Recommended
Likes
Comments
Share
Hey fellow growers week 8 update in the books! Not much happened this week besides having to raise my light to its max! The pistols were showing signs of orange pistols but it looks as though they are burning 🔥 so measured my light to plant and was sitting at 15 inches so I got it back to 18 inches but if these plants stretch any further I'm going to have to cut a hole in the top of my tent for the light!! So I finally had a week of ease. Thanks for viewing my grow and be sure to smash the like button and drop a comment I'm on here a lot prob more than I should be. Sorry for the bad pics this is a closet grow and its pretty tight quarters with no light so I have to work with what I got! Well until next week Best of luck and Happy growing!!😎🌱💚💪💪
Likes
12
Share
Just water and molasses as the trichomes are cloudy but no amber's yet but very frosty and smells amazing 17/1 chopped her tonight she had 24 hours of dark before.
Likes
39
Share
Las altas temperaturas han persistido es por esto que el riego ha sido más seguido variando siempre entre fertilizante y agua. Esta vez ya se utilizó Flawless Finish para este último proceso, una vez secándose el sustrato se comienza con la cosecha. Ha sido un buen cultivo. Veremos como termina esto. Seguimos ! 👽💪
Likes
2
Share
This plant is growing well, I transplanted them this week into 3 gallon pots from 1 gallon pots. Structure on this plant is pretty nice and visually pleasing to the eye lol.
Likes
2
Share
Got back from 2 weeks holiday and immediately lollipopped and defoliated all 4 plants heavly. Will wait a few days for them to recover from the battering I gave them before flipping to 12/12. This plant is at the back of the 4 in the timelapse.
Likes
22
Share
BIPLANE IS ALREADY FLYING !!! SEE YOU SOON MEXICO
Likes
25
Share
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.
Likes
65
Share
@3lementa1
Follow
August 23: Just finishing up about 36 hours of darkness, then I'm going to wash the buds, then hang them. Harvesting a bit early due to time constraints but it looks good. The smell is very dank, not a tropical skittles smell, much more like wood glue as I've seen mentioned in other reviews, although I'm starting to occasionally catch a sweeter tropical scent as well. I wanted to leave it a little longer. There were still a lot of white hairs when I started the dark period, but a lot of them seem to have developed into swollen calyxes so I'm pretty happy. I was a little worried they were making seed pods after last time, but I broke one open and all that was inside was red hairs. I'm going to keep an eye on the RH while they're drying and get them into jars and try to wait as long as possible before I start sampling. I can tell this is one of those batches that's going to get better and better if left alone for a couple months. Just did the wash, did 1.25 cups of 34% food grade H202 and a squeezed lemon in a 5 gal bucket. Another bucket of just water to rinse. Then I had a fan on it while hanging in the sunlight from a skylight in the bathroom for 30 min, then put the fan further back and on oscillate, then turned it down an hour later. Left it in there for a few hours, then hung it in the grow tent with everything removed except an oscillating fan, pointed away from the buds. I have the whole plant hanging in the middle of the tent and the tent is holding at 60% rh. Next run I'm going to do 2 buckets and only top once. I might leave them a bit longer in veg too to maximize the height in my grow space, and I'll get a proper 500w bulb instead of continuing to run 1000w bulbs at 50% to lower the heat a bit. The weather will be cooler and I'll only run one air stone in each bucket which should help with res temp. I'll probably foil-wrap the buckets again as well. I should be able to get another run done by the end of the year. I have a White Widow fem seed I've been waiting to use but I'm not sure what else I want to grow yet. Maybe Granddaddy Purp. I'll take some micro pics of the trichomes this week and start curing, and I'll post a proper review in a couple weeks. Happy growing everyone! August 24: I took it out of the tent to inspect. No mold or mildew. The middle of some buds are still pretty wet. I'll keep an eye on it. Wet weight on the stem is 158 grams/ 5.5oz. I harvested a couple branches last week and hung them up. I just ground up one of the buds, left it overnight and vaped some today. There was a bit of Chemdawg Tangerine in the grinder already but overall I got a lot of thick vapour, instant effects, and a really great tropical taste. I busted out the microscope camera and I realized I had a couple buds that fell off before I washed the plant in the H202, and a couple buds that came off in the washing process. It doesn't look like washing the buds took off any of the trichomes. I do seem to find less debris in the buds, not that there was much there before. The trichs look great. Just a light toasting of amber. The washed bud actually seems more dry than the unwashed bud. August 25: there's a real chlorophyll smell coming from the drying room today, it was much terpier yesterday. Leaves are getting crunchy, stems are still fully bendy. I ended up taking it down in the evening. The drying room rh dropped from 60% to 55% and the buds were starting to look too dry based on my last grow. I put it all in a paper bag for the night and I'll put it in jars tomorrow morning. Broken down most of the way it came out to 48-49 grams. From the bud structure, I definitely feel like it would have benefitted from more grow time if I didn't have to travel. More to come. August 26 - the edges of the buds are getting really crispy and the buds are getting tighter. I checked the paper bag earlier and it was 65-70%. I got the impression it was time to put it into jars. I'll keep the lids off for a bit.
