Transplants been done into final containers(20l)and started LST.They doing really well,they've started sexing so I reckon from next week I'd say week 1 flower.Havent fully saturated the medium as yet with fertigation ,want that stem thicker before I do that. Weathers been decent but the wind has been strong on 1 or 2 days.

Everything’s looking great with these two really happy with these perfect height for me, I’m defiantly going to be doing a lot of Mephisto strains in the near future. ✌️🏻 Still looking good, starting to frost up now also added an 4” air intake and hung it up to blow air across the canopy.

So there were a couple little things I did to the tenth I removed some of the very low but that we're definitely not getting anywhere close to the canopy in fact they're only sticking up about three and a half for in above the trellis net so got rid of those guys and I moved the air conditioner Inlet to the top of the tent other than that the girls are doing really well

Day 60 12/12 buds seem to be slowly fattening up and colas falling over i believe she is a 63 day strain so i am reducing ppm of water each time i feed most likely got another week to go as she doesnt look completely finished as of yet Also thinking whether i should change lights to 11/13???  Like 2   Share

🌹Start to End week 6🌹

Day 35 and plants are going good alot of lst last few days some more to go photos of individual plants will be uploaded later

Inizio Terza settimana e tutto va bene,💪🔥 crescere forti belle mie.... Anche loro la prossima settimana entreranno in fioritura.... andiamo belle piantine mie crescete belle e buone

Fattening and stacking! That’s what’s up 😎🔥 The girls are doing well, no issues other than the tip burn (went a little hard on the nutes then dialed it back) I was very busy this week and had minimal time for the garden, the automation is key for success! I really should look into an auto water system to complete the process, but I love the time I spend and watering is one of those times you can get up close and personal and really view your plant and how it is doing from top to bottom. Only about 3 weeks left give or take, I can’t wait. The terps coming from these plants have kicked it up a notch and are intense! Like walking through a pine forest… that also has weed growing 👃🤤🌲, lol. Started with the Bud Candy from Advanced nutrients for the Mag/Sulphur and to help with the terpenes and fattening. I had impressive results with my last GG Autoflower using this product in the last 3 weeks, hopefully we can get a similar result. 🤞

Hello Diary! This time on the "Farm" there are two new strains from Royal Queen Seeds, Watermelon Auto and Purple Punch Auto. In this diary we will dedicate ourselves to Watermelon. 😀 I would like to thank James of the Royal Queen Seeds for sending me these strains. 🙏 LET'S START FIRST WITH THE FARM SET-UP: Box - Secret Jardin DS120W 120x60x178 Lights - MIGRO 200+ Ventilation - Blauberg Turbo - E 100 Filter - Primaklima filter PK 100/125 Fan - Oscillating Koala Fan Humidifier - Beurer LB 45 Soil - BIOBIZZ Light - Mix Pot - 11L AirPot Seed - Royal Queen Seed Nutrition - BioBizz and RQS Organic nutrition A few words about Watermelon Automatic. The breeders from RQS set out with the intention of crafting a strain that lights the taste buds on fire. To achieve such a tantalizing terpene profile, they selected two of the most flavorful parent strains available: Tropicanna Cookies and Lemon OG. Both of these varieties are packed full of limonene, myrcene, and other fruity and earthy molecules. Watermelon Automatic emerged with a genetic makeup of 75% indica, 20% sativa, and 5% ruderalis. The speedy autoflowering strain managed to inherit all of the tasty terpenes from her ancestors. These are the characteristics, we will now see what it will look like on my small farm. LET THE DIARY START OFFICIALLY: 14/01/2021. Planting. After cleaning the Farm (GrowBox), I prepared everything I needed. Soil is a Light-Mix from BioBizz, Air-Pot's, Organic Additives that I mix with soil. From the beginning of this hobby, I use only organic fertilizers. I used 11L pots, to which I added 50g Easy Boost Organic Nutrition, 10g Easy Roots Rhizobacter and 5g Easy Roots Mycorrhizza Mix to the soil and mixed everything well. After that I soaked the soil well with water, made a small hole, laid the seed inside and lightly covered it with soil. After planting is completed, they enter their new home. As I wrote earlier, in addition to Watermelon, there are two more Purple Punch Auto on the Farm to keep him company. The temperature in the Box at that time was 23 degrees and the humidity was slightly below 45%, so I will have to put humidifier to raise humidity. I set the lights 35cm from the pots as Migro recommends. 14 - 17/01/2021 I sprayed the surface of the soil with water a couple of times to keep the soil moisture at the surface. 17/01/2021 Watermelon Automatic sprouted. There was a seed coat left on the stalk so I had to remove it by hand, but a nice photo motif. 22/01/2021 I watered the plants with a small amount of water to which I only regulated p.H at 6.4. Farm: 24.7 degrees - 55% humidity I'm quite late with the publication of the diary, the reason is the large number of photos I take and then I need to find time to put everything in a pile, along with the notes and type everything nicely. No matter how much time I spend on the diary, it relaxes me and makes me happy. See you soon.

