Día 20!!! Estamos en el punto de comienzo de la 4 semana de floración ! Esa en la que notamos como el cultivo nos da el cambio que queremos y a partir de los dos vemos como Nuestras flores evolucionan de una manera u otra dependiendo de clima,genética,nuestra mano con ella etc.. Vamos a comenzar la media floración bien cargados con la paleta de nutrientes alta en potasio y nitrógeno! Siempre añadiendo también,nuestras mañanas de agricultor. Tuve el fallo de abrir el tupper de lombrices y echarlas a el cultivo y no poderos grabar el proceso. Fue algo rápido que hice con el armario apagado..lo tuve que iluminar por un minuto para añadir la bola de lombrices unas 60!!! La siguiente tanda de flores si empezara a sacarle provecho a estas amigas!! Deciros que el cambio en altura es muy grande no para aún de crecer! Y las últimas están engordando mucho las flores a pesar de el corto periodo se ve que nuestra selección de amnesia haze,es un fenotipo muy especial.. Es de unas 8 semanas de floración y muy buena productora! Día 21 Primer día de la cuarta semana de floración tenemos una escalera Desde la puerta del armario hacia el fondo tenemos alturas que van 54cm/62cm/71cm/80cm Gracias a el control individual en altura de cada luminaria iré trabajando con el control de dividir el área en tres Alturas diferentes,así lo requiera cada planta. Una pequeña planta que está cerca de una rendija de ventilación tuvo unas pequeñas picaduras de tips”. Observaré si no es de un periodo anterior de antes del fumigado.. Si no es así trabajaré un poco de jabón potásico y ajo! De momento el olor es muy sutil. Algunas flores empiezan a producir resina de manera temprana. Dia 22 Va todo sobre ruedas,un verde lima en las hojas,las puntas tensas y bien firmes esperando el regado de mañana! Una humedad de un 55% en el armario,cerrándolo con un 59% una vez echo el seguimiento,inspecccion de este en el día de hoy. Seguimos con una semana de humedad en el exterior del 90% y toda una semana por delante de más lluvias. Seguiremos controlando la humedad como hasta ahora con los riegos. Guardo paciencia en las plantas que aún no llegaron a la red,para poder tener un control visual de todas las puntas! Me alegra ver la cantidad de flores que están produciendo por casi todas partes de la planta y la resina que empieza a producir alrededor de estas,es un gran fenotipo de amnesia haze,con gran rendimiento productivo de flores y resina. Todo un hacierto para quienes buscan genes de sativa bien marcados con un corto periodo de floración.

Sehr dunkle Blätter. Sehr frostige Buds. Langsam erkenne ich, dass sie bestimmt kein Highyielder wird. Aber krass wie viele Trichome zu sehen sind!

This was a very stressful week as there were too many variables at play all at once; even my camera refused to cooperate for the first few days. The freshly transferred plants were starting to droop and I was unsure if it was transplant shock, nutrient burn, or because of the incomplete grow tent. My first batch of nutrients were mixed into a gallon bottle and was weighed by a friend using his scale; this set was enough to last weeks. For this new batch however, I didn't have my scale and used the table spoon as my measuring tool; needless to say when my TDS meter finally arrived, both runoff and the remainder of the mixed nutrients read 2800. Fortunately my light setup seemed to be inefficient still and the plants weren't drawing much nutrients and only ended up with a very light burn on the older growth. All pots were flushed back to recommend levels and the light lowered until the lux values read appropriate. This week ends my daily comments and I'll stick to this end of the week format going forward.