Likes
9
Share
Likes
38
Share
Hi:) it’s day 72 today. 2 days ago I feed them with nutrients for last time. I will flush every single girl with 15l water plus canna flush And then water with terpinator only for another 12 days and happy harvest :) can not wait. I also welcome to see my new project baby’s from fast buds :) nice strains are coming! Bless guys, see you soon !
Likes
19
Share
Hola hemos tenido problemas con la cámara del celular y no hemos podido tomar muchas fotos por lo mismo . Esta es la Segunda semana de floración de este seguimiento , me parecen bastante rápidas la formación de sus flores y ya se está viendo una formación de resina en las flores. tenemos una SBR que se espigo más que las demás intentaremos ir controlando su crecimiento con algún cropping. Hello, we had problems with the cell phone camera and we could not take many photos for the same. This is the second week of flowering of this follow-up, the formation of its flowers seems quite fast to me and a resin formation is already being seen in the flowers. We have an SBR that spikes more than the others, we will try to control its growth with some cropping.
Likes
25
Share
@kizdog
Follow
So this week I saw some decent bud development! There are a couple of colas with tips a little too close to the light, but they aren't getting super high PAR measurements so I think they're good. I added PK 13/14 this week, so I wanted to see some interesting changes. Not as much as I thought, but some flowers are noticeably much fatter than a few days ago. Had an issue with the top layer of my coco getting dry which I realised to be from the 15L dehumidifier I had in there, right next to my pot 😳 So that's now on full power in the room outside of the tent. The heat can be a bit of an issue, reaching 27-28c briefly some days. There's been a couple of fluctuations in the humidity, from 55% RH to 70%, so I've straightened the ducting and tried to perfect my ventilation and environment as much as possible. I'm debating buying a co2 bag to help my plant deal with the heat and intense light. The trichomes are really starting to show, with the 60x magnifier I can see so many cool heads. It just seems that my buds aren't really filling out beneath the pistils, causing me to worry. This week there were so many photos that even after picking out my favourites I ended up with 111 of them! Also, it's worth noting that the nutrient amounts I have listed are in *ml/1.5l. Happy growing! KIZDOG
Likes
3
Share
@Sators
Follow
Day 29 – Holding Strong Indoors While Awaiting the Sun After two bright and sunny weeks, the UK weather has taken a turn—temperatures have dropped and grey skies have taken over. For the second day in a row, the plant has remained indoors on the windowsill, patiently waiting for the return of warm, sunny conditions. Despite the limited direct sunlight, the plant is showing steady vertical growth and structural development. The inter-nodal shoots are beginning to stretch confidently, and the canopy is broadening out with healthy fan leaves. It’s clear that the root zone is well-established, as no wilting signs appear and the medium remains nicely moist—no need to water for now. While it may seem like a temporary pause in outdoor activity, this rest indoors is helping the plant conserve energy and avoid potential stress from fluctuating cold and wet conditions. Once the weather stabilises again, it’ll be back to soaking up real sunshine. Observations: Location: Indoors (windowsill) due to cool outdoor temps Temperature: Noticeably lower; unsuitable for outdoor stay Soil: Moist, no watering needed Growth: Internodes extending, foliage thickening Patience remains key, and this CBD Auto 20:1 continues to impress with its resilience. Day 32 – Stretching Skyward with the Sun After a few overcast days indoors, the sun is back—and so is our CBD Auto 20:1, basking once again in full-spectrum natural light! The shift outdoors today was met with bright, clear skies and a lovely warm breeze. The plant is thriving in these ideal spring conditions, showing confident vertical growth and a strong central stem that’s gaining both height and girth. The leaf spread is wide and lush, with healthy serrated edges catching the sun from every angle. What stands out now are the multiple lower branches developing evenly—clear signs that this plant is preparing for the flowering transition in the near