This week i turn off 1 Fan cuz it to strong for flower left 1 outside on. Flower get bigger everyday make me feel so nicely i add more nutrients to 1000 ppm before add Terpinator hope they're flowering well. Next i will add more diary new crop(Ethos seed with athena line) hope you guys enjoy it Thx you happy grow friends.

Day 49 of flower. Lovely! The Buds begin to bring flesh to them self. They grow up. The smell is a little bit diskret till now. I mean the strength of it. Sweet! SWEET! Glorious. I know for the most of north and south (maybe) it's an old wallpaper from Yesterday. But for me, its the first time I smell sticky Watermelon Zkittlez on my Fingers. AMAZING. (If in normal zkittlez is no watermelon smell) than:Like a voice of an God. "BONUS! DOUBLR XP FOR THE REST TIME OF THE GROW! YOU CHOOSE! MORE YIELD? UNIQUE COLORS?" "God(of Ganja maybe)…?" "YES? MY GROWMI?" "can i have both bonus?" WHAT THE FUCK! TRY TO DEAL WITH A GOD? What followed know is unknown. Just you heared some screams in the night. Not the funny ones. except you re an sadomasochist. Than you had really fun. I got still some aphids. But less than ever before. Still 3 weeks of flowering.. I can wait. The yield will not be big. I don't care about. I care about mouthwatering strong healthy weed. Thats why i grow. (and, i love to see them grow. But that was unexpected). WATERMELON ZKITTLEZ. I Love this plant. The colours. The height, the smell, and the sticky buds. Day 52 of flower. TRICHOMES RE MILKY the most 75% ca. The Buds re hard. The smell has changed to Haschisch. The fruity smell is still there, but getting less. Lets see. Phylaxien re 50% brown. Down under(Australia?). 20% and the lowest 5% brown. 18 days still to go. BARNEYS FARM, once again you satisfie me.. Hello @ day 54 of flower. The buds re becoming harder , and now they begin to grow up. In height. The colors of buds. Brown phylaxien, till bottom. She got 16 days to go now. Lets see if we take some amber trichoms till the harvest. The chop will be in stages, because Iwant the maturity ( is this right?) In every bud, and light helps. Day 55 of flower. The Light Spektrum has been Modified. I kill switched the blue Spektrum. In previous Grows it helps to increase the trichom productivity and faster maturity. But warning! If you kill the blue light to early, she stretches a lot.. Thank you for reading. I hope you enjoyed it. Day 55again. Aphids found! Damn! Should i defoliate the infested leaves? Day 57 of flower. I will not defoliate. I will wash the buds. Stay strong baby, youre my first photo period plant. And this is my first plant without any influences from a ruderalis.. And she is a beauty. By the way still some glass trichrome DAY 58 OF FLOWER. nothing happend Phylaxien went brown. Some new came... The buds re still hard. But they grow up.. 😛 24.09. 59 days of flower. Everything pretty. 25.09 AMBER trichomes starting on top buds. 60 days of Flowering. 27.09.... The Buds. Not soo big. But soo solid! I ve the pheno with the hard buds and slow growing but heavy earthy and INDICA lasting one! WITH THE HARD STEELBUDS YES, HAPPY!! Fruity smell is like zkittlez, but with an heavy earthy tone. Still not many Amber trichoms. But Hey we are in FLOWERWEEK 9!!! And 8-10 weeks the Breeder said. Did a defoliation cause prepare to harvest soon. And to get to the lowest benches some light, so they get harder. Trichome check says. WAIT! Gave water ph 6,5. Trichomes re mostly foggy. Still some clear Trichomes. AMBER ist not so much. Maybe on every bud 1%. Harvest, were coming closer... Boah SMOKE REPORT: First bong hit. Häh? Something happend. 30 sec later... Ok here we go, should i take another one? Its so smooth... Three minutes later... Damn my eyes, im so fxxxxxx relaxed, i liked to take a nap. Smooth A Smooth Criminal (AYE) The Buds re heavy. And the hardest i ever had. 30.09. 65 day of flower. Did a little prechop. The Rest still can ripen.

Cada tres/cuatro días empecé a regar con 500 ml de agua, el domingo va a ser el primer día de comida q le voy a dar ferti de crecimiento. Ya empezó a crecer para arriba y a ramificar bien. Apliqué hasta ahora en cada riego micorrizas de Namasté

Quite the week, finally got to transplant into a larger container, hopefully the roots open up and explore soon. First round of LST completed as well.

