Plantitas sanas hoy se pasan a 12/12

Overall happy with this solo cup grow, wish I could have got a little more but I ended with 6.3 grams dry weight, bud looks amazing. Post more of a update after I smoke it in a few days! Thanks for following & happy growing friends!

I made some begginers mistakes in week 4 but this lady Is strong and bounced back 3/02/21 i snapped a big fan leaf :((

She's moving along at a nice pace. Bulking up while giving no real issues. Has some nice mass to her. She's a wee bit taller. And if I could redo something it would be applying HST to her after preflower. Lovely dank lemon kush smell developing. Super sticky to the touch and building a boat load of trichomes. This is my 2nd SweetSeeds grow. And I'll 100% be doing this strain again. (As I know what it's like, its being curing 45 days now). Xpert nutrients have been a gift in their application to its ease and fast results, I simply can't praise them enough. Has brought my bud quality up easily 2-3x and Increased bud quantity. Although, that's me knowing by looking at the plants. I roughly weight stuff, I know I got 1850 dry grams from 45 plants. 13-15 were 8L pots and small such as this. So, this was 1 of the biggest yeilders out of the lot.(crop is finished and burnt my way through 2/3rds of it, I've about a halfo of this for my night time smoke, while my last 6 plants from this crop have been curing 3 weeks now and will soon be smoked) biggest crop I've done. 45 plants was a feat, a real task keeping track with whos on what and using xpert nutrients made it much smoother and any slight ph mistakes or overf/under feeds didn't destroy 1 plant to the point were it was culled. Big thanks to ALL my sponsors. Whom I truly thank as I wouldn't have any of this without them. And to you my viewers. Whom I'd have no sponsors without. I thank you. DISCOUNT FOR XPERT NUTRIENTS 20% OFF CODE:ggst. Free EU SHIPPING Also, any new growers or struggling to purchase seeds and would like a few different strains. I've lots there. (Offer open to those who don't have lots of stock). Just DM me. Please be patient in response.

