Всё отлично. Появился слабый запах. Средняя температура 23 градуса

Hello everyone 😊😊😊 This week bring the problems with humidity, I started to add to much steam and some small scorching and discoloration occur. However I remove humidifier and everything back to normal. Girls grow up like nothing happened, tomorrow I will proceed small defoliation like I'm doing it in every grow. Have a fantastic night, You lovely girls growers 😊😊😊

Legend Timestamp: 📅 EC - pH: ⚗️ Temp - Hum: 🌡️ Water: 🌊 Food: 🍗 pH Correction: 💧 Actions: 💼 Thoughts: 🧠 Events: 🚀 Media: 🎬 D: DAY, G: GERMINATION, V: VEGETATIVE, B: BLOOMING, R: RIPENING, D: DRYING, C: CURING ______________ 📅 D15/V11 - 30/04/24 ⚗️ EC: 0.7 pH: 6.0 🌡️ T: 21 °C H: 50% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D16/V12 - 01/05/24 ⚗️ EC: 0.7 pH: 6.0 🌡️ T: 21 °C H: 50% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D17/V13 - 02/05/24 ⚗️ EC: 0.6 pH: 5.8 🌡️ T: 20 °C H: 50% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D18/V14 - 03/05/24 ⚗️ EC: 0.8 pH: 5.6 🌡️ T: 22 °C H: 60% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D19/V15 - 04/05/24 ⚗️ EC: 0.8 pH: 5.5 🌡️ T: 22 °C H: 60% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D20/V16 - 05/05/24 ⚗️ EC: 0.7 pH: 5.5 🌡️ T: 22 °C H: 60% 🌊 🍗 💧 💼 🧠 🚀 🎬 1 TL video ______________ 📅 D21/V17 - 06/05/24 ⚗️ EC: 0.7 pH: 5.3 🌡️ T: 22 °C H: 50% 🌊 🍗 Calmag, Grow A-B 💧5L 💼 🧠 🚀 🎬 1 TL video

Day 43 - Commence the flowering! Flower sights are becoming clear now, with lots of pistils appearing along the top of branches. Watered with 1.5L with a run off of 120ml(8%). Day 44 - Watered with 1.6L today. Run off of 200ml(12.5%). Day 45 - She's getting thirstier again. Watered with 1.6L with run off of only 65ml (4%). Can really see the height gain by the day... Hoping the tent will be tall enough. Day 46 - Watered with 1.8L today with run off of 100ml(5.5%). Had a few warmer days outside causing more water evaporation. Will move to 2L soon if run off stays low. Day 47 - Watered with 2L with run off of 260ml (13%). Flower sites really starting to stretch out now. Day 48 - Watered with 2L run off of 260ml(13%). Will continue to water with 2L and only note when changes are required. 2L seems to be the sweet spot for this week. Day 49 - That brings us to the end of Week 7 and the first week of flower. Bud sites are now really established - I'll be increasing nutrients to 1.5ml/L for Advanced Nutrients and 0.75ml/L on CalMag. Total growth of 12cm this week compared to the usual 7cm over the last couple of weeks. An extra 5cm of growth can be attributed to pre-flower stretching.

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.

Unsere Cinderella bleibt, trotz eines kurzen Zwischenschub, eher eine der zierlicheren Pflanzen. Aktuell baut sie weiter und kontinuierlich ihre Buds auf. Alles bestens bei unserer Prinzessin. Alles in allem eine eher ruhige und gute Growwoche. 😏

For those who follow me could see that I was absent and I apologize to you and the ladies in this tent. These seedsman northern lights are tough. I was out of town for work during their prime stretch phase and all they got was straight water added to the res. Two of them are specimens still and the one without the floraflex feeding cap isn’t getting the nutes distributed they way the plant likes so today I’ll modify one and see if I can make her happier. In the end I know they’ll end up strong but it was during the crucial stretch period and they needed more than they got. All we can do is move on and try to make them flourish. Thanks for looking. Have a great day.

