Oct 5-11 Vegetative steering? Aiming for: leaf Temp -80f CO2 -1250ppm VPD +1.04 (65%/75F) Vegetative Steering 6P1/ 2P2/1P3 Each P1 water event is 15 minutes apart. Seems to far apart. I think i Need More water events, with less time in between events in order to get a strong veg signal? Watering for 2min(110)ml May need 3min waterings(currently not getting runoff) I have to hand water every two days. Day 11 flo 18.5inches tall 12inches from light(moved to 16) 1300ppm Day 18 Defol Sprout chickpea(2days) Soaked 1cup for 4 hours then rinsed. Completely covered then Soaked overnight. Rinsed then poured water out and layed jar on the side for one day. Blended with water(aloe vera and coconut) Day 19&20 foilarspray Alfalfa/Chickpea SST with Kelp,aloe,coconut,silicate,microbes brewed for 1.5 days Day 21 Fed the Tea blend Leaf temp 80 65kluxx Co2 100 Plants look like they responded well to the foilar. The flowers at this stage are my best performance yet .crop steering may be working?

Week 1 of flower over going great plants are a nice size the tent is full up now I've moved a runtz muffin plant the 2 mac 1 and the mimosa to a small veg room so they can veg for longer and be ready for the next diary. It's quite hot round here atm and tent is hitting 27 degree not ideal but that's typical English weather sometimes good most of the time shitty happy growing team 🙂 any advice and help would be much appreciated send me a message any time I love the feed by Future harvest highly recommended see yous next week for my week 2 flower update thanks for all the help from my sponsors @Hydroprowashington @Anesiaseeds @divineseeds @monkeynutrients

Hello, Grow Diaries family! 🎉🍌 I’m beyond excited to share the harvest report for my incredible Red Banana Pudding! This journey has been nothing short of amazing, and I can’t wait to dive into the details. Let’s get into it! 🚀 🌿 The Harvest After a wonderful flowering period, it’s time to celebrate the fruits of our labor. The Red Banana Pudding has reached its peak, and I’m thrilled with the results! 🌈🍑 Visuals: The buds have developed beautifully, showcasing an array of stunning colors and a perfect density. The aroma is incredibly sweet and fruity, promising a delightful smoke. 😍 🌟 Harvesting Process • Timing: Harvested at the perfect moment to ensure maximum flavor and potency. The trichomes were checked and showed an ideal mix of cloudy and amber for peak effects. ⏳✨ • Technique: I followed a meticulous process, ensuring each branch was trimmed with care. The process was smooth, and the final product is a testament to the love and effort put into this grow. ✂️💪 Fun Fact: Did you know that Red Banana Pudding is renowned for its unique banana-like flavor with a hint of creaminess? It’s a true treat for the taste buds! 🍌🍰 🌿 Post-Harvest • Curing: After trimming, the buds were carefully hung to dry in a controlled environment, maintaining optimal humidity and temperature. The curing process will enhance the flavor and potency, making for a truly exceptional smoke. 🌬️💨 • Batches: The buds are being sorted into batches to ensure even curing and to preserve the quality of each nugget. The anticipation is building as we wait for this next phase! 🎉 Pro Tip: Proper curing can significantly impact the final taste and smoothness of your buds. Make sure to store them in airtight jars and burp them regularly! 🍁 🌱 Looking Ahead The Red Banana Pudding has set the bar high, and I’m excited to see how it turns out after curing. This has been an incredible experience, and I’m grateful for the support and engagement from the Grow Diaries community! 💚 Sneak Peek: Stay tuned for upcoming content, including taste tests and smoke reports! You won’t want to miss out. 😉👀 🎥 Catch the Full Journey For a detailed look at the entire grow process, including the harvest, be sure to check out my YouTube channel, where I share in-depth updates and tips. Dive into the full experience and see how it all came together! 🌟🎥 Thank you for following along with this amazing journey. Your support means the world to me! 🌍💚 Happy growing and see you in the next update! ✨🌿

If you're not already following my youtube channel go subscribe now! Appreciate it people. Now for these girls. Day 38: All very healthy and well, I said I wouldn't be doing any topping this round and i haven't. Been doing a lot of LST/Bending (haven't used any ties as i dont want holes or marks on my rdwc system buckets) but if anything else im challenging myself. As you can see, plants look quiet bald after defoliation but definitely bounce back better if done right. Opening up the plant so its more bushy and exposing potential bud sites, not rocket science just basic logic. Hope everyone is doing well and staying safe during this time. Once more, Go Subscribe to my YouTube channel.. link on profile. Stay tuned.

Primera ves cultivando una cepa de esta calidad, algo ansioso por obtener los mejores resultados posibles con estás genéticas. Básicamente elegí la Grandpa's Stach R2 y la Grandpa's Cookies #6 S1 solo por sus tiempos de floración, espero que sean buenas tanto de sabor y resina, cómo también de producción. G1, brotaron las semillas, solo 1 semilla brotó chueca, por lo que tuve que ayudarla con un alambre y va un poco atrasada en comparación del resto. G3, primer riego con pH 6.1 y EC 0.6, y micorrizas Great White. G5, creciendo bien. G11, riegos cada 2 o 3 días, a punto de pasar a etapa vegetativa.

