrient feeds - Normal LST training - Lights running 18/6 - Retied up her main cola - increase in CAL-Mag feed.

Hi Growmies, She continues to develop nicely. The rootball continues to expand and nested itself right above the airstone. She is very thirsty, finishing a good 10l over the course of 5 days. I have opened my last atami rockzbastic tester and added a ml per liter. Seems like the buds start stretching around the colas now, so pretty much half time +- a week.

WOW LOOK AT DAT!!!! MADE A HINDUGOD TEA FOR DAT PLANT ON DAY 44!!! ON DAY 45 PLANT DRANK UP DAT VERY VERY GOOD TEA!!!! ON DAY 46 DID A MASSIVE DEFOLIATION AND TAKING OF BUD SITES!!! IT WAS ABOUT 50-60% OF DAT PLANT DAT IS VERY VERY MASSIVE!!!! SUN AND RAIN GOD WORK VERY VERY GOOD TOGETHER DIS PAST WEEK DAT IS VERY VERY GOOD!!!!!!😎