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.

📆 Semana 6 Blue Zushi está mostrando su lado más exótico esta semana. Los cogollos han comenzado a compactarse con fuerza y se nota una producción de resina que va en aumento. Visualmente, empieza a asomar ese tono azulado que tanto llama la atención en esta genética, sobre todo en las puntas más expuestas a la luz. A nivel nutricional, sigo con la base de XpertNutrients y ya se nota el empuje adicional de Sticky Fingers, que está potenciando claramente la formación de tricomas y dando un pequeño salto en la intensidad del aroma, que empieza a volverse más dulce y fresco. Los Adlite están funcionando a la perfección: gracias a su uniformidad, incluso las ramas laterales están sacando cogollos densos y con buena pinta. Temperaturas estables entre 22 y 25 °C y humedad en torno al 55%, controlada con buena ventilación para evitar condensaciones y problemas en la fase más delicada. En cuanto a olores, empieza a destacar ese perfil afrutado y ácido con fondo kush, muy característico de la Blue Zushi. Los tricomas están en su mayoría lechosos, por lo que aún queda recorrido antes de pensar en cosecha. Una planta vistosa y con mucha clase. ¡Seguimos creciendo fuerte! 💪

6/8 Haven't had to water yet (besides the two tens and I should've held off). It's an overcast day. Perfect for the plants. I've noticed more off shoots of 3 pronged leaves so a few plants will reveg but thats fine. I'm happy with how things are going thus far. These are certainly very resilient strains. I've done some SLIGHT LSTing. EDIT: IT'S BEEN A NICE DAY TODAY. A LITTLE OVERCAST BUT SUNNY AT TIMES. PERFECT WEATHER FOR THE GIRLS. THEY ARE LOVING IT OUT THERE! 6/9 And the girls are lookin' Fiiiiiine. In all seriousness everything is doing pretty good. Even that overwatered pink kush runt in the 10gal is coming out of its little funk. Some of my FIM's turned out amazing! With the reveg of some of these I'll definately have my hands full. Very grateful for smart pots and well draining soil! We've gotten some harsh rain but the girls all seem fine. It's the wind today that's a little worrisome. I may stop over later. I COULD put up tarps around the cage as wind blocks (and have before in the past) but it increases the humidity of an already extremely humid day. These girls are strong. I'm sure they'll be fine. I've found that the tarps typically hurt worse than they help. 6/10 56° at 9am. Shook the plants off. Medium wasn't soaked though. Luckily we had some wind. It's not raining now but it's going to have showers for half the day. Tomorrow is supposed to be in the 80's and sunshine so if that comes through things might workout alright. I still haven't had to water this year besides that one gallon on the tens. If I do something I'll update. I'm considering light stepping the two pink kush's in the 10's. I'll need to do more research. 6/11 BEAUTIFUL DAY! Windy too which helped dry the grow bags. Plants are growing at a rapid rate. I've yet to have to water. A few more days like this and I'll have too. It was in the 80's and is still 75 at 5:30. Bags still have heft to them and I can still feel moisture. They got tons of rain. I'll keep an eye on them. Thus far I'm pleasantly surprised (knock on wood). 6/12 Everything looked great this morning. It's a little overcast and 69° @ 8:45. I mixed water planning on watering but decided against it due to the weight I was feeling. My wife said it rained hard last night for a little while but the topsoil was dry. It did look disturbed though. Luke it got PELTED with rain. The medium looks dry but there is still some weight to the grow . I'll be back over later and I'll check things out. Overall plants have made a great transition even in this bi-polar weather extravaganza. EDIT: WENT BACK OVER AT NOON AND EVERYTHING WAS LOOKING WONDERFUL. ITS 80° AND SUNNY WITH A STRONG