Eccoci entrati nella 3°settimana di fioritura.queste papaia cookie mi stanno sorprendendo.belle e sicuramente buone.hanno una struttura ben forte. Stanno iniziando pure a profumare in modo spettacolare.buona buona davvero.. Quando sarà pronta vi dirò anche com'è a livello di gusto e effetto stupefacente 😂🤣😂🤣

08/29/2018 Been a hot week but the girls don't seem to mind,90s in the day 82° at night and sticky,muggy weather. Their leaves all pointing ☝️,lets me know they are happy ☺️ .watered with plain water they were pretty dry pots weight was very light. Will feed and water in in morning sleep well and medicated😎 08/31/2018 Just a note today #1 is very green compared to the other 4 plants, could be potted plants running low on nitrogen? My soil has plenty according to soil test. I know last year's crop in soil was pale like other 4 plants, maybe biochar is helping soil retain it's nutes better? Year 2 for biochar, first year could have tied up some nutes....hmmm? Ps Last feeding today Fox farms big bloom at heavy feeder dose 1/2 cup per gallon, should see nice gains this week! 🙏🙏🙏. Pss. G GTH #4 loosing her smells, #3 smells of Skunk and coffee ☕,#2 minty chlorophyll orange,#1 menthal,skunky but very lite scent. Should I pollinate a branch of each? Oh my God the pressure! Do I have enough pollen? Oh sorry for rambling on just smoked lemon sour diesel and thoughts very racy😀 Got to garden see you next week 😎😎😎😎😎😎😎😎😎😎😎😎😎

Great week continued flowering did notice diet went from one feed to two feeds growing beautifully starting to see crystals on leaves or whatever makes leaves sparkle there is a lite smell but nothing to crazy

Buding in progress ✌️

the small ones take their rhythm😄 this week I start with bio-grow 2ml / l alternating day if not day. They begin to notice odor inside the closet, filter works ok👍😅

🙃

Giorno 3 annaffiata con 2,5L di acqua

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 Status First day feeding the Fantasy Feast girl with this base mix. Too early to tell how she’ll react, but so far everything looks clean and balanced. Ca + N from Calcinit and P + K from FERMAKOR should be plenty for a gentle start. Citric + FPJ round it off nicely. We’ll see how she takes it over the next few days before deciding if she even needs the urea and micros. 💧 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. 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 Day to day tasks & actions 🌿 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 19.10.25 VW26 – Fed 3l of #1 → 2l runoff 20.10.25 VW26 – Fed 3l of #1 → 2l runoff 21.10.25 VW26 – Fed 3l of #1 → 2l runoff 🍶💧🍶💧🍶💧🍶💧🍶 💧 Nutrients in 30 L #1 (Veg Strength) 🍶💧🍶💧🍶💧🍶💧🍶 💧 Calcium Nitrate (Calcinit / Nitcal): 45 g = 1.50 g/L → ≈ 225 ppm N + 150 ppm Ca 🍶 PK Concentrate (FERMAKOR Base): 30 ml = 1.00 ml/L → balanced 1 : 1 P : K support 💧 Home-made FFJ / FPJ (Fish + Veg Batch): 30 ml = 1.00 ml/L 🍶 Citric Acid (Chelation & pH Balance): 1 tsp (max) = 0.33 tsp/L → add only after checking pH 💧 Target pH: ≈ 5.8 – 6.0 (drop test – yellow-green zone) 📦 TOTAL: ≈ 105 ml / 45 g inputs per 30 L (≈ 3.5 ml / g per L active mix) 🍶💧🍶💧🍶💧🍶💧🍶

Thanks God🙏😄

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.