Unfortunately, I had to find out that my account is used for fake pages in social media. I am only active here on growdiaries. I am not on facebook instagram twitter etc All accounts except this one are fake. Flowering day 42 since time change to 12/12 h. Hi everyone :-) The buds will certainly develop further :-). They keep getting thicker and smell more delicious :-). This week there was 3 watering with 1.2 l each time and the whole tent was cleaned. Otherwise everything was cleaned and checked again. I wish you a lot of fun. Stay healthy 🙏🏻 You can buy This Strain at : www.Zamnesia.com ☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼 Strain Gelato clone from mother (Zamnesia ) ☝️ Genetics: Wedding Cake x Gelato x Gelato 33 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Fertilizer: Green House Powder Feeding ☝️🏼🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.5 - 5.8 .

I've been waiting for at least some trichomes to turn amber. I prefer to harvest when there are at least a few amber. I took the PL2 3 days before the PL1. Flushed them for a week only

This week, the plant is feeding heavily and has grown well. I super cropped the main stem to help with the plant becoming too tall. It has taken very well. The plant was becoming very tall so I thought this would be something to try out. Here's what I did this week. 18.7.25: I watered with 2ltrs of dechlorinated water PH'd to 6.4, containing the following nutrients; 💜 2ml Ecothrive Trace PH: 6.4 PPM: 365 22.7.25: I watered with 3ltrs of dechlorinated water PH'd to 6.6 with; 💜 1 TSP Sea K PH: 6.6 PPM: 485 25.7.25: I watered with 2ltrs of dechlorinated water PH'd to 6.5, containing the following nutrients; 💜 2ml Ecothrive Trace 💜 1/4 TSP Ecothrive Biosys PH: 6.5 PPM: 361 28.7.25: I watered with 6.5ltrs of dechlorinated water PH'd to 6.0 with; 💜 7ml Trace 💜 1.5 TSP Ecothrive Biosys PH: 6.0 PPM: 351 Thank you for checking in this week and hanging out in the comments 😁💚✌️🌱🙌

Day 22: Getting bigger! Day 23: was at 4 nodes. Topped it down to the 3rd. Ready for her to explode Day 26: lower nodes are growing larger as expected from topping. Fed GH nutes half dosage 2 days ago. Day 27: LST. I'm going away for 5 days

Update week 1 day 4 of bloom , this week we put the net to make the technique that calls scrog we see next week what is the resul

I put 4 or 5 new LST clips on her to open her up and she has already grown a LOT since doing so 4 days ago!!

Welcome to my Slurircane Diary sponsored by MSNL & SPIDER-FARMER Sponsored with their SE5000. Veg Days 26-32 Days 36-45 Plant is pushing along well. Good solid growth. Done lots of the last toppings this week. No need to defoliation or LST at this point. Her shape really is perfect. And, I know by know when a plant needs LST. Maybe I'll bend the nodes out lightly after I uppot this wk to an 11L Lights. SE5000 was used and supplied by Spider-Farmer for most of this grow. (Thank you Bella) and for early veg. The SF-1000 was used. So, all SF baby. Great lights. Forgot how much faster this spectrum pushes the plants along. Co2 850-1300ppm. Growth is good. Healthy. Need to be on the ball with this co2 growing. Shit happens so fast. A very light mag def one hr and 4hrs later its full on. Crazy fast for the autos. Haven't been keeping up required co2 levels. And sadly. I pushed this thing into pre flower (how Idk) but, the DLI was been reached. And she was shutting herself down. This is her last through week of veg. I've tried revegging her the the last 2 weeks. But, nothing is happening. She's good. Really nice long nodes. And she'll be a great plant. (I'm 2 weeks ahead, weeks will be updated more frequently)

