Day 36 Ladies look great on the start of week 6. Yesterday’s feed went in well and they both seem stretching their nodes. Day 37 Watered them with water only today. They look happy and healthy. The red stems on the taller lady are genetics as kindly confirmed by Fast Buds. 🔝 Day 39 Water day today / mixed different cocktails for both with specific needs. Run off Ph and EC improving :) Day 40 All looking good today 💚 - both plants have some slight rust spots on some leaves but I think it’s Cal/Mag deficiency and yesterday I both gave them some. Today the spots seem to have remained the same so maybe it’s solved. Day 42 Ladies are stretching their tops during these days and filling up slowly but steadily. All looking good till now for the Gelato Sisters 👯‍♀️

So, I’m excited. New lights today. Horticultural grow lights quantum boards built for me by growerslights.com I don’t have to time or knowledge to build one but I wanted one. Growerslights builds and tests for you for $50. Money well spent. This light is the shit. Full stop. So bright, so efficient. I’m getting a lot more light for 80w less per hour and that’s on full power. I’m going to start at 1/3 and slide up a little over the next few days. It’s the hlg-650h ok commercial done. I cannot wait to do a full grow under this monster. As far as the current plants. They’ll do their last week and a half under it. I’ll move the mars hydros to a small cloner I got. Flushing now until harvest on the weekend of the 30th-31st

Both plants are doing excellent. This is the end of week 6. BHB will be ready by mid-late week. CBD still has a couple weeks at least, I think. Really bulking up! BHB is ripening. Branches bending. 80-90% cloudy trichomes. BHB is slowly having it's nutes reduced and fresh water added. By weeks end, it will be fresh water only. Not much else to report. Researching dry ice extraction for the CBD. Will probably use fresh plant without drying to save the terpenes. Once the extraction is done, the trichomes will immediately be put into a MCT oil where it will be decarbed.

Great grow from start to finish, very resilient plant and would of given her some more TLC if I was to grow her again.

FOLLOW THE GROW———>https://youtu.be/SjZ-eizIP7o Growth has been steady and lush considering the fact that there has been a 2 week heat wave. For the plants in the bucket the 2 smaller ones are phenos of my previous Fanta Sea RBX grow, and the bigger one is a Sherb clone from my previous grow as well

Thing's are still going well, feeding is going well and they are eating at 2.2 e.c, plenty of food and boost in the solution with no burn, I may increase over recommended amount, had some weird stretching on two of the plants, not sure if something is wrong or just the genetics.. seen first video for example.. Ended up having a fair amount of stretching from the two Jaffa Cakes relative to the washing machine so I've out up the second support net but used it to further hold down the branches. They are drinking lots at the moment, fill recommended dose of A/B/B-52/BigBud, drinking a total of 5-6ltr per 48hrs, e.c coming on around 2.4 to 2.6 however plants seem to be absolutely loving life :)

Buds getting big. Very good sweet smell. Remembers a little bit the Radical Juice smell.

Do not pay attention to the temperature on the thermometer in the middle, it lies by a couple of degrees. I have a good thermometer on top of the box that shows the temperature. Day 29: After a terrible fracture, we see that the plant is beginning to recover. I'm honestly disappointed because it makes it very difficult for me to train mainlining and it will also increase the amount of time it takes to grow. Day 30: It looks much better already, I could superprune the right branch, but I don't want to stress it. I will try to bend the right branch harder, I will bend the left one a little in the morning the next day, maybe early. Day 31: This morning I cut the lower leaves, photo in the evening and continued the LST training after the injury. Photo in the evening. Day 32: I am completely sure that the plant has moved away from the stress, but we can see on the left circle, the right bud (and side) slowed growth. Day 34: I saw traces of salt on the tips of the new leaves, so now I pour water with regular 15 PPM.

Harvest day 70 since the time change to 12/12 hrs. Hey guys :-) Finally the time has come . The lady was harvested. After the trichomes have been checked (70% milky 30% amber) as always, it was left in complete darkness for 48 hours before it was neatly trimmed by hand. After trimming, she was put back in the drying tent on nets. There they are allowed to dry for the next 8-12 days at 62% humidity before they are put into the jar to ferment with 62% boveda packs. After about 4-6 weeks in the jar I will swap the 62% boveda pack for a 58% boveda pack where it can be ready for another 4-6 weeks to enjoy :-). As always, the remains of the leaves are used to make Ice o Lator and oil. Of course, as always, there is a final update during the fermentation process. Until then, I wish you all a lot of fun with this update. Stay healthy 🙏🏻 and let it grow 👍. 👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼 A thank you for this wonderful strain goes out to Herzog https://instagram.com/herzog030?utm_medium=copy_link and the Exotic Seeds team You can buy this Nutrients at : https://greenbuzzliquids.com/en/shop/ With the discount code: Made_in_Germany you get a discount of 15% on all products from an order value of 100 euros. You can buy this Strain at : https://www.exoticseed.eu/ Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.8 - 6.4 👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼👆🏼

