Всем привет друзья! Растние растёт не по дням а по часам. Набирает жирок на шишках полным ходом. Очень хорошо кушает Цветёт и пахнет Всем мира и добра и хороших урожаев!

Going well gonna end up transplanting sometime this week or next week just trying to give it some time to recover from the topping in the added nutrients. Just want to see how she’s going

I'm greatly impressed!

Soooo, da mir die lieben einen Ersatz Steckling zugeschickt haben sich aber mein erster einigermaßen erholt hat, dachte ich mir wir starten hier noch ein kleines Projekt auf meiner Fensterbank über den Sommer Hinweg. Würde sie jetzt gern noch eine Woche entspannt ankommen lassen im neuen Topf und dann schon mit dem LST Training beginnen. Muss sagen den Bio Tabs Dünger habe ich diesen mal nicht abgewogen und einfach mal von allem etwas in die Erde geschüttet. Denke da muss ich mir dann eh in den nächsten Monaten Gedanken machen wie ich die Lady am besten düngen werde :D Habe den Steckling mal vorsichtshalber aus dem Zelt genommen da er mit den Anschein macht gezwittert zu sein oder in der Blüte angekommen zu sein was ich super komisch finde Bin sehr gespannt was hier auf meiner Südseite passieren wird. 24.3 : da das Wetter hier bei mir die nächsten zwei Wochen eher schlecht ist und ich der Dame eine gute Licht Zeit gönnen will steht sie jetzt die nächsten Wochen noch mit im Zelt, solange ich dafür noch Platz habe. Denke ab Mitte nächsten Monat sollte aber die Sonne so lange scheinen das es kein Problem sein sollte sie auf die Fensterbank zu stellen, ab Mitte Mai kommt sie dann komplett raus.

🌸🍊✨🍭🌸🍊✨🍭🌸🍊✨🍭🌸 Back at it with Kannabia — huge thanks for the NEW EXCLUSIVE Upcoming Kannabia's seed Launch 🙏🍨🍊 Grateful for the trust and for everyone following along, I’ll run her clean and showcase what she can do. Dessert-party goals: berry–citrus sherbet terps, creamy finish, tight stacks, easy trim, zero drama. Veg 24/0, clean manifold + LST, flip on a happy, even canopy. Coco’s fresh, seed goes in now. 🚀 Added on 12.10.2025 🌞 Light conditions: Limited direct light for the first 4 weeks — ~4 h/day on weekdays and ~10–11 h on weekends due to tent sharing and work schedule. 🌸🍊✨🍭🌸🍊✨🍭🌸🍊✨🍭🌸 💭❗💭❗💭❗💭❗💭❗💭❗💭 ❗Events & thoughts worth noting❗ 💭❗💭❗💭❗💭❗💭❗💭❗💭 10.08.25 GW1 Sowed seed, soaked starter pot with #1 12.08.25 GW1 Seed popped hip hip hurray 28.08.25 VW2 Stopped using GreenBuzzBloom, took it out of the schedule. 01.09.25 VW3 TriPartMicro 10→30ml, TriPart bloom 10→30ml 12.09.25 VW4 Applied nemadodes against thrips and fungus gnats. 20.09.25 VW6 topped and trained for first time, decided against a full manifold as I lost a few weeks already. 