8/19 Rained again last night. No damage but medium is drenched. The 9lb kush I've been struggling with seems to be improving. I spent a lot of time on her yesterday and at least an hour this morning defoliating and pruning her. New growth and flowers look promising. I'm cautiously optimistic. I defoliated what needed it. I needcto qpplyvorganocide again. I can see random signs of septoria leaf spot. I really have been off my fame lately. I'm back on it now. This week the garden will be rearranged and I'll pull that big GDP back and better support the blueberry for flower. That NYCSA is a beast. It's resilient as all hell and just continues getting bigger and fuller. Despite pr9blems in the garden this girl seems absolutely fine. At least I don't have that defeated feeling anymore. I've got flowers on a few different plants. I'll try to get a couple pictures. I may take rapacaps advice and add a cheap plastic roof for later flower. I'm not sure if the explosive flower growth is due to the liquid kool bloom but I think I'm going to switch back to tiger bloom as it works better with the other nutes. I'll jeep this updated but I've got work to do. 8/20 Well it Rained again last night. This is getting discouraging. Now my other 9lb kush has the bottom branch all droopy like there's a borer or something. Realistically with the temp swings and the weather I think it's a firm of root rot or pythiym damage which isn't good. I posted pictures of the stalks and would be grateful if anyone has any advice. I'm go8ng back down to look again for a borer hole but i didn't see one. What it looks like to me is that the petroleum jelly I put on the stalks (to battle ear wigs) seems to keep them moist or something inviting mold or fungus. I'm kind of at a loss. I don't really know where to go from here. I don't know if I should just replant the severely damaged plant away from the rest of the grow, bag it and get rid of it or leave it be and hope for the best. I certainly don't want anything spreading. I'm getting tigerbloom today as my plants still need to eat and I'm nervous about the liquid kool bloom. It's probably fine but still. I'll update after I put in more work and research more today. Any advice helps. UPDATE: No borer holes. The stalk looks fucking horrible. It's supposed to rain today. I'm going to give it one more day then I'll amputate that branch and get rid of the other plant if I don't see an improvement. Perhaps I'll plant it in the ground. Don't really know what to do. Family bar b que today so my options are limited. 8/21 FED TWO GALLONS TO THE GARDEN. ONLY USED .5TSP/GAL OF LIQUID KOOL BLOOM. Did not feed dieing plant. Back to super hot weather 80° at 9am. Did a lot of research last night. I also went to several commercial growers and asked advice. What I came up with was a fusarium infection of pythiym infection (Crown rot). I looked at all my stalks and they all have bark and are darker where I applied the petroleum jelly. I'm also NEVER using DE again. It fucking ridiculous amounts of water. Everyone swears by it bit it's not going in my garden again. Since use I can just watch water sit right on the GD soil. I tried to get some examples of what I'm talking about with the stems. I amputated that lowest bottom branch I trained (which was huge). I didn't have time to dispose of the other plant before my wife's doctor's appointment. I'll update when I go back over. I'm sure this won't help and may hurt but I used Bee Safe 3 in 1 on the wound and around the stalks of the plants I saw discoloration on. I didn't touch the NYCSA even though I see some discoloration. I may just be seeing things. That plant I'd super healthy and I don't want to risk losing it. It doesn't seem to have the stem rot like the others. At least I'm not the only one having problems. I hears some pretty bad stories. Still. I'm heart broken. I'll keep this updated after I go back over. FUCK. I MAY just go back to indoor. UPDATE: Got back from the appointment and the rest of the plant was all droopy just like the other 9lb kush (and the branch amputated). I wondered about that because other branches looked worse. I got the totally dead 9lb kush out and found some root rot. AFTER wheeling the bag out I found earwigs and other insects where the bag had been. Awesome. I used h202 to try to wipe down anything that looked Fingal in the stem. It sucks because it seems like that liquid kool bloom pushed them over the edge into flower. Cotton balls where there was nothing. So that's both my 9lb kush plants and the largest plant of the year the GDP that have all bit the dust. If you grow cannabis you know how I'm feeling. I KEEP TRY8NGVTO UPLOAD THE MINUTE VIDEO I TOOK BUT I CLICK ON SOMETHING ELSE AND IT DISAPPEARS. WIFI SLOW. HAVE TO WAIT FOR 5G 8/22 What do I say? Fusarium? Pythium? Stem rot? I'm going to have to get a tent to do some indoor to get the medicine I need for me and my wife. I took the last 9lb kush out and disposed of it. Well it's still in the bag. I'm hoping maybe it might come out of it (beyond hope and far away from the others (but I'm going to toss it today). This blows so hard. Flowers are just starting to develop. I like the liquid kool bloom. It seems to make flowers explode when there was none before. At least on the plants I have left. Actually even the dieing ones started flowering. I'm really concerned considering that one plant (at least) has septoria and every plant has that petroleum jelly on it. Cautio to people that use that. It seems thats where the rot started or is. In spots I spread the petroleum jelly. Anyway my NYCSA has the smallest amount of "funky looking stuff on the stem" so I'm hoping it will make it. Cotton balls starting to appear. If I lose the whole fucking crop I'm gonna go ape shit. UPDATE: Spoke with a few others and did more research. I removed my braces on the bottom of all the plants. It looks like the pjelly and the brace allowed for some type of contaminate. Other