So langsam legt sie mit der Trichombildung los und der Geruch verändert sich deutlich 💚

Hallo zusammen 🤙. Sie wächst sehr schön und macht keine Probleme. Rabattcode für den BIOTABS-Webshop https://biotabs.nl/en/shop/ GDBT420, damit erhalten Sie 15 Prozent

Okay so after 48 hours instead of 24 of darkness. These ladies were begging to be chopped with how much more intense the smell got. Cheesy , sweet , skunky , and a floral incense kind of scent. Made lots of finger hash just getting them off the plants , already smoked. I’m about 75% done with chopping all the major tops. This time I decided to cut off the branches and dry on an eight tier 24” diameter rack off Amazon. All 8 tiers are full with gorgeous top colas. I’m drooling. Can’t believe just how much bud this is turning out to be. They are dense , and oozing. Not going to get a wet weight because this is just too much. But holding the rack it’s like 20 lbs or more. My scales don’t go that high. Lol. Gotta say it, I think my buds look 10 times better than the advertisement photos g13 lab’s mozzarella. My 2 cents and honest opinion. Please do give me your opinions. I know I didn’t show the full grow because life gets busy. My next grow I want to control the humidity and heat levels a bit better. Or just humidity and run co2 to withstand higher temps. I have every angle of the grow under my tips now. It feels amazing to have this kind of harvest after the dedication these plants received. I’m Convinced…. rdwc with a water chiller , is by far the best way to do hydro. When it’s dry I’ll add the final weights. My nutrient reg is this. Jacks 321 , botanic are cal mag plus, hydroguard,PK booster is flower fuel(purple can off Amazon) and unsulfured molasses. If you don’t have an ability to keep water at 70 degrees then only use jacks hydroguard and cal mag. You’ll still do well but that molasses , that sauce is the boss.

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.

CRAZY NIGHT: We were in Montreal around 2006/7 to promote an entrepreneurial business set up by my brother. The business centred around fightgear and fighter promotion in the mixed martial arts industry. My Brother (NX), myself, Stephanie 1 and Stephanie 2 (real names) and some big name fighters were in town to hang out with some clients, bring the fighters to a few venues to meet fans, run some demo classes, and sell some shirts. These two girls are bombshells, and apparently NX has a sexy night planned with the both of em. The Stephanies are all over eachother all day long, playing the role of stupid bimbo to a tee. While these girls are day drinking, we are trying to get everyone settled into hotel rooms, give enough time to meet clients for dinner, and then we would head out to the bars in Montreal where we had booked appearances. A typical weekend promo, nothing should go wrong.... (continued next week) THE DIARY STUFF: Well, Fastbuds, they never called me fastgrower!! You sent me these seeds MONTHS ago, and waited on my grow season to start. Much appreciated, and in turn, I will grow your little ladies with the utmost care and respect they deserve. Lets see the full potential of these fast finishers, cant wait for you to tell me whats in em! All seeds popped within 48 hours of germination in paper towel method. So far, off to a good start!

Week 8, and my custom fit SCROG has been installed! ❤️ At Day 50 I separated my 7 gallon girls and my 5 gallon girl. Once done, I began the very easy process of adding my “floating” SCROG. I use ratchet straps, just like the ones that come with lights to secure the four corners of the screen to the top of my tent. This allows me to adjust the screen height as necessary when 1) first installing and 2) once the full stretch of flower has occurred, I can tweak it a bit to balance the canopy as best as possible. It’s not 100%, I still get some over achievers, but I find it useful as another option. I like to do a major defoliation before I set the ladies in. Typically till this time, I have done almost no defoliation, just LST and some HST techniques. I adjusted the ladies placement to allow growth out all sides of the screen, set the screen height and began tucking and bending. The defoliation and bending allows light to penetrate all those side shoots that would have amounted to nothing, and they become top shoots as they grow up and form an even canopy. I don’t like to weave, it can damage the new shoots and cause growth problems, but the goal is to get as even a coverage as you can while allowing for plant growth in all directions. Once complete, I will give the girls about a week to recover and grow those new shoots. I like to have about 80% coverage of the screen, before I change my light cycles to flower 12/12… and if they are healthy and strong. I’ll decide this weekend if it is time ❤️👊🇨🇦😎 Happy Gardening!

Checkout my Instagram @smallbudz to see the Small budget grow setup for indoor use, low watt, low heat, low noise, step by step. 04/01/2020 - Did the last defoliation, removed about 1/4 of plant material. 06/01/2020 - Fed her 1.5l of 6.5PH water with 0,3ml Cal Mag (Atami) 0,25ml of Grow, 0,6ml of Bloom and 0,5ml Max, and 1ml of each: Heaven, Alga-mic and Vera, noticed some run off, I use about 1/3 of the nutrient dosage on the chart, to achieve about 200/300PPM (500 scale).

