Vegetation: To keep temperature and moisture on optimal levels at around 23°C / 65% I'm using two mechanical timers. - 24/7 on: Fans and water pumps (+Ventilation after 3.11.) - Timer 1: Lights and Humidifier 18h on / 6h off - Timer 2 (BROKEN 3.11.): Ventilation 18h (15min on / 15min off) / 6h off NOTES: Everything looks good and the roots have appeared from almost every (11/13) rock-wool cube. From now on I'll mostly water the plants from bottom by adding the wanted amount of nutrient solution on a plate, and then placing the plant on top of for ~15seconds This week I'm also starting to prepare the hydroponic systems (2x NFT-GT90, and 1x EBB-flow I think) and stronger nutrient solution since my plants are becoming ready to be transferred. Spreader-mat is the base of my plants when I have transferred them in to the hydroponic systems. DO NOT place more than one layer of the spreader-mat as it is not meant to be used like that! As you're cutting the mat for NFT's, be aware to have some extra for your peace to reach nutrient solution below the tray. That way you won't get noise from water dropping when systems are turned on. Day 15 (1.11.) Day 16 (2.11.) First watering with a bit stronger nutrient-solution (~ EC 0,6 / pH 5,9) than before, starting with 50ml/plant and watering once from above. Slowly increasing EC to 0,8. I cleaned and assembled 2 out of 3 hydroponic-systems which I'm going to use. I'll do the same also to the last system, but it currently has my plants on top of it so I'm going to do it later. I want to make sure that my plants have built healthy and big enough root system before transplanting to hydroponics. I'm waiting for the rock-wool cubes to be bursting of roots so they won't drown on their first day in hydro. Also, as the plants are bigger before the transplant, I'm able to fill my nutrient-solution tanks full with correct strength nutrient-solution for Mid-Vegetation from the start, therefore no need for that much adjusting later on. Day 17 (3.11.) I noticed my other timer which controls the lights had stopped working... The lights were on when they shouldn't have been, I noticed it an hour after they were supposed to turn off. I think I caught up to it early, but it may have been on for maximum of 2 days straight. No worries there since on vegetation-phase the plants don't necessarily need any sleep (Even though you should avoid quick changes like that!). Roots have appeared from the bottom of every cube and plants are looking pretty healthy. I think they are almost ready for hydroponics. Day 18 (4.11.) Few plants are showing symptoms of nutrient deficiences or some sort of sickness, not certain what exactly. I'll be keeping an eye on it. I'll be transferring in to hydroponic systems in maybe a week, so I don't want to stress my plants more than what's necessary. Increased my solution strength to 0,9 EC with a bit more Cal-Mag than before, and watered the plants for 50-150ml each plant depending on weight and size. I'll be slowly increasing the strength by around 50% during upcoming week. Thanks for tips! Day 19 (5.11.) Day 20 (6.11.) Plants are recovering well from deficiences and I just transferred all of them to hydroponics. I don't have the water pumps on for 24/7 just yet, at this point I water them a couple times a day by keeping the pumps on for somewhere around 15min at a time. Lights are now set to 60% and I also added a tower fan to circulate the air and shake the plants. Day 21 (7.11.) Lights are now set to 70% since the Led's and plants are spreaded wider in the tent than before. Distance to plants stays the same at 75cm.

Any idea what other nuits i hould get

Pilot continues to stand out for its excellent flower development and exceptional resin production. By week 7, the colas have stacked tightly with swollen calyxes, creating dense spear-shaped buds covered by a thick blanket of trichomes that already extends well onto the sugar leaves. The plant has maintained a very balanced structure after training, with strong lateral branches supporting uniform flower formation across the canopy. Resin production is becoming one of its strongest traits, suggesting excellent potential for both premium flower and extraction. At this stage, the plant is entering the final ripening phase while maintaining vigorous health and impressive visual appeal. Seeds by World Breeders Cultivated by Piperoots 🇲🇦 🌱🔥

Day 36 Stretching has slowed but not stopped. 28-29” today. Feeding 3L per plant now. The orange haze seems to be flawless, the other 2 needing a little extra calmag and N, but early flower can be expected. Humidity holding at around 50-55% little higher than I want but plenty of air blowing inside and strong extraction, so no problem. Would like to see the bud sites fill out over the next few weeks, before swelling. White pistils everywhere very exciting to see these blossom. Lovely mild fruity smell already from the tent