Days 50 - 56 Last week, I had a major lockout issue with my plants, so I’ve started monitoring both the irrigation and runoff water closely. I had to do three rounds of flushing, but after that, my lady started to recover, which was a relief! Since I'm going on vacation for the next 10 days, I’ve been working on setting up an autonomous irrigation system, which I successfully implemented and built yesterday. It uses three 12V water pumps controller by Arduino Uno via H-Bridge motor drivers, each dedicated to one plant. The system runs from 9 a.m. to 11 p.m., delivering around 250 mL of water per plant per session. This means each plant will get approximately 2.5 liters of water per day. I’ve mixed all the nutrients in advance. I know the ideal scenario would be to add the fertilizers just before each irrigation session, but unfortunately, that’s not possible. Still, it’s better than nothing. The system has been running smoothly since this morning, and so far, the cycle works fine. I’ll improve it further when I get back from vacation. To prevent any future lockout issues, I’ve extended the irrigation cycles throughout the day to ensure the coco stays consistently moist.

It’s a nice grow so far in terms of expectations reality on the seed breeders. Great stuff again. I had a real germination nightmare this time around though - lots of strains failing at seedling so the numbers and strains became more 😂. So the tents are mixed up again to auto on one side and photoperiod on the other. In this tent as well as Afghan and a red gorilla - there is sweet zensation , banana krumble and red hot cookies and a peyote skittlez. Water in using ro solely through the grow. There has been one issue. I tried a “pro” substrate from biocanna this time and I have those little fleas. Really annoying and my aphids are late so kind of annoying - takes the pleasure off a bit. Any good organic solutions let me know please on comments

Welcome to Zamnesia Spring Cup 🏆 Hey everyone 😊. A nice week starts before the harvest 😍👌. It smells incredibly delicious and looks beautiful. . You can see from the leaves that they suck their last energy out of the leaves 😉. There will be an update before the harvest 🙃, until then I wish you all a good start into the new week, stay healthy 🙏🏻 and let it grow 🍀🌱 You can buy this Strain and Nutrients at : www.Zamnesia.com Typ: Sour Diesel (Zamnesia) Zamnesia Spring Cup 🏆🏆🏆 Type: Runtz ☝️🏼 Genetics: Zkittlez x Gelato 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205 W 💡💡☝️🏼 Soil : Canna Bio ☝️🏼 Nutrients : Monster Bud Mix ☝️🏼🌱 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 6.0 - 6.3 💦💧

Anyone know how much longer I should leave this ?

Compared to powerplant, LSD is very slow to get going. By the end of week 2 of flower i expect more established bud-sites, however i have been told that LSD will get busier towards the later stage of flowering. We shall see. But in terms of plant health, there are no deficiencies (not that you get any with NFT), very uniform nodal spacing - no stretch, very large stems at the bottom and the root mass is exactly what i expect. The temperature has now dropped to 14c at ''night time'' so ive had to introduce a small heater to keep the temps up whilst theyre asleep.

29.6 I think I have missed a week but girls are growing like crazy now. I topped that topped one again and pinched also couple new shoots. Let's see how that turns out never done that before. Gonna switch to flower once these get recovered from that pinch. That topped one is also super cropped. I bend it to half from main stalk and tied to a stake for support. But yes very healthy nice growing plant no problems all good. 3.7 Flipped to flowering today. Next update is flowering week 1 seven days from today. (10.7.) Both doing very good. Topped girl has got good even bushy shape, like it. Other one has not gotten too tall. They actually are the same height. Happy growing!

Day 79, 28th of November 2020: Hi there! Here we go let's say half way. Plants are pretty these Original Sensible Seeds genetics are fantastic! The 2 OG and the Runtz Gum is very strechy. Black Ghost is pretty shorter bushier plant. Runtz Gum and Do-Si-Dos OG approx the same height Do-Si-Dos OG is taller a bit. Wedding Gelato is really cool little, bushy anf nice buds forming not problem with her all she is quiet. Do-Si-Dos OG has some deficiency and leaf gets dry but nothing very serious..... Fertilization is still the same every second day with the rationand mixture above stated. The lamp is on 11.15 min and off 12.45 min. Last week was 15 min longer light cycle.... So every week 15 min shorter light cycle until the 5th week. So far -45 min. It switches on at 6 am and off at 17.15 pm.

Day 49. Those buds are now really starting to swell up. They also produce a very lovely smell🤩 A few days ago I also changed the light colour from blue and red to only red. We'll see how the buds will react to that.

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.

Tuesday 30th . Flushing started today.

Hello growmies 👩‍🌾👨‍🌾🌲🌲, 👋 Like than others, she don't like the hot temperature, more and more Yellow leaves, look done soon, but the buds don't really look ready, don't bump.. 💧 Give water each 2/3 days. 1,5l Water + RQS Bio Flo Pack 1,5l Water + RQS Bio Flo Pack + Sugar Royal PH @6 - Bio Flowering Booster Pack Thicker Flowers 1 ml/l Bigger Flowers 1 ml/l Sweeter Flower 0.7 ml/l 💡Mars Hydro - SP 3000 80% 45 cm. 🔥 Thanks community for follow, likes, comments, always a pleasure 👩‍🌾👨‍🌾💚🌲. Mars Hydro - SP 3000 💡💡 https://www.mars-hydro.com/sp-3000-samsung-lm301b-greenhouse-led-grow-light Zamnesia - Gelato Auto🌲🌲 Discount code -20% with GROWITGD code 🔥🔥 https://www.zamnesia.com/7688-zamnesia-seeds-gelato-automatic.html

La medida de riego es por semana 1, riego por semana

Not much to say the one on the right seems to be going into to flower or stretching more then the on on the left we turn the light up to 100% this week nows just a waiting game. Plants are a bit green we shall see

Raised EC to 1.9-2.0 ish pH 5.8 Raised the Lights to the maximum height. Tops-to-Light-distance around 25-30cm Buds are bulking up daily! This run is smooth as hell. No deficiencies, no pests, plants look happy from beginning until now.... Lets hope the last 5 weeks will be ok!