2024-09-07 This was a very effective Week, it started with Rain an Wind then it turned over to very hot and sunny exactly what we need here. The Outdoor tangie still looks super fresh and green, only minor signs of getting ready the colas are very glitery and you see alot of potential already super frostyhere. the revegetating Plant looks fine too. she produces some flowers.too.

The temperatures, humidity, and watering volume(if measured) in grow conditions are all averaged for the week. The pH is soil pH. Any watering done by me is well water which is 7.6 pH and 50° F. Any listed nutrients are topdressed @ ml/gallon of soil. Day 1 we started with lots of sunshine and clear skies.Then we had a pop up severe thunderstorm with grape sized hail. Thankfully it only lasted a few minutes. Day 2 we have clear skies and sunshine. The temperature is mid 70's. You can see the hail damage that occured day 1. The #3 plant was topped by a hail stone. Luckily it only got the top and didn't take out the side branches growing out of the 4th node. This was very fortunate a topping above the 4th node done by nature. Day 3 we had rain and thunderstorms through the previous night and into the morning. We had sunshine, clear skies, and temperatures in the upper 70's. That was followed by severe thunderstorms, rain, and a touch of hail from 4p.m. to 6p.m. Day 4 we had relief from the rain. Temperatures were in the mid to upper 70's and lots of sunshine. We have a few days of sunshine in the forecast 🙏 Day 5 we had lots of sunshine and clear skies. Highs in the upper 70's and 49% humidity. We needed the dryness. 🙏 Day 6 we had clear skies and sunshine. Temperatures were in the mid to upper 70's. Day 7 we had partly cloudy skies and temps in the middle 70's. Overall this week was a success. We thankfully avoided any major damage from the hail. The girls more than doubled in height and really kicked out some branches after topping.

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

Legend Timestamp: 📅 EC - pH: ⚗️ Temp - Hum: 🌡️ Water: 🌊 Food: 🍗 pH Correction: 💧 Actions: 💼 Thoughts: 🧠 Events: 🚀 Media: 🎬 D: DAY, G: GERMINATION, V: VEGETATIVE, B: BLOOMING, R: RIPENING, D: DRYING, C: CURING ______________ 📅 D85/R13 - 09/07/24 ⚗️ EC: 0.1 pH: 7 🌡️ T: 26°C H: 65% 🌊 3L 🍗 💧 💼 Flushing 5dd 🧠 🚀 🎬 ______________ 📅 D86/R14 - 10/07/24 ⚗️ EC: 0.1 pH: 7 🌡️ T: 26°C H: 65% 🌊 3L 🍗 💧 💼 Flushing 6dd 🧠 🚀 🎬 1 video, 3 pics, 6 macro pics ______________ 📅 D87/R15 - 11/07/24 ⚗️ EC: 0.1 pH: 7 🌡️ T: 26°C H: 65% 🌊 🍗 💧 💼 Flushing 7dd 🧠 🚀 🎬 ______________ 📅 D88/R16 - 12/07/24 ⚗️ EC: 0.1 pH: 7 🌡️ T: 26°C H: 65% 🌊 3L 🍗 💧 💼 Flushing 8dd 🧠 🚀 🎬 ______________ 📅 D89/R17 - 13/07/24 ⚗️ EC: 0.1 pH: 7 🌡️ T: 26°C H: 65% 🌊 🍗 💧 💼 Harvest 🧠 🚀 🎬 ______________ 📅 D90/D01 - 14/07/24 ⚗️ 🌡️ T: 26°C H: 65% 🌊 🍗 💧 💼 1st day drying 🧠 🚀 🎬 ______________ 📅 D91/D02 - 15/07/24 ⚗️ 🌡️ T: 26°C H: 65% 🌊 🍗 💧 💼 2nd day drying 🧠 🚀 🎬

Transplanting today into 3 gallon with some dry organic amendments. Coco, perlite, gaia green, EWC, Mycorrhizae will be the weapons of choice. Currently under 4000K light might change to 3000K as only 2 x 3 or 5 gallon pots will fit under the preferred veg light. Main focus has now shifted to this new run will try and get her ready for flower 2-3 weeks from today. Cheers to all fellow growers.

I wish I had more to say but these ladies are just happily chugging along! My humidity is either spiking or that probe is having... ? complications. I'll open up the windows to dry it out down there, it's not crazy to think the sub-irrigation and high transpiration of flowering is dumping water into their lung room. 🤔🤔 Also it was raining and snowing the last two days, so maybe a de-humidifier will have to get budgeted 🤓 I've never had mold issues and I don't want i start! Again, they're coming along effortlessly! Coming soon I'll probably top dress and get rid of the rice hulls, as well setup the automated watering because they're drinking so dang much! Thanks for reading and take care!