Girls are trucking along without much issue. I did have a bit of PH flux due to my PH meter calibration being off but no biggie, she didn't show too much signs of stress. These girls are starting to stink which I'm happy about, hoping for a really cheesy harvest :D

Not sure if these girls are ready for the chop yet?? Still sucking up water quickly 🤷‍♂️🏻

Day 21: I still have my garden on a 6-2 light schedule and my two plants that i stunted do to overwatering are slowly making a come back. I am going to keep them as i am a optimistic person so im hoping for the best but to say the least it will help me learn how to deal with different problems as they arise and teach me how to manage a garden this size. I only low stress trained for 1 day which was the day that i took the pictures a few days ago. I didnt feel confident when i started it mostly because of the size and felt like i was starting the process to late. If its not to late feel free to let me know and ill try to start it again, other than that as always feel free to drop some tips and happy growing. I also added a video at the top for quick viewing. 😀

So I'm flushing this week, Sunday I used Flawless Finish and watered heavy early, and did a 2nd plain ro flush 6 hours later, I did the same thing Monday. Tuesday I did not give any water at all, Wednesday I flushed the same way with Flawless finish, but water 2 times after that night, I let everything dry Thursday and Friday, It is Saturday, Today I have used only RO water, I am done adding anything. I think I could call it good, but I am going to keep things going after today, tomorrow/Sunday, and Monday, I will not water again, Tuesday the light will not even come on and I will give it a couple days of dark to finish. I could use some tips on how to get some better pics. I try, I really do, but I'm not getting the pics my eyes are seeing, so in the center of the area is all yellow and marooning leaves, and the buds have a pink tint in that area. The trics are getting there, but not yet, I figure by end of week they should be right... almost all cloudy now, a few clear left, but barely any, the few amber here and there, but I'm also not taking a piece to check from the top either, I gettin a look at a few small little buds, near the top, but not the top, I feel like I'm close... , So anxious had to phone a friend to tell me why to wait today... lol, I'll test my runoff ppm's tonight just to be sure, but the way the coco is taking the water makes me think its clean. I'm always ready at the end, Garden of Green seeds have ALWAYS made me look like a great grower. I'm excited, The smells, is very strong, it has a sweeter smell, next week I should have harvesting pics... Thanks for checkin it out

Well, another week has passed and it has been growing not exactly as I expected, but they warned me about using only base fertilizers with an inert soil and a higher ambient temperature, I could have a not so good result, well, it's one more experience and I liked it and let's see how it will be until the end of the cycle because the next one I already ordered a starter kit from the advanced nutrients line! Let's Go!

Hi, topman! There is week was really difficult! Damage from buds of fat and unreal brown 🍃 on my Amnesia (A.)… So, we are continuous! 1/2 bloom from behind. See more>>

Cali crasher is growing well under the Hortibloom Solux 350. She got neem oil sprayed this week when the next grow space got infected with russet mites. So I treated everything not flowering to be safe. She didn't get training after the spraying. It was stressful enough as the leaves are showing. She did get a fresh solution change for first time. I Should see a lot of new growth comming in the next few weeks. Everything is about as good as expected. Thank you Hortibloom, and Doctor's Choice. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

