Bruce Banner #3 Fast is doing her thing. She is growing great under the Hortibloom Solux 350. She got defoliated, and some root pruning. I will likely be changing light times next update. Thank you Hortibloom, and The Original Sensibile Seeds Company. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

Week 6 - The Purple Power Is No Longer The Tallest In The Forest But It’s Still The Prettiest. The Purple Power Has Been Dethroned By 4 Of The Other Plants. Everyone Except For The Gorilla Glue Is On Bloom Nutrients. Height: Gorilla Glue: 19 Inches Purple Power: 28 1/2 inches Girls Scout Cookies(3gal): 30 inches Lemon OG: 34 1/2 inches Girls Scout Cookies(5gal): 34 1/2 inches Stardawg: 33 1/2 inches These Plants Are All Correct Measurements Size May Look Different In Picture Because Of Pot Size.

Not much to say, everything seems okay!

Last week went well. She is growing up at a good steady rate. Hope it continues like this for another week in veg and I think it will be a decent sized auto for being in a 3 gallon container. I started lst training and because of how fast it grew,.it started to split the plant in the middle at the base of the branches. To avoid it splitting and causing damage, I did some supercropping to help even out the canopy some. That's the main goal of the week is evening up the branches.

29/3 the grapefruit is coming along nicely, buds actually smell like grapefruit! Lsd is so impressive! it’s on fire! The west coast ogs are still quite a bit behind..looking online, a lot of people seem to get these buds growing huge! Hopefully they get there.. BCN critical xxl popped 1 day after the LSD but has been the slowest to flower..It's just going into flower now. Light has been at 75% for the last week or so and is at around 23inches above. Have been feeding all plants alternating water/feed/water/feed 1 litre every 2-3 days. So far so good! 4/4 bcn critical xxl isn’t looking very happy at all..she’s fully flowering now but all of her new growth has been loooking droopy for the last week…not too sure what’s up there..

63 days!!!! The girl got a lot of sun this week, the air temperature also rose above 30°, so the girl has to be watered every day, all because it is a northern balcony project with not very good conditions, but in general, her current condition really satisfies me:) a real decoration of the balcony:):) good luck to everyone:)

Hello Growers and Tokers! 👋 👩‍🌾 🧑‍🌾.🔥💨 A lot to talk about this week.. Got my lights installed and oh my have they grown. Royal Gorilla has taken a major growth spirt this week, new growth everywhere and getting taller. I spread her out a bit doing some LST. She took it great and ket growing. Amazed with how these lights are working for them. Most likely will do some defoliation next week to clear some space, more light penetration and have the main colas grow. Happy with how this girl bounced back, she had time to recover when they were all under the 150W CFL... and now she's at an even height with the others. Watering every other day.. Hope your week goes as great or better than mine, have a good one growers!

I love this plant. She is so strong and grows with a lot of vigor. I am a little annoyed as I have been quite busy so I have been feeding the room the same mix and I think this one is started to show signs she is pissed off at me . There are the start of nutrient burn on her tips. I do not like this. I do not want this. So I I'll make her a slightly different feed this week and reduce the EC by a bit. Back down to a 1.5-1.6ec . Lights are at 40% drawing 180w. Lovely..😎 Uvb is not on yet as I have been away working and don't want to scare my wife away from the great job she does feeding when I'm away.. so I will deploy it as soon as I'm back and can be around to observe the effect.. it's all new to me so a bit of a lesson to carry forward to future grows... Thanks for passing. Grow well 🌿💚🌿🙏🏼

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.

