Start of week 9 - Day 56 from start of bloom Giving her just straight pH'd water with a bit of the hydro-sparkle. I will change out the res with Clearex in 3 or 4 days. Most likely harvest 1 week after that. Total ~66-70 days

Bloom Week 3(Almost 4): This girl looks happy and there are buds everywhere. In the past week the buds have really started to get larger. She seems hungry, every few days a leaf shows some deficiencies (Yellowing/fading), but it’s only 1 or 2 leaves at a time. I’m not too worried about it, but may up the nutrients a bit as the manufacturer says that you can double the numbers for heavy feeding. This is a large hungry girl, and she drinks a lot. I’m loving this plant and it looks like we’ll get a nice yield from her if she continues being healthy.

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.

Despite the worm 🐛 eating some of the leaves...I am very happy with the plants vigorous growth. Had to resort to a spray solution to rid the bugs.

6/7 flipped to flower leafs lil droopy due to over watering a lil bit but it’ll bounce back and everything else looking good tho I think the flowering stretch is going be wild haven’t grown one this tall before going have to move the light up some more soon

Entrada dia 30 (sin marcación de desarrollo de plántula) : Señores y Señoras, un mes desde el comienzo de vegetativo y creo que cuando miréis el vídeo que he colgado no vais a creerlo, por que yo tampoco me lo creería, ni por un millón de florines filipinos. Os explico, todas las cuentas de crecimiento, nutrición y desarrollo expectables se han ido sencillamente a la basura y os explicó por qué. Primero, estamos en un ritmo que en cerca de seis dias, los cuatro cultivars están tomando la friolera de 24 litros, o sea que estamos con un ritmo de 4 litros de absorción diarios y eso sencillamente y por aritmética nos va con un litro por grow. El calor ha sido impiedoso la pasada semana y incluso ahora que la temperatura ya ha caído en torno a cinco grados (en temperatura máxima), la increíble tasa de absorción de agua se debe ahora esencialmente al increíble tirón que la cepa afgana fast de Sweet Seeds, ha tenido en los últimos días. Hubo cambio en el ciclo lumínico pasando ya a 12/12, y en este limbo entre final de vegetativo y empiezo de floración, en los últimos cinco dias los cultivars han ganado como 25 centímetros en altura y la multiplicación de ramas laterales ha sido exponencial. Sencillamente os invito a que echéis un vistazo a la entrada del pasado viernes y que registréis, la diferencia de crecimiento en tan solo 5/6 días. Con ello, cuestión número 1 : hasta que talla seguirán las chiquillas afganas "tirando"...todo lo que tenía pensado de cultivars sobre los 65/70 centímetros se han ido al garete y tendremos cultivars de talla de metro muy próximamente y con ello un armario abarrotado y sin un palmo más de espacio. Cuestión número 2: que vamos a hacer con el olor de esta cepa?!? En entrada de pré-floración, ese olor dulzón (casi al puro skunk) ya se hace sentir tremendamente en la habitación donde está el kit del armario de grow. Ya he instalado el ventilador de ozono y algo de olor se dispersa pero si la realidad en pré-floración es esta, cuando empezemos a ganar cogollos, hojas de azúcar y tirón de terpenos, no se a lo cierto, lo que será necesario para evitar la dispersión del olor y eso en un apartamento en un condominio, no es algo que pueda ser despreciable y habrá que intentar crear algún cultivo de plantas de compañía en mi terraza de modo a que se pueda ocultar el fuerte aroma que esta cepa tiene. Cuestión número tres - nutrientes necesarios y consumo de solución nutritiva. Como os he dicho, ahí vamos con nuestro Quadgrow, "chupando" por via de los "smart mat" que caben a cada una de las macetas, más de 20 litros en 5 días...empezé la entrada del diario haciendo aritmética simple, o sea que cada uno de los cuatro grows se toma un litro al día. No hay misterios, grows con crecimiento tremendo, sujetos a calor elevadísimo y humedad relativa que en los días más próximos, llegó a los casi 75% (os había dicho en otras entradas que estuvimos con humedad muy baja, sobre 40%, pero en la última semana y con el tiempo de "levante" (vientos de norte de África y con humedad llegada del Mediterráneo) hemos tenido días de casi 80% de humedad. Si en invierno, 80% ya es una humedad respectable y que no puede prolongarse mucho tiempo, por las condiciones de aparecimento de hongos, en verano, si sumamos a temperaturas sobre los 35ºC, humedades a los 80%, tenemos el "cóctel" perfecto para cualquier ser viviente (sea animal, vegetal o de otro reino biológico) tenga necesidad casi permanente de água (el calor y humedad, tienen la función reversa de causar deshidratacion rapidísima y con ello, hay necesidad biológica de reponer el agua perdida. Estos factores son también determinantes para que nuestra hidroponia y su reserva de 25 litros, sea suplida a los grows en cada 6 días, cuando mi idea sería que habría que rectificar solución nutritiva tan solo a cada diez/doce días, pero la verdad es simple y salta a la vista, a menos de cada semana es necesario hacer nueva cuba de solución y dejar que el sistema radicular de los grows se encargue de marcar el ritmo de riego. Como podéis también ver, esta semana ya hemos empezado a aplicarle la "forma" deseable para sacar renta a los grows. Ya ha sido colocado el entranzado SCROG para que podamos direccionar el sentido de crecimiento de las ramas laterales y también ha sido puesto en práctica, una primera defoliación, para limpiar exceso de hojas y sobretodo por la necesidad de la no existencia de áreas de sombra junto al sustrato de coco y evitar que puedan crearse hongos patógenos, pese a que mis grows siempre son "brindados" con micorrizas y trichodermas, justo para evitar cualquier disgusto a causa de un "menos pensado o deseado" Botritys, Fusarium o "amiguete" del estilo. Para final, que Dios Jah siempre nos proteja a todos, en los grows, en los que mal nos desean y a los que nos pueden hacer daño sin que algo tengamos echo para tal. Green greets y la semana que viene, espero volver y para enseñaros algun esbozo de floración inicial.