Day 135 14/09/24 Saturday De-chlorinated tap water pH 6 with Plagron products. Day 136 15/09/24 Sunday Light top up of 2L de-chlorinated tap water pH 6 only. Day 138 17/09/24 Tuesday Feed today using de-chlorinated tap water pH 6. She is stacking now 😁💚 Picture and video up, ✌️😎 Day 140 19/09/24 Thursday De-chlorinated tap water pH 6 only today. Day 142 21/09/24 Saturday Another feed to push this week they seem to be handling it 💚. Fattening up on the buds now and pistils starting to mature. Day 143 22/09/24 Sunday (End of week) Damn!! Noticed I have leaf rollers!!! Damn caterpillar, from moths. So I have removed affected leaves and areas.💚

Good morning little miss sunshine. Using heatmat at 24°C for the first week. Light Power: 40% Soil in the final pot: I use 80% Dope Soil - florganics & 20 % garden compost. The soil was used by two grow sessions before. In the last one I added the compost. For this grow I added a 1/2 cup Dolomite limestone in the middle layer of the earth. To prevent Ca, Mg deficiency. Covered with 5cm old mulch. Watering with 2,5L tapwater and let it flow DAY 6 Cover open and she can feel the first breeze. DAY 7 Welcome in the final 25L pot .

Hello my fellow growers I hope you are all having a wonderful holidays and a wonderful day in general! Anyways I have been very busy recently so I couldn’t post a weekly update but I will be posting some more pictures later this week as I will be manipulating the plant a bit more to maximize my cola potential but beyond that nothing much is happening just watering her on the Monday/Wednesday/Friday schedule and letting her grow

**Encontrarás la traducción a español al final de la descripción** From/Desde: 08/03/19 || To/Hasta: 14/03/19 From day/Desde día: 15 || To day/Hasta día: 21 You can find the Gorillas Diary here: ** Podéis encontrar el diario de las Gorilla aquí:** https://growdiaries.com/diaries/25675-makingmoney-with-gorilla-mm-vs-gorilla -----IMAGES & VIDEOS----- Video 1: 7 days TimeLapse, +/- 1 image each 180 secs @ 30 fps, you can see how beauty is the dance of this babies and how are they growing. This is a fast timelapse adjusted to 1 minute for instagram, if you want to see the 3:21 min complete video (1fx60s 30fps) it's uploaded on the gorillas diary named abobe. Video 6: An overview video of the babies, moments before i performed the first topping/man-linning/prunning/LST on the biggest gorilla. The other one is recovering at time from those ugly color marks she has on them leaves. As the leaves seems not healthy i decided to not perform the man-lining on this one until it has a pair of healthy main leaves on which i can trust to guide. -----WEEK SUMMARY----- I traveled to Venice this week and i have very few photos, also i returned with a terrible flu, so i'm not going to take too much photos for the next week too, i'm so sorry. The Money Makers are growing healthy and equitative, with very short nodal distances as you can see in photos 4 & 5, i'm not going to perform the same main-lining technique i'm doing with the gorilla, i'm going to test some things. With the Money Makers i'm going to perform something similar to the man lining but with 3 or 4 floors, i'll be twisting the main branch to create a circular horizontal proppagation with 6 or 8 branches. First i will fix the heights of the floors and then i will push them horizontally. Let's see where they go ;). -----WATERING CALENDAR----- 12/03/19 - 700 ml with all week nutrients @ 0.95 E.C. PH5.9 12/03/19 - FOLIAR - Used about 25 ml of (200 ml water with 1ml Pro Active, 2 ml Plant Vitality + and 0.1 ml Foliar Spray) *****ESPAÑOL***** -----IMÁGENES & VÍDEOS----- Vídeo 1: TimeLapse de 7 días, +/- 1 imagen cada 180 segundos @ 30fps, observad la maravillosa danza de las nenas y cómo crecen. Esta es una versión rápida de 1 minuto que cree para instagram, si queréis ver el vídeo completo de 3:21 min (1fx60s 30fps), está subido en el diario de las gorilas que nombro en la cabecera de la descripción. Video 7: Un vídeo general del armario, está grabado momentos antes de realizar las técnicas de cultivo sobre la mejor de las gorilas. La otra se sigue reponiendo de esas manchas feas que le salieron en las hojas. Ya que las hojas parecen enfermas, he decidido no hacer el man-lining hasta que no tenga un par de hojas saludables en las que poder confiar para hacer el guiado y alimentar los brotes. -----SUMARIO SEMANAL----- Las Money Makers están creciendo sanas y equitativas entre si, con distancias internodales cortas como podéis ver en las imágenes 4 y 5, no voy a realizar el mismo man-lining que estoy realizando sobre una de las gorilas, pues voy a probar cosas. Con las Money Makers voy a realizar algo similar al man-lining pero respetando 3 o 4 pisos de las plantas, giraré el tallo principal para crear una propagación horizontal circular de las plantas con 6 u 8 ramas. Primero ajustaré las alturas de los pisos y luego las expandiré horizontalmente. Veamos hacia donde van ;). -----WATERING CALENDAR----- 12/03/19 - 700 ml con todos los nutrientes semanales @ 0,95 E.C. PH5,9 12/03/19 - FOLIAR - He usado unos 25 ml de (200 ml de agua con 1ml Pro Active, 2 ml Plant Vitality + y 0,1 ml Foliar Spray)