9.7 D85 Harvest day✂️ Last flush 10L Water PH 6.5 EC 0.3 Return PH 5.9 EC 3.4 Very high EC of soil. Above 15% amber. Triochoms at top cola start degradation. Defoliation&wet trim. 23inch tall. No training. 121g wet (but now freaking stems and leafs like people do 😂) 32.2g (73% return)

Hello all and welcome to the much anticipated beginning of vegetation for these five Epsilon F1 Autos from Royal Queen Seeds. Allow me to introduce Ally, Normani, Lauren, Dinah, and Camila. All five girls have pushed put their 2nd node (3 fingers) and node 3 is on the way out. I expect all five girls to take off from here, and so the next seven days are going to be big. I will start fertigation today. For comparison purposes the Day 1 here means Day 1 of veg. For Ally, Normani, and Lauren this is day 11 since breaking ground, for Dinah day 10, and for Camila it is day 9. For the rest of this grow I will increment days from here but it's really easy to work out days since breaking ground as it is a simple matter of day + 10, 9, or 8 respectively. Day 1: Fertigated 2l. Day 2: Right ok. Can you actually believe this response in 24h? The poor girls were STARVING. Wow look at the change in color! Wow look at the growth!! Ally is most advanced, Camila least. It is fascinating so see them develop! They are growing faster and faster now. So let us talk about the elephant in the room a little bit. Phenotypes. At the moment there is absolutely no evidence to suggest that this crop will be anything other than uniform. Nevertheless there are some clear differences in some of the girls. So let's have a look shall we: Ally (center), Normani (closest to the middle purple basil), and Lauren (opposite side to Normani): These three girls are not quite identical, but it is a pretty challenging game of spot the difference. Dinah: Okay so Dinah is coming in noticeably darker than her sisters, with a little more tendency to claw, and with quite a bit larger and more angular serrations. Her first leaves are also a different shape. Camila: Little Camila had a twin, but I killed her with some overzealous tweezing before I realised what I had. She came in with only one cotyledon, and she came in last. Her first leaves are quite different to the rest of Fifth Harmony. She is also showing slighty more narrow leaves. She is lastly also very slightly more pale than her sisters. Are these phenotype differences? I mean in terms of the environment, feeding, watering, substrate, temperature, light, airflow... well these girls are all in the same pot, so unless I am particularly haphazard in my mixing and fertigation (which I can assure you I am not) I do not think it likely that these ladies have significant enough environmental difference to account for these quite clear visual differences. I am absolutely fascinated to continue to witness this, and it has only now occurred to me what a great privilege it is to be able to grow the world first F1 cannabis hybrids, and what an astounding honor to be one of the very first hobby growers to do so! The fact that RQS made this happen by not only supplying the seeds and other merch and goodies, but also sending expedited international shipping so as to fit within my arbitrary timescales is almost unbelievable. When these guys (on their website) say that it is their belief and mission to forge the path to worldwide legalisation, they are not hollow corporate whispers, it is their core of being. Cannabis everywhere is truly blessed to have such a worthy and proactive ambassador. Bravo RQS! I have adjusted the timer such that the main tent is now getting 20/4 upped from 18/6. After monitoring DLI at 18/6 for a week I am unhappy with the overall level but because of the varying heights of the plants I am limited in what I can do in adjusting the light height. Some areas were only getting 20 DLI. So I have rearranged to have the taller plants on the edges and the lowest in the middle and doing it this way all plants are getting between 35 and 50 DLI at 20/4 - although one or two cola tips here and there are getting 55. Will monitor for a week. Day 3: Well look at this growth again!! These ladies have responded to feeding really well. Fertigated 3l. Day 4: Growth is accelerating fast, these ladies will be ready for their first training soon. I am starting to formulate an idea what to do. I am thinking of topping Ally and LST on the rest. Day 6: Fertigated 3l. Ladies growing fast now. Will soon be time to start training. However! The secondary nodes are developing strongly. Hmmm Day 7: Fertigated 3l. Defoliated the three fingered leaves from Ally and tucked the five fingered under other plants. End if week summary: Well when they said "hybrid vigour" they were not joking. Look at day 1 and day 7 side by side after approx 6 days into veg growth. Wow.

420FASTBUDS FBT2106 WEEK 7 This beautiful lady is maturing nicely with some amazing purple flowers. It's starting to give off a sweet smell so one could only imagine as she gets futher into flower. The other unfortunately isn't going to make it. I've continued to let it grow and see if maybe it would snap out of the funk it was looking like. But it still has not and seems to be not getting worse. Every now and then you end up with some funky mutations. All in all Happy Growing

Flower kicks in party hardy

Harvested 2 of 8 plants today. 90% or more trichomes were white with a few amber here or there. All pistils brown on the 2. 2 more plants should be ready within 2 days. The others are still a week out.

