This was an easy grow, and had some amazing results. This is some of my best homegrown to date ❤️ the ladies were easy to manage, no PM, pests or disease. The root balls were enormous, wasn’t much soil to recover. They got heavy in the end from the weight but managed to stay upright for the most part. They were big stretchers , prepare for that, scrog was a good way to go but some of the eager beavers got away from me, which ended in some massive colas. Overall easy to grow, no surprises and you won’t regret the results! 10/10 ❤️👊🤤

Failure, turned herm or is

No purple yet kind of bummed out about that but we'll see what happens the buds are getting fatter so I'm happy about that nice and hard the smell is awesome can't wait to smoke this

After checking the grow yesterday (2021-01-01), I noticed some of the yellowing I've seen in previous grows that served as early warning signs for an impending grow failure. I checked my reservoir and found it was down to about two gallons left and the pH had shot up to 7.1. I then checked my AutoPot runoff in the tray and found it was at 7.2. I then took my Remedy CBD out and flushed it with 10 gallons of pH 5.8 tap water until the runoff measured about pH 5.8. The plant has been returned to the tray and the pictures you see this week are the following day and I'm continuing to measure at the tray more closely now as well. I've continued to pull off some of the larger yellowing fan leaves but, other than that, I've kept this grow as simple as possible. The flowering stage is continuing as expected and the pictures show about how far along we've come.

another week on full dose. 3-4 weeks remaining.

Week 4 - Sometimes You Got To Lose To Gain Phase 2 - I took off the fan leaves so that the plant would redirect its energy into the stem and branches rather than the leaves. I also cut of the top heads so that the energy would go into the development of the 2 heads below.

Added bud factor X and bud ignitor, hammerhead , 2.5 liters each 3 days , budding ist nice and getting thicker

6/24 this may be the last week. The screen recordings are of both plants (purple octane and rs11) they're both close. I also went back and did some math and the last week of veg, should've been first week of flower. I may let her go for 10 weeks. We will see how she looks throughout this week(trichs) 6/25 looking super close. All cloudy besides maybe 10% 6/29 will get in there with a microscope again. just waiting on her to ripen. can't tell if she's done, or at rhat point where she looks so good that she's done but then that last week the plant explodes. well see and yall will definitely hear about it.

05/17 - received last "week 4" nutrient mix. Next watering will introduce overdrive. Buds are looking a little smaller than expected - especially that the Northern Lights is a 6 to 7 weeks. Will most likely be pushing right to 7 maybe 8. 05/24 - May have mislabeled Bubblegum and Northern lights; Based on the "bubbled gum" being clearly more mature than the other 2 and I had some seed dropping issue I thought I had cleared up. It is what it is - but one plant has much more orange hairs than the other 2, and I had 1 "fast version" The Northern Lights. Top nugs on "Bubblegum" are nice and tight, fed last nutrients on 05/24 - will start flush on next watering. Trichomes seems to be clouding up - generally speaking. The "northern lights" and Pink Berry will keep on AN feed schedule - possibly to 9 weeks. (there's virtually no browning hairs at the start of week 6).

Week 7 day 3. I stopped giving soluble nitrogen today. 1/2 reduction in soluble pk. Adding solubles in water drops my ph perfect so I don’t use ph down in flower. Now today I start adding a little ph down as the 1/2 strength soluble pk brings water to about 7.4, so reduction to 6.9

Going nice;))))

Week 4 middle floração and they are looking beautiful….

Day 15- 4/10/21: Welcome to the first day of the 3rd week.... Happiness.... big one. They look amazing.... really so some changes: Lamp is set to be on 150W approx 60% of the full power..... enough..... they love this ViparSpectra XS2000.... So Do I..... Himidity stays on approx 60% Ventilation is fine every 2 hours switched on for 5 min.... Watering like 0.06 l per day.... Started some fertilization also with Bat Guano, Biobizz family /before someone ask why I use BioBloom and Top Max in veg just beacuse lol/ And... Epsom salt.... Ratio can be found just scroll down.... And yes, I do it on Tuesday and Saturday except the Epsom just 1x a week the rest then 2x for now. All of them are beautiful and the first LST has been done basically just bent them to the right or left haha for now except Afghani Gold and Spliffs Strawberry because they are basically just 2 weeks old so too young to be trained. I assume Blue Berry has a little funny deficiency but I am sure she will be okay anyways I will colour her back lol with some magic nutrition 🤣🤣🤣 I am happy ;) As you can see 2 of them are smaller /Afghani Gold, Spliffs Strawberry/ because they are younger: planted 1 week later as the first germination failed. Pictures sYs everything so not much more to say... ;)

