inizio 3°sett. una delle 3 piante l'ho toppata..a vederla sembra cresce più lei che le altre

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.

Hey everyone 😃. This week she has done great 👍. It was done again on all the drifted topping and sprayed one last time with neem oil so that the last trips are finally gone 😁. We haven't had any pests for so many years and all of a sudden we have such little shit parts 😅. This week it was poured twice with 1.2 l of water. GHSC enhancer was added during a pouring (1 g per l) The tent was cleaned every day this week and the plants were checked for health. The humidifier is filled once a day. Next week I will decide how I will continue the training because I have space again in the flower tent 😀. Until then, I wish you and your families a good start into the new year 2021 🙏🏻. Stay healthy and let it grow 🍀 You can buy this Strain at https://www.amsterdamgenetics.com/product/kosher-tangie-kush/ Type: Kosher Tangie Kush ☝️🏼 Genetics: Kosher Kush X Tangie 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Fertilizer: Green House Powder Feeding ☝️🏼🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.5 - 5.8 .

All good! My DWC experiment worked out better than expected! My soil grows are great!!!

8/25 -Plants responded well to the increase on volume of water fed. Im really liking the +50 mLs a feeding (every other day) -Only a few of the oldest leaves have started wilting. This is normal and expected as those leaves have been used and abused the worse. I left them on originally because it seemed the plant was pulling nutrients from those two leaves specifically if there was any kind of deficiency. As I took care of the Ca/Mg/Fe issue a few weeks ago those spots went away. -The canopy is so damn thick defoliation doesn't allow for light penetration down to the coco. 🤷‍♂️🏻🤷‍♂️🏻 -I really shouldn't complain since these plants are definitely going to harvest big. Very excited -Building 4 separately raisable platforms so I can start growing my Fall plants. Only have 1 light, limited space for my grows but I don't want to waste a month of vegetation. If the platforms work as designed I am very confident ill be able to grow staggered harvests. The goal is to always have weed ready and cured for me to smoke. Buying from dispensaries is getting to be too expensive. -Went back and re red some online forums about growing in coco as I had no experience going in. All the forums said to essentially flood the coco on a daily basis. I have no idea how that is successful--when I tried that I almost killed my plants. Listening to the plant and reading its signals is WAY more efficient for me. The time lapse allows me to look at the plants normal day/night trends. SUCH a good idea plus it makes for a really great video at the end of the grow. 8/26 -NEw nutrient solution made. Same nutrient concentration and strength. -Cheese lowered 1.5 inches on its stilts. Its definitely stretching according to the Time Lapse -Cream Cookies smell is getting stronger and stronger every day. Cheese is the first smell to start developing. -Slight color change starting to occur on Cream Cookies. -Its beginning to become more obvious that Cream Cookies is transitioning focus from maintaining older leaves birthed in early vegetative growth and transitioning to only focusing on bud production. Lower growth is beginning to wilt out. A Natural lollipop if you will. 8/30 -Cream cookie buds are really really really starting to thicken and fill out. Looks like the final buds are going to be quite dense. The smell is really developing on cream cookies. Cant really put my finger on the exact smell but there is a definite strong cheese odor followed by a strong earthy smell. No sweet/citrus smells yet. -Cheese is flowering completely differently from cream cookies. It seems three of the main cola branches are going to yield absolutely huge buds. These main cola bud sites are stretching and small flowering nodes dominate the landscape of the branch all the way from the soil line to the canopy. It seems like the flowers are going to really fill in around the branches. -Lower branches of Cream Cookies starting to become more rigid, taking on rigid character of the main stem. Makes me think that the buds are becoming sufficiently heavy that the plant needs to reinforce some branches to avoid bending over and falling. Love to see it. -Slight signs of stress observed, going to reduce concentration of bloom nutrients to 11 mL/gal. Still should have all the nutrients the plant needs just in a less concentrated solution.

