The Grow Awards 2026 🏆
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@Salokin
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Absolutely stunning buds
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@Pblc_10
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Heute wird die blüte eingeleitet und ein paar Fotos folgen noch. Zu sagen gibt's nicht viel nur das sie sehr gut aussehen, alle Tops auf einer Höhe sind und die seitentriebe auch bereits neue seitentriebe bilden. An 2 Stelle ist mir vor n paar Tagen ein trieb abgebrochen aber innerhalb der paar Tage sind schon 2 dafür nachgewachsen aus dem Stück was noch hing. Wie immer würde ich mich über Tipps freuen ✌️🍀
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@Dabking
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86 days from seed in soil until chopped. Roughly 40g dry weight. I ended up pressing most of it into Live rosin, however I kept some in flower form to smoke. Personally, I'm not big into the scent or smell of this strain, but it stays true to it's sativa roots and everyone who has tried it has really enjoyed it. I'm not a big fan of this strain, purely based off the fact that my nose doesn't like the smell of this plant. It smells like chicked-peas (the stuff hummus is made from). It's very odd I know. However every one who has smoked it, including myself has enjoyed it. But if I'm picking and choosing, then this one would be near the bottom. I ended up turning a vast majority into live rosin and it is much, much better. Amazing for listening to music and cleaning the house👌
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@Adam420
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Every week I love this plant more and more. I have given her molasses this week No deficiencies and her pistils are healthy as well as leaves.
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@Caertner
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Wusa. Bonzai chillt. Blüten warten auf Pollen, doch der kommt nicht... hm. Langsam wird es eng. Die Farben sind einmalig... Schönster Herbst (im Frühling) ;)
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Notes for flower week 9 (12/15-12/21, days 56 to 62) Watering Days. All feeds with nutes use either a whole ratio, or combination, of "Veg Mix" and "Bloom Mix"concentrates. These are/will be DILUTED in water until a total ppm of add-in is reached using a (Total Dissolved Solids) TDS Meter measured in PPM (parts per million). The "Veg Mix" concentrate will eventually be added-in larger, then smaller, ratios while the "Bloom Mix" concentrate will eventually replace the "Veg Mix" concentrate entirely. The ppm and ratios will be listed when I feed. Veg mix recipe is on week 3. Bloom Mix recipe is on week 5. Day 128/58 (last feed was day 124/54) Tested and Calibrated my ph pens. Fed 3 gallons of de-chlorinated tap (starting with 251ppm) mixed with 402ppm of 100% Bloom Mix Concentrate. Due to this soil showing a possible calcium deficit, I am still using 1ml per gallon add-in to test on all plants using this soil, so I added 3.0ml of CaliMagic (General Hydroponics 1-0-0) and then I ph balanced before feeding. The ph on this feed was balanced to 7.0 (7.13 last feed). I used knitting needles to help both aerate the soil and create new water pathways for the roots. (a practice I am making a new feeding standard for all my plants) I got ~20 cups of runoff (~27 cups last feed). Higher runoff volume was expected with the feed volume increase as well as previous knitting needle aeration. Runoff was tested at 6.15ph and 1800ppm (6.21ph and 2100ppm last feed). Top soil tested at 6.4,6.48,6.39,6.42 for an avg of 6.42 (6.42 avg after last feed)- next feed will be 6.8 to 7.0 ph as I'm still liking where the ph is finally at. I dont see any issues with the feed's data other than the possible calcium deficit Next Feed should be 2.5 gallons of de-chlorinated tap water ph balanced to 6.8 in +4 days (132/62). I expect I will run 400ppm and 2.5ml of CaliMagic (General Hydroponics 1-0-0) again, but no more HP2. I expect to start flushing her out with lower nute levels from that next feed point. Day 132/62 (last feed was day 128/58) Tested and Calibrated my ph pens. Fed 3 gallons of de-chlorinated tap (starting with 277ppm) mixed with 397ppm of 100% Bloom Mix Concentrate. Due to this soil showing a possible calcium deficit, I am still using 1ml per gallon add-in to test on all plants using this soil, so I added 3.0ml of CaliMagic (General Hydroponics 1-0-0) and then I ph balanced before feeding. The ph on this feed was balanced to 6.8 (7.0 last feed). I used knitting needles to help both aerate the soil and create new water pathways for the roots. I got ~17 cups of runoff (~20 cups last feed). Runoff was tested at 6.0ph and 1710ppm (6.15ph and 1800ppm last feed). Top soil tested at 6.42,6.45,6.34,6.33 for an avg of 6.385 (6.42 avg after last feed)- next feed will be 6.8 to 7.0 ph as I'm still liking where the ph is finally at. I dont see any issues with the feed's data other than the possible calcium deficit Next Feed should be 2.5 gallons of de-chlorinated tap water ph balanced to 6.8 in +4 days (136/66). I expect I will run 400ppm and 2.5ml of CaliMagic (General Hydroponics 1-0-0) again. Im flushing with these lower ppm feeds through harvest.