growers think I'm being too bleak. They think things will turn out okay. They are more knowledgeable about cannabis than me but I'm with these particular plants everyday. They're probably right and my anxiety is just getting g to me. It's scary seeing a healthy plant completely die in such a short time. After removing the other 9lb kush I could easily see extreme rootbound roots still too the size of the 1 gallon they came in. The bag was PACKED FULL of tight roots so they definitely made it down. The plant however just fell over when I pushed it. I had roughed it up a big before. Anyway I'm praying to the cannabis gods to not take what I have left. 8/23 Fucking pouring again. This sucks. I've gotten loads of advice and made another friend on here. I forgot my phone so I couldn't take pictures this morning. My spirits are up a little seeing that others are at least attempting to help. I'm headed to the grow shop after a night of research to grab supplies to battle this. I'll update later. EDIT: I picked up plant doctor at the grow shop. It was 50% off and I couldn't find anything with trichodermia. However, I've heard good things about this plant doctor. It's systemic and can be used as a root drench and a foliar spray. BIGGEST selling point for me is that it SPECIFICALLY lists fusarium, grey mold. Pythiym crown rot, black mold and all kinds of other shit. The thing that sucks is it's raining and it's not supposed to stop for a few days. That's going to make application more difficult. Oh well. I think I may do a root drench on the one plant that has a wilted bottom branch. I'll keep this updated. Thank you everyone who reached out. Especially growing grannies and my commercial buddy who is always here for me. However he has no experience with this so I'm kinda on my own here. EDIT: I couldn't find trichodermia and I don't have time to wait around and order. I found plant doctor which literally lists it treats all the possibly pathogens my issue could be. Even has a section for medical Marijuana. I did a root drench on the plant up front in the middle AND I did a foliar spray. Might as well get the septoria too. It's systemic but it gets in faster through the leaves I guess. It started sprinkling and I want to test this stuff out before I go ham with it. I did give some to the to other plants bit left my best AND THE TWO SMALLER ONES alone for now. I'm not seeing those issues on the NYCSA and I don't want to risk damaging it. I chose tge root drench as it's raining and the instructions for fusarium WAS a root drench. Thank you all for your help. I will close out tge question once I know it's figured out. Wish me luck. DID A SHORT VIDEO BUT WIFI IS SUPER SLOW SO I NEED TO WAIT TO UPLOAD IT. Went back over. Finished foliar spraying the other two and left the NYCSA and two Littles alone. Hopefully this works. I did I short video. Who knows if it uploads. UPDATE: Went back over and finished foliar spraying. Took a bunch of pictures and did a video but it didn't upload. I'm hoping this will do it. Plants actually look good. And they're flowering nicely! It's too bad I had to do a foliar bug this us supposed to combat PM and septoria as well. 8/24 It Rained last night but hasn't Rained today yet. It's supposed to and uts overcast. I'm really considering putting a roof on my grow (like rapacap suggested) for flower to decrease mold chances. Plants looked happy. I saw no negative effects from the Plant Doctor. I even sprayed a branch of the NYCSA and the stem and a little around tge roots. I finally feel like I can take a breath. I've been working so hard and worrying about losing g everything. I may have been able to save that 9lbkush but I don't think bit was worth taking the chance. The sun is peaking out now. My buddy at the grow shop called and set a side general hydroponics armor si 0-0-4 silica supplement cause it was 90% off. I pad like a buck sixty lol. I'll incorporate that next feed or water. Whatever comes first but it will be good to get it in the regimen. I was worried plant doctor might hurt but the girls seemed to kike it and I went ham on the worst plant. I mixed according to medical Marijuana guidelines on the label (Theres another label on the internet, it's not on this one, it's at the very bottom and just recommdations from commercial growers. I hope this stuff works. Things look better already though. That liquid kool bloom is the bees knees. That's making flowers pop up like crazy! I think I'll stick with it. I was going to use beastie bloom and cha ching later on (and still might) but I hate the lockout bullshit. I've done a bunch of videos but most don't get uploaded as i forget to upload when I leave and wifi is slow here. Anyway at least I've got a few good ones left and pleating the words of my commercial poll buddy, "barring anything catastrophic you should be fine. I know your anxiety gets the better of you sometimes." Couldn't be a truer statement. I'm still getting a tent and doing indoor though. I'm going to need to. 8/25 Did some slight defoliation. I think today I'm going to reorganize my grow space. Things are looking better though. Plants look healthier. Flower is on and they are going to beat hell. I'm glad I took a cutting from NY 9lb kush. I also took one from the NYCSA. THose are tge little ones. The 9lb kush is flowering pretty good. Too bad it's just on a 3 gal. The NYCSA us in a 10 gal grow bag though and is doing amazing. I still see septoria on the leaves. I'm sure I'll need to reapply plant doctor but thus far I'm impressed. Things LOOK better. I don't even remember the last time I watered. It Rained last night. Looks sunny today. I'm going to feed tomorrow. I want the soil to dry out though. We usually don't get consistent rain like this. It's a first for me. I'll update later if I get stuff done.still wondering if I should amputate that wilted branch or give it a bit. It's still attached right now. I'll get some sealant and do some more research.

