Bonjour à tous. Le 5 septembre jour 31 pour ma Boy. Elle grandi doucement, je lui ai fait un Topping et j'ai laissé que 2 étages pour essayer la technique du Mainlining. Je lui donne 1ml/l de bioroots et j'ai augmenté la dose du biogrow à 1ml/l. Elle commence à avoir de bonne racines c'est cool. Voilà c'est tout pour l'instant. Merci d'être passé me voir, laissez moi un like si le coeur vous en dit. Peace and Grow for All..🌱🌿🌲

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Day 0 - She's in a red solo cup, that has been cut in 1/2, and has 5 small holes in the bottom! The idea is that she's building a tight root ball, and will explode upon transplant! Can also slip a sandwich bag over top, as a humidity dome! Day 7 - Thinking that she should have the small pot rooted by day 10.

Great nose and terps. Cookies beats out Humboldt in quality. Yield was very low but that could have been growers error

Started flushing today, day 55, seeing what looks like trichomes going amber but my scope arrives tomorrow so I’ll finally get to see exactly what is going on. But I’m sure the scope is gonna show that the trichomes are screaming that they’re ready lol

Cereal Milk (YLife X Snowman) Gave them a full day of darkness and flushed for two weeks with phd water after flushing with Advanced Nutrients Flawless Finish! UVB light did increase trichomes and it appears it sped up trichome ripening, not 100% sure on the ripening tho. WILL UPDATE AFTER DRYIN WITH DRY WEIGHT! 2/18/25 UPDATE..Cereal Milk weighted in at 39 grams so nearly 1.5oz. The scent is not so strong but it’s there and so far it’s smelling like gassy bad breath smh unless my brothers breath had my nose pallet out of balance lmfao. I’ll cure for a short time and coma back to that!

Huge thing 26/01/2025 - defol 27/01/2025 - flushed Coco to lower the strength feed from 1.3 to 0.9 EC

Esquejes

Finally harvest time arrived 🤗 It’s been a great run, though I had to improve a lot along the way. But as usual there was a way to get things done and finished up😎 After a long heatwave I decided to chop the whole tent, just a bit before I actually wanted to. But I see amber trichomes and heavy buds, so I think it’s safe to chop now, so here we go. 🤩 Can’t wait to taste this after so long watching over it🤤 More details to come.

Very happy with how this lady has performed, amazing quality buds, very sticky and dense flower with a concrete smell that I love so much, which is that kind of fruity sweet flavor that this lady is able to produce, it's been a beautiful journey, I'm gonna enjoy a lot this flowers. Very recomended guys!