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I made these seeds myself, letting the Male pollinating the Female in the same tent. I dropped pollen with a paintbrush on 2 different occasions, then shook the male over the female a couple times as well. Harvested most the seeds after the female plant died of thirst, around Bloom Day 65-67, but some earlier around Bloom day 53-55. These seeds were soaked then direct sowed. Originally using 6 seeds but settled on 10. Success germination rate of 100%. Bred by Dark Horse Genetics, purchased Chem Berry D from Parkland Flowers then reproduction by moi. Who knows where this project will go. I collected a whole bunch of seeds, they seem to be very healthy.
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Day 28 from cutting they are EATING GOOD! I feel they were a bit hungry but are so happy now. They are reaching for the sky! Watered on Dec 14 with a ppm of around 900 of 6ml /gal A+B 6 ml FS 2ML golden tree. I'm seeing some signs of a few things that I have pretty much eliminated down to either a nutrient deficiency or a need to transplant either way this weekend I'm going to do it and we will see what the results are!
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@Kushizlez
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Day 24-31 (Day 25) The smell in here is absolutely ridiculous. My last grow didn’t smell even close to this bad in early flower. (Day 27) Stretch is finally all done. #6 in the back is very stout and barely stretched compared to everything else. I doubt it will yield much but I’m excited to see the nice tight colas on it. It seems to be still getting adequate light and raising it up is hard to do with a scrog net so I will just leave it. If it wasn’t getting enough light it would be stretching right? The early frost is really shocking to me. My last indoor round definitely wasn’t this caked and I’ve never had an outdoor plant on this level either. That’s also true in terms of smell too. (Day 29) I’m still debating whether I should feed anything in flower or just leave it. The only deficiency I’m seeing is purple stems from P def which could actually just be from light intensity rather than a lack of P. I’ve done some thinking and I’ve decided to only feed my small plant. What I’m most curious about is if a PK boost will actually make any kind of a difference in flower when it comes to bud size and smokability. So to test this theory I will be top dressing a teaspoon of 0-18-0 bat guano, a tablespoon of 1-4-2 Destiny launch and a half strength watering of 0-0-15 kelp extract. I’m trying to avoid N all together as I just toxed my guinea pig plants with another experimental flowering PK boost that had a very small amount of N in it. This plant in particular actually has very early signs of N def and probably will fade harder than the rest. (Day 31) Shit. Looks like #1 is starting to herm. It’s definitely not environment or light leaks so maybe it’s just genetic or the recent leaching stressed it out too much. Either way, it’s only a single lower branch and I’m prepared to cut her down if I start seeing anymore. I double checked every other budsite but couldn’t find anymore. In my experience true herms usually start pushing bananas out of the main tops and plants like mine can usually be salvaged with little to no seeded bud. But then again it’s day 31, when these things usually start to happen. I’m 50/50 on this one. I will be watching it everyday like a hawk if anymore show up. The breeder I’m using, ‘Jordan of the Island’s’ is notorious for having unstable genetics and this will be the last time I run any of his stuff. The quality is good, certainly better than most European and Dutch genetics I’ve run but I know I could do better where genetics are concerned. I can’t wait to start hunting my archive dosidos x gelato 41 and in house sugarcane.