Day 21 today. These two are doing really good so far and I haven’t had to do much with them. Hoping I can get another week of veg before flower, other than that we are looking good

the roots broke the plastic basket😱 Very strong genetic, very recommended👽

@MephistoGenetics, Hi all the happy people here in GrowDiaries. This is my second cultivation ever and it will be fun to try a bigger space than my closet grow. First, I'm just going to say I'm done with the construction of my new growroom. The room is 2.14 meters by 1.7 meters and has a ceiling height of 2 meters. It provides a floor area of ​​3.6 square meters. I use a 54 Watt Lightwawe T5 for germination and 2 Pcs 400 Watt HPS lamps. I have a channel fan that replaces the room air about 40 times an hour to get a comfortable environment in the room, the air enters a fresh air intake from the outside. The air is purified through a carbon filter to then leave the room to the rest of the basement. Then I use that heat to heat the rest of the basement. I will use 10 pcs 15 liter Autopots to grow with and a 100 liter water tank that supplies the pots of water and nutrition. I will grow completely organically in soil and will watercure my buds to get the best possible medicine for me. But there are no cultivation rooms to be displayed here, so I continue with what is most important. Today I have put my seeds in paper towel and hope the seeds have germinated within a few days. I am very excited to see how the new growroom will work and how this Illuminauto 21 - Sour Crinkle will turn out. Illuminauto 21 - Sour Crinkle (Grape Crinkle x Sour Crack) Two of our fastest and frostiest varieties collide to make a sweet and sour delight! Expect super frosty, compact nugs that won't be a toke for novices. Destined to be a great strain for extraction work too! Plant size - Small - Medium Cycle time - 60-65 days from sprout Indica/Sativa - 80/20 Frost level - Extra Ridiculous https://www.mephistogenetics.com/product-page/illuminauto-21-sour-crinkle ................................................................................................................................................................................................................................................................................................................................................. 2017-08-21. Started to germinate the seed. ..................................................................................................................................................................................................................................................................................................................................................... 2017-08-23. Seed germinated and put in small pot in the humidity dome. ......................................................................................................................................................................................................................................................................................................................................................... 2017-08-27. Slow and steady she grows. --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-28. Transplanted in 15 liter autopot. Check the roots on this girl ----------------------------------------------------------------------------------------------------- 2017-08-29. New movie of the girl. ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-29. Hello to you who read my diary, I just want to say that I am pleased that you have chosen to check in with me and in my diary. I just want to say that I do this for myself and for a steady flow of my medicine. Everything you read and see in my diary is 100% honest and I will never distort or beautify anything here. I document my crops so that I can learn from my mistakes and also to look back at those different crops. I try to update with pictures every day and with text if something special has happened in the garden. This is my strainhunt for the best medicine and the beginning of my journey with cannabis and the cultivation of it. ----------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-30. Cleaned the room this morning, just vacuuming and cleaning with chlorine solution. Im testing the fan to control temp and humidity, it works great. Added some pics and a movie. Everything is looking great right now. ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-31. 3 new pics. --------------------------------------------------------------------------------------------------- 2017-09-01. New pics and a video from the grow room today. ------------------------------------------------------------------------ 2017-09-02. New pic. ---------------------------------------------- 2017-09-03. New video from this morning. --------------------------------------------------------------------- 2017-09-04. Week 2 starts now, new pics. ----------------------------------------------------------------------------------------------------------------------------------------- 2017-09-05. KL 08.00. Cleaned the room this morning, just vacuuming and cleaning with chlorine solution. KL 12.00. The girl got 2 liters of water with nutes in it, added a video. --------------------------------------------------------------------------------------------------------------------------- 2017-09-06. KL 08.00. The girls woke up after their beauty sleep, the leaves are always a bit down after 6 h of darkness, but they will stretch now when the HPS lamp starts. Everything looks good and I keep trying to tuck the leaves so they get the maximum amount of light where needed. Added pics and video. -------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-09-07. Day 17 from sprouting. I have never tested PH in my grows, when growing organic in soil iv learned that it adapt PH by it self. But im curious by nature so i had to test. Kl 10.00 Tested PH in the soil, it was 6.9 and tested my tap water and it was 6.8. Added video of the girl. Kl 22.30. New pics. ------------------------------------------------------------------------------------------------------------------ 2017-09-08 KL 08.00. Good morning, added new video. 2017-09-08. Kl 23.50. Gave every girl 3 liters of water and nutes, added new video. ------------------------------------------------------------------------------------ 2017-09-09. Kl 21.00. Defoliated a lot and added pics. ----------------------------------------------------------------- 2017-09-10. Kl 08.00. Last day of week 2. New video. 2017-09-10. Kl 23.00. 3 new videos.