THese Girls did not turn hermi But they turned Krazy and have been Stretching way more than there parents did and is flowereing like a week longer to start than its hermi parents.. i even trimmed it to bare ones when i started 12/12 and kpt it tied down to trellis hight for two weeks before letting it get virticle. then to my surprizi in only two more weeks its grown over 6' wich is higher than y lights will GO. had to Bend it down asmap last week now i have to crack the stalks again to barely keep them 8 in below my lights im down to Three inches and they have stopped stretching and have maintained the 3 inches hoping to get lucky and not get light burn Im Going to try and tie it down lower but already have way to much horizontal branches from bending it down every day this week wich is blocking a lot of light to anything below 4 inches from the top isnt getting the proper light and space to flower they bloom alot better when they are virticle to the light and not tied down virtical making the flowers only get the one side of the flower instead of all of it This Grow has been the most challenging one like Nothing Went as it was supposed to ive grown this strain times prior one from seed and two from clones and this grow was 2 Cloned branches with Flowers in the 4th week.So im thinking this is the reason why the speedy extra growth is because the clones were flowers back to veg for 5 weeks then flowered again thats the nly thing that is different also they have Zero male flowers unlike their Hermie mothers

Strain: Chocolate Haze (Royal Queen Seeds) Medium: Coco bricks (Action budget bricks – hell yeah 💰) Light cycle: 12/12 from seed Grow Style: No training, no stress – just flow Grow Medium Prep: 500L of coco – never again in one go 😅 The Kickoff 🚀 This run started off wild and direct – no veg time, straight into 12/12 with Chocolate Haze. I wanted a quick turnaround and thought, hey, why wait? I germinated 14 seeds, hoping for at least 9 strong ladies. Ended up with 11 survivors – not bad! First few weeks were a bit chaotic: stretching due to low light (I tucked the seedlings under mature plants, which I do not recommend 😆), and the coco prep took way longer than expected. But hey, that's the game. Early Veg/Bloom — Lessons Learned pH: Started a bit high; some light green leaves at first EC: Too low at 1.3 — they weren't having it. Upped to 1.7 and then to 2.1 later Environment: New extractor dropped temps way down (25°C vs my usual 30°C). Thought it would help, but growth felt slower Coco quirks: They looked overwatered at times, but coco is tricky like that. Eventually, roots hit the bottom and they took off Around mid-March (3 weeks in), pistils showed up – officially the start of flower. I topped them once just before full bloom kicked in. Always a strange move, cutting healthy plants... but they bounced back beautifully. Nice and bushy now. Week 2–5 Flowering 🌸 These ladies are small but mighty. Not tall, but full of energy. The canopy is tight and even (except for one shorty), and they've been stretching like crazy — classic sativa move. Had to raise the lights twice in two days. I’ll probably do some defoliation soon to slow things down a bit. Environment is now dialed in: Temp: 30°C with lights on RH: Holding nicely in that humid sweet spot CO₂: Set to 500ppm (passive mostly, no full-on enrichment) Feeding is now solid, color has recovered beautifully, and the buds are starting to form nice stacks. I’ve kept it low-stress — no nets, no heavy training, just letting them do their thing. Observations & Setup Tweaks 🔧 Ventilation: Running the fan at just 30% now. Tent takes 18 seconds to vacuum seal, which tells me airflow is minimal – less CO₂ loss. CO₂ System: Minimal usage at 500 ppm. I’m not going all-out with gas bottles; it’s just there as a buffer. Structure: These Chocolate Haze plants don’t get tall, but they do fill out nicely. Perfect for a space where height is limited. Auto side note: One of the autos in the same tent is way taller, but less dense. Makes me appreciate the Chocolate Haze structure even more. Current Status (April 17) 📆 We’re deep into flower now — week 5, and it shows. Buds are swelling and resin production is kicking in. Nothing major to report (which is kind of the point of this grow — set and forget). Just a slight dry issue with one auto, which I adjusted on the Blumats. Besides that? Happy plants, happy grower. 🌞 Check the latest pics — they speak for themselves. Final Thoughts (So Far) 💭 This Chocolate Haze grow has been chill, efficient, and surprisingly hands-off. The direct 12/12 schedule really works when you're going for a fast cycle with minimal hassle. And even though I’m usually more into hybrids, this sativa-dominant lady is winning me over — the structure, the vigor, the smell… mmm. Now we wait for the real magic — the last few weeks of flower. Trichomes incoming. 🍫✨ Stay tuned for harvest updates — it’s gonna be sweet. Feel free to drop any questions or thoughts. Always happy to share the love for the plant. 💚 Peace

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.

🍼Greenhouse Feeding BioGrow & Bio Bloom 🌱GARDEN OF GREEN SEEDS ⛺️MARSHYDRO The ⛺️ has a small door 🚪 on the sides which is useful for mid section groom room work. 🤩 ☀️ by VIPARSPECTRA (models: P2000 & XS 2000)

Just winding down. Gonna go lights off for a day or two now at week 10. Tangerine dream are close to done and grape ape are throwing bananas for past week so it’s time.

Would love to hear from everyone..

Esta cosecha fue muy buena con excelentes resultados de flores muy compactas y demasiado resinosas , la genética en sí es muy resinosa con olor muy característico , con sabores terrosos muy marcados .

We have gone a little lighter in coloring again but I am adjusting lighting a little more on her and defoliating a little but so she can use her energy in places she needs too.