***** Week 11 growth - February 13 to 19, 2021 - Week 2 Flower ***** This girl is looking very nice but she is the shortest of the bunch. She has not growing out as wide and tall as the other girls in the tent but that could have changed with an extra week of Veg. 8 weeks from seed was quite quick to throw a girl into flower so it’s all good.....just noting it👍😃 2nd SCROG layer in now....finally😞 Lots of work to do in cleaning up the lower leaves next week. Will do larger leaf strip and lolipoping when they start focusing more on bud development. Light is at 24” only pulling 310 watt, and the meter at the tops of the girls is roughly 28,500LUX. It is feeling like it’s a little strong for them but it’s close......the curling leaves is slowly increasing on the tops. By the end of the week we are at 400watts and reading 38,500LUX, this should be roughly 980 umol/s/m2.......over 900 and less than 1,000.......should be good for going into week 3. Nutrients switched over to flower schedule and following week 2.....but so-called back a couple of items. Adding some other items beyond IPP line so backing off some of the ppm to compensate. Still only one “feeding” per week. Early flower so hitting the microbes a little harder this week and next and then slowly start backing off. I like Remo’s Natures Candy for sweetener because it has humic, sweetener and old school molasses, amongst other things to feed the microbes as they are in coco. Bud Fusion being used now for pk boost.........no more “red kool-aid”😂 Still adding Rezin from Green Planet becuase it seems to boost my trichome quantity.....Terpinator likely this week as well......increase some of the sulfer to increase aromas. Little more detail....... Feb 13/21 - Day 8 - 3.5L watering with CalMag @ 1ml, Nature’s Candy @ 1ml, Resin @ 1.5ml Feb 14/21 - Day 9 - 2nd SCROG added today.....finally. Plucked a bunch more leaves in the process - watering with microbes only today. Recharge has some molasses in it so just adding that. - 4L water for these girls with Recharge @ 1/2 tsp/gal - 320ppm and 6.0pH Feb 15/21 - Day 10 - today is big feed day....its been 7 days. - 3L each girl with all the IPP line as listed plus silica @ 1ml, Nature’s Candy @ 1ml. (Bud Fusion was 0.2gr/L) - 1325ppm and 6.0pH - Girls gave run off at 3L today so didn’t push past that. Feb 16/21 - Day 11 - some feed left from yesterday so added 6L of plain water to dilute it and watered into the girls tonight. - 3L full feed of nutrients for each girl - 800ppm and 6.1pH Feb 17/21 - Day 12 - 3L each girl with Terpinator and CalMag @ 2ml, Nature’s Candy @ 1ml, Recharge @ 1/2 tsp/gal - 775ppm and 6.1pH - increased light power to 350 watts. Now at 32,500LUX.......take it slow over the next week and keep creeping up. Leaves have a bit of a taco shape coming out and looking fairly serrated at the edges.....pushing the light intensity on the tops👍 - leaf colour on the girls is very good......tips are not burnt either. Feb 18/21 - Day 13 -3L each girl of plain water today - added beneficial bacteria and enzymes @ 1.5ml - 330ppm and 5.9pH - was looking for a little lower pH as I have not been checking runoff. - have to do a leaf strip this weekend......start of week 3. - light power increased again, 400 watts now. Feb 19/21 - Day 14 - day out day.......they have not had one in a bit. - humidity was higher today as door to grow room closed today to assist clones with more humidity. So that takes us through two weeks of flower now. Not knowing this strain enough yet, I suspect feeding will stop at the end of week 6. That leaves four more weeks. I will treat the next two weeks like mid flower for nutes, and the following two weeks as late flower. Feed supplements accordingly. She is a nice plant and looking forward to seeing how her buds form. Looking good ETS!

Flower week 6 (3/1/2022 - 9/1/2023)

Change Friday Very smelly

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.

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Me sorprendío esta variedad OG. Kush auto. Es una voraz y golosa con el agua 😎 toma bastante yo que le doy 100ml al los 2 días otra ves me volvía a pedir estaba casi seco el sustrato cuando volví a echar otros 100ml 🌲😎 Gracias Seedstockers buena variedad.

Fed her some Guao this week. Her leaves are looking a little yellow which I assume I need a dose of nitrogen.

Weekly Update on the Runtz 🌱 Hey everyone! Just wanted to share how the Runtz is coming along. She's thriving under the care of the Plagron nutrients 🌿, reacting beautifully to every feed. Since my last update, she’s sprouted several new nodes and is showing incredible growth! https://plagron.com/en/tools/grow-schedule-calculator She’s definitely growing like a sativa 🌳, with those long, stretchy branches. To manage that, I’m planning to enforce some solid training techniques to keep her short and wide, just the way I like it 💪✨. I’m loving the whole experience so far, it’s been such a rewarding journey 💚. I’ve attached plenty of pictures for you all to check out 📸. Please drop a like, leave a comment, and share any feedback or tips you’ve got! 🌟🙌

This lady eats and drinks a lot, she,s drinking 30L per week of nutritive solution with 1.8/2.0 EC without complaining, she's looking very healthy .