8/10 buds are fattening up nicely. Moved plants under growlight to attempt to take better pictures. Cant wait to see what she looks like at the end

6/17/20: 15 days from seed. 11 plants look absolutely fantastic. 2 are a bit undersized, although they're probably the second wave of sprouters and are expected to be a bit behind schedule. 1 has twisted leaves and doesn't seem to be growing as well as the others. I moved one of the 6" clip-on fans into the tent yesterday to increase airflow. Discovered this morning that shutting the window of the grow room and sealing the tent completely with the humi set to midway results in a quite humid grow tent/room the next morning; RH was at 82% when I checked in! 6/19/20: Day 17. Watering day. I'm going to add 0.25 tsp of Dyna-Gro Grow to the mix. Maybe too early, but a little bell in my mind is saying "It's time!" Every plant is popping new growth, even the weird twisty ones. I think that means the conditions are dialed in and they're happy. I probably shouldn't upset the apple cart, and maybe this will end up being the place when I look back on this diary that will make me say "And that's where it all started to go wrong," but ... I just want to give them a tiny little kick. We'll see how they like it! 6/21/20: Day 19. Watered/fed again. Plants are crushing it since I started adding the DG! 6/23/20: Day 21. Conditions are getting a bit cramped in the Solo cups for a couple of the kids. I think a couple might get potted up today. Exciting!

V8, supuestamente hoy haría transplante a los maceteros definitivos, pero, hace 3 días que las plantas están presentando hojas débiles y dobladas hacia abajo, en un principio pensé en que podría ser exceso de agua, pero creo que es exceso de nutrientes, básicamente exceso de nitrógeno, ya que las hojas están con un verde muy oscuro y algunas están presentando manchas color café. Así que hoy les hice lavado de raíz, con agua EC 0, hasta que el drenaje fue de cercano a 4 EC. Esperaré unos días a ver si se recuperan, si no, simplemente las eliminaré y empezaré de nuevo, ojalá se recuperen. V9, al final si era exceso de nutrientes/nitrógeno, menos mal que se recuperaron con el lavado de raíces, pensé que morirían, ahora veré como siguen para decidir si hago transplante hoy mismo. V10, se realizó trasplante a macetas definitivas y un riego suave. Las plantas están todavía en recuperación, esperaré unos días más para empezar el LST. V12, riego. V13, se realizó una pequeña defoliación y LST.