WIND. THAT'S WHY I FIGURED THE PLANTS WOULD NEED TO BE WATERED. APPARENTLY THOSE THUNDERSTOTMS WITH SHEET RAIN HAVE KEPT THEM WATERED. AS PREDICTED THE TWO 10GAL POTS AT THE FRONT OF THE CAGE WERE A LITTLE LIGHT AND THE TOPSOIL WAS REAL DRY. MY MK ULTRA IN THE 30GAL LOOKED LIKE IT COULD USE SOME WATER AS WELL AND I FINALLY GAVE SOME TO THE 10TH PLANET IN THE FRONT ROW. BOTH THOSE PLANTS WERE BIGGER THAN THE REST AT TRANSPLANT AND IN A SLIGHTLY LARGER CONTAINER. THE FRONT ROW SEEMS TO DRY OUT FASTER FOR SOME REASON. I HAD 3 GALLONS MIXED UP TO START WATERING BUT AFTER CHECKING EVERYTHING ELSE I DECIDED TO GIVE THE FRONT ROW (THE ONLY ONES THAT WERE LIGHTER) A LITTLE WATER. I USED TWO GALLONS FOCUSING ON THE KUSH'S IN THE 2 10'S. THIS WAS MY WAY OF MEETING IT IN THE MIDDLE. IVE LOOKED AT PREVIOUS DIARIES AND I THINK I MADE THE RIGHT DECISION. NO RAIN IN THE FORECAST FOR A WHILE. I NEED TO REMIND MYSELF THAT PLANTS THIS SIZE USE MUCH LESS WATER THAN WHEN THE BAG IS ALL ROOTS. 6/13 It's windy as hell! I would've thought that the bags would be dried out by now! I went around and it seemed like they still had weight. It was also cold last night and is 63° and sunny at 11am. It's not getting any hotter. I DID water the two plants in the back row as they seemed a LITTLE lighter than the others. I split a gallon between those two and didnt water the rest. I figured I'll let tje wind dry them out some more. I know what they feel like when they are totally dry. I don't want to get to that point but it's easier to fix than over watering. I'll update later today. EDIT: I FORGOT MY PHONE BUT I USED ANOTHER TO TAKE A VIDEO BYTCI CANT ADD IT. PLANTS STILL HAD SOME HEFT BUT WERE LIGHTER THAN EARLIER. I DECIDED TO WATER AFTER A PRETTY THOUROUGH ANALYSIS. I GAVE EACH PLANT A HALF GALLON EXCEPT THE 50GAL WHICH I ABSTAINED. WIND IS STILL HIGH. I even got on my laptop to try to add a video but it won't allow me to do it here EITHER. Come on grow diaries. Up your game. 6/14 GROW DIARIES STILL WONT ALLOW PICTURES OR VIDEOS. TRIED MY LAPTOP BUT STILL NO DICE. Weather has been sunny but in the 60's. I'm glad I watered. I can tell the plants liked it. Everything looks amazing 10th planet 2 in the second row is getting massive. I noticed something with the pink kush in the middle of the back.i originally FIMed it but I didn't think it took so I fimmed it again a little later on. Go8ng through the plants I found that there's a point that has like three tops on it but the thick stalk continues up and there are FOUR or FIVE more TOPS!!! I've never seen anything like this! I'm interested to see how this one turns out. Man I wanted to put some pictures up. Everything is doing so good. Maybe when I start a new week it will let me. I need to start low stress training and I need to put up trellises. Plants have also survived sustained high winds. EDIT: WENT OVER AT 5PM AND WATERED THE TWO TENS WITH A HALF GALLON EACH. THE OTHERS "LOOK" REALLY DRY BUT I ADDED MORE SOIL TO THE BAGS A COUPLE DAYS AFTER TRANSPLANT (A WHILE AGO. DONT KNOW IF THAT HAS ANYTHING TO DO WITH IT. I ASSUME ITS THAT THE PLANTS HAVENT FULLY FILLED THE BAGS AND THUS TAKE LONGER TO DRY OUT. I PLAN TO CHECK WEATHER (NO RAIN UNLESS ITS CHANGED) AND WILL WATER EVERYTHING TOMORROW. STILL CANT ADD PHOTOS. PR9BABLY WONT BE ABLE TO START A NEWXWEEK EITHER TOMORROW. I HAVE A BUNCH OF GREAT PICS. OH AND IN ONE BAG I SAW WHAT LOOKED LIKE CORYLEDON LEAVES. I PULLED IT OUT AND IT WAS LIKE A TUBER. I DUG DOWN AT THE EDGE OF THE GROW BAGCWND WHETE THEY HAD BROKE SURFACE AND PULLED THEM OUT. ITS FUCKING BIRD SEED. I SAW THE BITCH THAT MOWS THE LAWN MOWING INTO MY CAGE. I'LL BE SPEAKING WITH HER. LUCKILY I KEEP A GOOD EYE ON KY PLANTS. PLANTS THAT WRRE SHOOTING OFF 3 PRONGED LEAVES SEEM TO BE REVERTING BACK. IF THERE WAS REVEG IT IS CERTAINLY NOT HURTIMG ANYTHING. CANT WAIT TO SHOW HOW THE GIRLS HAVE GROWN!

