Defoliation, more hishtress. Some pistils got burnt by rains. Rocié con preventivo también esta semana. esperemos que haiga suficiente

They go fatter day by day, still clear trics, and some nuggs are littel under developped further down stem, but massive colas covering the whole surface, smells like fruity candy and sticky as hell, resun production is insane. I just dont eant to get mold drying this, any yips? Whole plant or chop of piezes and hang or dry net, colas are real fat and rock hard.. counted round 35 top colas

8 Days 60 55-60 Hum, 65-70 temps

Raíces bien pobladas, trasplántadas a maceta definitiva de 7 litros, utilizamos micorrizas Myco Jordan 1gramo por planta y fertilízanos con enraizante deeper underground.. daremos algunos días más de vegetación y pasaremos a fotoperiodo 12/12 👨‍🌾🏾

Day 1 down...will connect the blumats tonite 😁. Blackberry moonrock and girl scout cookie were damaged during transplant but look good and bounced back nicely. Was waiting for them to recover to flip. Light compost tea bubblin since 8 pm yesterday to help start the process. In the next day or 2 ill get the last trim and take the last few clones. At the end of week 2 ill quit sprayin labs and em5. Grow cam still sux but its all i got at the moment so ill have to make due with it and my cell.

Week 4 flower : everything’s looking nice still got the lights about 7-9” from top of canopy without any issues . The humidity has gone up to 50% in day and I can’t really get it any lower I’ve already got a dehumidifier so don’t want to get another one . I would like to lower to 40-45% and lower for last 2 weeks but can’t see that happening . I’ve started the pk from end of week 4 (day 28 )at 1ml per litre this took my ec to 2.2 I will see how it goes and maybe up it to 1.2-1.5 and I’m going to use the pk for 7-14 days then I will start the flush I also lowered the silicone to 0.5ml per litre 3x blue cheese plants are on the left but has spread over and 1x sunset sherbet on the right

Just transplantere into the autopot system and the girls didnt even slack for one day before bouncing back and starting to grow some more🤩😍 After two days we put up a trellis🙌🏼

Filling in nicely has a great smell starting to frost up. My haze beast smells very sweet like fruit loops cereal. Light took a crap almost 10 days ago only 9 months old. Its a medic grow smart 8. After dealing with getting it replaced in the middle of a grow I am done with them. They make a great light, but the service is terrible. You are forced to work with someone in China who will respond to you at 2am. I had to call, text, email, FB msg and msg through IG to get a response and someone to replace my light. It should be here Tuesday. I bought a Mammoth mint today and am going to run that from now on. 11/20 Grape God has a smell of grape and rubber is the best way I can describe it. The haze beast smells Identical to fruit loops almost caught up to the GG in height.

Purple Berry Kush by Spliff Seeds 🏜️4.7 Days off 🏜️5.7 🤘🦄 🏜️6.7 excellent recovery, really excellent. @weed__mee what do you think? 😁🤘🦄 🏜️7.7 Cutting done according to manual, contrary to how I act initially. patched up to the third node above and below, I await developments, today irrigated 🤘 🏜️8.7 🤘 🏜️9.7 🦄 🏜️10.7 Why do I always start so late? damn me! i'm really off with the timelines i wanted to adopt. never mind, I'll make up on the next plants worthily 🤘 __________________________________________ ❓ Are you new to the world of the cultivation and don't know where to safely buy your seeds? 🦄Fast and anonymous shipping. Take a look at their very nice graphics ✅https://www.spliffseeds.nl ______________________________________________ 👀 Are you looking for a good lamp to start with? 👀 🌞Viparspectra has something more than the others, take a look at their site. ⏩ Use "GDVIP" for an extra discount or "ViparDreamIT" for an extra 5 %% discount 👀 Search for it on Amazon ✅Amazon US: https://amzn.to/30xSTVq ✅Amazon Canada: https://amzn.to/38udUVe ✅Viparspectra UE: bit.ly/ViparspectraUE 👀 Watch my ViparSpectra XS1000 unboxing on YouTube, leave a like and write to the channel 🦄 ✅http://bit.ly/UnboxingViparSpectraDreamIT ______________________________________________ 📷🥇 Follow the best photos on Instagram 🥇📷 https://www.instagram.com/dreamit420/ 🔻🔻Leave a comment with your opinion if you pass by here🔻🔻 🤟🦄💚 Thank you and enjoy the growth 💚🦄🤟