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😁😁😁 Hi grow mates 😁😁😁 As day 43 arrived we are opening 7th week of my grow journey. Like you can see from the photos girls started to blooms wildly. Purple Lemonade is getting absolutely purple, flowers gets density and aroma. Cinderella !! Wow !! Here is an interesting one. She is huge, I never had so many flowers sites on one plant. She's tall girl 118 cm !! Bruce Banner, she is a real mystery. She started to blooms like all her sisters, but looks a little shy. I think she need just more time. From previous experiences, I know that the "shy" ones gave best results. Fingers crossed 🤞 Day 44 Purple Lemonade 81 cm Original Cinderella 118 cm !! Bruce Banner 90 cm I wish you all, All the best 😇
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Hi everyone :-) This week the buds developed super ;-) All are beautiful 😍. Super genetics 👍. Blue Cheese pheno 1 is slowly coming to an end :-) This week I will start to use up the remaining nutrients and harvest in 10-14 days ;-) Everyone else needs something else :-) have fun with the videos, stay healthy 🙏🏻 and let it grow 🌱
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Great grow. I experimented with topping and topped to earley which hurt my overall yield but after all was said and done I ended up with just over an ounce of really good top shelf pot!!!
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You don't become confident by shouting affirmations in the mirror, but by having a stack of undeniable proof that you are who you say you are, outwork your self-doubt. Nitrogen fixation is a chemical process by which molecular nitrogen (N2), which has a strong triple covalent bond, is converted into ammonia (NH3) or related nitrogenous compounds, typically in soil or aquatic systems but also in industry. The nitrogen in air is molecular dinitrogen, a relatively nonreactive molecule that is metabolically useless to all but a few microorganisms. Biological nitrogen fixation or diazotrophy is an important microbe-mediated process that converts dinitrogen (N2) gas to ammonia (NH3) using the nitrogenase protein complex (Nif).[2][3] Nitrogen fixation is essential to life because fixed inorganic nitrogen compounds are required for the biosynthesis of all nitrogen-containing organic compounds, such as amino acids and proteins, nucleoside triphosphates and nucleic acids. As part of the nitrogen cycle, it is essential for agriculture and the manufacture of fertilizer. It is also, indirectly, relevant to the manufacture of all nitrogen chemical compounds, which include some explosives, pharmaceuticals, and dyes. Nitrogen fixation is carried out naturally in soil by microorganisms termed diazotrophs that include bacteria, such as Azotobacter, and archaea. Some nitrogen-fixing bacteria have symbiotic relationships with plant groups, especially legumes.[4] Looser non-symbiotic relationships between diazotrophs and plants are often referred to as associative, as seen in nitrogen fixation on rice roots. Nitrogen fixation occurs between some termites and fungi.[5] It occurs naturally in the air by means of NOx production by lightning.[6][7] All biological reactions involving the process of nitrogen fixation are catalyzed by enzymes called nitrogenases.[8] These enzymes contain iron, often with a second metal, usually molybdenum but sometimes vanadium. Green clover (Fixation) White clover (Fixation) Red Clover. (Fixation) Yellow Clover. (Fixation, deeper roots) Sweet Thai Basil. (Terpenes) Italian Basil. (Terpenes) Chamomile.(Oil production) Borage.(Pest attraction taste) Lavender.(Pest attraction smell) Marigold(Pest attraction visual) Mycorrhizae are beneficial associations between mycorrhizal fungi and a plant’s root system. Mycorrhizal fungi spores germinate in the soil, creating filaments (hyphae) that penetrate the root cells, thus establishing a symbiotic relationship. This collaboration leads to the development of both intra-radical and extra-radical networks of filaments, enabling efficient exploration of the soil for enhanced access to nutrients and water. Consequently, these vital resources are transferred to the plant, resulting in numerous benefits for crop cultivation. Various mycorrhizal products are available in diverse formulations (powder, granular, and liquid), concentrations, and qualities. Ongoing advancements in products, technologies, and research are reshaping our understanding of mycorrhizae. Despite these positive developments, certain misconceptions persist. In the following discussion, we aim to clarify the truths and dispel the myths surrounding mycorrhizae products. MYTH #1 A HIGHER NUMBER OF MYCORRHIZAE SPECIES MEANS BETTER RESULTS. Contrary to common belief, having a higher number of mycorrhizae species in a product does not translate to better results; in fact, it often yields the opposite outcome. A plant can sustain only one association with a particular mycorrhizal fungi species. Introducing multiple species creates competition among them, which is not advantageous for the plant. The initial colonizer does not ensure the highest success; instead, it gains precedence. It is recommended to select a product with a concentrated