The Grow Awards 2026 🏆
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@GODAXE
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2024.09.12 D64 Its been two busy week, as i trim the 1 pond mother, get aknowledge that my wife use my grow sniper two pruned is badly infested rose bush, since 2 week and never proper clean it whith alcool.😱😱😱😷 in result a massive PM & mithe contamination in my grow tent... 😱😭😷😭 all plant have been shoot with H2O2 at 0.5% and set ouside for 2 day, wich turn to be rainy as f***, until i clean and serilized everything, twice and run the hepa filter .😷😰 the plant look ok, lightly over wartered, but no more pest or PM sign as they return in the tent.. 3 days later PM hardly bonce back, no choice to use more agressive treatment so they all have been shoot with saffer's defender 3 in 1. after 3 shoot in 24h and another tent desinfection we should have get rid of it 🙏 8 day laters everything look fine👍, all damage leaf have been removed, i also prune some unrelevant lower and inner grow
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Starting to gain a lot of trichomes and I’m loving the purple colors
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@DreamIT
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🐩👤Sirius Black👤🐩 by 🌍🌱WeedSeedsExpress🌱🌍 👤 29.3 ... 👤 30.3 ... 👤 31.3 ... 👤 1.4 Begin to see a swelling of the flowers, it was time: D begins to feel a slightly sweet scent but we wait a little longer to feel the veterinarian characteristics of this beauty. Viparspectra always works to the maximum, I am enthusiastic about this lamp, I can't wait to mount the XS1000 too. in a week I will soak another seed, I hope to catch the colored one: p 👤 2.4 👤 3.4 👤 4.4 __________________________________________ 👀Are you looking for a good lamp to start?👀 Viparspectra in my opinion has something more than the others, take a look at their site. ➡️ http://bit.ly/pro-seriesproductspro-series-p1500 ⏩Use " GDVIP " for an extra discount💯 ____________________________________________________________________________________ 📜👀 A look at the details of what I'm growing 👀📜 🐩👤Sirius Black👤🐩 by 🌍🌱WeedSeedsExpress🌱🌍 📋 Details 📋 ⚧ Gender ▪️ Feminised ➰ Genes ▪️ 70% Indica / 30% Sativa 🎄 Genetics ▪️ Sirius Black 🚜Harvest ▪️ 450 g / m² 🌷Flowering ▪️ 63 - 70 days ✨THC ▪️ 25.0% ✅CBD ▪️ 0.5% 🏡Room Type ▪️ Indoor 🌄Room Type ▪️ Outdoor 🕋Room Type ▪️ Greenhouse 🎂Release Year ▪️ 2020 ____________________________________________________________________________________ 👀📷 Follow the best photos on instagram 📷👀 https://www.instagram.com/dreamit420/ 🔻Leave a comment with your opinions if you pass by here🔻 🤟🤗💚Thanks and Enjoy growth 💚🤗🤟
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Great week going into 4 weeks. Started LTS 3 days ago Gelatos have responded very well
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@Zengrower
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The top buds are still fattening up but slower than last week. In the lower branches there are also many smaller buds that have started growing. I guess the plant is fattening up those as well. The flowering time of this strain is between 9 and 10 weeks, so it still has at least 2 weeks to fully mature. The top buds are looking nice and frosty, and the smell is outstanding! More pics will be added after wednesday. I lost my Sanlight dimmer key and waiting for a new one to arrive. And taking pictures with the growlight at 100% is no bueno 😐 🌿🌿🌿 Mid-week update Allright so my dimmer is replaced and I can take more pictures of this frosty lady ✌️ The trichrome production on this plant is more than I have ever seen sofar. My microscope broke down and I'm waiting on a new one to arrive so I can inspect the trichromes more closely. We're entering the ninth week of blooming so the plant should be ready within 2 weeks.