It's time for a thrilling week 4 flower report on my magnificent Medusa F1 from Royal Queen Seeds. This girl is an absolute monster, and I'm not just talking about her size! She's bursting with buds that are starting to resemble baseballs scattered throughout the garden. It's like a home run derby in there! Now, let's talk about the power of mass defoliation. I carefully stripped away those excess leaves, creating space for the buds to shine. It's like giving them a VIP pass to the spotlight. By removing unnecessary foliage, we channel the plant's energy towards bud production. It's like a backstage makeover, where the stars of the show get all the attention. The result? Bigger, denser, and more potent buds that'll knock your socks off! I mean my Medusa's buds are growing so big that they're starting to look like baseballs. But hey, let's be grateful they're not golf balls, or else we'd have quite the game to play in the garden! I want to give a special shout out to Royal Queen Seeds for providing me with this incredible opportunity to grow the Medusa F1. Their genetics are truly exceptional, giving us the chance to cultivate plants that are nothing short of spectacular. Thank you, Royal Queen Seeds, for being the game-changers in the cannabis world! Stay tuned for more updates on the awe-inspiring journey with my Medusa F1. Until then, keep growing, keep smiling, and enjoy the amazing genetics that Royal Queen Seeds has to offer. Wishing you all bountiful harvests and an abundance of green goodness! As always thank you all for stopping by and for supporting me on this journey, i am super passion about growing and fell blessed to have you all with me on this new journey <3 <3 <3 Genetics - RQS MEDUSA F1 Ligth - LUMATEK ZEUS 465 COMPACT PRO 
Food - APTUS HOLLAND 
 
All info and full product details can be find in can find @ https://www.royalqueenseeds.com 

https://aptus-holland.com/
 
https://autopot.co.uk/ 

https://lumatek-lighting.com/ With true love comes happiness <3<3<3 Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so <3<3<3 <3 <3 <3 Growers love to you all <3 <3 <3 Medusa F1 Medusa is a true F1 hybrid created from pure, inbred cannabis lines. She boasts uniform grow traits, mouthwatering aromas and flavours, and plenty of potency. If you're looking to bring stable, elongated plants into your room, tent, or garden, look no further. Mouthwatering Aromas, High Potency, and Mid-Size Plants Though she won't turn you to stone like the mythical goddess after which she's named, Medusa F1 is bound to get you plenty stoned in her own special way. Combining genetics from inbred lines deriving from Sugar Magnolia, a thick and sweet indica, and American Beauty, a fast, fruity hybrid loved for its well-balanced, positive high, the result is an autoflowering F1 variety that produces fresh flavours, a unique cannabinoid profile, and large yields. A very aromatic cultivar with a vibrant concentration of terpenes bearing notes of fresh mint alongside an upfront peppery kick, backed up by hints of fresh fruit, berries, and tangy fuel. Her thick, frosty flowers consistently produce high levels of THC and CBG, as well as high concentrations of myrcene, ocimene, farnesene, and caryophyllene. As a result, Medusa F1 has strong effects that relax and stone the body from head to toe (brought on by particularly high concentrations of myrcene and farnesene) while motivating the mind with an uplifting, creative, and motivating kick (thanks to high concentrations of ocimene). Medusa F1 seeds produce elongated autoflowering plants with long, strong branches and well-spaced internodes. Plants regularly grow up to 80–85cm tall and boast a fast flowering time of just 42–45 days (72 days from germination to harvest). Thanks to her genetics, Medusa F1 produces plenty of thick flowers with big, swollen calyxes that make for very easy trimming. Medusa F1 is very stable, handling stress and unfavourable growing conditions with ease, though she is somewhat susceptible to Botrytis, so make sure to keep tabs on the humidity in your grow room/garden

The transition is officially happening—the plant has now fully entered the flowering phase!🌱 The stretch is kicking in, and it’s growing rapidly, really taking off this week. It looks incredibly healthy, with vibrant green leaves and strong development. Thanks to the LST, it has spread out beautifully, allowing for even light distribution and great bud site exposure. I’m really happy with how things are progressing and excited to see how the buds start forming in the coming weeks! This one is looking very promising.💪😎

I used both the soaking in a cup and paper towel method to germinate. I’m using fox farms ocean with no other fertilizers until week 3 or 4. I let it finish germinating in the window indoors. I water with R/O water PH 6.0-6.2