Really happy to harvest this girl. Made sure I pushed her to the max. Just about 70 days. She was done around 65. 14hrs into pre fower and beyond. I find that with High ppf with less hrs. Makes for much better phenos. Really happy to say. This is SUCH A 100% TOP strain. And it'll be 500% a auto that I'll repeat Mind you I've hardly ever repeated any strains. Except mimosa X orange punch auto and super lemon haze. And a few CBDs. So, if anything that should speak volumes to me saying this is a tip top strain. Going to run her with one of their new autos, apple strudel is meant to have very high terps. All about the taste. And this Apricot Auto from Fastbuds has this in spades.

Fed all four twice with half a gallon nute water, PH 6.3, day 43 and 49. Video and photos from day 50.

Piante sane toppato quelle che sono arrivate al 6º internodo

This week I Supercrop all the plants and spred them out over both lights. One more week of Veg and they are ready to explode Check me out on Instagram @growmorestressless

So Day 60 of 12/12 and the girls are ripening perfectly. Trichomes are mostly cloudy but I think they need a few more days for sunset sherbet and another week or 2 for the Plat. GSC. Obviously the amnesia haze will go for another 3-4 weeks. Hope you guys enjoy the update ✌️🏼

watering with liquid karma, bud candy with a touch of molasses inbeween feeding ending the week adding some fox farm Cha Ching transitioning from beastie bloomz

Potted up as she was Rootbound Still only feeding biobizz grow

Chop day will update with weights when trimmed and dry I think about 500g. Dry

Fun one to grow even in veg its exciting because the foliage is fuckin Jurassic like it's a beautiful thing. Had some high ph towards the end so I would say theres plenty of room for improvement but all around this was a decent grow and this strain is a classic

Mon: Day 71: Chopped small plant. Day 73: Watered big plant Day 76: Watered with just phd water.

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.

WEEK 8 (Day50-56) Week No. 8 went quite smoothly. One of the plants still has a slight deficiency due to the intense light, while the other has stretched way too aggressively. At one point, it was almost 15 cm taller than its neighbor, which I didn’t like at all. So, I took a rather bold approach. Using supercropping, I brought the plant back to approximately the same height as the others. I bent the shoots and stabilized them in the new position using plastic training clips and some tape. This was done just before the photos were taken, so they don’t look their best at the moment. However, I’m confident it will work out well. Other than that, I haven’t changed much. The lighting remains at 24 hours, and I slightly increased the amount of fertilizer again.

Flowers filling out nicely this week!! She is fattening up very well!

Acapulco Gold has been forming some promising looking buds 👌 I have had to increase waterings this week as the plant is becoming increasingly thirsty. The branches are very heavy for the plant now, and they're beginning to buckle under the weight, so I might have to stake the plant. Because it's got so big now. I turn the plant round each day to evenly distribute light. It's become difficult due to the bendyness of the plant now, so I have to be very careful now whenever I move it. The plant has done really well this week, actually, and hopefully, we can be done in the next few weeks, which would be great. This has been the fastest and biggest plant I have grown yet. I'm very impressed. I have increased the waterings and am trying to give correct nutrients. However, I am also using Ecothrive dry amendments as always, and because of this, I don't know how many nutrients to add. The plant is so big now, I don't think I am feeding enough. If you have any ideas or suggestions, I'd appreciate it. Leave it in the comments 😁 I am having trouble assessing the nutrient requirements as the plant has always been a light green, but it is really beginning to go yellow. Here is what I did this week. 12.9.25 I top dressed the plant with Ecothrive dry amendments. The following amounts were used for this 8 Gallon pot; 💚1 TBSP Ecothrive Life Cycle 💚1 TBSP Ecothrive Bloom 💚 2 TBSP Diatomaceous Earth Here is what I did this week. 12.9.25: I watered the top dress in, with 6.5L of dechlorinated water PH'd to 6.0 with; 💜 2 TSP Sea K 💜 2 TSP Biosys 💜 8ml Trace PH: 6.0 PPM: 597 13.9.25: I watered with 2L of dechlorinated water PH'd to 5.9 with; 💜 .5 TSP Bud Explosion PH: 5.9 PPM: 678 15.9.25: I watered with 6.5L of dechlorinated water PH'd to 6.1 with; 💜 1 TSP Bud Explosion 💜 1 TSP Sea K 💜 8ml Trace 💜 1 TSP Biosys PH: 6.1 PPM: 685 16.9.25: I watered with 4L of dechlorinated water PH'd to 6.4 With; 💜 7ml Trace 💜 2 TSP Sea K PH: 6.4 PPM: 552 The fungus gnats have really increased since I did a watering of the whole tent. I have some more sticky traps set out, and I will not water for several days. Once it has dried the top soil, I will add some more Diatomaceous Earth to the top 5cm. Thanks very much for checking out my diary this week and for hanging out in the comments. Advice or encouragement is appreciated. It's been a fun week! 😁💚🤞🌱👌🧡

Thick root system. Currently she is competeing for grow space against the larger Bermuda Gold

Jour42 defolliation Stretch 10 centimètres Jour47 arrosage avec de l'eau ph6.3 à laquelle j'ajoute 1ml par litre d'eau de topmax biobizz

Beginning of the 10th week of flower. Shouldn’t be too much longer now. I will add some bud and trich pictures this week.

I made too many mistake to comment light was to high early in the grow I forgot to transplant, I fed it veg nutrients for 2 weeks into flowering and RH went down to 25% at the end and stayed at 25% through trying to dry

(Have been thinking about it, decided to just do both runts under one diary and just using the Green Sensation on them both. Had only used growdots on the other one, but will be bringing the other runtz into this diary aswell) Beginning to add the Green Sensation nutrients this week. Really curious to see how she looks in the next 2 weeks now that its being added!. But these Runtz are growing well, looks great to me so far nothing crazy , bit different pheno then my other grow but I'm happy with both .. Can't wait to see how they flower fully. Not much else was done, I do regret not training but wanted to let it do its thing , didn't have the space for anything big (I never go for massive, one of these days I'll veg longer tho just for the experience of it) Had cut off a handful of leaves that were laying on each other. Did alil form of lollipoping but not extreme. And only plan besides Green Bay is the Recharge will also be used 1x weekly. Lights are currently around 32 DLI roughly 700/750ppfd off the top of my head. I'm thinking around 40 I may push to peak but we will see, no added CO2 besides environmental atleast its above 500 pretty steady raises to 8/900 amd alil higher when I'm in talkin shit to them. The water input is picking up in frequency aswell. Watering every other day still due to how cold it is they are drinking slow but their just about 3/4s of a gallon currently.. Temps have been way lower this run then I really wanted just last heater I had decides to quit on me.. big area so tough to replace that thing and of course it was just out of warranty lol by 2 months. The one is getting some purples on it this one's pretty light green , ec is in range after a quick lil media test, had been curious if she was hungry so decide to check did alil runoff when watered prior to feeding the plagron. Ec was fine and PH was alil low so bringing that up as I feed. Besides that tho , their smelling really sweet.. literally like a pack of runtz already ...anxious to get to smoke some of my first try at a runtz plant! As always I appreciate everyone's time checking these things out.. thanks for your support and encouragement. And another big thank you to Zamnesia and Plagron for throwing this together!! Been a fun contest so far.. Beans: https://www.zamnesia.com/uk/ https://www.zamnesia.com/us/