🌳.

First time here… have a rough idea though lol Week 1

The End is near. Can’t wait to harvest and dry them. Next 2 Weeks I use to flush them. I think then they’re ready. I’m very proud of the purple BigBud. She’s purely looking incredible. What do you think ?

Lights are bak on tents 🏕️ bak in action so am Goni need tae hope a don’t get visit dae land lord or coppers so al need tae behave av got a big mouth n always thot send it on now a feel as if a can do without the bad vibes n jealousy that festers amongst so called pals this is ma ting now am just Goni keep smashing the grows until hopefully av got a couple a people a can show the ropes n fire a tent up or we’ve spoke bout doin a full room but need safe place no regrets no. Remorse a believe that growing n smoking cannabis really helps my mental health’ so a don’t believe am doing wrong 😑 n can’t stop won’t stop fuck yer system free the weed peace ✌️ chedderbob112 s2340420 🏴󠁧󠁢󠁳󠁣󠁴󠁿

Strawberry Cadillac W6 12/14-20 Important dates 11/9 Germination 11/25 Transplant to 1.5 gal, 12/1 Topped, Pinned and removed 2 large center leaves 12/5 Repositioned pins and removed lowest fan leaves 12/16 Topped 4 tops on each plant except Cadillac1 (first topping) and put manuka honey on the cut. Nutrients: 12/16 1.5 ltr Aptus Regulator 1.5ml Aptus strtbooster 2.5ml Flora micro 5ml/g Flora grow 5ml/g Grow Time 5ml/g Plant Juice 2 TBSP/g 6.32ph, 825ppm, 60.9 12/19 Pics 1.5ltr Aptus Regulator 1.5ml Calmag 2.5ml/g Recharge 2.5ml/g 5.71ph, 310ppm, 64f The Strawberry’s received 1.5 liters 2 times on 12/13 &19. 12/16 On 12/16 after harvesting Apricot Auto, I had to move Cadillac1 off the shelving unit and put her on lower crate. She is as tall as the other plants positioned on the top shelf. I topped Cadillac1 but since she is asymmetrical, I don’t think topping will create 2 tops. Time will tell. All the girls bounced back after the topping. Strawberry Cadillac #1 27” #2 18.5“ Strawberry Trop Cherry #1 18” #2 13” Straw-Lectric Lemonade #1 15” #2 14 Happy Holidays Stay green, growers love 💚🌿 💫Natrona💫

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.

Getting better. Going in to week 4. Will harvest and smoke this girl

Day 35 - Ladies are way taller than I could have ever imagined & starting to get extremely dark pruple😍 make sure to check back for daily updates & happy growing friends✌️🏼🌱

week intel: im felling in love with them everything is good . this week was time of second net layer , the first layer was for spreading the branches and doing LST now the second layer is for supporting branches for later weeks when the buds gain weight and gets heavy the net will hold branch stand up without benting. stresses: im just gonna cause a little E.C stress to raise the terpens. i found their max tolerance is 1.9 E.C so im not gonna reach or get close to that amount again and beside this wont cause any more streses untill week 6 that will do second pruning and we are done with trainings then. feeding: as always im feeding plants 3 times per week with nutrients , no plain water at all, just with nutrients with adjusted p.h at this order : day 1 : i feed them heavy with silicate +base nutrients(calcium & micros + Bloom) and karbo about 950 ppm - 1.8 e.c to cause a little e.c stress. day 3 : i feed them low dose for start of Green House Feeding Booster around 267 ppm - 0.6 e.c alone cuz this bad boy is very strong. day 5 : i feed them with medium dose of Top-Max around 160 ppm - 0.3 e.c to let them recover the stresses and eat the previous nutrients untill next feed at next week and the next 2 days will rest and eat :D just remember never feed them plain water besides the first week of germination always feed water with nutrients to feed them right p.h every time and to avoid excess water problems, and let them eat the previous meal for 24 hours and dry the soil, so at total only feeding nutrients 3 times a week other days let them dry and rest

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.