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Early veg. Stage Do si dos og by Original Sensible Seeds day 23  lollipoped and stripped the ladys they slept for 36 hours to trigger the far red ... so my ladys are in flowering now still don't feed them with nutes its still enough in my soil .. starting with nutrients in about a week i think they only get some HyPro spray mix HyPro Generator and some HyPro Rootsstimulator 3 days in bloom, and 4 days after defoliation damn where do all these leaves come from 😂 but everything is going well, no defects or other problems to find that was it again Soil: Atami light mix & Plagron Grow Mix mixed! Temp: 25,5 °C Lights: 12/12 Humidity: 54% Ph : 6.0 Water: 1l 23°C CO²: No Mercy Tabs Tds/Ppm: 400 ec 0.8 Nutes by Hy-Pro Fertilizers ml on 1 liter... HyPro : Spraymix 5ml HyPro : Terra vegi & bloom 00ml HyPro : Rootstimulator 5ml HyPro : Generator 00 ml HyPro : Epic Bloom 00 ml Light distance: 24 inch=61cm dimmed to 60%= 600par 1x MarsHydro TS 3000 Air Van: 800m³ Prima Klima AKF : 800m³ can lite 4x 140mm controled Be Quiet pc vans 3 l water cooling airco Diamant... 3.3l humidifier 1.8l dehumidifier Humidity control: Inkbird IHC-200 Temp control cooler/heater: Inkbird ITC-308 My grow room is variable in size 120cmx120cm² Custom Grow space for sog 150cmx150cm for scrog   S.O.G. Sea of Green Thx to Original Sensible Seeds,  HyPro Fertilizers, BTB Grow Supplies, Mars Hydro as our exclusive sponsor of our group The High Community
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@SamDo
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Hello, nouvelle session, et 1ere expérience cette fois ci en coco. Avec une nouvelle gamme d’engrais de chez Canna, ainsi que le substrat en coco de chez Canna aussi J’ai constaté que les graines de Quick Critical+ ont germées très vite par rapport à la terre, ici, à peine 72h pour les 1ères. Et un joli 100% pour la germination!! Merci dinafem!👍🔥 J’ai pu aussi constaté que le réglage du PH et de l’Ec prennent ici toute leur importance,, puisque pour mes 1er arrosages j’ai oublié de contrôler l’Ec, résultat, légère brûlure sur le bout des 1ères feuilles,, j’ai immédiatement corrigé en contrôlant et en ajustant l’Ec,, les choses devraient rentrer dans l’ordre maintenant. Voilà pour cette 1ere semaine de découverte de la culture en coco,,, A la semaine prochaine... Happy grow...😎
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@DBanned
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June 12, 2020 Week 7 I added some manure to all the pots. 2 of the plants aren’t growing much so Im leaving them to grow, and see what happens. Plants were a bit too wet from previous thunderstorms, now waiting for them to dry out so I can try and bring their ph down. Thank you and happy grow🌱 June 14, 2020 Plants started to dry out so we added ph down water and authentik Veg nutrients 4-3-2 by nutri+. Ph’s mix equivalence was around 5.8 So we brought the ph up to +/- 6.4 For ph Up we used sodium bicarbonate(baking soda). And used 1 litre of water per pot. Thanks happy grow!!!
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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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DAY 21: Hi all , been a busy week in the real world this week for me ( baby no 9 due anyway now !) . The light has been performing well with nk signs from the plants that they need to get more light and the smaller Gorilla cookies seem happy to Bush out just above the pot top . Must be plenty of light for them. I have no idea what's happening with the #2 Northern lights at all , it is in stasis I think.. Its sister is going crazy and needed a 90° bend at the 4th node to keep her tamed. She has grown past the super cropped bend already and begun heading upwards with her 5th node again. It has given the lower growth time to pull even and compete for the main bud status. The Gorilla cookie are spreading themselves out a little better now and hopefully once they hit flowering , the stretch will power them to send out their best tips for flowering. The Grandaddy,s Mimosa is doing well too and on par with the #1 northern lights for size. She is also showing female hairs at the bracts now which is great to see as it a first run out of my own seeds under this light. I am so far very impressed with this little looking but well powered light and wonder how good their biggest xs light could be in my grow room. Be safe and well growmies
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@Ruuddata
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Well I'll say I didn't put as much time into it as I should have but it was quite or a pretty fair grow considering it's my first time growing anything.I've learnt alot and looking forward to my second grow
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@BloodBath
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Sour Wiz is still in veg. 7 weeks. Looking fantastic. EAsiest strain to grow so far. 0 issues and respond so everything well. Once I can sex I’ll separate and start planning to flower. Skywalker OG is still going great in week 9 of flower. STARTING to see a lot of bud structure and white hairs. Northern Lights is still surprising because it was so mutated and now its thriving.
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Gagarin is comin' ___)))))
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@Paulolo03
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DAY 63, the grow box is now fully functional again, new extractor, new handmade softbox, back to 18/6 schedule, max temp=33°C, RH=50% (I know it's a bit high for flowering stage but I check carefully the plants and so far, nothing is wrong) 3 plants are frosty, I can see the trichomes with the microscope so I stopped the nutrients for them and flush with water pH 6,2, do you guys think I'm doing well ? For the 7 others: - 1 hasn't flowered, I keep her but I know shell never give nothing. - 6 are growing and I keep giving nutrients (Biogrow, Biobloom, Topmax and Bioheaven)
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@BatGuano
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D37 - I totally stopped defoliation as there will be no more new leaves from now on. The girls don't need any LST either. All I need to do is just water them and wait for them to mature! No crispy leaves, no nutrient burn, no flies, no bugs no problem at all. Only AK2 is a little bit behind on bud development but it is possible that it might need more time in the flowering The nutrients are still double the recommended dosage.
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