April 20, 2024 Happy 420 Everyone! A new diary for a new contest by Seedsman! Sit back, because there's a lot to talk about today. Just like all of my grows, this run will have daily updates with pictures, a weekly video and as much detail as I can muster in the stats. Let's get started. First off, let's talk about the setup. I have 4 plants in my main tent that won't be done for a couple more weeks. So these ladies will be starting out in an AC Infinity Germination Center with their Germination grow lights, a heat mat and a small computer fan to keep the air fresh. The DLI will be around 12 mol/m²/d. They will be planted in root Riot Plugs until they show roots. Then in their final 3 gallon fabric containers. Then into the Mars Hydro 2x2 tent with the TS600 light. 100 watts of pure power. Haha. This should only be for a couple weeks. Just enough time for them to be well established. Then they will go into my AC Infinity 3x3 tent with the S33 grow light. 240 watts of power. I have 2 oscillating clip fans running a slight breeze at all times. I'm using a 4" exhaust fan with filter. I'll be using the AC Infinity bottom feed wick system. I've been using it for quite a while and I find it to extremely efficient. More about this later on in the grow. Let's talk about the strain. Sour Diesel Auto by Seedsman. This strain should be with us for the next 8 to 10 weeks. In my experience, add another week or two just Incase. We can expect a really good yield if I don't screw anything up. Up to 650/m². She has some environmental requirements. Heat is the main thing. Slightly humid for the veg stage and dry for the flowering stage. Being a sativa dominant strain, she will grow tall. I'll be implementing LST and light defoliation for this plant without a doubt. That's about it for now. I'll describe characteristics throughout the run. Finally to our actual ladies. I'm germinating 5 in a glass of water. I plan on keeping 4 total. That's all my tent can fit. So I'll do away with the 5th and work with the 4 best seedlings. They should sink overnight and start to open up. As soon as I see the tap roots, they go in the Root Riot Plugs. That's all for today. See you tomorrow. Oh, and thanks for reading. Wish me luck on this journey. It is a grow off after all. Lol April 21, 2024 4 of the 5 seeds have sunk to the bottom of the cup with my assistance. The 5th one I still floating. However, I don't see any tap roots, so another day or 2. I may pop the sunken seeds in the Root Riot Plugs tomorrow afternoon. The 5th seed may be the reject. If it doesn't pop in a couple days, I'm calling it a loss and working with the 4 other seeds as I originally planned. I could also go down to 3 plants, but I frankly would like the even number of 4. 1 per quadrant. We shall see. I wonder if I should do three 5 gallon plants or four 3 gallon plants. We shall see. The biggest obstacle will be the tight space I have to work with for the next 2 to 3 weeks while the plants already in there are done. I plan on dry trimming for a faster dry. Normally, I like to hang the whole plant. This time around will be wet trimmed and hung in parts. OR placed in my bud drying rack. That's large enough to hold all 4 plants' buds. I should also mention that these seeds are in constant darkness until they go into the plugs. Kind of obvious, but these diaries are not only for my records but set up as an educational piece of work. The environment is looking fine. The air temp is 82°, but the water is definitely no where near that warm. I did have to drop the exhaust fan down and increase the heat mat temp to get the water temp up to a proper temp. Germination Center Environment: I'll be keeping the temp around 82° and the humidity doesn't matter for now. When it matters, I fill the bottom of the Germination Center with water. It helps perfectly with the humidity for growing seedlings. It will also help regulate the temp to around 78° to 79°. April 22, 2024 All 5 ladies have sunk to the bottom of the cup. Now it's just a matter of time for the taproots come out. Somehow, the Germination Center was cold this morning. Like 68° cold. So I took the riser off the dome and cranked the heat mat to bring the heat and humidity up. That being said, the seed water is much cooler than I want. I like warm water for germination. Oh well. The heat mat should fix things in a matter of hours. Everything else looks good. Germination Center Environment: Currently it's at 77° and 94% humidity. It should level out to about 80° and the humidity should stay about the same. I also took the fan off the dome. I'll put it back on when they pop out of their plugs. April 23, 2024 All 5 seeds popped. They all have tiny taproots just starting to form. This is when I plant them in the plugs. They should take a couple days to break surface, but definitely germinated. Now it's just a matter of choosing the 4 best looking seedlings. They are now in the Root Riot Plugs with the