26.09.25 VW7 Topped her one more time for 8 mains 27.09.25 VW7 Topped up the pot with perlite instead of clay pebbles this time, just trying things out, TriPartMicro 30→40ml , TriPartBloom 30→20ml 10.10.25 VW9 have her a haircut, umm be trimming the side shoots tomorrow, rest in the video 📹 12.10.25 VW9 done some extra trimming to clean up a bit and chose two extra side shoots to nurture info mains, so kept the 8 original mains plus 2 rest in the video 📹 17.10.25 VW9 FfJ/fpj fish mix 30 → 60 ml 20.10.25 VW10 Feed tweak: added 3 g Calcium Nitrate/ 30 L (≈ 15 ppm N + 10 ppm Ca) 24.10.25 VW11 did a defoliation and trimming session 📹 27.10.25 VW11 Epsom Salt 0 → 2.5, Calcium Nitrate 3 → 9 g 01.11.25 VW12 CalMag 60 → 30ml, TriPartBloom 20 → 30ml, Magnesium 2.5 → 3.5g 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 🌿 Day to day tasks & actions 🌿 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 31.10.25 VW11 -- no feed no water (*RUNOFF reused for tomato plants) 💧💦💧💦💧💦💧💦💧 💧 Nutrients in 30 L #1 💧 💧💦💧💦💧💦💧💦💧 💧 TriPart Micro: 10 → 30 → 40 ml  = 0.33 → 1.00 → 1.33 ml/L 💧 TriPart Grow: 0 ml  = 0.00 ml/L 💧 TriPart Bloom: 10 → 30 → 20 → 30 ml  = 0.33 → 1.00 → 0.67 → 1.00 ml/L 💧 Cal-Mag: 60 → 30 ml  = 2.00 → 1.00 ml/L 💧 Home-made FFJ/FPJ (new batch): 30 → 60 ml  = 1.00 → 2.00 ml/L 💧 Calcium Nitrate (Calcinit): 3 → 9 g  ≈ 15 → 45 ppm N + 20 → 60 ppm Ca 💧 Magnesium (Epsom Salt / MgSO₄·7H₂O): 0 → 2.5 → 3.5 g  ≈ 0 → 8–9 → 11–12 ppm Mg 💧 pH Down: Citric acid (BuxXtrade) — adjust to ~ pH 5.8 – 6.0 📦 TOTAL: ≈ 110 → 180 → 170 → 190 ml liquids  + 3 → 11.5 → 12.5 g solids per 30 L  ≈ 5.9 → 6.4 ml/g active mix per L 💧💦💧💦💧💦💧💦💧 ⚙️✂️⚙️✂️⚙️✂️⚙️✂️⚙️ ✂️ Tools & equipment ✂️ ⚙️✂️⚙️✂️⚙️✂️⚙️✂️⚙️ ✂️ 2× MarsHydro SP3000 ⚙️ MarsHydro 150mm ACF Ventilator ✂️ Trotec dehumidifier (big unit) ⚙️ Mini no-name dehumidifier ✂️ Kebab skewers (LST – stainless) ⚙️ Wire + roast skewers (LST assist) ✂️ Scissors (HST) ⚙️ Vacuum (for spills & cleanup) ✂️⚙️✂️⚙️✂️⚙️⚙️✂️⚙️✂️⚙️✂️⚙️ --- 🍊🍧🌬️🍬🍊🍧🌬️🍬🍊🍧🌬️🍬 Mystery seed (Kannabia Seeds) — NEW EXCLUSIVE 🍊🍧🌬️🍬🍊🍧🌬️🍬🍊🍧🌬️🍬 Species: Hybrid (GF / swift-flowering line) Genetics: TBA (breeder sheet pending) THC: TBA Effect: Euphoric, relaxed, creative (target profile) Flavor: Berry–citrus sherbet, sweet candy, creamy finish Flowering (indoors): ~6–7 weeks target (GF) Resistance: High (aim: no drama) Indoor yield: TBA Outdoor yield: TBA Structure: TBA Notes: Brand-new exclusive from Kannabia’s GF line — I’ll update specs when the breeder card drops. Goal is rich sherbet terps (berry–citrus + cream), low leaf-to-calyx, easy trim. Stage harvest stays on the table if tops finish early. YouTube Link: https://youtube.com/-m8h?si=A7x4Zlr2kj-_ga31

