Ok so it’s been along time since my last update as life has been busy for me.I have moved these 3 ladies outside sometime the end of June or early July and they have thrived.Ive topped them a few times after the initial topping and have added 3 scrog nets to keep the colas spread open over time and keep em below my fence top :).Some really nice colas and smells amazing I just know my neighbor is jealous 😆 kidding we smoke and bs together often.Ive been feeding them twice a week 4ml per gallon of advance nutrient line and they love it.Ive noticed they are starting to really thicken up this past week as its sept 19th today.I have some rain coming next week but it’s been a drought in Ohio so no worries about bud rot or mold until now.Im debating on adding a roof structure this weekend before the rain hits.What are opinions on polycarbonate roof top ??

First day in Flower! It's been... very interesting 2 weeks.. now that I survived tha, im having some lockout due to being unable to take care of my plants for the past 5 days and someone having no idea had to do the job, I'm not afraid of showing these mistakes I'm always looking forward to the outcome so I'm still having some hopes for this og kush, not everything here went as planned and that's why I want to focus on finishing up the grow and starting new ones, better ones as soon as possible, I will definitely never grow autos again as I'm just not a fan of them having to be on 18/6 schedule and I like having co trolley over my plants as sometimes things can go wrong. Og kush had a lockout after flush it grew beautiful but still ate up some of the upper leaves. Runtz.. yeah I like him he is a beautiful little bonsai he didn't get lockout too much but also did I'm looking forward to seeting the stretch on him if it so happens. Cherry gusher, a tiny pheno I got this time I'm looking forward to growing 4 next time and hunt down a pheno. They say outdoors you have to play with God and indoor you try to play God.. we are not perfect and that's why I'm looking forward to the finish line. Will i scrog? I have the net setup but I'm not sure if I will get enough stretch. Day 3 I noticed some light white spots on bottom leaves of the plant after a flush I did recently, I diagnose this as magnese or magnesium deficiency, I'm going to up the cal mag to 8 ml and a+b to 10ml per 5 L of water along with additives extra 0.5 ml just as a touch up. Also I noticed we are at 47cm at the tallest branch after topping and lst and this thing is an absolute bush.. I could probably hide behind it if I was a kid playing hide and seek!.

The tricombe production on this strain is ridiculous! It looks amazing under my microscope. The heads are mostly milky coloured so this may be finishing sooner than expected. The space in the tent is getting a bit tight so I'll be glad to have more room when this lady has done her thing.

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(9th feb) So these girls are now entering week 5 and with small space comes challenges as these girls have really started too lift off growth wise as you can see 2 of the girls icc are tall and the remaining shorter girls are toronjaz all happy and healthy... still no defoliation I have chosen not too took these girls only a topping and leaf tuck here & there and wow they are loving life under aptus nutrients 🌱 They are thriving into this week where I will be tucking a few more leaves before flip in roughly a week or so time 🙏 Finally grow diaries has let me update with images and videos and I'll be updating my fastbuds diary tomorow too These girls are sailing through each week and I'm really happy using aptus nutrients I have topped 1/2 and all have responded great under aptus nutrients which I'm really loving using atm. These girls will have another 2 weeks untill flip too 12 hours light but these aptus fed girls I expect too boom in flower 😍😅 We shall deal with that issue when it arrives 🤣 Happy growing! 💚

Hello, Day 47, 48, and day 49, Flower Phase , PGK, Everything looks fine, seems ok for the moment. RH is high these days, very near to harvest and i am going to finish this grow after 10-12 weeks or Day 70-84. also gave 2nd dose of NPK (0.6-3-3).Thanks. Week 7 Flower Phase Day 46 - 19/12/22 Day 47 - 20/12/22 Day 48 - 21/12/22 Day 49 - 22/12/22