Super easy trim✂️ The buds are super dense & sticky🤩 For the smell it’s cherry & blackcurrant with a gassy touch the Cherry Cola Diesel ⛽️🍒

Week 8 of flower Well this plant is really filling out. I definitely roasted the edges of the her fan leaves but she is still chugging along nicely. She should start to ripen up in the next couple of weeks. 😎😎

Didn't change anything to the feed because she seems happy Did remove quite a bit of fan leaves, as I'm planning to send her into flower soon Not exactly mainlining, but it definitely is a very beautiful canopy

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.

Happy 4:20 everyone! 🙌 I hope everyone's doing well and please remember to stay safe! The buds in my plant are getting bigger! Two of the side branches of Pistachio could not hold the weight of the buds (you can see when they fall on the timelapse!) so I had to "hang" them to the tent, yikes! 👽 I also increased the amount of Silver PK by 0.5 but I believe the PPM was a little too high, so next week I'll try lowering the dose of CalMax to see if that helps. Some of the trichomes on the leafs are starting to turn ambar (while the rest of the plant are transparent or very milky) so I suppose the girls are getting there! They need a liiiiittle more time since there are still some immature hairs, specially on Matcha. The leaves of Pistachio are also turning lighter in color and I've been removing them everytime one pops up. Anyway, see you all in my next update! 👍

This is the girl's final week. The wife will be happy the stink is coming to an end. Will be stripping off all the useless leaves at this point, getting them ready for a quick trim. The ppm in the planters is down under 200 ppm now Kannabia genetics made these easy to grow. I had no problems growing these 3 different strains out. They all flourished except for 2 of the smaller ladies. They were a little overfed as I treat all girls in the tent with equal amounts of everything. Those girls still did well, just not as well as their bigger sisters. The Kritical will be coming down first as most of the pistols have oranged over and the trichs are clouded over. The Super OG will be the next to come down. The buds on these girls are so hard I think you could knock someone out, if you through it at someone's head lol.... The Hellfire OG will be the last to come down as their still throwing pistols. Mostly still white and gaining more weight. I gave 3 of the seeds to my bud and he grew his out under cmh lighting. Plants stayed much more compact and he just finished his trimming. Under the HID the plants get much larger and buds twice the size. I gave him the same feed my girls got through his entire grow, mixed and ready for him, so it was mostly lighting that made the difference. My climate controls are also much better, but he is very happy with the amount he trimmed from each plant. Grade A looking weed for sure.... Thanks for the looks and like my frinds. 🙏

Day 22 begin medium full fertilisation (around 500ppm) 2,5 lt x4 pots Day 28 first LST