All feeds with nutes use either a whole ratio or combination of "Veg Mix" and "Bloom Mix"concentrates 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 smaller ratios and "Bloom Mix" concentrate what will eventually replace the "Veg Mix" concentrate entirely with the ppm and ratios listed when I feed. Veg mix recipe is on week 3. Bloom Mix recipe is on week 5. Day 56 Took some glamor pics with black background - not really for vanity (although there's a little) but for contrast. I see more of the lockout issue better in the pics this way. - on that note, the ph seems to be working as it's been two days since defoliation and knitting needle ph correction, and the progression is way slower than it was on the last leaves at 3rd day of identifying. So with that, room VPD of 1.07kpa seems stable enough with temps about 76F/65%RH/33%ILV I released the binds today to let her grow without them until they crowd each other too much and I need to restrain - so in a couple of days at max. Day 62 Transfer day. Although at first I didnt think I would be able to until Saturday, I got pots and plant saucers today, so I ended up going ahead and doing it. Started by calibrating/testing both meters. Double checked the soil mix from yesterday as the last time I used wood ash the ph rose the day after... however this time it was fully mixed to I wanted to know if there would be a higher ph - it was the same as yesterady - 5 reading avg of about 6.35 - the slurry of 1:1 soil and 7.7 ph water was tested at 6.3 also. Made about .75 gallon of 75/25 veg/bloom juice water at 500ppm feed water. Tried to ph read the soil in the pot and seen it go from 6.6 down to 6.35 (took video) in the dry soil, so I decided to use the 6.35 new soil reading and ph balanced the feed to that. Used the needles since it was 7 days since the last feed and I am using such a small amount. Poured over needles in 8 places and pulled each out to let water down. the vacuum pulls the water down when I lift the needles. Then I mixed 5tsp of Dynomyco to the 5 gallons of new soil and mixed really good. I placed a layer of perlite on the bottom of the 10 gallon pot and then layered in some soil. Then with the help of my wife we pulled the plant out of the pot and placed it in the 10 gallon. I place back in the tent and added about a quart of plain de-chlorinated water evenly over the new and older soil to help bind them. I reduced lights by 100ppfd to have about 505 and 500 at center colas and 430 lowest on outer ring with most at 450 and 470 highest. Soil to light is 35 inches and the plant is about 14 inches so about 21 inches from leaves to lights. I left the ring off today and will rebind as needed tomorrow after she rests. Today the leaves look wilted and limp. Also reduced humidity to 60% so 58 to 65% should be the range and the temps are 73F with the lights lower. PPFD was higher with the new growth - unbound and tucked in for better cola/light position, it reads 570 to 580 on outer colas and 590 at both center branches Day 57 Getting 1 more day out of free range growth before I tie her back against a ring. So in that time I decided to take a few vanity pics. Overall the ph block seems to have slowed or stopped and she's back to growing again. Will be thinking about flip at the end of this week or so. VPD same stats 76F/65%RH/33%ILV - ppfd right at max so I'll likely tie her off tomorrow. 605 600 in center and 580 to 590 at the outer ring. Day 58 VPD stats mostly steady again today - 76F/65%RH/33%ILV - ppfd was checked after LST, measured 600 at each center cola and the outer ring measured between 550 and 590 most at 580 So as I said, I did LST today to bind her more out while the 4 center 4 colas fill the middle. I had to bind to the pot base instead of the ring as the colas are still a little short to reach for binds at the ring just yet. There's a lot of space to fill and a few (about half) of the out colas are sideways for now. Had a break at the center cola when I tried to pull it back for bind. I knew to hold the branch at the node but forgot to do it here and heard a "snap" ... taped the crack and moved on - will monitor obviously Day 59 Did more light LST to ensure the branches are growing where I want. PPFD was mostly the same as yesterday only now there are more colas around 560 than 580 on the outer ring with the center colas at 610 and 590 (front cola was tied down to spread more away from the ring and fill center better. vpd same as past week or so 76F/65%RH/33%ILV Last feed was on day 54 and the soil still seems damp so I will check again tomorrow for the next day. (Day 61) The broken branch doesnt seem to have affected either side of the split as both sides seem to have grown a little with little to no wilt or drooping leaves. Im hoping it heals okay and doesnt delay flip to recover more; still monitoring. Day 60 Did some light LST today by releasing the lower binds to the pot and attached as couple to the outer ring now. So far I only have to bind a few as most are already holding where i want them to. Took the tape off the split and seen I didnt seel the gap closed when I taped it so now Im considering a drop of super glue to bind the branch back in hopes it grows onto the other side again. If not at least it would be more secure than it is now. And since it's a main split for 4 colas, I dont want too restrict it by binding at the split and potentially cutting off the nutrient pathways. ppfd after LST was 610 and 600 after more LST and the outer ring is still ranging 550 to 580 with more at 560 now. VPD same as I havent messing with any of the variables. 76F/65%RH/33%ILV Soil is a bit dry and it's been 5 days since the last feed flush, so I have about 3 gallons of tap burning of chlorine now for a feed tomorrow morning. Might still update again later if I find superglue... found some superglue - tried to take pictures but I cant hold, squeeze the applicator, and film with just two hands. So the idea gets through, I did both sides. On a side note I discovered a root popping out of the soil from the top. Covered it up but wasn't sure if I should be concerned. Day 61 VPD same as it's been for most of the last week - 74F/65%RH/33%ILV PPFD was recorded after I turn the plant a quarter turn for the smaller colas struggling to get over he ring's edge to have more light. Most colas at 580 with a couple at 600 and a couple more at 550 - center colas are hitting 615 and 620, but I have plancs to reduce in the next couple of days now On that note, the root growing out of the top tells me that she's hungry and needs more root space, even if that means growing through the top of the soil. So I plan to transplant to a 10 gallon and flip after the recovery. After reviewing more of NugBucket's journal I realized this is why he moves them when growing 16 colas. New pots should be here Friday so I should be able do it on Saturday. So I prepped soil (using more Happy frog with mycorrhizal fungi already growing in it for a few weeks) with de-chlorinated tap water Started by ph testing the soil and the water (4 readings on soil at 5.03 avg) - added about 1/2 cup total of wood ash to bring up the ph , mixed and tested again - added water at (about 7.7 ph) and tested again... last 5 readings in soil was 6.24,6.3,6.35,6.37,6.38 avg of 6.328 - covered and let rest until needed. Since I plan to transplant in a few days I felt it would be best to 'lightly' feed tomorrow, again on transplant day, and again 2 to 3 days later. Since my wife was taking pics at this time, I could only find this one to show the roots growing into the perlite then we planted it in the bigger pot. -------- (Day 62 root base picture from above) I have a hypothesis that says these are so short because I intentionally tried not to move the plant without the base stand to keep it from grinding these up and allowed them to grow in the last 2 weeks. This is that test picture/results. I like the idea of better/more drainage, but thinking I am doing more harm each time I hear those gravel pieces crunch as it cuts those and forces the plant to look somewhere else for root space. Notice how the small root lines have no finer pieces or laterals grow out from these - I believe that is because they are so new in growth and that the perlite chewed up the smaller laterals even with little to no movement over the last two weeks I would like to see a root ball experiment that exposed the roots throughout the grow but for now I can see these roots do grow into the base perlite and need to be handled carefully if you want them to grow more freely or with a standard pot size. As you can see Im not root bound but my plant thinks it is and is growing roots out the top.