In week 5 of flower and decided to start documenting my indoor 2x4 grow setup. We currently just finished day 3 of week 5. I have my lights running from 9:15PM - 8:45AM. I am not sure how I messed up on my timer but that's been my schedule since flipping to flower. I have an A/C in my bedroom that I duct into the tent. I have my A/C set at 62F and the tent gets to around 71-75F with the lights on. Lights off it ranges from 68-70F. I have a small dehumidifier in the tent that needs to be replaced because it is not efficient. I have an intake fan running at full blast at all times and my exhaust fan is automated to turn on based on temp and humidity. Week 5 has brought on a lot of strong dank smells and a whole lot of weight to the buds. They are really starting to thicken up! I have not had too many issues with this grow so far and luckily, the tent in clean and bug-free. Lots of resin and terpene production going on and you can smell and see it increase daily! I am following General Hydroponics Flora Series 6-Part grow chart. I am currently following the medium strength chart. I'll measure everything out exactly as the chart suggest then dilute my mix until I get to my desired PPM of 1000-1200. I PH around 6.2-5.8 and then add my microbes. I changed up my watering technique mid grow due to an issue I dealt with and now watering 2x a day. Lights on and right before lights off. If my lights didn't run overnight, I would like to add in a 3rd watering in the middle of my light cycle but 2 a day is working for now. I water until there is a good amount of runoff. I measure the PPM of my runoff compared to the PPM of my inflow mix and will keep watering until the runoff is 300PPM or less over my input. So if my mix is 1000 PPM and my runoff is 1600PPM, I will go back and water or as I like to think about it, rinse off the coco until my runoff PPM is at 1300-1000. It is a little tedious but it's a habit I formed and it does not take much longer to ensure your PPMs in the root zone is perfectly where I want it. I defoliated right before flipping to flower. Then defoliated 2 weeks later, and then a minor defoliation on week 4 of big fan leaves. I most likely won't be taking off any more leaves for the rest of the grow unless they are really blocking the light. I am planning on harvesting in week 8 or 9, depending on when the plant is showing it is ready. For General Hydroponics line, it has been the same nutrient strength/mix from week 3-5. Next week, Week 6, we start lowering the strength and adjust the amounts as we get into the later stages of flower and eventually will be flushing. For my flush, I will be using GH Florakleen, GH ripen, Mammoth P, and Bio-Fizz. Excited to see how these girls turn out! I'll be adding my outdoor grow as well as a new veg tent that I setup yesterday in my room. Stay tuned!

4/29🐼👍 I gave her about 2 L of water yesterday with a little bit of bud factor X I think about 2 mL into that and I don’t think it needed it but I’m trying it with some other plants and I had good results but that also could have been a result of the way I mixed up my regular general hydroponics nutrients which are my favorite. 5/5 🐼👍🔥💫

On my next round I am going to make sure that I make additional soil when I start a grow so I can keep topping the soil off to take advantage of all the root barbs popi g out

Casey's Rollex OG sprouted on the second seed. The husk was caught on the leaf, and was wet. Which caused the burn from the light on the tip. Regardless she is started and doing okay. She is still very young. Nothing more to report yet. Thank you DutchFem Seeds, and Spider Farmer. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

Start of week 6 of flowering for rhino number 2 Smooth as it can be will give her one more strong feed then will start flushing !!! The fade on her is beautiful loving it !!