Day 37 - Everything looks good.... they are drinking so much.... i built a bit more stable light setup, and i'll need to buy afew more plugs and stuff, to fill it out ...... i organised all the 2700k globes, ready to swap in..... still waiting on the exhaust fan, so i'll keep em in "grow" mode another week or 2 .... i'm vaping a leaf or 2, and drinking "green tea hot chocolates" .... it is so delicious in hot chocolate .... my health has picked up since starting the vape/drinks... the 21 thc/19 cbd is supa healthy ... Day 38 - Getting them ready for Flower, noticed they are lacking in nutrients, so i started em on the heavier dutch master gold flower nutrients. Day 40 - Added some pics. (they look droopy because they in night mode, just turned on lights for pic) - Started them on 12/12 flower, still working on getting all the lights, gear, and globes, for the right spectrum and amount of light.... atm got - 7x 2700k (click) , 2x 6400k (osram), + 60w light panel .... i'll go get some more gear today and hope to expand it to 10x 2700k , 2x 6400k ...... I put the exhaust filter fan on seperate power, so it doesn't go on/off with the timer, but stays on all the time.... it totally fixed up any odour problems, haha ....... Added some different pics for my light spectrum ... etc..... the outside winter temp is now at 40-60oF (5-15oC) so with the 12/12h, the temp inside the tent is dropping to 60-80oF (18-22oC), abit low, but flowering is supposed to be in winter, so idk, see how it goes..... I'm new to growing, so idk how this will work out....... just working it as i go.... i noticed afew spots on a leaf, so i upped the neuts abit more, they are still drinking like fish, huge amounts.... Day 40 late - new vids - Got the extra gear and installed it all... redesigned the initial setup, refined it with proper measurements, had to get my steel rule out, lol....... got the 12 leds in and running, 10x 2700k clicks, and 2x 6400k osrams, with the panel..... it's lookin beautiful and got the exhaust on 24 hrs now, all working perfect with 12/12 timer.... they are forming a few spots on leaves, so hammering the nute water into them now... they are drinkin 1-2 litre of nute water a day each.... (nute water = Dutch mater gold one grow/flower, 800-1000 ppm 6 PH) 😎 Some details about lights.... i did some maths on it, and included some handy pics..... because i'm using cheap leds, i'm keeping the distance at 25cm, they are leds so they won't burn, and it massively increases the lumens/lux/Par, and with my home built light setup, the leds are spread out enough to keep it lower.... worked out good..... something of note is that all the led globes are built/made in china... however different marketing/selling companies from around the world... and the german osrams are 1w leds ... by far the most superior, but anyone can design and send the requirements to china to build em, haha) it's not a contest, we all work together.... haha.... the person with the best led light globes gets my business, because i want the best for my babies.... :) (let me explain- 1w led vs 0.5 w led, the watt of the led projects the light, lumens, LX/PAR etc much further the higher the watt of the led....my 600w panel has 0.5w leds, the philips has 0.75, the osrams have 1w leds..... ) each globe philips (dutch)- 10.5w internal - 14 leds 0.75w 1055 lumens each globe osram (german)- 10.5w internal - 10 leds 1w 1080 lumens each globe click (cheap)- 9w internal - 16 leds 0.56w 800 lumens light panel - 70w - 600w 30 red - 8 red 12 blue - 8 white 7500k 1 ir - 1 uv = 20x blue 6400k - 38x red 2700k internal - 60 double leds - 120x0.5w 6000 lm

Start of week 7 for the OG Kush and blueberry. Second repeat of week 5 feeding for the super lemon haze as she's on a 10 week schedule. OG's are super sticky, smelly and packing on thick dense buds, blueberry is bulking up, but not nearly as much as the oG. The SLH is also pumping out nice buds, that are very sticky. Very happy with this grow so far.

Always seemed like it needed cal/mag because of the neon green color. I did give it to them but didn’t make a difference.

Overall successful grow… will try to get bigger buds on my next grow for sure with different techniques…. Other than that 42fastbuds is legit