future. It’s rewarding to witness how much energy the plant can absorb on days like this. The outdoor environment clearly encourages a more upright and assertive growth posture compared to the last couple of indoor days under diffused windowsill light. Observations: Light: Full sun exposure, ~7 hours direct sunlight expected Development: Lower branches maturing, stem thickening, leaf canopy expanding Mood: Energised, reaching, vibrant We’re now well into the vegetative peak, and the structure is shaping up beautifully. Let’s hope this weather holds—it’s perfect for what comes next. Day 34 – First signs of flowering! We’ve entered a new chapter—today marks the visible appearance of pistils, signalling the official start of flowering! This beautiful CBD Auto 20:1 from 420FastBuds.com has been developing steadily, and it’s been an exciting journey transitioning it from indoor windowsill care to full outdoor exposure. Last night’s rain disrupted my plans to leave the plant outside overnight, but perhaps that was a blessing in disguise—timing and adaptation still matter. Today, however, the sun is back in full swing, delivering strong warmth and excellent light. The super soil is doing its job wonderfully, holding moisture and nutrients efficiently. The plant is clearly enjoying the rhythm of nature. Growth has stretched upwards significantly since the last few days, and side branches are expanding too. Unlike in a tent where watering might happen every 1–2 days, this outdoor grow has taught me the art of patience—watering is done only when the soil truly dries out, which depends on weather, sun, wind, and positioning. Huge thanks to 420 Fast Buds for this amazing strain—resilient, beautiful, and rich in promise. Can’t wait to see what the next days bring! Day 35 – Settling Under the Open Sky This CBD Auto 20:1 lady has now officially begun spending her nights outside under the open sky. So far, I haven’t felt the need to cover her, and she’s handling the shifting weather conditions with impressive resilience. Some nights are slightly cooler, but the days bring back that familiar warmth – and she clearly loves it. Her structure is becoming more defined, with side branches now fully visible and stretching confidently towards the light. Since she’s grown outdoors from the beginning, the natural rhythm of sun and wind has made her strong, well-adapted, and noticeably more robust than my previous indoor tent grows. It’s truly fascinating how dynamic and engaging outdoor growing can be. There’s a deeper connection to the process – monitoring the skies, respecting nature’s timing, and witnessing each subtle change. Plus, it’s certainly a more economical setup! The pistils are now popping with greater clarity, signalling the transition into flowering. It’s incredibly satisfying to watch her shift gears and get ready for her next stage of development. My super soil continues to do all the heavy lifting – no feeding schedule, just pH-balanced water when the topsoil is dry, which depends entirely on whether she’s basking outside or sitting in the shade indoors. Massive thanks to 420FastBuds for this incredibly vigorous and well-adapted strain. She’s growing with confidence, and I can’t wait to see how she flowers under these natural conditions. Let’s keep the rhythm going – one sunny day at a time!
Likes
18
Share
Мой первый - Grow Boxing, и самое сложное уже позади. Я думаю, что впервые человек учится на ошибках, и у меня было этих ошибок минимально .. Так или иначе, я считаю свой первый рост успешным .. и мне очень приятно видеть цветы на своей девушке 💚🌱
Likes
5
Share
อีก 4วันจะเริ่มทำดอก วิกที่1
Likes
68
Share
@715creeks
Follow
looking really good now. i removed some of the larger fan leaves at the top and trimmed the bottom to tidy up :) still loads of white hairs, a few have turned brown but not too many.
Likes
15
Share
@No_Clout
Follow
Flowering is starting well, starting to see trichs so I’ve gave them their first feed with bloom nutes (C4) which is also 95% organic which is always a bonus imo and I’ve not grown anything using organic products so I’m anticipating to see the end results. Their all 3ft tall or just under which is abit taller than usual but overall we’re looking fine, did some minor defoliation and lollipoping on the bottoms 1/4 of all 3.
Likes
38
Share
@Haoss
Follow
I have to dry the buds in the dark, at 20 degrees, 50% humidity