Week 4 All are growing good. 3 nodes, correct and solid stretch . Daylight 6h30 / 21h25 = 14h55 Rainy days - 19°C … globally bad weather in May Low water Weekend: changing pots — 17L for all + 20L for BreakPadBreath…Geo textile Soil= Patchamama (rich Mix) + Coco + Worm humus Adds = algamycor + guano + mycorrhiza Topping on GMO and Flash Back: 4 nodes Now the plants have a reason to be stressed 😬

Hi guys!its getting kind of boring but again a rainy day.They need sunlight bad,the coming days the sun will shine so we will see what happens. Cheers! Finally we have sunshine!The smallest one,a gg,just will not grow i dont know whats wrong with her and she is already in flower. The rest is doing fine i think. Cheers!

Y nos fuimos a floración!! 🍀👨‍🌾🏻

Gracias al equipo de AnesiaSeeds, Marshydro, XpertNutrients y Trolmaster sin ellos esto no sería posible. 💐🍁 Coco Jambo: Con una composición genética 60% Sativa y 40% Indica, Coco Jambo es tu billete dorado a un verano sin fin, ofreciéndote una escapada a un mundo donde el sol nunca se pone en tu felicidad. Con unos niveles de THC que oscilan entre un relajante 30% y un estimulante 34%, Coco Jambo es un faro de euforia que guía a sus usuarios en un viaje a través de olas de serenidad y vibrante alegría. Su aroma es una celebración de los sentidos; imagina el momento de euforia al abrir un coco y descubrir que rebosa de las frutas tropicales más suculentas. 🌻🚀 Consigue aqui tus semillas: https://anesiaseeds.com/es/product/coco-jambo/ 💡TS-3000 + TS-1000: se usaran dos de las lámparas de la serie TS de Marshydro, para cubrir todas las necesidades de las plantas durante el ciclo de cultivo, uso las dos lámparas en floracion para llegar a toda la carpa de 1.50 x 1.50 x 1.80. https://marshydro.eu/products/mars-hydro-ts-3000-led-grow-light/ 🏠 : Marshydro 1.50 x 1.50 x 1.80, carpa 100% estanca con ventanas laterales para llegar a todos los lugares durante el grow https://marshydro.eu/products/diy-150x150x200cm-grow-tent-kit 🌬️💨 Marshydro 6inch + filtro carbon para evitar olores indeseables. https://marshydro.eu/products/ifresh-smart-6inch-filter-kits/ 🍣🍦🌴 Xpert Nutrients es una empresa especializada en la producción y comercialización de fertilizantes líquidos y tierras, que garantizan excelentes cosechas y un crecimiento activo para sus plantas durante todas las fases de cultivo. Consigue aqui tus Nutrientes: https://xpertnutrients.com/es/shop/ 💻 Trolmaster Tent-X TCS-1 como controlador de luz, optimiza tu cultivo con la última tecnología del mercado, desde donde puedes controlar todos los parametros. https://www.trolmaster.com/Products/Details/TCS-1 📆 Semana 5: Comienzan a formarse los cogollos, las hojas se llenan de resina cada dia y el olor es bastante fuerte. Parece que ha terminado de estirar. Practico una defoliación intensa para airear los futuros cogollos y dejar mas espacio en el cuarto de cultivo. Agrupo de nuevo las macetas en su lugar optimo para asi rellenar por completo la carpa @marshydro. Me quedé algo corto de nutrientes pero estoy muy contento con los resultados, cada vez le voy encontrando mas su punto optimo. Siempre es mejor quedarse corto que pasarse.

Awesome grow more to come from rocbuds I’m gonna post more here and stay off IG

Day 36. Still no feed.... Again, difference in size growing many autos is HUGE pain. One Northern Lights is smallest plant I ever grew, I doubt I would I achieved it with loads of LST ;))) Will try to lift that midget a bit ... Some flower, some not, Diesels are still the only strain I would grew, but most probably not once ;))) they look amazing !!! 10 out of 10 ! Green Crack still the obvious looser at the moment and is still mostly in veg ... Next watering will be full of goodies for them !!! Couple leaves off here and there, couple branches cropped or repositioned, still waiting for stretch to be over before installing some support. Day 37. One more girl took SuperCroping like champ and at the moment has very even canopy. All garden looks fine, hope feed won't spoil that joy ;))) Day 40. Girls still on water, but during every two days, so it's again pain ... Whatever pot size I take - girls start to go faster, than my laziness wants :))) Cleared bottoms of first row, next watering will clear other 5, just want to see are they ok. Some strains hates any job done to them and stops developing.... Would be stupid to slow them down in final stretch ... Happy Growing !!!

Zbliżamy się do końca. Dziewczyny dostają już tylko wodę. Pojawiają się mleczne trichomy, czekam mniej więcej na stosunek mleczne-brazowe 80-20%. Gubią dużo liści (szczególnie ethos) , dziewczyny się zjadają :-). Ravenberry ma piękne jesienne kolory. Temperatura w dzien w tym tygodniu nie przekroczyla 25C w nocy 18-19C. wilgotnosc 40-50%