ESPAÑOL: Hola chicos !, espero que se encuentren muy bien. En esta semana hubo un notable crecimiento de las chicas, todo va super bien !, aun no comienzo a aplicar fertilizante de crecimiento, pretendo aplicarles ya en su primer transplante a maceta Airpot 10.8 litros que sera dentro de una semana para luego ponerlas a florecer, esta semana añadi 1 ml de cal-max de grotek para para aumentar ec a 0.4 ya que trae una pequeña dosis de nitrogeno para darles un empujoncito. esta semana tambien se incorporo la Cookies Usa en reemplazo de la Kryptonite que no sobrevivio y que por lo demas es una chica muy fuerte... saco sus hojas a la luz en un par de horas despues de ponerla en sustrato, maravilloso ! eso es todo por esta semana amigos ! INGLES: Hi guys! I hope you are doing very well. In this week there was a remarkable growth of the girls, everything is going super well!, I have not yet started to apply growth fertilizer, I intend to apply them already in their first transplant to a 10.8 liter Airpot pot that will be within a week and then put them to flower, This week I added 1 ml of grotek cal-max to increase ec to 0.4 as it brings a small dose of nitrogen to give them a boost. This week Cookies Usa was also incorporated to replace the Kryptonite that did not survive and is otherwise a very strong girl ... I bring its leaves to light in a couple of hours after putting it on substrate, wonderful! that's it for this week folks!

Thts things starting to get interesting now

Had a bit of strip not much to say about this week again apart from flowering is happening finally and it's getting there with small bud sites popping out everywhere

Amazing week for girls they look happy I'm happy too 😀

Hello Everyone 👏, As you can see, are all Cherry Colas growing, they all have a tightrips in their pots for now, for recognition. Will make nicer pictures of them in a few days. They are now 4 days from germination🙏. The humidifier had been added, so I had to adjust the room a lil bit. Seedlings don't need much nutrients, neighter do autoflowers. with normal soil I would recommend to only give water for 1-2 weeks, since it holds nutrients in it as well. But since I'm using Cocos for this grow, I might have to add some basic nutrients in the upcomming week. For this week I gave/give only water turns and Startbooster turns. Update day 5: - Lowerd the lights to avoid stretching. they are now at 75cm distance from lamp to pots. I want them at 40-50 cm, but I don't want to rush it. - Added another layer of cocos to avoid the soil from drying up therefore the roots from dying. This will happen because of lowering the lamps down, the soil will get exposed more to heat. As you can see, the humidifier is doing his thing haha. Pictures and videos where taken without the lights + fans on. because of that, it will look like this. Still fun thought. Enjoy 🙌

Eccoci qui... Tutto va per il meglio, questa settimana ho eseguito Lollipopping e Defoliation per far si che le cime principali sprigionino al meglio il loro vigore. Siamo verso la fine del progetto ora bisogna solo aspettare la fine... Grazie a tutti per il supporto🔥🌲❤️

Update week 4 Bloom

Ready

🌱 Start: 17.07. 🌱 Hello everyone! This is my very first grow and I'm thrilled to share every step with you! 🎉 I'd appreciate any tips you might have to help me achieve the best results! 😊 Equipment: I've geared up with an Indoor Grow Kit from MarsHydro along with some BioBizz supplements to ensure my plants get the best care. 🌿 🌼 Seeds: I opted for Fast Buds seeds after hearing great things about them. They were delivered super fast—just two days! I’m especially excited to test the C4 strain. 🚀 I've begun soaking the seeds and setting up my space. Eagerly awaiting the transition to the next stage in a day or two! 🌱 📅 Update: 19.07. All three of my C4 seeds sprouted 1-2 cm within just 1.5 days! 🌱 It’s often recommended that autoflowers be planted directly into their final home, so I'm following that advice. I'm working on improving the air circulation in my tent to ensure the best environment for growth. 🌬️ I'm currently using 0.2L cups with big holes over the sprouts to maintain higher humidity during their initial two weeks. 💧 🎉 UPDATE 22.07. - THEY ARE ALIVE 🎉 My C4 sprouted on 20.07., and I'm overjoyed to soon share photos and a video of my little green buddy! 📸🎥 PS: My plant enjoys 2 hours of chill jazz music every day! HAHA 🎷🎶