This is the whole flowering cyclus posted in one week.

23/10/2025 18:10 20.1°C 55%RH After a very cold and rainy week today temperature raised above average,air is pretty dry and plants smells more than ever This strange hot day made hunters come back after a chill period with no shots in the background,also this time was really near my spot(i thought he was finding us😰)

Hello Growers 👋 👋 👋 At last I am doing an update 😇 It's Day 49th big changes occur in my tent. She is a cracker 😇 😇 😇 after that small L.S.T. she released her potential. She is so so so huge, all that tops you can see are a side branches 🤯 🤯 The Gelato growing very healthy and very fast, this is one of my best looking plant so far. I'm very happy to see her in that condition, it's looks like the harvest could be very big 😀 😎 😀 Please have a proper afternoon rest 🙏 You Lovely Girls Growers 😇 🌻

Still swelling but starting to slow down and swagger. It's kolas are becoming so large that it's really starting to weight down the plants small height and stature. Trying to get away with not holding it up but I will see how the further biggest kola starts to lower more how it'll end. I'm starting to lower the feed and get ready for the last 3-4 weeks I'll be giving these plants. Some more foliage will be removed eventually in the coming weeks and also I'll start to change the feed up a little. You can really see the difference in the two phenos. One's a lot like a leafy gelato and the other is OG all the way with great dense kolas. I'm expecting the Gelato type pheno to take 9-10 weeks and the OG one seems to be showing it's age more rapidly with it's pistil development and colour change beginning to start while the other seems untouched and continues to shoot newer whiter pistils!

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.

Auto Northern Dragon Fuel is growing good. She has started to produce her first pistils. I did some defoliation, and lollipop the canopy some. Just getting her ready for the stretch. Everything is looking good at the moment. Thank you Medic Grow, and Super Sativa Seed Club. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

Four are females, two males and another two I still don't know The males I've already cut out and I believe that this week I'll know the sex of all! xD

Just topped her

Week 16 from Seed | Week 5 Flower The White OG – Seedsman Seeds Hello beautiful people! We’re officially in week 5 of flower, and oh my dear, our girl is flourishing with power and grace. Her structure is spreading beautifully through the canopy, and bud sites are exploding in all directions — it’s a bird’s eye view of glory and promise! 💫 This week’s feeding continues the Aptus Holland Clean Program, with a mix fine-tuned to perfection: Regulator System Clean RO Water Conditioner All-in-One Liquid Breakout Powder (yes, we’re still pushing for those dense flower formations) Details for the week: • pH: 6.23 • EC: 1.58 • Water Temperature: 18.8°C Every branch is showing its potential. Buds are stacking up, frosty and full of intention. She’s turning into a real medicine maker, and we can feel the energy vibrating through her leaves. From above, she looks majestic — a full canopy with multi-dimensional depth, and the side views confirm she’s a queen in bloom. We’re just here witnessing her greatness, supporting with love, light, and nutrition. Next steps? Let her ride this flower wave and continue to support her path with intention and consistency. No major defoliation this week — we let her breathe, spread, and show her full character. Massive thanks to Seedsman Seeds for the amazing genetics, to Aptus Holland for their clean, efficient program, to Future of Grow for the stunning lighting (Black Series 600W ), and of course to the whole GrowDiaries community, friends, growers, lovers, and even the haters — you all help push this garden to new heights. Don’t forget to follow the journey also on Instagram — we’re running the Dognabis Cup, and things are heating up! Good vibes, friendly competition, and lots of passion in every frame. Much love as always — until next week, stay rooted and radiant. See you in the next chapter, my dear friends. Let’s grow. As always thank you all for stopping by, for the love and for it all , this journey of mine wold just not be the same without you guys, the love and support is very much appreciated and i fell honored and so joyful with you all in my life 🙏
 With true love comes happiness 💚🙏 Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so 💚