Oh yeah!!!! Apple Strudel is finishing strong 💪. Her buds have swollen up nicely, are a beautiful lime green & super frosty. She smells really potent! Started to flush her a couple days ago so she'll be getting the chop here in a few days. Excited to see how she taste after a dry & cure.

She has made it to day 35😍 I was away for most of the week. When I got back I did some more lst and took a couple leaves off. If I didn't stretch her out the plant would have been huge. The plant is also starting to flower now. 😍

Seguimos con el Seguimiento pasado con el proceso de Floracion. dando un cuidado diario y constante Led: Tesla 540 W Carpa: Indoorbox Sustrato: Bio bizz

FERMAKOR BARREL MIX – BASE IN USE (Testing on the Fantasy Feast girl we pulled out of another diary https://growdiaries.com/diaries/274722-grow-journal-by-yan402 ) (FERMAKOR BASE SYSTEM KOH VERSION diary https://growdiaries.com/diaries/278391-grow-journal-by-yan402) (Urea & Micros on the way — first week running without them) 🍶💧🍶💧🍶💧🍶💧🍶 💧 30 L Barrel – Current Working Mix 🍶💧🍶💧🍶💧🍶💧🍶 Step 1 – Calcium Nitrate (Part A) 7 L warm water (~35–40 °C) → added 45 g Calcinit, stirred until fully clear. That’s the calcium + nitrogen backbone for the feed. Step 2 – FERMAKOR PK Base (Part B) 15 L water in the main barrel → added 30 ml FERMAKOR PK Concentrate, mixed well. This forms the main P + K part of the formula. Step 3 – Combine Solutions Slowly poured the Calcinit mix into the barrel while stirring — no reaction, still crystal clear. That confirms the mix is stable and precipitation-free. 🌿 Step 4 – FPJ / FFJ Batch Added 30 ml homemade FPJ (fish + veg batch) ≈ 1 ml/L. Color shifted to a light-amber tone — looks alive and active. 🍋 Step 5 – Citric Acid Balance Added 1 tsp citric acid after everything was blended to fine-tune pH and help chelate micros later on. 📦 Step 6 – Top Up & Check Filled to the 30 L mark with plain water → pH tested with drops, showing yellow-green — roughly 5.8 – 6.0 range. Nice clean look, stable smell, no residue. 💧 Current Base Ingredients (Active Mix) Warm Water ≈ 22 L total Calcinit 45 g → N + Ca foundation FERMAKOR PK Base 30 ml → P + K support Citric Acid 1 tsp → Chelation + pH balance FPJ / Fish Emulsion 30 ml → Organic enzyme booster Result: clean amber mix, mild and balanced. I’ll let this version run for a week before adding anything. 👀👀👀👀👀👀 Observations and changes 👀👀👀👀👀👀 27.10.25 VW27 noticed some min burnt tips so I decreased Calcium Nitrate 45 to → 40g, decided to add two more elements micros and Epsom salts just to make sure they got everything, Fetrilon Combi 1 (Micros): 0.5 g, Epsom salts: 8 g 28.10.25 VW27 she seems devoid of any deficiencies, seems ready for the flip to 12/12 02.11.25 VW27 girl is looking good so I decided to stop making daily videos and do a standard once a week update. 09.11.25 aVW28 7 days since flip,stretch in full swing, first pistils showing, leaf color deep and healthy. Slight tip burn early week → gone after pH stabilized. Feed stayed clear, no residue, roots clean and sweet-smelling, did what I hope is a last cleanup and pruning🎥 10.11.25 VW29 added Phosphoric acid pH down to the schedule for flowering stage. 14.11.25 FW1 FERMAKOR PK Micros 40 → 50 ml 23.11.25 FW2 got some burnt tips, observe and act accordingly in case it worsens, diluted by 25% for this week. 05.12.25 FW3 about 2 weeks ago Calcium Nitrate 35 g → 25 g, FERMAKOR PK Micros 50 ml → 60 ml 12.12.25 FW4 Calcium Nitrate 25 g → 20 g, FERMAKOR PK Micros 60 ml → 80ml 16.12.25 FW4 Calcium Nitrate 20 g → 17 g, FERMAKOR PK Micros 80 ml → 110 ml 20.12.25 Calcium Nitrate 17 g → 15 g 26.12.25 Ffj fpj 30 →0ml 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 🌿 Day to day tasks & actions 🌿 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 Fed about 5l a day of #1 and on the weekends I do a pure FERMAKOR PK flush 2l runoff (*RUNOFF reused for tomato plants) 💧💧💧💧💧💧💧💧💧 🌱 Nutrients in 30 L #1 – FERMAKOR (progression kept) 💧💧💧💧💧💧💧💧💧 Calcium Nitrate (Calcinit / Nitcal): 45 → 40 g → 35 g → 25 g → 20 g → 17 g → 15 g = 1.50 g/L → 1.33 g/L → 1.17 g/L → 0.83 g/L → 0.67 g/L → 0.57 g/L → 0.50 g/L = 207 ppm N / 253 ppm Ca → 184 / 225 → 161 / 197 → 115 / 141 → 92 / 112 → 78 / 96 → 69 / 84 PK Concentrate (FERMAKOR Base): 30 → 40 ml → 50 ml → 60 ml → 80 ml → 110 ml = 1.00 → 1.33 ml/L → 1.67 ml/L → 2.00 ml/L → 2.67 ml/L → 3.67 ml/L → balanced 1:1 P:K + light micros (from extract) Home-made FFJ/FPJ (Fish + Veg): 30 ml → 0 ml = 1.00 ml/L → 0.00 ml/L Epsom Salt (MgSO₄·7H₂O): 8 g = 0.27 g/L → ~26 ppm Mg + ~35 ppm S Fetrilon Combi 1 (Micros): 0.5 g = 0.017 g/L → Fe 0.7 ppm · Mn 0.7 ppm · Zn 0.3 ppm · Cu 0.3 ppm · B 0.1 ppm · Mo 0.02 ppm Phosphoric Acid (pH down) + Citric Acid (chelation): as needed → First set pH with phosphoric acid, then add a little citric only if you want extra chelation Target pH: 5.8 – 6.0 (drop test yellow-green) 📦 TOTAL (corrected): Liquids (PK + FFJ/FPJ): 60 → 70 → 80 → 90 → 110 → 140 → 110 ml per 30 L = 2.00 → 2.33 → 2.67 → 3.00 → 3.67 → 4.67 → 3.67 ml/L Solids (CaNO₃ + Epsom + Fetrilon): 53.5 → 48.5 → 43.5 → 33.5 → 28.5 → 25.5 → 23.5 g per 30 L = 1.78 → 1.62 → 1.45 → 1.12 → 0.95 → 0.85 → 0.78 g/L YouTube Link: https://youtube.com/-m8h?si=A7x4Zlr2kj-_ga31

