Las flores más lindas del condado son las de strawberry banana, que hermosa genética! Perdón por no cuidarla y alimentarla como correspondía 27/04 Se riega con 2.5 litros de agua + calmag + top auto. PH:5.5 EC:0.9 29/04 encontré una placa de saltahojas del mismo color que los tallos, por este motivo fue muy difícil darme cuenta. Se estaban chupando la sabia de mi planta, al menos 6 capture con mis dedos. 30/04 se riega con 2,5 L de agua + Monster Bloom 0.1g x L. PH:6.2 EC 0.8

Floracion (Tiempo estimado 64 dias) Primer Semana de Floracion 08/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz , 12 hrs de obscuridad. 09/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, subir demaciado la intencidad del ventilador fue contraproducente ya que las hojas sufrieron quemaduras por frio, se a empezado a regular un poco mejor la temperatura pero el intractor y extractor de 4 pulgadas no estan eficiente, empeze a provar con hielo embotellado para bajar temperatura de la solucion nutriva, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz , 12 hrs de obscuridad. 10/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz , 12 hrs de obscuridad. 11/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz , 12 hrs de obscuridad. 12/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz, 12 hrs de obscuridad. 13/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, se cambia extractor por uno de 8 pulgadas con filtro, se mantiene la temperatura a 21 grados con la lampara a 75 % de potencia, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz, 12 hrs de obscuridad. 14/01/2024 - 5:00hrs y 22hrs: Se verifican parámetros básicos del agua, mantener cuidados específicos. Agua de osmosis: Ph 6.0, PPm 1000-1250, Ec 2.0-2.5, Temperatura 20°C - 26°C, Humedad 75% Ambiente: Temperatura 24 °C, Humedad 65%, Ventilación 15%, 12 hrs de luz, 12 hrs de obscuridad.

"Hi, I received my pH meter this week, so from week 6 onwards, I'm aiming for a pH value of 6.0 - 6.5. This week, I noticed that the plant in the small pot received too much fertilizer. The other two 7.5-liter fabric pots also received double the recommended amount according to the feeding schedule, but they don't show any signs of over-fertilization."

Another day another week and coming along nicely only difference this week is I have started pumping some overdrive through them now seems as it’s week 6 flower. 2 weeks on that then hopefully ready for a flush with pure water and a few days dark then harvest time. I’ve got a feeling the papaya is going to be ready before the cookies waiting for.my microscope for my phone to come then will update with some pictures of the trichomes.

9/21: I harvested 2 more of the #4's, and my 3 hybrid autos last night. After washing them, I hung them to dry in a room with very little airflow and average temperature of around 78f-80f. The humidity has been pretty high, so hopefully they dry slowly. After 4 days of hanging to dry, I've been alternating the first #4 that I harvested between a brown paper bag and a 1 gallon jar every day to slow the drying process and will probably do the same with these 5 plants. 9/22: I fed the 4 x #2's, flushed the 4 x #10's, and watered the remaining 2 x #4's and the 2 x #3's with some liquid soil only. They're pretty much ripe and ready, but they'll have to wait another day or two until I have some time to spare. 9/23: I harvested the last 2 x #4's and one of the #3's today. Buds washed and hung to dry- 9/25: ...late night and early the 26th.. Harvested all 4 of the #10's and the last #3. Yowsa, those #10 buds are heavy and sticky! I moved the last 4 plants into my tiny tent..all the #2's. For their last week, they're gonna be about a foot underneath 360w of quantum boards in roughly 5 square feet of space (36" x 20"), which breaks down to about 72w/sq ft, so I'm venting my bigger CO2 bucket into the tiny tent for the next week.

3 of the ladies are in flush will be cutting them down within the next or 2 & the other 2 probably have another month left! Fingers crossed for harvest!🤞🏼✌️🏼🌱

Day 42, everything is chuggin along pretty healthy. Definitely some seeds in most of them which bugs me. The whole tent reeks tho which is nice. Some of the citradellics look like they are gettin pretty close so I'll start keeping an eye on them. I had to take the pics again and was strugglin so they arent my best. I have to go thru them still so I got the video up and tmm or as soon as possible I'll get the still shots up✌️ 1 is seeded but healthy, havnt really smelled it but its sticky af. The plant has a beautiful structure but the buds are kinda ugly lookin despite the pink pistils. 2 is tryin to make it's way it's got some hideous lookin leaves but they are kinda cool in person they are the thickest leaves I've ever seen and the stems of the actual leaves are thick and almost perfect rectangles.