presence of a single mycorrhizae species known for its effective performance, rather than opting for a product with multiple species at lower concentrations. MYTH #2 ECTOMYCORRHIZAE ARE EFFECTIVE FOR CANNABIS PLANTS. Although ectomycorrhizae can colonize five to ten percent of plant species, cannabis is not among them. Ectomycorrhizae do not penetrate the root cells; instead, they develop around the roots and on the exterior. For cannabis plants, it is essential to seek out endomycorrhizae. Endomycorrhizae are capable of colonizing 70% to 90% of plant species, including cannabis. Unlike ectomycorrhizae, endomycorrhizae penetrate the root cells, forming structures like arbuscules for the exchange of nutrients and water with the plant. MYTH #3 WHOLE INOCULANT (PROPAGULES) PERFORM BETTER THAN ONLY VIABLE SPORES. The propagule count specified on most mycorrhizae products indicates the presence of spores (viable and unviable), hyphae, and root fragments. However, it is crucial to note that only viable spores, those with the capacity to germinate, can successfully colonize a plant’s root system. Spores are to mycorrhizal fungi what seeds are to cannabis plants—a fundamental component enabling fungi reproduction. Consequently, even if a mycorrhizal product boasts millions of propagules, its effectiveness hinges on the presence of viable spores. Without viable spores, the product will not contribute to plant development. Therefore, the genuine value of a mycorrhizal inoculant lies in the quantity of viable spores it contains, as only viable spores can efficiently initiate symbiosis. MYTH #4 ALL METHODS OF APPLICATION YIELD IDENTICAL RESULTS. To establish the symbiosis, mycorrhizal fungi spores must be close to the plant roots. The optimal recommendation is to directly apply mycorrhizal inoculant to the roots, either in powder, granular or slurry form. This method ensures maximum proximity between the spores and the roots, facilitating a rapid establishment of symbiosis. Particularly with crops like cannabis, which have a short growing cycle, employing this technique is the most effective way to obtain optimal benefits. Alternatively, techniques such as blending the inoculant with the soil are effective, but there may be a delay in the establishment of symbiosis. This is because the roots need to grow and come into contact with the dispersed spores throughout the growing media. MYTH #5 MYCORRHIZAE CAN ONLY BE GROWN ON LIVING PLANTS. While the predominant method for commercially producing mycorrhizae involves growing them on the root systems of living plants (in vivo production), it is not the exclusive nor the optimal technique. In fact, this production approach has notable drawbacks that the “root organ culture” method just does not have (in vitro production). In vitro production occurs in meticulously controlled, aseptic laboratory conditions, allowing for the consistent generation of products that are viable, highly concentrated, species-specific, and free from pathogens. Achieving such precision and quality is impossible when relying on the cultivation of mycorrhizal fungi on plants exposed to external conditions. In conclusion, it is crucial to take all these factors into consideration when choosing the appropriate product for your crop to fully harness the wide array of benefits provided by a high-quality mycorrhizal product. STRONGER PLANT – Stress resistance. FASTER GROWTH – Improve plant structure and shorter veg time. INCREASE YIELD – Overall more biomass. IMPROVED QUALITY – Increase cannabinoids and terpenes content.
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The ladies don't seem to be hungry that much. I slightly introduced them for the first time with some nutrients from General Hydroponics and CalMag.
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A big hello to all the cannabis growing gardeners...and all the other visitors that came across my grow journal. This week i need to change the reservoir again, the plants drink solution just as I add fresh water the EC stays at 2.7 and i need to add PK and Calmag so that's why. The weather outside is very cold this whole week around -18 degree Celsius at night...this made my reservoir water go under 15 degree Celsius. Since i ran the Spider Farmer UV lights i noticed some purples on my cannabis plants i think it's their doing....i run it now for two weeks the UVs ---------------------------------------------------------------------------------- The SE 7000 is hanged at 28 cm. over the canopy and runs at 520W. This whole grow's main sponsor is Spider Farmer. You can easily obtain all the great grow equipment we use at: spider-farmer.com A big thank you to Jessie and the whole Spider Farmer crew for supporting me with the newest technological advancements in horticulture. Thanks to them what i do here is possible. Thank you Seeds Mafia for giving me the opportunity to try out your stock. seedsmafia.com/en/feminized-cannabis-seeds/moby-dick-feminized.html Plagron did send us their Contest package for the Power Buds competition . Thank you for your visit, please leave a like and hope to see you beck here in about a week.
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