Das Problem bei recycelter Erde ist das man nicht weiß was noch drin ist nach dem spülen. Die Erde hatte microorganismen und Dünger vom letzten run, den ich soweit ausgespült habe. Danach hatte die Erde immer noch einen ec Wert über 1.2... Aber woraus bestehen die 1.2 ec? Im Nachhinein sah ich das es wohl microorganismen waren die den ec hoch hielten...deshalb hatte ich erstmal nicht gedüngt nach dem umtopfen. Die Erde war auch noch relativ nass und musste trocknen. Dafür hab ich die Erde auf einer Folie ausgebreitet und 2..3 Tage liegen lassen...aber ihr kennt es , die Zeit läuft und das Zelt ist leer was ein nogo ist :) Somit habe ich die Töpfe befüllt und micorrhyzza dazu gegeben. Wie ihr sehen könnt habe ich dann die Lampe auf 80 % gestellt und die blüte eingeleitet. Damit kamen bis auf die acp. Gold die lady's net ganz klar da die Nährstoffe fehlten. Ich versuche sie mineralisch wieder schnell fit zu bekommen und möchte dann mit Bio weiter düngen. Ich verwende verschiedene microorganismen die ich flüssig oder in Pulverform verabreiche. Heute 15.11. Bin ich am Ende der 1. Bt. Woche angelangt. Hab also noch was vor mir bis zur ernte.

Left it over the weekend with no water and it looks like we got some great growth. The fungus mosquitos came back unfortunately, gonna need to figure out a better solution. Next week we flower!

Hello, J’ai recoupé les extrémités des 4 branche pour créer 8 nouveau site de buds, plus qu’à attendre pour recouper et faire 16 sites… la végétation se passe bien dans l’ensemble, je vais la voir une fois par jour, elle est heureuse et pas compliquée 😎

Divine Seeds 2025 Auto Contest 👉Sponsored Grow👈 AK-47XL Auto W6F2 The weather was rainy with thunderstorms early in the week becoming hot, humid and overcast. I fertilized with I49 grow 1 tbsp/gal & 2 tbsp I49 Flower. I added this as a preventive measure since I’m seeing issues with nitrogen usage in the lower leaves even though she is in super soil. AK47 must be a heavy feeder. With the extreme heat and rain, my AK-47xl. She grew a foot and is now 31 inches tall. She demonstrates resistance to fungal diseases and bug damage. In the background noise on the video is Cicadas. When they hatch, they crawl onto a tree or plant and molt. The adult has wings. This is the empty body casing. This year there are some but not a lot as in many years of their 17-year cycle. As always, thank you all for stopping by, for the likes and most of all growers’ love and support. Stay green, growers love 💚🌿 💫Natrona💫

Week 6

I'm going away for 30 days about a week into this grow. I'm going to automate weeks 1 through 5 by using the Blumat watering system along with the automated fan from AC Infinity. Hopefully, these will keep things going while I'm gone. I've never used the Blumat products before and I'm excited to see their potential. If I succeed, I'll return to happy 5-week old plants. If not, I'll have to start a new grow...which is what I was going to do anyway. I have nothing to lose but a couple of seeds. Let's get this automated grow started. Day 1 - I placed the seeds directly in a fist-sized clump of Coast of Maine Seed Starter soil that was then placed in a 3-gallon pot full of Coast of Maine Stonington Blend. This will ensure the seedling doesn't get exposed to the nutrient-rich soil too soon. I set the light 2 feet above the top of the pots so they have room to grow into the 18" to 12" range. I also set the light strength to 60% during germination. The temperature in the tent remained 75 degrees and humidity was 70%. I also covered the soil over the germinating seeds with mason jars to act as humidity domes. Day 4 - Both pots sprouted this morning. I immediately removed the mason jar humidity domes. I also increased the light to 70% strength and installed the Blumat watering system to help me keep things growing while I'm gone.

End of week 9 flush week, cut the blueberry ladies and put them in the mesh drying rack. Will update in 2 weeks with first smoke and dry weight, assuming she's dry in 2 weeks. Flush week for the Super Lemon Haze, she'll get chopped this coming Sunday.

Tiny Potter grow for the contest is coming along nice. She just stretched a lot. She is progressing into flowering nicely. She is really root bound badly. So draining is extremely slow. I feed her twice a day to try to keep wet, and ph in check. She is growing great. Curious to see how she finishes. 🤞 for another trophy 🏆. She has done great under the Mars Hydro FC4800 light. Thank you Mars Hydro. 🤜🤛🌱💡. Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

- Defoliated the bottom half pf the plant at the start of the week removing all leaves and little stems so the plant can put more energy into the buds on the main stem. - Some of the outer leaves are getting burnt from the strip lighting. Nothing I can really do about this, next grow ill make sure the plant doesn't get so big. - Looked like the plant was getting some slight nute burn so I decided to back off from the Canna PK this week. I might bring it back in week 17 if shes looking hungry. - Installed a feeding tube to avoid spilling nutrients on the buds and reduce the amount I have to move the plant in and out of the bucket. - Tested my runoff Ph and its at about 6.5. Should I lower the Ph of my nute mix to compensate or is this normal? - Buds are coming along nicely, smell is very fresh and light.