Ganja Farmer Seeds - AK 2.0 XL auto Day 19 from sprout Starting on week 3 soon Light: ViparSpectra XS2000 Watering every other day to every 2 days Started LST on the GaniaFarmer seeds. They have much faster growth than the Fastbuds growing in the same 4x4. I decided to LST only and not top the Ganja Farmer seeds. See you next week!

they have started to flower on schedule

Poco se puede agregar de este grupo, todo sigue viento en popa y el olor para que hablar. Disfruten el proceso tanto como lo hago yo.

This grow was incredible—hands down the most enjoyable in years! The harvest may not be massive as I’m still fine-tuning my system, but it’s more than enough for me. The aroma is phenomenal, absolutely mouthwatering, and brought tears to my eyes while trimming. I’m thrilled to taste the final product!

👋Top is a clean cut, no confusion for the plant, road ahead is clear, by completely removing the main growth tip, the auxin source is eliminated. The plant permanently halts vertical growth from that main stem and immediately sends its energy and hormones to the two new, evenly spaced branches just below the cut. Fimming slightly different because a small tuft of the top growth is left behind, the auxin disruption is temporary and less severe. The plant recovers more quickly and sends its energy to multiple surrounding growth points, often creating four or more new shoots from the same spot. It will eventually regain some vertical dominance after a few weeks if left to its own devices, but with a little more LST, bending the apex to the same height as the rest of the internodes, this shatters dominance, hopefully creating around 8-9 main shoots growing at equal height once recovered and grown out. Reduced environmental intensity for now and let her focus on dealing with this new stress for a week or two. When H+ ions are added to soil, the first nutrient displaced from exchange sites is typically aluminum (Al3+), if it's present, followed by calcium (Ca2+), magnesium (Mg2+), and potassium (K+), because aluminum and these base cations have different binding strengths. The order of displacement depends on the lyotropic series, where ions with a higher positive charge and those with weaker binding strengths are displaced first. The specific order of nutrient displacement is determined by the lyotropic series, which ranks the strength with which cations are adsorbed by soil particles: Al3+: Most strongly adsorbed, so if present, it will be displaced by H+ ions, leading to increased solubility of aluminum and potential plant toxicity. Ca2+: Displaced next, as it is more strongly bound than Mg2+ or K+ but less than Al3+. Mg2+ and K+: Displaced after Ca2+. The displaced nutrients can be lost from the root zone through leaching, becoming unavailable to plants. As H+ ions increase, the proportion of acid cations (H+ and Al3+) on the exchange sites increases, while base cations (Ca2+, Mg2+, K+) decrease, resulting in a lower soil pH. The amount of photosynthesis (water splitting) directly determines the availability of H+ ions (protons) in a plant. 90% of water is for cooling of photosynthetic apparatus the other 10% is split for its H+ among others things. Carbon sugars, like glucose, do oxidize in soil through a process primarily driven by microorganisms, which break down these sugars for energy. This oxidation converts the sugars into carbon dioxide (CO2) through cellular respiration, a key part of the soil carbon cycle, though some carbon may also be incorporated into soil organic matter. The rate and extent of sugar oxidation depend on factors like oxygen availability, the presence of Fe oxides, and soil redox conditions, which can all influence the process. My understanding of why we flush. Just plain water, what does it do? Strips the medium of salts and nutrients making it empty. What does that do? Triggers nutrient recycling within the plant. What's nutrient recycling? It is a natural part of plant senescence, which can be triggered once you know the switches. A 24:1 carbon-to-nitrogen ratio will also trigger. Why won't it trigger autophagy for me? Nitrogen needs to be gone, gone, gone almost. Ammoniacal (organic) nitrogen takes 4-5 times more water to separate it from soil particles than nitrates so what happens is most people jist flush the nitrates, leave all the ammoniacal in there and this prevents autophagy initiating. Nitrogen decays differently depending on its form during the dry. Ammoniacal nitrogen will oxidize in the air, leaving no trace. But nitrates do no decay and turn volatile and smelly and remain trapped until smoked, no matter how long you cure it does not oxidize. This is why you need to trigger it and begin the denitrfication process prior to harvest to get rid of all the nitrates. Otherwise, you will smoke it. Flush till autophagy begins, just make sure you add no nitrogen afterwards. Micronutrients for trichomes. Don't leave the medium empty for 2 weeks, that does nothing but reduce yield 10%ish. Trichomes are another thing. Trichomes themselves are not directly affected by flushing; rather, flushing affects the plant's nutrient uptake, which influences the development and final state of the trichomes. Trichomes are filled with antioxidants in the last weeks, which is what makes them cloudy. A lot of the processing of antioxidants requires energy and nutrients (mostly micronutrients ), so you don't want that soil empty for 2 weeks, you just want the carbon nitrogen ratio 24:1and no higher. She still wants what she needs to ripen. Processing antioxidants is energy-intensive; heat and light accelerate the rate at which THC converts to CBN. This is why you lower DLI, lower temps. By doing so, you reduce the oxidative workload caused by photosynthesis, which opens up the oxidative capacity for the production of antioxidants. THC is mostly processed at night when the plant's oxidative capacity is generally moreso "free and available" for work

They were super easy to grow but took ill very quickly and didn't bounce back all that well but no great impact on the harvest, I'm still really happy with what's on the scales and I learned plenty from this round.