And the flowering journey begins on this perfect exemplar, i mean she is growing as perfect as they can possible came, she is in did a very stable and outstanding girl and i am very curious to see how she goes from here <3 <3 <3 Man she is growing fast and getting taller and taller , loving this one As always thank you all for stoping by, for the love and time you guys spend on my stuff, i fell blessed and humble, many thanks to you all <3<3<3 Genetics - Fast Buds Tester 2309 Ligth - LUMATEK ZEUS 465 COMPACT PRO 
Food - APTUS HOLLAND #aptus #aptusplanttech #aptusgang #aptusfamily #aptustrueplantscience #inbalancewithnature #trueplantscience #fastbuds #dogdoctorofficial #growerslove With true love comes happiness <3 <3 <3 Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so <3 <3 <3 
All info and full product details can be find in can find @ https://2fast4buds.com/ wen released 

https://aptus-holland.com/
 
https://autopot.co.uk/ 

https://lumatek-lighting.com/ Have a bunch more diaries going on, fell free to drop by and say hi <3 <3 <3 <3 <3 <3 Growers love to you all <3 <3 <3

4 weeks in and all is looking stellar! The stacking on the BHB is stunning, while the Cheese is producing some respectable clusters and the OJ is defining up top and needs a bit of a clean underneath. All the others are producing from top to bottom so as long as light penetration is adequate, I'll let them go. BHB#1 has a most interesting aroma and I'm impatient to see her develop! Blueberry Headband (1) from Humboldt Seeds, Cheese (1) and Orange Juice (1) from Dinafem Seeds. https://www.dinafem.org/en/orange-juice/ https://www.dinafem.org/en/blueberry-headband/ https://www.dinafem.org/en/cheese/ Lighting https://www.horticulturelightinggroup.ca/products/260w-qb-v2-led-kit Soil Amendments https://www.gaiagreen.com/product-page/all-purpose-4-4-4 https://www.gaiagreen.com/product-page/glacial-rock-dust https://www.gaiagreen.com/product-page/mineralized-phosphate http://www.seasoil.com/ Worm castings Sunshine Mix #4 Epsom Salts Molasses

Day 89 - Harvest day has finally came for this lady & I beyond impressed, to only be in a 2 gallon pot she has put off some massive rock solid buds that smell amazing! Very strong stable genetics that’s can handle really anything you throw at it, would highly recommend especially to first time growers because this strain is so forgiving! Stay tuned for the harvest update & another run from spliff seeds because I will definitely be getting some of their strains🔥💪🏻 Thanks for following & happy growing friends!✌️🏼🙏🏼🌱

~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~ 09/04/21 🐱 boy are we ever starting to stretch...too much in fact, im not liking the node spacing with this strain (far too wide)..we lowered both lights in the tent to get this to stop (we never need to do this) and turned up the fans to really beat on these for a few days..hopefully this will strengthen them up and we can avoid steaking them...we'll update again midweek, thanks for reading and happy growing everyone!! 🐱❤️💡🌱 ~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~ 09/07/21 😺👌 We seem to have gotten the stretch under control, lowering the lights really seemed to have helped (or she's finished lol), the fans have gotten them pretty strong in the last few days, everything is lookinng great..a few leaves with mechanical/ wind dammage but nothing too majior and the high wind has been benificial... this is a very lengthy strain, had i known i would of done a few things differently with the others but still very happy overall..thanks for reading if you made it this far and happy growing everyone!! 😻