temp at 77° and humidity at 95%. The dome is on without the extension for now. Once they show leaves, I'll install the extension and turn the light on. I'll be leaving the light on for 24 hrs. While in the Germination Center. Once out and established, I'll change it to the normal 18/6 light schedule. I was considering starting at 18/6 from the beginning, but I've tried that and feel like it wasn't as successful as 24 hours. Especially because these are autos. The kickstart of light makes total sense. We will see if my theory is correct. Germination Center Environment: Temp: 77.4° RH: 95.4% VPD: 0.15 kPa April 24, 2024 Nobody hopped surface yet today. I don't even see green in the plugs yet. I'm definitely not worried about it. I expect them to break surface in a couple of days. Maybe tomorrow or the day after. Honestly, I won't mind if they take a little bit longer and I can keep them in the Germination Center for a bit longer. It will work out best for my whole grow operation. Small as it is. I gave each seed plug a bit of filtered water today. Just to keep the moisture up. It shouldn't matter too much. The plugs are pre-moistened, so there shouldn't be any issues there. I'll be turning the lights on when I start to see green. They will be on 24 hours for the first week. Then into the main light at 18/6 for the rest of the grow. The environment is a bit bouncy while I work to get the system right. The heat mat is perfect a it's setting, but the fan needs to be messed with and the dome port needs to be adjusted as well. So far it's not too bad, but the temp keeps dropping below 75°. I'll keep a closer eye on it while I get it to acclimate to the proper total environment. Germination Center Environment: Temp: 80.4° RH: 94.7% VPD: 0.19 kPa April 25, 2024 Some ladies are starting to show green! Today we have 3 of the 5 ladies breaking surface with the shells. One of them is absolutely going to have helmet head. Or whatever it's called. I'll be needing to fix that. I'll wait til tomorrow to see how things go. The other 2 are still working their plugs. That being said, I reinstalled the dome extension and turned the lights on to 20% power. The DLI is around 10 mol/m²/d. I'll increase the light power in a day or 2 when the rest of the babies pop up. We should end up with the DLI of 12 mol/m²/d when we start seeing leaves. The environment hasn't been the best. Not my best start by far. I can't keep the temp at a good range. My night time temps are super low and then I get a decent day temp, but then it gets too hot. I'm going to have to figure out the heat mat I think. It's back to normal now, but was like 65° last night. Not good. With the light on now, the temp shouldn't be a problem. Germination Center Environment: Temp: 72.6° (too low) RH: 76.8% VPD: 0.64 kPa April 26, 2024 So far I have 4 ladies fully showing with the 5th lacking any movement. She mush not have actually popped. Or maybe a little late. I'll give it 2 more days and see what happens. Anyway, I think I already have my 4 plants now. They will be labeled A through D. Everything looks great for now. The environment is looking great at 80° and a humidity of 82%. I won't need to mist them at all at this rate. Maybe when they get into the nursery bags I'll need to mist. We shall see. I'll be leaving the light at 20% for another day or two. Then I'll increase the intensity to 12 mol/m²/d. It should start this run out swimmingly. One of the babies had a helmet, so I gently removed that this morning. Other than that, nothing else for the day. Germination Center Environment: Temp: 78.7° RH: 80.0% VPD: 0.69 kPa April 27, 2024 This is when I normally would start a new week, but these ladies are only in the very early seedling stage. Not on veg. Honestly, I would love for a seedling stage week. Now I'm kind of stuck until I see the first set of true leaves. Another few days no doubt. So it throws off my schedule. Oh well. I'll do my best to keep track. I have 1 seed that rooted, but never grew up. I'm calling it a loss for now. So 4 of 5 seeds made it out of the plugs. I also have a 4th one that is super wonky. I'll keep it for now. If it looks all messed up over the next few days, I'll have to toss that one as well and just work with 3 plants. Hopefully it won't come to that. The 3 seedlings that are looking good, look really good. Roots already starting to get exposed. They will be going in the 1/5 gallon nursery bags in a matter of days. Maybe even tomorrow. I don't like too much root to show before transplanting. So that may be a thing tomorrow. I'll increase the light intensity when they are transplanted. It makes the most sense based on the speed they grow. The environment is pretty good. Hovering at a temp of 80° and 87.4% humidity. I also gave them a small misting to keep the humidity up and the babies getting all the water they can get without overdoing it. Germination Center Environment: Temp: 81.2° RH: 88.9% VPD: 0.41 kPa