160 days of life harvested on day 63 of flower. I don’t have photos of her vegging but she started off great. About two weeks in, she started having some major issues. Her leaves started atrophying, curling up at the borders, growing 3 finger leaves, all new growth was deformed and twisted and growth in general almost stopped completely, to what I suspect was from broad mites. These fuckers are nasty! I dm’d my local grow shop and tried out some Neem Oil. I diluted it in water like they recommended and sprayed that baby every day for one week, then every other day the following week, then down to once a week. I sprayed her leaves stem and surface of the soil. I also cleaned the entire grow space with some bleach solution. Doing this allowed her to really bounce back, growth started to take off again! So I vegged for a few more weeks and trained her as much as I could to keep her uniform but short, she responded well to this. During flower, she was very happy. I had two main issues during this time, one was being too hot in Nitrogen and a week of very hot temperatures which burned her a slight bit, although she didn’t seem to mind much. I also could’ve continued a once a week spray of Neem oil because I think they might’ve started to come back on the lower and younger leaves that weren’t getting much light. Overall it was a dope grow and hope to do better on the next one!

Radical Juice Auto – Two Phenos, One Mission 🌱🔥 Still two totally different phenos here: One is small and bushy 💪 The other one is tall and stretchy 🌿📏 The small one shows some nutrient deficiencies, but I’ll leave it as is – looks okay overall 🤷‍♂️👌 What’s crazy? The buds on both are incredibly dense – something you rarely see with autos 😲🔩 Even the tall pheno is packing weight! Can’t wait to see how they both finish – follow along for the final stretch! 🌟✂️ Radical Juice Auto – Zwei Phänotypen, ein Ziel 🌱🔥 Es sind immer noch zwei völlig unterschiedliche Phänotypen: Der eine ist klein und gedrungen 💪 Der andere hochgewachsen und gestreckt 🌿📏 Der kleine zeigt leichte Mangelerscheinungen, aber ich lasse das jetzt so – insgesamt sieht’s okay aus 🤷‍♂️👌 Was wirklich krass ist: Die Buds sind bei beiden unglaublich dicht – sowas sieht man bei Autos selten 😲🔩 Sogar der große Phäno legt ordentlich zu! Ich bin mega gespannt aufs Endergebnis – bleibt dran! 🌟✂️

For my first run I am happy with my results even though the yield was very low . The banana cake is frosty and has a great nose on it . The bud has white ash and overall it tastes great . I will be doing another grow soon and Im going switch it up . Going to be a great next grow so don’t miss it .

This week made a few oopsies . I gave un-ph’d water to one of the plants “moving to fast” . Started defoliation during this week to attempt to redirect plant energy into establishing a full canopy since flowering has initiated. Whilst defoliating I broke a branch that had to be taped to save it. Humidity went out of whack when I stored 4 prepped 5 gal pots for transplant in the tent sooo I’ve got to buy a dehumidifier bc at one point all my plants fell out in a fit . STILL haven’t filled these pots out, & I’m kinda sure/unsure it’s time to re-amend the soil for flowering. I’m conflicting on waiting until beginning/middle of week 7 so I can flush week 11 & 12 . I think that covers it pretty well Week 5 in the 📚 📕 📖.

Vamos familia, actualizamos la novena semana de floración de estas Thunder Banana de Seedstockers, salieron las 3 de 3, 100% ratio éxito. Aplicamos varios productos de Agrobeta, que son increíbles para aportar una buena alimentación a las plantas. Temperatura y humedad dentro de los rangos correctos dentro de la etapa de floración. La tierra utilizada es al mix top crop, por cambiar. De 3 ejemplares seleccioné los 2 mejores para completar el indoor, cambié el fotoperiodo a 12/12 y también apliqué una poda de bajos, se ven bien sanas las plantas, tienen un buen color progresan a muy buen ritmo por el momento, las flores han tricomado que da miedo, no sé si aguantaré una semana más o me las quito ya, veremos el finde semana. Agrobeta: https://www.agrobeta.com/agrobetatiendaonline/36-abonos-canamo Hasta aquí todo, Buenos humos 💨💨💨.

Es neigt sich dem Ende🤩

this is a very easy one to grow with an enormous bag appeal true her all cycle, a must in any garden, her trichomes production is out of these world, as are them grams on them fruits, a true must for us all to grow

The buds are spread everywhere and they are nice and frosty in next 2 weeks she will get fat.

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.

Dropped temperatures to 55-60F, added 2 hrs of darkness, and adding only water from 250 ppm - through finish. I guess I have to make them purple? Most trichomes are cloudy, so there isn’t time to freeze them to color. Going to chop in two days and call it a grow! Dumped half the res and dropped ppm to 0 and added FloraKleen. Will chop in a day or two. The bells toll…