I Messed Up A DAY Here. So one of the days is dated wrong. I tried to correct it the best that I could. 7/24 I decided to label this week as flower. It's more like preflower though. GMOs are stretching like crazy. Due to the rain we weren't supposed to get some of my plants are a little over watered. That's why I love the fabric pots. With the winds we get the bags dry out fast. The GMO's would've needed water anyway if we didn't get this storm. Event Horizon seems to be the furthest in flower amd the most over watered. WE'LL get a LITTLE more rain today and tomorrow but then hopfully my bags will dry out. They are heavy as hell right now. Had we not got rain for what seems like forever. Several plants would've needed to be watered if we didn't get this rain. Still the plants are currently overwatered. All the pics and video so far are from this morning after the horrible pounding rain of yesterday. Like I said before, I need to; defoliate for better air flow, add secondary supports or a vertical trellis, considering using a preventative pest application (e.g. BT), LST and spread branches apart and start using nutes. 7/25 Wasn't supposed to rain today. Like .001. It poured this morning and is still raining VERY LIGHTLY at 2:30. We got an inch yesterday. The total for these 3 days was suppised to be under half an inch. Anyway I went over around two and everything looks great! Things are clearly overwatered and heavy but the plants look happy! Most have their leaves out and everything! I love growing in bags because they dry out so quickly! I don't mind watering more. I defoliated one event horizon and the few yellow leaves I coukd see on other plants after shaking them off. The seedling in the 50 is far behind the others in flower and just showed its sex. I'm fairly certain that one is red runtz. Whatever it is is going to flower much later than the rest. It's going to be good if I have couple early finishers. I did a video but I'll have to upload tomorrow. I have a lot of work to do And not just in the garden so I'm hoping I can balance things out and get this stuff done. Caught three TINY inch worms. I'm wondering if me manually hunting has cut the adult population down and I'm just getting fresh born ones? If that's the case I wouldn't need to spray. 7/26 Plants looked pretty great today. I think me manually removing pillars has made a big difference. It's windy out too so it won't take long for those bags to dry out. Which is good because what wad supposed to be a half inch of rain turned into 3 straight days of rain. I'll be back over to work on the garden today and I'll update then. 7/27 Plants are looking pretty good. Good weather ahead and the bags are starting to lose weight. Found a pillar wrapped in a dead interior leaf all wrapped up. Found a couple more early this morning amd killed them. I did some slight leafing on some plants. I don't like doing that outdoors but since these are monster cropped they have far to many leaves. Airflow is improved. I'm not seeing any nutrient deficiencies yet. Plants are a vibrant healthy dark green. Soon I'll add a base nute like big bloom or ancient amber (I think that's the one, it's applicable to big bloom). I cam see some plants trying to start flowering and I've got one (in the 50) that has just shown sex. Hopfully this will give me some time between harvests. I'll update as I go along. DAD CALLED IN THE AFTERNOON AND SAID HE THOUGHT A PLANT MIGHT BE STARTING TO DROOP. IT WAS MY GMO CANARY THAT GETS HIT ON ALMOST THREE FULL SIDES BY WIND (ONLY ONE PLANT). I CHECKED THE WEIGHT AND IT WAS LIGHT. IT WAS DROOPING TOO. I WATERED THAT ONE PLANT WITH A GALLON AND WATCHED IT PERK BACK UP. I CHECKED THE WEIGHT ON THE OTHER PLANTS AND LIKE I THOUGHT THEY WERE STILL HEAVY. I PUT MY FINGER IN THE SOIL AND IT CAME AWWY COVERED IN DIRT. MY SEEDLING IN THE 10 WAS KINDA LIGHT SO I GAVE THAT HALF A GALLON. I USED THE OTHER HALF AS "A CUP OF KINDNESS" ON THE PLANTS THAT SEEMED LIGHTEST TO CARRY THEM OVER. I PROBABLY SHOULDVE WAITED BUT I DOUBT IT MATTERS. ILL CHECK IN THE MORNING. I ASSUME ILL HAVE TO WATER