This week has been good both plants are growing great with no problems in there transition to flower they jus started to stretch so I hung the 600 watt lamp at 24 in and will lower it as they flower but a very productive week so far. Gonna add nutes at the end of this week so they will have some nutes to fall back on when bud sites appear

Was another easy week - lots of healthy growth. Simply watered when dry, did some daily LST and leaf tucking. The green crack is definitely the fastest growing out of all the plants, and the one runt LSD25 is a bit smaller but still chugging along.

Marker is thriving, enjoying its meals as usual. The only change is its delightful berry scent, rather than the expected gassy aroma. Keep up the good work, and let's see how its flavors develop further! 🌿🍇

Další týden a už jen trénink . Hned jak zaplnim. Cely prostor přidám ještě síť a přepnu. Have nice day my Green friends 🍀❤️

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.

7/4 SUN was poking out a little bit. Plants loved that little feeding and seen to he noticeable larger this morning. I'm considering starting the nutes. At least the organic ones as well as upping the water intake I've been scared to water with all this rain and my experience last time. I plan on applying BT this afternoon and doing some work on the bottoms of the plants. I also saw a chipmunk in my cage so I have some spots in my fence that need to be patched. I know I can't compare this year to orher years as these are seeds and all the other years were clones. I CAN say for certain that my plants are healthiest they've been out of any of my journals. Previous plants were much larger but I was fighting numerous fungal, pathogens and pests at the sane time. Ear wigs would've lollipopped most buddies by now but I've seen no sign of them. I'm going to apply more poison where they were and add some rat traps inside the cage for the chipmunks. Once I fix the cage I think I'll be good. UPDATE: Went back over and fixed the holes on my cage from high winds. I found an old wire trap or cage and just cut sections and ziptied them to the existing wire and to the structure thus covering any open holes. I'll need to put lathes aroubdvtge outside because if a rodent REALLY wanted in they could get in. My belt had been wearing thin but I use shit until it breaks (yesterday the heal came off my shoe lol) so I was working hard sweating my nuts off and my belt gives out totally. At least ive got the major stuff done. I took a few videos too. I'm imagining it was this little bit of sun that gave these plants that boost of growth but I'm wondering if the added nutes had anything to do with it. Bags weren't light and I could feel moisture in the soil so I didn't water. I'll check again tomorrow morning. Since I didn't see many plants or even leaves for that matter with damage I decided to hold off ob the BT and the plant doctor. Only time will tell if that was the right decision. 7/5 Plants look fantastic. I see a few more holes in leaves sporadically amd I'm hoping it's pillars. I've seen lots of lightning bugs on my camera though and grasshoppers are abundant. Not one growth shoot has been chewed (knock on wood) which is what the earwigs had always done. I watched a video from last year and by nowcthey had lollipopped all lower leaves. It may not be the best weather growing season wise but despite the rh consistently in the 90's I still don't have pm or fungal pathogens. Need to get the BT out. Didn't water as we've had all that rain. I'll water either tonight or tomorrow morning. Sunny high in the 90s low is 66. Tomorrow looks good too. UPDATE WENT BACK OVER AROUND FIVE. IT WAS 88 DEGREES SO I WANTED TO CHECK THE GROW BAGS. THE POTS ARE FINE. IT WAS HUMID AS HELL. ONE PLANT WAS SLIGHTLY DROOPY BUT VERY LIGHT AND DRY. I FOUND TWO OTHERS THAT SEEMED LIGHTER THAN THE REST BUT HADNT DROOPED. I MIXED TWO GALLONS OF WATER WITH 1TSP KANGOROOTS AMD PHED IT CLOSE TO 6. I FED THE 3 PLANTS THAT WERE SUPER DRY LIKE A HALF GALLON AND SPRED THE REST OVER THE OTHER EIGHT PLANTS. THEY WERENT DROOPING BUT THEY WERE VERY DRY. I PLAN ON A FULL WATER TOMORROW. I WOULDVE DONE IT TODAY IF THE TEMPS WERENT SO HIGH. ITS RAINED A MONTH STRAIGHT SO I HAVENT HAD TO WATER. I MADE A COUPLE VIDEOS BUT I'LL HAVE TO UPLOAD TOMORROW. 