*LOS FERTILIZANTES SON HACIA LAS OTRAS PLANTAS NO TERMINADAS NO LA QUE SE CORTO ESA SOLO AGUA* *reemplazo bio bloom por monster bloom como los dos son PK la planta se sobrefertiliza* semana 10 y se va de corte la primera contento de terminar mi primer diario entero en esta plataforma cogollos llenos de resina muy contento con la producción en 68 días desde germinación *la planta en total creo un poco menos que el doble de lo que se corto pero fui sacándoselo de a poco antes* ahora solo queda esperar secar y las otras que vienen en camino 70.85 gramos en humedo contando tallos y una hoja de viento por rama espero marcar unos 15 en solo cogollos y ya secos LST en las dos ramas principales de una de las que viene siguiente muy compacta en lo personal me gustan los cogollos con casi nada de hoja (de esto dependerá cuanto raspe en la garganta) por lo que el humo entra sin dejar ninguna molestia muy suave y sativo

Day 65 - Starting week 10 and she’s definitely starting to fatten up a bit since lowering the lights for her. Already getting close to another round of water so most likely tomorrow, she’s drinking quite a bit lately. Day 66 - She was just about dried up already so gave her 2 gallons of plain pH’d water. Gonna start checking out the trichs soon, I’m thinking she’s down to about 2-3 weeks left but when the trichs tell me she’s done, I’ll chop her. Day 67 - Not much to do with her today, just some updated pictures and checked out the trichs for the hell of it and still mostly clear with a few milky scattered throughout. Day 68 - She’s gonna be ready for some water tomorrow, other than that, just been checking the trichs and tucking some leaves when I put her back in the tent. Day 69 - She was ready for water today and thinking she’s got about 10-14 days left, I went ahead and started the flush according to the Technaflora schedule. So mixed 5ML of MagiCal and 80ML of Sugardaddy with 2 gallons of water. Day 70 - Ending week 10 and she’s getting down to the wire. Still looking at about 7-10 days and everything is on track. Very few clear trichs in there, most are cloudy with a few amber scattered throughout.

Doing her thing. I gave her quite a heavy trim, noticed a LOT of leaves around main cola. Hopefully light can penetrate into the main cola now. Trichomes going cloudy now.

Day 17 and she is growing nicely, but hope the side branching will pick up a bit for training. Keep freaking out thinking I have mites again but I don’t see them on my leaves. Plus I think I have grasshoppers nibbling on all my gals leaves. As of Saturday Fozzy Bear (we wanted it Fozzie but official paper work says otherwise) joined the family and his new big brother Buddy. He has already grown a few inches since we got him but god is he ever cute, and god bless Buddy for taking his playful shit since

Gave them a good strip out! Was a jungle in there,undercarriage included! Smells still amazing one slightly more sour than the other. Ones bud structure is different to the others also. But looking great. Took quite the stretch ! Starting to slow up a bit now thankfully as running out of room !. Exited to see what the next weeks bring. Hopefully a realy nice harvest to come !

Hey guys :-) . This week I will use LST again, and everything radically shorten 🙈. Not because I want to, but because I still have to save some time and height because there is still no space in the bloom chamber for 35 days 😂. It grows great so far, and as with the last grows it is beautiful with it 😍👍. I wish everyone a nice week 🍀🌱. Type: Sour Diesel ( Zamnesia ) ☝️🏼 Genetics: Diesel x Northern Lights 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Flower Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 220 W 💡💡☝️🏼 Earth: Canna Terra Professional + ☝️🏼 Fertilizer: Canna Terra Vega , Canna Terra Flores , Rizotonic , Cannazym , CANNA Boost , Pk 13 / 14 , Canna Cal / Mag , Canna Ph - Grow , Canna Ph - Flores ☝️🏼🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 6.0 💦💧

Seed to harvest day 67 Sticky buds Fruity smell Good strees performance Total Used power 400w

planta que creció con normalidad, al pesar del tiempo de cosecha que era un poco mas largo que el resto se desarrollo mucho mas acelerada en la floración que el resto, bastante sensible con el fertilizante y teniendo dos de esta misma sepa crecieron totalmente distintos.

Day 15 ready for the transplant tomorrow. Just watered each with 1/3 cup of water. It was the first watering since the initial one 15 days ago. My basement is very humid. All 4 are growing pretty strong. The 2 on the left and right are the Guavo Autos and the other 2 are Sticky Soul Photos. They will continue their life outside starting tomorrow. Day 16 and all 4 plants have been transplanted into their final 3 gallon pots. What I did was water each cup yesterday with 1/3 cup of water. Today I drilled some holes in the 3 gallon pots. I filled it with a small amount of build a soil light mix and the rest with happy frog. I poured 2 cups of water into the new soil. I made a hole. I added 2tbspns of Mykos to each pot. I slid the plants out of the cups into the hole. I watered those in with 3 cups of water each. A little ran off through the bottom. I’m going to keep them in the shade for a few days then toss them in the sun. Stay tuned! Day 20 and we are looking really good. Check the video above.

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.