The Bananas are hanging! Stay tuned!

She put on so much weight this week I flushed her and now feed with ripen untill next week Mid week 11: still cloudy trichomes Maybe i let her go a few more days after the ripen scedule

The banana mango must be on roids! It’s doubled the size Of the others. If you are looking for a desert plant that handles 100plus F without being bothered - this could be your gal!

***** Week 12 growth - February 20 to 26, 2021 - Week 3 Flower ***** These girls have been happy all week and CL2 has looked happiest still. CL1 pheno came out of the gate stronger and taller from the beginning but I have been looking for a little more out of her so while I was giving GSC x 707Headband some fulvic acid in her feed I gave some to CL1 also. She has reacted well to it, or it certainly hasn’t brought about anything negative. Used Gold Storm at 5ml/L👍 CL2 is just freaking gorgeous and may be a keeper, in early growth anyways😃 Love her size, node spacing, leaf to calix ratio, thick branching, early trichome production......all on point so far🔥When I took a leaf the other day the underside vein appeared to be slightly starting a color change......should be some purple in there somewhere with that genealogy😍 Light is at 20” and pulling 480 watts at the end of the week. Stated off with 400 watts at the start of the week but keep pushing it up this week. I don’t want to break 1,000 to 1,100 PAR by very much as I am not supplementing with true CO2. I have an Exhale bag to raise it a couple hundred ppm. Feel the need to keep the intensity high for penetration lower in the canopy. Will lower the amount of time in daylight if stress gets too high. Push to 11/13???? Nutrients are following IPP HOG 3 Part pretty closely. Just playing with macro nutrient ratios but otherwise supplements are at full week dosages following week 3. Have been seeing great resin production last runs so staying with Rezin as part of their feed schedule in flower. Terpinator......I think I see a lot of sulfer benefit here so it stays in the grows as well. Recharge seems to be working out well but we did the change mid grow from Microbial Mass. Since in coco have to feed the microbes so they reproduce and really dig Nature’s Candy with Remos additives in there👍 To help keep the root zone clean we add Enzymes😃 I have been debating a lot lately about the addition of CalMag to these nutrient lines and it’s necessity but since in coco I keep adding some......noticed a couple of spots on MM2 so have added it back in a bit more this week. Little more detail....... Feb 20/21 - Day 15 - Full feed today.....it’s been five days. - tap water with Silica @ 1.5ml, IPP line at full strength. - 1400ppm and 6.1pH - CL2 given 4L with good runoff. - CL1 was given some fulvic acid in Gold Storm. Help with giving her a chance to stretch a little more. Little more node spacing.....bushier girl. - 5ml/L added to feed for 1490ppm and 6.1pH. She was given 4L with good runoff. Feb 21/21 - Day16 - Dry out day Feb 22/21 - Day 17 - watering with supplements and light feed today. We are in mid flower now.....need to keep the macro nutrients up. - Epsom salts @ 1 Tbsp in 20L. Purple on stems is getting prominent......could be cold temps but also giving magnesium. - Terpinator @ 3ml, Rezin @ 1.5ml, Nature’s Candy @ 1ml, grow @ 1ml, micro @ 2ml, bloom @ 2.5ml, Recharge @ 1 Tbsp in 20L. - 1400ppm and 6.0pH. - 4L Feb 23/21 - Day 18 - keeping up the silica this watering - silica @ 1ml, CalMag @ 1ml, Ultimate B+ @ 1ml - 600ppm and 6.0pH - 3L Little to no runoff this watering. Feb 24/21 - Day 19 - full feed again today.....girls are big and growing hard......keep it going💪 - IPP line as listed for full line. - Terpinator @ 3ml, Rezin @ 1.5ml - 1425ppm and 6.0pH - they are taking the high ppm feeding well. Feb 25/21 - Day 20 - Had some feed water left from yesterday. Added plain tap water to get 20L. - 810ppm and 6.1pH - 1.5L......don’t want to over saturate the medium. Feb 26/21 - Day 21 - Nothing today. - Will feed early tomorrow as it’s Saturday. - Let the root zone get some oxygen is my thought and water to nice runoff first thing in morning. Week 3 behind us and going into 4.....middle of flower and girls are feeding hard. Pushing the lights hard now as well so need to keep the ppm up👍 Little more variety in these two phenos but certainly not negative differences. In the end I think CL1 might have bigger colas than CL2 because she is getting some wide/thick bud tops. I do like the appearance of 2 better though because I suspect trim is going to be better as well😎 Again though......I am make sure nothing happens to the clone of CL2 and Mandarin Mimosa 1 right now💪👊 Good week ETS.....let the swelling begin🌟

Beginning 5 weeks of flowering, I will soon share a video of the two bitches

On day 11 of flowering. I spent a few days without being able to see them, and the people that take care for me gave them just water, so they are a little hungry. Gonna rise the feeding and do another micronutrients + potassium silicate + fungicide + aminoacids + neem oil foliar spray. I put and old scrog on top of the 2 big ones to open them more and give support.

Major THC all over it

This is the final week! My wife will be having a baby on 3/11/19, so I need to harvest on 3/10 no matter what. The trichomes are looking good. Mostly cloudy with a few amber and a few remaining clear. I could probably push this another 5 days or so, but since this is already a pretty heavy indica, I think this it great time to harvest, particularly given the circumstances. Really happy with the level of frostiness on these buds...they look super dank!. Can't wait to harvest and cure these babies :)

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.

I feed them with earthworm humus and red bird guano

Langsam wird es buschig. Ich hab mit Draht einfach die Äste auseinander gezogen. Düngen war bis jetzt nicht Nötig, nur ein wenig Wasser. Bis jetzt wurden die beiden Mädels mit 100watt beleuchtet. Demnächst werde ich die Leistung erhöhen.

Great réaction to stress. Flow exactly started thé 28th day. Let’s see. Started bio bloom too.

Teniendo el sustrato preparado con antelación un par de días antes.. nos animamos a germinar, tengo una tremenda ilusión con esta pequeña, me hace muy feliz verla crecer!🌱 Ojalá todo salga bien y pueda acompañarla hasta el final en este precioso viaje 👽❤️🌱 Nos hemos marcado tres objetivos en este cultivo: 1-hacer un cultivo seguro y no ser detectados👮‍♂️🥇 2-conseguir una cosecha en menos de 2 meses con éxito 🏇🥈 3-gastar la mínima cantidad de recursos posible con el máximo rendimiento posible🤑🌍⚡🥉

Hallo Freunde 👋 Do-Si-Dos F1 Hybrid Auto von Zamnesia ist 28 Tage Alt und in Blüte gegangen! Ich bin ehrlich überrascht wie schnell sie performt, und schaffe es nicht sie so zu trainieren wie ich es wollte 😕😉 trotzdem versuche Ich ihren Stretch zu nutzen um noch etwas Struktur zu bekommen! F1 ist zu schnell 😅😂✌️🍀💙🍀 keep Green and grow High ✌️🍀💚🍀

Wow she's still growing nicely!! 27cm more this week! She's looking nice.