Transplanted up to 7gal air pruners, rootzones look 👍. Just some last bending of branches to do this week, working towards leveling the canopy, getting close to flowering switch so I will start increasing the hours of darkness 1 incrementally 1 day at a time giving the plant ample time to prepare for the massive hormonal changes. This mimics nature slightly better given hours of darkness changing over the many months. Doing a sharp 18/6 to 12/12 feels like the plant really gets caught unprepared. Added far-red LED to simulate sunrise and sunset 30 mins each side. We have blassttttttt offff. The Cannabis flower is a special one for many reasons. Not only for the relaxed, joyful, euphoric and creative sensations it brings, but for how it specifically expands our consciousness. When the user (i.e. receiver) is tuned into the cannabis frequency, that is, tuned into the plant's intention aligned with our own, awareness often grows into areas of the unknown which instantly changes our vibration. The reason cannabis does this so well is due to its alliance with Gaia and the human template. It's why THC, the primary psychoactive component in cannabis is so welcomed by the endocannabinoid system of the brain. That system is innate to the cannabis plant. It’s familiar and this instantly harmonizes the frequency within our DNA field and the pineal. This means that cannabis can interact in a multi-dimensional framework within the human’s field and change its own consciousness in the process. Psychoactive plants are particularly exceptional at changing their own awareness by using the human being as a conduit, but cannabis is one of the best hence its widespread use throughout the world. This is how incredibly aligned it is with the human. But if the user doesn’t tune in, all that is experienced is a buzzing which travels though the head and body with nowhere to go. Nature’s psychoactive components are designed to transition our current reality, and they do this while synchronizing perfectly with the human field to send the user down another path that is quite different from everyday life. It can shift those seeking other levels of consciousness through portals to experience a different reality, one where common interactions are enhanced, especially since all senses must shift up. Sight, hearing, taste, smell, touch, and extrasensory perception are all enhanced. This makes food taste better, visuals appear more alive, heightened sexual experiences, and a nose that will track down your most desired scents. This is all completely dependent on the user’s intention to align with the cannabis frequency, one that requires permission to show you its beauty. On the flip side, it can also allow other less pleasurable frequencies to internalize, hence paranoia. So it can both expand and contract consciousness depending on the user’s alignment and intention. This is one reason why adults above 30 years of age (who are new to cannabis), can have very different experiences than those consuming it for the first time at a much younger age. This relates to differences in the maturity of sexual energy, wisdom attained, intentions, relationships, and many other lifestyle factors that influence how the cannabis frequency is integrated within. Getting high recreationally and expanding our awareness with cannabis in meditation can be two very different things. When the consciousness of the human being is in a state of expansion, cannabis brings a sense of wisdom that is unique because it delivers concepts through Gaia. These concepts end up being intimately related to our lives, since nature reflects a part of itself onto every aspect of us, just as we do to nature. It goes deeper than that. It can connect with not only our own lives, but other lives recorded on the planet through consciousness imprints while it gathers conceptual data. This includes data from those present on the planet and those who have past. Meaning it can retrieve information relevant to concepts it seeks to illustrate from today or from thousands of years ago. All psychoactive plants can do this through their unique interface with our field. Cannabis brings the underlying operating system to the surface. Shamans have used it for thousands of years for this purpose, to bring mindfulness where there is none so that we can see the world through an upgraded landscape that connects people to something more beautiful than what they know. Many of the shamans of today, those all around us, are just starting to realize it. So let us welcome what is now the full expression of cannabis, marijuana, weed, pot, ganja, etc, imprinting its consciousness on the world, embracing all the beauty it provides if we choose to tune in. Are we ready for new lessons?