Ok so, This is week 12 for this baby, and she just get the first Organic Compost Tea of the hole Season. She is a very Grateful plant who pardon me for all my beginners mistakes.

last feeding,ripping for 1 week then harvest my 1st grow yea😎 they turnedcolor durning harvest moon!!!! added veido today

🍊 Correction time! Alright guys, I have to admit — I totally mixed things up somewhere during transplant 😅 Turns out this one here is actually Sweet Mandarine Z, not Mental Rainbow. And the one that’s listed under Sweet Mandarine Z is in fact the Mental Rainbow 🌈😂 Unfortunately, GrowDiaries doesn’t let me edit the strain name anymore (thanks, GD 😩), but I wanted to make it clear for everyone following along. 👉 So just to keep it transparent: – This diary = Sweet Mandarine Z 🍊 – The other one = Mental Rainbow 🌈 Both are from Sweet Seeds, and both are turning out absolutely amazing 🔥 If you enjoy my grows and want to see even more updates, follow me on Instagram: @Dendegrow 🌿📸 I post there more often — with extra tips, tricks & grow insights 🌱💡 🍊 Korrektur-Post! Okay Leute, ich muss zugeben — ich habe beim Umtopfen wohl die Pflanzen vertauscht 😅 Diese hier ist nämlich Sweet Mandarine Z, und nicht Mental Rainbow. Und die, die unter Sweet Mandarine Z läuft, ist in Wahrheit die Mental Rainbow 🌈😂 Leider kann man bei GrowDiaries den Sortennamen nachträglich nicht mehr ändern (danke dafür 😩), aber ich wollte das hier klarstellen, damit alle Bescheid wissen. 👉 Zur Übersicht: – Dieses Tagebuch = Sweet Mandarine Z 🍊 – Das andere = Mental Rainbow 🌈 Beide stammen von Sweet Seeds – und beide entwickeln sich absolut großartig 🔥 Wenn euch meine Grows gefallen, folgt mir gerne auch auf Instagram: @Dend 🌿📸 Dort poste ich noch mehr Inhalte mit Infos, Tipps und Tricks rund ums Growen 🌱💡

This is my first grow and I’m excited to start. I will be growing in a space tote (2 50gallons stacked on each other with 2 150w lights and will be adding a 3rd soon ).Took the glookies seed 3 days to germinate via the paper towel method. Once it sprouted I immediately planted into its final home a 4 gallon pot. While the glookies were germinating I learned of a seed bank near my area which recently opened and they sold already rooted clones. So I purchased a doc og clone and planted it at the same time I planted the germinated glookies seed. I planted both and then watered until water started draining from the bottom. I used pride land’s premium potting soil as i was told that it stores enough nutes for 3 weeks.

As of day 21, the Blackberry plant is doing well! It is growing vigorously and will need to be controlled as it increases in size. The FIM has already helped a little, but I have started some LST with the Atlas plant trainer to start making the canopy wide and flat. A few of the newest leaves have the very start of yellowing in their tips, so I think this plant is maxing out at 1.1-1.2 EC. I am going to keep it around 1ec for the rest of vegitative growth, as EC can drift upwards in the reservoir very slightly while the airstone is running. Runoff, PH, and other parameters are right where I want them! I have a new gallon of Calimagic coming, so I am switching back to it this week in preparation for early flowering. Thanks for reading, happy growing, and stay safe! 👍🌱 Day 24: LST continues, the plant is growing quickly and is very lush. Outside of removing a few low growth tips that will never develop, I am going to try to leave as many leaves as possible. If this maxes out my humidity I will start taking a few lower leaves, and those that are too tightly squeezes in the center of the plant. Considering the plant's size as of day 24, I am hoping the flowering stretch isn't too strong or I will have to really work to contain this plant! Day 25: earliest signs of flowering. Day 26: runoff quantities were edging towards being too low as the plant has more foliage to transpire through, so watering adjusted to 5x per day, 15 second intervals. This is an increase from 60 seconds per day of watering to 75, and should accommodate the needs of the plant as it continues to grow.

Clip is from my YouTube channel. Didn’t have many pics of this week, was only filming clips for my grow channel.

Going into week 3 of flower in a day or two. I believe today is day 20 of flower. But they're looking beautiful! Some flowers are already starting to develop some trichomes. Excited to see what these babies will throw out!!