05/04 - defoliated some and removed a dozen or so sucker branches. Upped nutrients to manufacturer's recommendation, plants don't seem to show nutrient burns yet - PPM was near 1400. Overall not much stretching, could have let veg another week without much problem I think. 05/10 added a small dehumidifier (vivosun - 1.3L tank.. it's small). That bubblegum is really growing nicely. With training ( no training on this at all - only topped once) it would have been a beast. Didn't clone it either - because I'm smart like that.😂 Added 2ml/L of AN's B-52 on day 20. Just happened to be feeding nutes and would have been adding that in week 4 of flower - as per AN feeding charts. Real nice trichome production on all plants. They all currently smell kind of piney - but the Bubblegum is sweeter, the Pink berry is more of a tart-ish citrus/grapefruit-y. The northern lights was just very vaguely piney. not much smell.

ITA: topping a tutte le piante compresa la strawberry lemonade. Piccolo deficit della LSD probabilmente dovuto a una carenza di calcio/magnesio, ho quindi tamponato la soluzione con 0.5ml/l di cal-mag della biobizz. In seguito ho piegato i rami più grossi verso il basso i modo da far passare più luce, anche negli intenodi più bassi. La prossima settimana conto di toppare nuovamente gli apicali e fare una nuova LST ENG: topping to all plants including strawberry lemonade. Small LSD deficiency probably due to a calcium / magnesium deficiency, so I dabbed the solution with 0.5ml / l of biobizz cal-mag. Then I folded the thicker branches downwards to let more light through, even in the lower areas. Next week I plan to patch the top management again and do a new LST

Guava Sundae – Week 9 (Fast Buds Outdoor 2026) The weather was okay this week. Guava Sundae is now being fed more strongly according to the feeding schedule and is doing well overall. She has reached about 55 cm and is fully in flower. The aroma is already very strong. I checked the trichomes for the first time. They are still mostly glassy with some milky ones starting to appear. Nice development.

Strain is stable af. Wow this flower is great. Sebastian from fast buds was right, this gets you really stoned!! Thanks fastbuds!!!

Was a tough last few weeks lots of work to be done big problem with humidity finally sourced a good enough dehumidifier and added another 1200 light. Lemon skunks were suppose to be autos but no signs of flowering yet so I'm forcing them with 12/12. No room left in the tent now because photos are going into flower too

Start April 4th. Day 1 vega. Hey! Four seeds have hatched. One is smaller than the others. I planted the seeds in GroBag spilled with clean water ph 6. I'll be back with more information Day 2 I made a video, it shows that the seeds have taken root well. Leave your comments. I'll be glad to chat.

It’s Aliiiiiiive! Finally built my second matching hybrid NFT hydro system after getting the autos out of the main tent. 6” Rockwool cubes on draining racks in 8 gallon totes with an 8 gallon res. Waiting on some parts from amazon to add the second pump and feeding tubes. Hoping to veg them for 3-4 weeks before I flip the schedule. Haven’t decided if I want to scrog them yet or not.

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.

Due to change in weather i moved the red critical Autoflower inside under a grow light and she responed very well. Hope the buds keep getting fatter and thicker. The smell is amazing and the colours on these buds are amazing

This will be my last 'grow' pic for this plant as I plan to harvest within the next few days. I just fed her for the last time (I think) and will let her dry out for a couple days and then time to chop. I'm really happy with this one! Buds are a decent size, tight, sticky and smelly! Love it!

Germination date 🌰 10/03/2021 Day 99 🌱 22/06/2021 Strain 🍁 Purple Matcha, Humboldt seed bank Nutrients 💉 Advanced nutrients PH perfect sensi grow A+B (veg) PH perfect sensi bloom A+B (flower) B-52 (through veg until week2 of flower) Voodoo juice (🖕🏻) Tarantula (🖕🏻) Piranha (🖕🏻) Sensizym (all the way through) Rhino skin (🖕🏻) add first leave for an hour Big bud coco (week2+ of flower Bud xfactor (🖕🏻) Nirvana (🖕🏻) Bud igniter (first 2weeks of flower) Overdrive (last 2weeks of flower) Flawless finish (flush week) RockHoldings Rockresinator(week2+ of flower) Vitalink calmag Set Up ⛺ amazon special 1.2m x1.2m 💡 spiderfarmer sf4000 📤📥 AC infinity 6inch 💧 10lt dehumidifier Notes🗒️✏️ We are done 🌱👍🏻 dripping in ❄️❄️❄️❄️❄️ Another beauty of a grow finished, I just hope I can get the cure right with no a/c. Humboldt have seriously smashed this strain. Great for beginners as it will take everything you give it. Stand by for the havest results and thanks for following everyone means alot ❤️🍁 Massive thanks to PharmaZ for sorting us out and helping us along, top bloke go follow 👍🏻 Stay turned and happy growing fam ❤️🍁🌱👍🏻