8/1 This wad the most fucked up morning ever. Didn't get much time with the girls. I was able to take a few pics when I got back amd a video this morning. Pillars are still around. I killed a couple but I probably should spray BT. I think we got rain last night. Bags are heavy. I defoliated a little bit more on the interior and found some small yellow leaves. Event horizon is still on point to flower first. I NEED to lst and add supports for flower bit I've got a lot of other things going on too. I'm going to TRY to spray BT tonight if weather permits and I should have the supports up this weekend. At least that's what I'm hoping. 8/2 Quickly watered as I had to fix a flat tire to get my wife to the doctor. Gave most a gallon but closer to 3/4 on one event horizon and the sherb pie. Half g for the 10 and I gave the 5 and the 50 a little water. I didn't give the 50 much. That holds water far longer. I'm glad I got it done. It was 90°+ and sunny all day. Earlier everything looked great. I think I'm gonna go check them and maybe add a few pictures. WENT OVER AND FOUND THE EVENT HORIZON I GAVE A LUTTLE LESS WATER TO, IN THE BACK COMPLETELY DEOOPED OVER AND DRY. I QUICKLY WATERED A GALLON. I CHECKED THE OTHER PLANTS AND SAW A COUPLE THAT "MIGHT'VE STARTED DROOPING BUT WERE LIGHT SO I GAVE ALL THE GMO'S HALF A GALLON. I WATERED THE CONTAINER PLANTS AND THE ONE IN THE 50. BETTER SAFE THAN SORRY. THEY WERE SUPER LIGHT. SOME ARE SHOWING SOME HEAT STRESS BUT I DONT BLAME THEM WHEN ITS PUSHING 100° OUT. I HOPE THIS PLANT WILL PICK UP BUT ILL HAVE TO WAIT UNTIL MORNING TO SEE. I GOTTA GO EAT DINNER AND IT WAS IN ROUGH SHAPE. CANT BELIEVE THIS. ITS THE FURYHEST IN FLOWER TOO. INTERNET TOO SLOW TO UPLOAD 8/3 This morning it was "maineing" out. Basically like raining but more of an alternating mist. The event horizon that looked DEAD is completely recovered! I'm so stoked. I've had a really rough few days but at least I've still got my girls. After this little bit of rain I'll do the supports and a spray of BT for the pillars. I'm noticing more damage and I don't want them arpund when they can burrow into buds. WENT BACK AT LIKE FIVE. THE 5 GAL WAS DROOPING AND THE 10 WAS DRY AF. OTHERS WERE ALSO LIGHT. I USED 5 GALLONS ON THE GARDEN AS SOME STILL "LOOKED GOOD" BUT WERE DUSTY AND DRY. I ONLY GAVE THE GMO IN THE 30 A HALF GALLON. DIDNT WATER THE ECENT HORIZON IN THE BACK AND THE GMO IN THE FRONT BY THE DOOR ASXTHE LOOKED GOOD AND STILL HAD SOME WEIGHT TO THEM. THIS WAS ANOTHER DAY IN THE 90s THAT WAS SUPPOSED TO HAVE RAINED. LUCKILY IVE GOT THAT INTUITION AND I CAN CHECK. CAMS HELP WITH THAT BUT ITS BEST TO CHECK A FEW TIMES A DAY IN WEATHER LIKE THIS. FAR TO HOT TO SPRAY ANYTHING. 8/4 Chose not to water as we were supposed to get an inch of rain, then a half in and now it says .1in. I'm going to go over and check on the garden and see what they look like. I took pictures but I'll have to wait to upload them. WENT BACK OVER IN THE AFTERNOON AROUND 2ISH. GMO IN THE FRONT WAS DROOPY. WATERED THAT A GALLON AND IT WAS UP BY THE TIME I LEFT. THE GMO ON THE END (MY CANARY) WAS SUPER LIGHT SO SHE GOT A GALLON. THE EVENT HORIZON I DIDNT WATER YESTERDAY GOT ABOUT 3/4 OF A GALLON AND I WATERED THE ONE IN THE 10 1/2 GALLON. SHOWERS ARE IN THE FORECAST AND EVERYTHING ELSE LOOKED PRETTY GOOD AND WASNT DEAD LIGHT. AS OF 3 EVERYTHING IS GOOD. I IMAGINE ILL PROBABLY NEED TO WATER SOMETHING TOMORROW. IT SUCKS HAVING TO DO THIS SEPERATELY BUT SOMETIMES THATS HOW IT GOES. I DONT EXPECT THESE 90 TEMPS WILL CONTINUE. ALSO NOTICING SOME FADING AS THEY TURN TO FLOWER. DEF NEED NUTES. AND ONCE THE TEMPS GO DOWN I NEED TO SPRAY EITHER BT OR SPINOSID. 8/5 It Rained last night so I didn't need to water. Everything was nice and heavy. Beautiful day today. Hopfully I can do an app of bt tonight. Weather man needs to get things right. It says we got .005in last night but I heard it and it was way more than that. This is a tiny town. WENT BACK OVER AND FED. EVERYTHING GOT 1.75 PINTS. THE 10 GOT HALF THAT. THE FIVE A LITTLE LESS. I DEFINATELY NEED TO SPRAY FOR PILLARS. I ALSO HAVE A BIT OF DEFOLIATING ON A COUPLE PLANTS THAT I NEED TO DO. USUALLY I'VE LOST TONS OF LEAVES BY NOW. I JUST NEED TO IMPROVE AIRFLOW. THE TRELLIS WILL HELP WITH THAT PLUS SUPPORT. I THINK I MAY BE ABLE TO SPRAY PISSIBLY TONIGHT (DEPENDING ON WEATHER) AND SUPPORTS AND DEFOLIATION THE NEXT FEW DAYS.

Flush week Total system power 230w Dim %10 UV-IR-FR Dim %100 PH:6.0 PPM 285