I flushed my monster plant we are starting late flowering so i wanna make sure that there is no nutrient build up. And to make sure that shes gonna end up like a Bomb. Smell is good but not too strong. So the plant is perfect i have nothing to say

Que pasa familia, vamos con la cuarta semana de vida de estas Papaya Zoap F1 de Sweetseeds. Vamos al lío, me quede con 3 por espacio, siempre pongo alguna semilla de más por si no abriese alguna por no perder ese hueco del indoor. También se trasplantaron a su maceta definitiva, en este caso de 7 litros. Y también superaron el shock por el trasplante se recuperaron 100%. El ph se controla en 6.2 , la temperatura la tenemos entre 20/22 grados y la humedad ronda el 50%. Hasta aquí todo, Buenos humos 💨💨💨

this is weeks 5 and 6.I topped them and trained the branches out to the side. Plus I broke one... I tried to save it but it broke again later

🗓️ Week 12 – Flower Week 8 (MAC n Cheese only) Stage: Late Flower MAC n Cheese is now fully into late bloom and continues to impress: 🌿 Development: • Buds are dense, frosty, and maturing evenly across the canopy • No significant leaf discoloration • Aroma profile is becoming increasingly intense – leaning towards creamy and earthy notes 💧 Feeding & EC: • Input EC: 1.65–2.0 • pH: 6.3 • Current runoff EC: 2.3 → Still well-balanced, no visible signs of overfeeding despite the elevated drain values Flush status: No flushing yet – plants are still feeding actively → Final flush with Flawless Finish planned in ~1 week ✅ Summary: MAC n Cheese remains healthy and consistent. Structure is solid, frost levels are high, and everything looks on track for the final push. Late-stage nutrient uptake is still strong without stress indicators – ideal conditions heading into the home stretch.

Removed ScrOg, I’m too ocd and damaged two colas. Two weeks was enough to space. Wish I put it on two weeks earlier. Currently removing flarf sites.

Domani dovrò andare a comprare il necessario per fare qualche clone mentre darò una tagliatina ai rami non necessari 🌱👽 Questa settimana ho integrato calcio e magnesio insieme a un infuso di banane che inizierò a dare prossima settimana Oggi ho cambiato a 14 ore di luce e dalla prossima passerò a 12…devo assolutamente tenere qualche clone di questa PPOG perché è una bomba 😛 Vedremo come si evolve più avanti non vedo l’ora 👉🏻👐🏻🤭🌴

Despite the scrog failing, I was able to train some branches to the outer band. Have a lens coming in tomorrow for trich inspection. Currently most mature plant (red) is looking to have some cloudy for sure. Red probably got her last heavy nutes this week. Cut grow big for white. Will do a semi flush with pH'd water with light cal mag and big bloom on next feeding followed by a final full flush. Ripening seems to be staggered 5-7 days plant to plant red -> white -> blue -> yellow Depending on how things look on the lower buds.I am definitely considering a gradual (ripe bud) harvest approach.

Watered straight water on day 130, runoff & pH still high at 5/3230, raised lights to 23" above the canvas do give better coverage but only getting between 17,000-35,000 lux so I'm under lit for flower, might be upgrading to HLG Scorpion R Spec LED. Added half a tsp NPK Microbes Bloom Stage today, hopefully this will help.

🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀 Welcome to week 6, dear growmies!! 😘 The little cake is growing alright! 💚 I can already see huge leaves, hihi!! 😬 DAY 37 Watered with 2ml grow + growzyme + humics + 3ml fastbuds + more roots 💧 Topdressing with Living Organics :shroom: Removed some pollen sacks on the lower floors.. 😂 Rolling my eyes, that's it. DAY 40 Switched on the red spectrum. ✌️ DAY 42 Watered with 2 ml grow + 3ml more roots + humics + growzyme + 2ml calmag 💧 Thanks for showing up and supporting me and the girls, bless you, growmies!! 😘 ❤️ Shouts go out to my sponsors @GreenBuzzNutrients, thanks so much for your support!! 💚 💚 💚 If anyone would like to try their amazing organic products, you can find a generous discount code of 25% in my weekly comments! 😜 🙏 If you want a recommendation which product to get first.. BIGFRUITS!! 😍 I love the tasty terps with this one!! https://greenbuzznutrients.com/ Thanks also of course @Kannabia, for the beautiful genetics!! 🧡🧡🧡 Pouring all my love into this grow, thank you for joining in, growmies!! 💚 💚 💚 😘 ❤️ ❤️ ❤️ Wishing you all the best for your beautiful gardens!🌱 🙏 Grower love!! 💚 _________________________________________________________ Strain Info: https://www.kannabia.com/en/feminized-cannabis-seeds/break-up-cake We need to talk You’ve got to celebrate everything in this life, and that includes love and heartbreak. Since you’re all familiar with Wedding Cake feminised marijuana seeds, we’ve put a Break-up Cake in the oven at the Kannabia Seed Company – because things don’t always go well, and we sometimes need a friendly seed to lean on. Break-Up Cake has a base of Girl Scout Cookies, one of North America’s best-known strains, which is earthy with a very potent indica effect. And we top it off with a delicious Cherry Pie which, in addition to giving it an elegant dark attire, adds a silky, deeply sweet flavour of cherries and berries. Look no further – it’s the perfect cake. This seed will be celebrated for its ease of cultivation and abundant production. It’s one of the best investments you’ll make this year. But if it’s going to be memorable for one thing, it’s for its sweet complex flavour that’s full of contrasts. If we have to break up, let’s do it sweetly and amicably, right? How to: Break-Up Cake Break-Up Cake is an “all-terrain” marijuana seed, which will adapt to the place you allocate to it. An ode to independence, it’s a plant with only the most basic needs that knows how to grow by itself. It’s a pale branching plant with tremendous dark green leaves, purple tips, and an icing sugar coating of trichomes. Its immense buds are some of the stickiest ones we’ve found in our seed bank recently. Indoors, it needs 60 days of flowering to give no less than 600 grams per square metre. Use a Screen of Green method without hesitation, or plant it using hydroponics if you want to obtain the full benefit of its potency. Outdoors, it reaches two metres in height with a harvest of 800 grams per plant, which is reason enough to give it a go. Like a good break-up cake, this plant doesn’t need to live with a partner, and knows how to live well in a Guerrilla plot. Between 25th and 10th October is its moment. Taste and effect of Break-up Cake Very relaxing but not causing lethargy, it’s a good indica-dominant plant. Its effect is mellow (we’re too old for childish games). It calms the consumer but it also gives rise to creative moments. Head on up to the top floor, later to make your way, little by little, down to the kitchen later (where you might want to give in to temptation if you need to stimulate your hunger). The flavour is full of nuances. It will remind you of a vanilla sponge or cheese cake: you’ll notice a cherry topping, something sweet that you can’t quite distinguish, and an earthy undertone on a biscuit base… You’ve got to sample it to know it. _____________________________________________________________________ SETUP: 80x80x180 cm Zelsius 240W Full Spectrum LED IR UV dimmable DW240H-A6-HS Heatsink color red LED Chips: 512pcs SAMSUNG LM301H + 24pcs Osram 660nm + 8pcs Osram IR 730nm + 8pcs UV 385nm Color mix: 2700K + 4000K 2,8umol/J Driver HLG-240H-C2100B Coverage: veg 5x3ft / flower 4x2ft Product size: 628x205x68mm Green Buzz Nutrients Shouts go out to my sponsors @GreenBuzzNutrients, thanks so much for your support! 💚 💚 💚 If anyone would like to try their amazing organic products, use code GD42025 for generous 25% discount (for orders of minimum 75€) ✨ https://greenbuzznutrients.com/ Biobizz Lightmix custom exhaust fan 320/270cm³/h Carbon Active Granulate 240cm³/h tab water pH 8 - EC 0,25 with Calmag to 0,5 Advanced Hydroponics pH minus Grow + Bloom to pH 6.2 🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀🍪 🍒 🍰🍩 🎀