First week of flower for this healthy and happy FFT. Really looking forward to Fastbuds releasing the names of these strains, because they all grow very differently. I'm guessing at #8 being cheese, but it will be a complete surprise on all the others. This girl is sitting pretty and taking up her designated space perfectly. A heavy defoliation on F1 opened up some tops to the light. There has been a massive growback in just 3.5 days of flower, as well as a massive stretch. I have all the headroom in the world, so I will let these maximize. All healthy, no spots or bugs, so these are just booming. They will get a final heavy defoliation on F21, and then maintenance plucking to maximize cola exposure.

Day 2 - LST and topping/mainlining where possible before flowering Both plants have broad leaves blocking light to the canopy

She continues to develop nicely. Unfortunately I managed to break two more branches, from both she recovered instantly and the branches started to heal already. (Need to be a bit more careful going forwards). The quick healing I would either account to the genetics, but would also contribute it to the rizothonic from canna, as her root system is also a lot further than the plants I grew before. She already smells super strong, can bare keep the tent open for long.

Good week, I think I am done tucking the scrog for this run, screen has filled out reasonably well and am happy with all the room variables. I did add some beneficial bacteria as my ph spiked a few times and my res tank felt a little slimy.. so fingers crossed that takes care of that.

Holky jsou připraveny na sklizeň dva dny tma a hurá na to😁🤨😉🍨🍧🍦 Každá je jiná těším se .🚀🚀🚀

I finally decided to cut my losses and focus on just one plant. It's time to go all-in on my "one plant, one light" goal. It feels kinda scary, but I'm also really excited to see how much attention this plant's gonna get. Pretty sure I kept a pheno that is going to be huge My Pound Cake plant's leaves are looking awesome, just like the pictures online. It's growing so fast, it's almost doubled in size in the past week. I'm really excited to see how big it gets by the end of its life. I messed up last week and overwatered my Pound Cake plant. It got really droopy and sad-looking, but luckily it's starting to perk up again. Definitely a lesson learned about keeping a closer eye on things.

-Sponsored by: 🏡GANJA FARMER SEEDS🏡-💡VIPARSPECTRA💡-💐GREEN BUZZ LIQUIDS💐-🛠️WEDRYER🛠️ 🏁18/6 hello growerz, with today I start the resumption of diaries on GD. I have 13 new genetics in germination and as many diaries. I start by putting the seeds in water for 24 hours, after a day I will put the two seeds in two different jiffies, one with humic acid from greenhouseseeds and the other with just plain water. Get comfortable and follow the updates 😉👋🦄 19/6 The seeds were divided and placed in two different jiffies, one with humic acid and one with water only. 21/6 after another 24 hours in the dark the jiffies were moved under the lamp. let's start the dances! 23/6 Nothing to report, if not the high temperatures of these days, uffff 24/6 still nothing to report 25/6 still nothing to say .-. 26/6 one of the two seeds has rotted qq I didn't realize the too high temperatures in the germinator and one is officially dead. but I have planted a new seed with which I will open a new diary. I remain hopeful for the second seed 30/6 the second seed is officially deceased, rep. great progress for the survivor, yeah! __________________________________________ Personal advertising (contains affiliate links) __________________________________________ 🦄 Huge collection of exquisite genetics since 2009! Anonymous shipping! ✅https: //bit.ly/Ganjafarmer __________________________________________ Did you know that Green Buzz Liquids fertilizers are 100% vegan? A complete line of products ready to give the best to each of your plants! Visit the site and see my journals to see how they work 🦄 🤯 And with the code "dreami t" you will immediately receive a 15% discount on your purchases ✅https: //bit.ly/GreenBuzzLiquidsPro __________________________________________ 👀 Are you looking for a good lamp to start with? 👀 🌞Viparspectra has something more than the others, take a look at their site. ⏩ Use "GDVIP" for an extra discount or "DREAMIT3" for an extra 5 %% discount 👀 Search for it on Amazon ✅Amazon USA: https://amzn.to/30xSTVq ✅Amazon Canada: https://amzn.to/38udUVe ✅Viparspectra UE: bit.ly/ViparspectraUE ✅Viparspectra USA: bit.ly/ViparspectraUS ______________________________________________ 🌈 Tired of blowing on your weed hoping it dries quickly? Check out the Wedryer website! You will find a well-made accessory that will help your weed dry in just 8-10 days without the annoying risk of finding mold or other annoyances! (no affiliate links) ✅https: //bit.ly/Wedryer_ ______________________________________________ 📷🥇Follow the best photos on Instagram 🥇📷 https://www.instagram.com/dreamit420/ Backup https://www.instagram.com/dreamit4200/ 🔻🔻Leave a comment with your opinion if you pass by here🔻🔻 🤟🦄💚 Thank you and good growth 💚🦄🤟

I've already smoked some of this sweet one😘

Very fast seedling process, seeds stayed soaking for 24h and in the water they were already showing the first white root hair, another 48h in the paper towel and the day I potted them up they showed cotyledons. They took around 11 days to reach third node and complete germination but honestly I belive it could be faster if in better enviroment, mainly the humidity which was low and I transplanted them a day late. From day 5 I started feeding them exact same nutrients and ratio from the first vegetative week but starting at 0.4EC and increasing by 0.1EC/day until 1.1EC

Update Day 14 Flowering: Pog is ambling along stacking her neat little buds up ready for long colas i hope. Temps here have been crazy hot for the UK. 34°c at points which is slowing them a little but with lots of airflow incoming , the rh is not too bad at 70% and i am watching for mould like a sheepdog for wolves.lol Another happy Barneys Farm Girl