Was a real pleasure to grow. Super easy with a low budget light and top nutrients. Got really nice plants and was really happy to find that I'd be happy am to do more strains from Divine Seeds. I've already started new strains in big pots giving me big phenos Delighted to have this in my collection. Took 10 days to dry. Only got about 2 weeks into the cure before it was gone. But, still has a lovely high & taste

Seventh week of flowering: I opted not to put a net to facilitate access to the room. As expected, the buds are starting to be too heavy. I hang them one by one, on hooks high up. The buds swell and still smell ! I increase the EC to 2.60 Good hydration, no dead leaves to remove. See you next week !

Day 85. Just before lights photo's for better true colour understanding, Bio Grow and AlgaMic is out, after finishing this cycle CalMag and Silica out too. Hope its not too early, but girls are really healthy, time to pump up the flowers not leaves :) Day 86. Girls just flying, very happy with Gorillas and Control Garden looks really funky, they stand under no direct light on them... and still flowers looks amazing. Got my new mobile, had to try out :) Next week very busy at work, no updates I think. Day 89. So again i made mistake, while watering them last time accidently left heater on, they overdried , plus temps where at +33c ... Bunny Gorilla looks bad, Gorilla Max got biggest pistil damage, half went brown. Thinking i took nitrogen too early out, but we shall see. On other hand all Control Garden took it well even Cookies with theirs waxy leaves stood thurst nice as such stress can be ... Planing to do defoliation next week, but if Gorillas started to eat themselves already will leave them as it is. Future will show .. Happy Growing !!!

Wie man sieht, haben die beiden F1-Samen ein enormes Wachstum gezeigt, während das Apple Flitter langsames Wachstum zeigte. Ich baue zum ersten Mal F1-Autoflower-Samen an und die Wachstumsrate ist wirklich beeindruckend. Nach drei Wochen habe ich Holzstäbchen zur Unterstützung hinzugefügt, und die Wachstumsrate der F1-Samen ist weiterhin beeindruckend. Sie sind bereits bereit, Blüten zu bilden. ご覧の通り、2つのF1種は驚異的な成長を見せたのに対し、Apple Flitterは遅い成長を示しました。私は初めてF1オートフラワーの種を育てていますが、その成長速度は本当に驚異的です。3週間が終わった時に木の棒を挿して整理しましたが、F1種の成長速度はやはり驚異的です。すでに花を咲かせる準備ができています

Day 37 We started with nutes today Then all day long outdoors From 6AM to 6PM Plus CFL afterwards They rest for 3 hours and then CFL again Btw accidentally snapped one part of one big leave but that okay Since we don't do defoliation on her We guessing it's okay she will recover soon Day 38 Since she's such a queen we wanted to upload a video showing how she starts flowering for the record, thanks a lot You can Always follow me at Instagram @cannagrowersiriuz Also don't forget to add your comment below, it is important to us! We want to learn, any tips, suggestion, more than welcome my friends Happy Growing Day 39 Some mins before installing ScroG Day 40 Wonderful, she's out of there already so huge, full of buds Day 41 she's actually doing great full of buds but those 2 first leaves are a little bit sad looking weird plus those black dots idk and it's turning yellow in between I decided to remove it and well, I'm hoping she's doing well what else I could think of guys any help or concerns? At the end of the day, she's overall healthy and strong Day 42 Time to feed the babies, so we added 900PPM (300ml) floranova grow Followed by 1590ppm (300ml) flora nova bloom to make sure she's got all nutrients balanced well, also added 400ml of plain water after that so they could get a nice run off. I think they're happy and we gonna check on them in a couple days to see how they go, Ph is around 6.2 which is great Temp outdoors from 7-@ 1pm around 25C to 36C Then back indoors Temp is 28C and drop to 22 at night and dawn so they're good and comfortable Keeping humidity lvls around 40/65% top Nice AC and Fan for air circulation Thank you all for your support

This week I found fungus gnats I added sticky boards and mosquito bits. A small amount of fading on oldest leaves. I did a small defoliation of the yellow fan leaves. I added bone meal to the top layer of soil and worked it in. Water at 6.5.