Ya es la décima semana de vegeta de estos esquejes y va todo muy bien, muy pronto se cambiara su ciclo de luz a 12/12 para iniciar la floración. El día sábado 25/07 se hizo la primera aplicación de Delta9 la cual fue vía foliar, a los 10 días ,es decir, el martes se pasara a ciclo 12/12 y se hará la segunda aplicación también vía foliar, la tercera será 10 días después de la segunda y será la única que se realizara a través del riego. Estoy dejando que se vuelvan bien frondosas para hacer un pequeño raleo el día que cambie el fotoperiodo y puedan estar listas para entrar a floración. La temperatura con el led apagado es la única preocupación veré alguna manera para sobrellevarlo durante la flora que es donde mas horas estará apagado. Por lo demás todo va bastante bien, las dos plantas van con buen aspecto y sin posibles carencias. Cualquier recomendación será bien recibida!!

😎09/26/2023----____👹YOOOO WHATS UP GANG!!!! BIG THINGS POPPIN FOR WEEK 3 LFG👹!!!!!!!!!!!!!________________ _____________________________________________________________________------------------------------________________________________--------------------____________________________ SOOOO TINGS LOL GOING ON THIS WEEK, FIRST AND FOREMOST DOING STANDARD WATERING EVERY 2.5 DAYS, USING THE FOOP NUTES VEG1 AND VEG 2 WITH SWEETNER. SECONDLY, I HAD HER FIRST TOPPING DONE AS YOU CAN SEE IN PHOTOS, SHE IS RECOVERING PRETTY QUICKLY FROM THAT AS WELL. AND LAST BUT DEFINETELY NOT LEAST, I HAVE UPGRADED SOME HARDWARE INSIDE THE GROW TENT, I HAVE STARTED USING THE MIGRO ARAY 2 +RED 120 W AND I MUST SAY THIS LIGHT LOOKS LIKE SOMETHING OUT OF A SCIFI MOVIE SUPER SLEEK DESIGN, VERY VERY VERY WELL CONSTRUCTED LIGHT, THE WHOLE THING IS AMAZING TO BE HONEST AND I GOTTA SHOUT OUT TO SHANE TORPEY OWNER OF MIGRO, YOU KILLED IT MY GUY THIS SYSTEM IS A KNOCKOUT. WONDERFUL WORK SIR!!! THAT BEING SAID THANKS FOR STOPPING BY IF ANYONE WOULD LIKE TO COMMENT OR GIVE ANY ADVICE AS ALWAYS IM SUPER THANKFUL FOR THAT THANKS!!!!!!!!!!!!!!!! LETS FUGGIN GOOO!!!!!!!!!!!

Nov 20th-27th Still Feeding at between 1.0 and 1.3 EC for the 12 Coco/Pearlite plants

Sorry for the lack of uploading ! These plants have been perfect from the start. Budding out nicely and haven't shown any signs if defficiency. All training has been stopped and I have started cutting back on the nitrogen for the 2 autoflowers. The peanut butter cookies is growing to be very bushy so I have done some light defoliation to help with light penetrative to the lower canopy of the plant

First week of flowering out the way all plants seem nice and healthy, there has been big improvements with the 3 tropicana and 2 mimosa what i had stunted over the past 7 days havent half shot up in size and looking nice plants now cant wait to get the next couple of weeks out the way and start to see these ladies fatten up

Subimos algo más los ml de terranabis,buena asimilación y engorde,gracias a enzynabis que busca el equilibrio de todo.

Note : + jegliches Zubehör wird in der GermniationsWoche aufgelistet . Ich hab keine Ahnung was es wiegt , da ich keine Zugwage hatte. Warten wir also ab was es an trockengewicht wirklich wird. Aber da ist viel Drann , bei 116cm größe ist selbst der kleinste Bud noch groß :)) Es sind nach 5 Tagen Trocknung bei 22°C und 55%rH genau 204g