Not my strongest specimen but hopefully she will strengthen over time

Wie man sieht, haben die beiden F1-Samen ein enormes Wachstum gezeigt, während das Apple Flitter langsames Wachstum zeigte. Ich baue zum ersten Mal F1-Autoflower-Samen an und die Wachstumsrate ist wirklich beeindruckend. Nach drei Wochen habe ich Holzstäbchen zur Unterstützung hinzugefügt, und die Wachstumsrate der F1-Samen ist weiterhin beeindruckend. Sie sind bereits bereit, Blüten zu bilden. ご覧の通り、2つのF1種は驚異的な成長を見せたのに対し、Apple Flitterは遅い成長を示しました。私は初めてF1オートフラワーの種を育てていますが、その成長速度は本当に驚異的です。3週間が終わった時に木の棒を挿して整理しましたが、F1種の成長速度はやはり驚異的です。すでに花を咲かせる準備ができています

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.

Me encantó la cepa y su facilidad de cultivo ! Aun que tuve muchos problemas ambientales y climáticos . Me atrasé unas 3 a 5 semanas con estas nenas , pero nos recuperamos bien ! Usamos malla scrog chilena #kanovicultivo , lo mejor que he usado en malla scrog , no se le comparan , su espacio preciso! . Las 4 comenzaron en pequeños vasos , luego de 1 a 2 semanas , trasplanté a macetero de 5.8lts , finalizaron 3 en maceteros textil 19lts y 1 en macetero de 20lts AirPot ! Comencé a brindarle 20hrs de luz / 4 hrs oscuridad , a la 3era semana 19hrs de luz y a la 5ta semana bajé hasta el 18 / 6 . Usé un panel QB de 480w regulables , chips marca Samsung de 3500k , chips epistar UV 660nm iR , el mix completo gracias a mi bro MKleds chile ! Se pasó ! De todas maneras recomiendo una potencia mínima de 600w ( QB LED ) para espacio de 120x .. Usé un bio estimulante chileno , que a mi parecer fue uno de los mejores que he visto y usado ! El grande #trichomemania , te cuento que este producto activa un mecanismo de defensa en la planta (SAR) , haciendo que reaccione y se trate de defender con mayor producción de resina , terpenos y tricomas ! Es increíble ! A los 24hrs tienes resultados , un saludo grande a los hermanos ! El mejor producto 10000000%.... Grande eva seed , buenisima esta cepa , me dí cuenta que si se deja madurar un poco más , su sabor es más frutal candy , exquisita cepa !.... Estamos probando con un papel de blunt organico 100% libre de tabaco marca *jamaican buzz*...al fumarla su efecto es notorio , enseguida viene el efecto psicoactivo y cerebral , se viene a la vista un tanto distorsionado el entorno ...la vision un poco más brillante , y a la vez relajado .. Hoy 18 de agosto estamos probando con un papel de celulosa organico marca lion rolling circus ( foto al final del album ) , quema bastante bien , al parecer ya está casi en su totalidad secado , combustión lenta , buen sabor afrutado citrico con toques candy diesel ...uuff efecto despues de 3 quemadas ya por los cielos , totalmente cerebral y estimulante , un gusto charlar con amigos ! Al manipular su fruto , la planta expele un olor afrutado con limon maduro y skunk , con finales de candy terra , una delicia , muy buena cepa , ahora mientras escribo me siento un tanto "mareado" con esa mitad de blunt ! Buenisinaaa!... ____ La verdad cuando comencé a cortar cada planta era como llenar "infinitamente" el armario donde dejaría secandola , se llenó casi la mitad y un poco más sólo con 1 planta cortada ! Increíble producción , yo estimo unos 90g por planta aprox , ya he consumido un buen peso además ...veremos en estos días que esté por completo su secado ! Esta riquísima , sus efectos fuertísimos ...100% ... ___ Una cosecha buenísima, muy parecido como obtengo resultados en comparación con el sodio , todo bien me gustó la experiencia !.... Además tuve la oportunidad de hacer extracción en seco de su materia vegetal . Obtuvimos entre un 18 a 20% de retorno ! Para mi primera vez , geniaaaal ! Su utilizó prensa de 12 toneladas , de apretó a 80°C por 4 minutos . . . Usen lemon king ! Una delicia .

Using Promix coco mixed with worm casting on the top layer and promix myco to help with seed start