7/6 Another super hot day. I hefted the pots and they still had some weight but I could tell they were dry. This rain has messed up my watering schedule. Well it made it so I didn't NEED to water. These are big plants now. I need to get a schedule to stick too. They're going to probably need a gallon a piece at least. I'm still nervous watering. Right now I'm just reading the plants. I added .5tsp kelp me/you to 1 gallon of water to help with heat stress. I fed an additional two gallons to the garden this morning including the two container plants in the back. They were dry on top too but I know they have water deeper down. Next watering I'll be more consistent and try to give them there 10%. It's great having the bags elevated. I can finally see when I start getting run off. I could even measure the ph of it instead of relying on that meter. Ill check the ph when I go back over. Still a few 🐛 holes but they are few and far between. I really don't want to spray for such a small problem but if I cant find them at night that's what I'll do. UPDATE: Another 90 degree day. I went back over and gave the garden a gallon of water as they were dry and it didn't rain. Tried to use a soil ph meter to check ph. First couple were 6.4, 6.5 then I got 7.3 and I accidently dropped it. Then I got somethings that were high eights and even one 9! Obviously the Meter shit the bed. I'll lower the ph of the water slightly when I fully water tomorrow and I'm going to measure the runoff. 7/8 I must've messed up the journal again as the dates are off. GAVE PLANTS A FULL WATERING. Each girl got a gallon. I couldn't upload my videos this morning as I had to break up a fight. 3 on 1. Didn't give me a chance to put the videos up. I'll take some stills then I can upload them. I took stills and they all uploaded but didn't fucking save. I'm nit going to keep trying to upload if it's not going to. Noticed a few more holes in leaves and one skeletinized leaf so I need to either spray the bt or something more versatile. I'm putting more poison around the cage and de between the bags. I'll go check things out tonight. Sick of writing a book and uploading to just hace them disappear 7/9 Did a quick video today. Noticed the bags were fairly light despite the plants being soaked amd the pallets wet. I was pressed for time. I gave two gallons to the entire garden. I hope that will hold them over until tomorrow. I'll need to up how much water I give them. Going with a gallon and a half next time. I see more pillar spots and a moth took off when I shook the plants this morning. So I'm gonna have too apply the BT. I figure if I go over before dark tonight I might be able to see aju nocturnal insects around. Luckily my dad feeds the birds and they are always there. I think they help with pests. UPDATE IT WAS A LITTLE COOLER TODAY BUT MICH MORE HUMID. I WENT AROUND SIX TO MAKE SURE THE GIRLS WERE OK WITH WATER AND TO GIVE THEM A TREATMENT OF BT. I WENT THROUGH THE GARDEN ANDCGOUND THREE LEQVES TO DEFOLIATE AND LITERALLY A COUPLE LEAVES ON TWO PLANTS WITH PILLAR HILESM WHEN I ARRIVED TWO BIRDS FLEW OUT. A HORNET CAME IN WHILE I WAS THERE. THIS DO LESS APPROACH SEEMS TO BE REALLY WORKING. I DODNT SEE NEARLT ENOUGH DAMAGE TO WARRANT SPRAY8NG MY EXTREMELY HEALTHY GIROS WITH ANYTHING. ILL KEEP AN EYE ON THEM AND CLEAN THEM UP A BIT. I DO NEED TO INSTALL THE VERY8CAL TRELLIS FOR SUPPORT. THEYRE PRETTY HEALTHY THOUGH. ONE PLANT IS ABOUT AS WIDE AS IT IS TALL. STILL......PLANTS ARE EXPLODING AND ITS GETTING TIGHT IN THERE. I NEED TO GET THE TRELLIS UP THOUGH. 7/10 I went over and was planning to water. Plants were wet and it's raining. Top of the medium was moist but the bags were light. ONE bag was super light but seeing that we are having showers all day and an additional half inch of rain coming tonight so I didn't water them. Especially since they looked great. Decided to to spray BT yet as the damage is so small and i think the birds have been taking care of the pillars for me. Now I'm wondering if I should've gave that ONE plant a little bit of water but it will be find. Did a video. I'm being careful not to over water. Last year this is when all my buddies were devoured by earwigs. And no senescence like the years before. I think it was hust those earwigs. I haven't lost shot for leaves. Even the stalks are bright green and look amazing.