Week 6 for Moby Dick, She was moved outdoors at the start of the week, shes been adjusting well besides the fact shes been having issues with aphids 😥 But shes been getting sprayed water every sun rise to keep them under control as well as me going in there & killing them when i can spot them every morning & evenings. Trying to get my hands on some pyrol products to clean her up nicely as well as clean up the outdoor space. But wow look at her size... really looking forward to her coming out with some flowers😍

Start of week 2 flower today, introducing big bud this week, gave them the full 4ml per litre recommend on the bottles and noted a small mute burn on a few of the leaves but nothing major. Switch to larger reservoir (25l -> 100l) and added bubbler stone as I'll be keeping the feed over 3/4 feeds, this should help keep the food solution oxygenated and fresher. Overall the plant is looking very healthy and seemed to transitioned to bloom food v. nicely.

Took the 3 other plants out side, 2 out in the country one in my backyard. So she has full range of the tent just switched from 14-10. So the stretch should start soon :) oh and I dont water it daily just when it drys usually 2days.

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.

An intense heatwave has been rolling through the grow environment, making it tough to dial in the VPD. The air is very dry, and since I don’t have a humidifier (yet), mitigating the high temperatures has me stuck between a rock and a hard place. Fortunately, I’ve reached flower, so a drier environment isn’t the worst thing in the world. But it’s definitely been a challenge! --- Quick rundown on everything else: Watering: 1500ml every third day Fertilizer: According to the BioBizz schedule Light intensity: ~1000 PPFD VPD: Around 2.23 kPa Temperature: ~30°C Relative humidity: ~40%

Land race Psychedelic this one did not turn Purple but she tastes purple and makes you feel like the color purple I think Franco and Prince are smoking this stuff in Heaven !

PSA!! PSA!! PSA!! WATCH those ZeroWater pitchers... when the filter goes, it goes FAST. Leaves you with a ton of undesirables, and AN EXTREMELY ACIDIC PH!! Acidity in the body leads to CANCER! will kill your plants fast as fuck too. ======================================================================================================== 2 Girls 1 Cup week 11? We should come to a finish this week... oh the excitement. Can't wait to see WG without her leaves. Going to have to cut each branch and hang individually due to the density of its structure. Got this far, don't want to risk moldy weed.. damn I'm gonna get bored while drying/curing not having a plant or diary to occupy the time. Day 77- currently flushing the girls. GC isn't ready for it, but she isn't in charge here. She should have stuck with WG when she extended a helping hand. Since falling behind, WG has thrown up a peace sign to GC as to say "see ya sucker". It's my favorite bud by far on WG. Bitch has got an attitude 🤣. RES sitting at 87ppm @5.9. Yellowing has started.. going to have to check trics more often so I get that sweet spot I'm looking for. ======================================================================================================== Day 78- these girls are starting to stink! Come on WG... ripen up so we can get this over with.. lowered lights power a bit today. RES climbed from 87 to 137. Drained 2gal, added 2gal RO. down to 38ppm. Forgot to mention the ice probe has been unplugged for over a week now. Been putting a 3/4 full 1L frozen bottle in the RES to chill. Rotate out every 12hr with a fresh. At lights on, and 12hr later. Full bottle got Temps too low for my liking. ======================================================================================================== Day 79- tick tock.. tick tock.. come on WG.. she's showing a little fade on her leaves. Seeing more of a calcium difficiency on her fans than fading honestly. Trichomes taking their time ripening as well. I'm SURE this strain ambers up.. taking their time for me though.. dont know how long I feel comfy flushing hydro though.. I did notice a few exploded trichomes up top, which has me thinking I need to go ahead and chop within the next couple days. If I notice any more ruptured anywhere else I haven't poked it with the scope.. I'm hanging the bitch that night. May give her 24hr dark period, since I've tried some other bro-science and it seemed to help. *edit* felt bad starving WG and she's not more amber coated. Gave her a bit of nutrition tonight. GHE aggressive ripen. M-2.8mL/g G-2.8mL/g B-4.5ml/g and 5mL calmag (using RO). Came out high @ 867 so I pulled 2L and dumped 2L RO in. Sitting at 613 @ 5.9. ======================================================================================================== Day 80- well, the 3 days starving the girls kicked their metabolism back in gear. I want more amber before chop chop. They quit eating and were drinking MUCH less signaling the end. Was down to topping off once a day, maybe a liter to a liter and a half. Since feeding yesterday, they've started eating and drinking like they were on week 10 again. Topped off 3.5L in the last 16hrs. TDS dropping with water level, even more when topped off with straight RO. I'm not giving em any more nutes. Last push for some extra weight before the end. ALLOT more frosty today than yesterday as well. ======================================================================================================== Day 81- Started flushing again. Maybe starting their metabolism again will help ripen these trics. If not, they're getting chopped @ day 84. Don't want to let em go too long and regret it. I may have f'd em up feeding again after the 3 days starving. Time will tell ======================================================================================================== Day 83- still waiting... 💤 Going to order some bubble bags. Freezing all GC and trim/larf from WG for some bubble hash. GC is frosty and all white like WG, just tiny popcorn shit everywhere since it's been neglected and abused over and over and over and over 🤣. ======================================================================================================== As always, thanks for stopping by and checking out my current grow. full timelapse added to this week 27-70 (looks better on YT.. https://youtu.be/8JdUkR36Wfc)

The leaves are droopy cause i went on holiday and my drip system didn't work for 10 days, but they are STRONG, they will come back easily. Great flower stretch and awesome structure.