Getting closer but not quite there yet. Still looking for some more amber trichomes. At least the clear ones are becoming fewer while the amount of white ones raises. Buds are very thick now and the smell is amazing! After the daily trichome check the magnifying glasses smell deliciously sweet and creamy like blueberry ice cream. Gonna leave her in her normal light cycle until I‘m happy with the trichomes.

Hey yall, Temps were high, but under control now. My girls were droopy despite having moist soil. After a good compost tea they bounced right back. Pistol hairs are showing, haven't grown this specific cultivar before so the bud structure is a but different than others I am familiar with. Let's see what she does moving forward. I am not a super fan of these genetics. Already have new seeds I am ready to start once these ladies are done. Over all the Strawberry Diesel from Beaver Seeds is not a noob grow, you need to have your grow dialed in. And really be careful with PM. I am keeping humidity as low as I cam while still maintaining a decent VPD. Challenges with this strain definitely turns me off. Looking forward to a new cultivar, already have some genetics from Michigan, those cats are really something else, they are hellbent on being better than the West coast. And they are in my humble opinion 😌 ☺️ Pure Michigan looks good, also Honey Sticks Genetics out of Maine is killing it, their Bananaconda 4 tested over 40% total cannabinoids. They want like 3k per cut, so that won't be my next, but looking forward to new genetics nonetheless. Anyways made some new ferments, remember to use equal parts organic sugar, Jaggery is best, that is the closest form of sugar to the sugar cane plant. Cover with paper towel, 2 to 3 days later let gravity give you all that juice, don't squeeze it to get more. Keep that juice in the fridge, that is your food. Then add water to the solids and keep at room temperature for 3 months to make a vinegar. That is your cleanser. Ask questions please 🙏 Love to see others trying KNF, or simply put Natural Farming methods.

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