THEN OR AT NIGHT. ILL GO BY THE WEIGHT. THE CANARY WILL NEED TO BE ON A SEPERATE SCHEDULE. THATS FOR SURE. Went back over at 6:30 and plants looked better than they have in a long time bags still have some weight. With the sunny weather we are going to have these plants will keep exploding in growth. Found one pillar but I wasn't there long. Seriously considering a spray of BT in the near future. EDIT: UNFORTUNATELY MY SPIDEY SENSE STARTING TINGLING AROUND NOON. MY ANXIETY WONT LET ME IGNORE IT (IM NOW EMBRACING IT) AND I HAD TO CUT OFF A CONVERSATION WITH MY WIFE TO GO TO THE GARDEN. I IMMEDIATELY SAW THAT ONE OF MY GMOS WAS STARTING TO DROOP. NOT LIKE BEFORE BUT IF I HAD BRUSHED IT OFF AND LEFT IT FOR FOUR MORE HOURS IN THE 90° SUN IT WOULD'VE BEEN. I GAVE THE GMO'S (BESIDES THE ONE I GOT YESTERDAY EACH A GALLON. I DIDNT WANT TO WATER DURING THE DAY BUT THIS WAS MY BEST OPTION. I GAVE THE TOASTED TOFFY A GALLON AND THE 2 EVENT HORIZONS EACH GOT HALF A GALLON, AS WELL AS THE SHERB PIE WHICH GOT HALF A GALLON. I DECIDED TO DO THIS BECAUSE SOME PLANTS USE MORE WATER THAN OTHERS. BEFORE ACTUALLY GOING OVER I CONSULTED MY PREVIOS DIARIES. I HAD THIS SANE PROBLEM LAST YEAR ON THE SAME WEEK OF THE MONTH! THATS WHAT MADE ME TRUST MY INTUITION FULLY. I LEARNED FROM THE MISTAKE OF LAST YEAR. THINGS ARE GOING GOOD. IM STARTING NUTES SOON AND I NEED TO SPEAY FOR BT BUT DONT KNOW IF IT WILL BE TONIGHT. 7/29 Apparently my intuition worked out well. Plants looked great this morning. I may feed today. I defoliated a bit and watered the 10g with a half gallon and gave another half gallon to the gmo on the end that dries out fastest and that I didn't water yesterday. I think I've got the watering down. Now I need to start nutes and spray bt. Need to wait for the rain first though. Suppised to get minor showers the next couple days. I'm gonna try to get the trellis up too. WENT BACK A LITTPE AFTER FOUR. HUMiDITY WAS 100% AND IT WAS RAINING VERY LIGHTLY. I MEAN AS LITTLE AS IT CAN POSSIBLY RAIN. ALMOST LIKE WHAT IT FEELS LIKE WITH THOSE MISTING FANS IF YOU STAND BACK A WAYS. I DIDN'T WATER. PLANTS WERE LOOKING GREAT! I DID SOME DEFOLIATION AND CAN TELL I NEED TO START NUTES. I CAN SEE SOME SLIGHT DEFICIENCIES IN BIG OLDER LEAVES. SOME SMALL INTERIOR LEAVES YELLOWED. NOT MANY. GRANTED THEY ARE STARTING TO FLOWER. I'LL PLAN ON FEEDING TOMORROW. THE NEXT FEW DAYS IS SUPPISED TO BE SHOWERS. I DOUBT IT WILL GIVE MY BIG GIRLS ALL THEY NEED BUT IT WILL BE A GOOD START. I DID A VIDEO BUT ITS RATHER LONG SO I CANT UPLOAD IT HERE. ITS COOL WATCHING HOW DIFFERENT THE DIFFERENT STRAINS GROW. STILL HAVE A BUNCH OF SHIT TO DO. IT WILL GET DONE THIS WEEK. 7/30 I held off watering today due to a supposed storm and rain we were supposed to be getting. I had early doctors appointments. I got back around 11 and the bags seemed light. After consulting last years diary I saw that I am underwatering. The root system weighs a lot! We haven't got the hundredths of an inch of rain but we got some sun. It's over cast now. I was there working for a few hours. I watered most a gallon. All the gmo's got a gallon. I gave the two event horizons about two thirds a gallon. About the same with the toasted toffy and the sherb pie. About 3/4 of a gallon as they seemed to have a little weight left. Looking at last years diary there were plants I was giving two gallons at a time in a 20 gal bag so I've been u Der watering a bit. I've caught it now and adjusted. I'm not losing leaves at the pace I have in the past. Even though some are in flower. I think I'm getting better. I fed for the first time today. Each plant got 1.75 pints. Except the 10gallon which got half the powerade bottle and the 5gal which got a qtr. By the time I left the plants were standing up nice and tall and looking amazing. Now I just need to apply bt and secondary supports. 7/31 Another eight day week. I'll have to do six days next week. Everything looked amazing this morning. I'm seeing less pest damage. Watering and feeding was the right move. Now I just have a little rearranging to do, add supports and spray if I decide to.