 Friendly reminder all you see here is pure research and for educational purposes only 💚Growers Love To you All and remember to keep that smile big and alive 💚

17/01 So I have had serious doubts about my 300W CFL grow light since day 1 so I decided to instead opt for a Mars Hydro TS1000. Looking forward to seeing if there's any difference! With regards to my previous grow question, my tap water, while drinkable tastes terrible and has a higher than normal amount of chlorine which i heard is terrible for plants. Hence the RO water. Got hit by a really cold spell last week and I struggled to keep the tent above 16 degrees C but it's starting to get back to normal now so hopefully will see some good growth :) 20/01 So I may have set her back by a couple of day's with the new light, apart from the apparent change in wavelength from CFL to led that can cause some stress I also gave her 100% on the dimmer. Just a quick note to any newbies out there, the Mars Hydro TS1000 gives you a recommended distance from the canopy for each stage of growth but not recommended power, if your girl is at my stage of growth use 25-30%. On the bright side she has adapted nicely and no lasting damage seems to have been done. Seeing signs of growth all over and she's back to praying :) 23/01 She recovered from the change of light nicely! She's growing like a superstar now and just got her first feed today. Gonna take it easy on the nutrients, really don't wanna stress her out anymore. I have been turning up the light strength daily and she's currently happy at 50%.

Been having problems with EC! And I thought I had it made.😏 The only thing I can figure is my mix of HP Myco, and HP coco coir, EWC, shrimp compost, perlite and a little powdered dolomite lime must be too "hot". I am using a bluelab truncheon that is accurate and my runoff EC is 3.6. Plants were still to dark despite my hopes. My well water is 400ppm so I will try to keep my input water 1.8EC and 6.2 - 6.5 PH, 21 degrees and my runoff 2.0 EC. I have put thru another 120 L of just PH'd water 0.8EC until runoff was 1.8 to 2.2. Their shade of green looks better but there are 4 that are still too dark so I will try more water tomorrow. EC'd, PH'd & took Temp of all inflow and outflow on 10 plants (this takes forever)😟. Watered again with 6.3 PH, 20 degree, 0.9 EC well water and put thru 3 gallons for 6 plants . Run off EC was 0.8, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 2.0! Their colour and hue is much better than it was, not so heavy and dull, and I believe that this flushing has saved them from being stunted and having more cell wall damage, as well as nitrogen toxicity and other bad stuff. You can see them coming around already from my blunders. Today Sept 28 is Day 73 and Day 14 of Bloom. I can hardly wait to actually feed them something in a couple of days.

11.10.2022 130 giorni dalla germinazione al raccolto 70 giorni fioritura in totale Pianta molto bella, sexy, 2 semi su 2 germinati con successo. di due piante, ho avuto 2 fenotipi leggermente diversi, entrambe le piante mostrano una struttura ibrida tendenzialmente sativa, con rami lunghi e boccioli densi e duri, ricoperti da tricomi. Ho laciato le piante crescere con un Lst applicato un po in ritardo, ma entrambe le piante hanno reagito benissimo e formato delle belle chiome a cespuglio. Profumo tendente al dolce, note di lavanda ed erbe aromatiche, una delle 2 in fase avanzata di fioritura profumava di ananas maturo, semplicemente uno spettacolo! La resa sembra buona, le cime sono di ottima qualita, aggiornerò con peso tra poche settimane!

been a great week for cookies shes turning into a nice Bush did some more defoliation and lst removed some lower nodes tried opening her up as much as possible will be dropping silicon and adding buddy next week thanks for reading happy growing guys

7/28 some light lead pulling removing bottom area and sites that I fill be waste of time taking energy from the tops still RO water and tea every other week