Hello and welcome to u all.. Hope ur well and had a great day.. 😁👍 Great 2nd wk of growth.. Roots are starting to fill out tray and vegative growth is going strong it seems.. Still a bit warm but temps av dropped loads last few days in my area thankfully.. Took alot of central n lower grow sites away this wk n just trying to open her up a bit b4 she stretches.. Flipped lights to true 12/12 today and will b planning a 70day flowering program (already 14days thru!).. Emptied out res and flushed top tray with 10ltr plain ph'd water @5.8 and 21°c so not to shock her roots.. Looking forward 2 my first crop from Humboldt's stock.. 🤞😎 Huge thanks to you all for your constant support, comments, follows and likes.. Stay safe n best of luck in ur gardening adventures.. 👍🍀

Que pasa familia, vamos con la séptima semana de floración de estas Papayton feminizadas de fastbuds. Vamos al lío, el ph se controla en 6.2 , la temperatura la tenemos entre 25/21 grados y la humedad ronda el 50%. El ciclo de floración puse 12h de luz, el foco está al 100% de potencia. De momento van engordando y marcándose unos aromas bastante dulces y afrutados. COMENTAR: que una de las 3 salió macho. - os dejo por aquí un CÓDIGO: Eldruida Descuento para la tienda de MARS HYDRO. https://www.mars-hydro.com Hasta aquí todo, Buenos humos 💨💨💨

Was away 18/6 allday 19/6 *Water day / Looking thirsty -Temp 25-27day/21-23night -60% RH (2+-) -950ml to Biobizz Topmax, Bio heaven, and Bloom (1ml/L) biobizz grow 1ml/L 20/6 -Temp 25-27day/21-23night -60%RH (2+-) 21/6 - I did some defoliation/trimming and removed a couple of branches that i didnt believe in. -Temp 25-27day/21-23night -60%RH (2+-) 22/6 Some pistils are starting to show, they look happy, but soon thirsty. -Temp 25-27day/21-23night -60%RH (2+-) 23/6 *Water day + i denoted lower shoots and romoved a couple branches and small leafs -Temp 25-27day/21-23night -58% RH (2+-) -1050ml to Biobizz Topmax, Bio heaven (1ml/L) Bloom (2ml/L) 24/6 Removed a couple of top fan leaves that were shading some tops. It looks good an healthy -Temp 25-27day/21-23night -55%RH (2+-) 25/6 -Temp 25-27day/21-23night -53%RH (2+-)

Start April 4th. Day 1 vega. Hey! Four seeds have hatched. One is smaller than the others. I planted the seeds in GroBag spilled with clean water ph 6. I'll be back with more information Day 2 I made a video, it shows that the seeds have taken root well. Leave your comments. I'll be glad to chat.

•She was started for fun. •Not much to say about her just letting her do her. •Week 3 fead her with 2ml off grow auto from living Soils.

Hello everyone, It was a disappointing week with 2 of my biggest buds getting budrot i cut them in half. I presume there will be more to come but it is what it is. I started flushing and the runoff is under 400 ppm i also started removing leaves so that the plants have less nutrients to consume. From today I gonna keep humidity at 45% not higher than that. Let's see how they look next week, thanks for stopping by and have a nice day. Regards, Growfather

Anche lei inizia a riprendersi come la matanuska

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.

Day 71. Girls just perfect ;))) As any grower i would want, bigger, fatter, stronger, but they are in that range anyway, now main thing not to screw up ;))) Girls on nute, water, water+calmag, water+silicaAcid, water+molasses rhythm and just love life ! Day 72. Got more presents, thank You Zamnesia ! Asked for 4 strains, got 2 ;))) Still 10 beans and full grow by one house, like i always try to do. Always wanted to try out Runtz, all grows that i saw - was sick ! Kalini Asia - new taste and strain for me 4sure ! Day 76. All is good , they are missing CalMag from those lights a bit and with such amount of buds, but should be fine. Todays watering was only with CalMag, ph 6.5. Next watering full nute blast, should be fun to observe, they are starving a bit , so i hope for huge grow rate after. Tried 4 month cured weed at a friends, he had to chop girl on week 6 of flower, with nutes still being fed. After an hour head pain , ash was still black ... I would never try not to flush .... Happy growing !

This week was hottt. I have been out sic l8ly sorry 4 no updates. The girls r still growing strong. With very little maintenance. I gave them each 5 gallons of water with nutrients on Sat, (early morning since it was a heat wave) I defoliated (the lower branches became shaded out) and now the little bushes are taking upon a more tree like appearance. They are all just under the 7 ft roof, with training. They were hitting the roof and getting wet (morning dew), so i put more fans inside, (also the 90+ outside temps). No problems with heat. I will start making preparations 2 switch them 2 flower at the end of this month :)

Booommm! Llegó la hora tan esperada Farmers nuestras flores llenas de resina acabandose de formar, la verdad que estas genéticas ayudan mucho al desarollo del cultivo espero que os guste!! Un banco seguro y confiable para una locura de olores y terpenos!!💚

So this was the week changed the light cycle to 12/12. I also went to town again and defoliated, lollipopped and ScrOGed them

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Hello Growers and Tokers! 👋 👩‍🌾 🧑‍🌾.🔥💨 We'll got progress going! Pictures taken on day 42 of flower. The smell is something that i'm loving. Although one smells stonger and sweeter than the other, they both are smelling great. I had my doubts about the nugs not being big or hard but it seems like the green sensation is doing it's job. There's been a good progress since i've started using Green Sensation. Glad to see that. In flower I feed with only water and 2ml/L of enzymes. Once about 10 days. Resin prodcution has gone up, buds are denser and a bit bigger. Which is good given that most of the pistils are still white and they fatten up more when they rippen. As long as things keep a stable progress, i think i'm good.

Plant ran low on nitrogen during stretch. This was cause by the potassium and phosphorus out competing the nitrogen. I solved the issue with a 3 day dry back.

Moon rock auto has been progressing more into her flowering stage. I have been keeping up on her kst and selective defoliation when needed. Not much has changed beside she is just getting bigger. I don't forsee this plant getting really big. I could be wrong. Nothing more to report on. Thank you Medic Grow, and Divine Seeds. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

this week was great, the V1 arrived through a lot of logistical nightmares. its the final test before mass production- i will post another dairy for it but please have a look at the pics above. ive created a stylish subtle, modern way to grow 4 plants. this will be great for all levels and will save big on energy and nutrition. you just have to prune, it can even draw water into itself. anbd its 4 plants!!! stick here and youll see it in action. ive decided to change the order in tents. now we have super strong Purple berry Kush with the returned and super strong sweet seeds Sweet cherry pie. so one tent is the strong, and the other tent is now perma auto flower, which serves for additional veg for girls who fall behind their grow peers. hope that makes sense. i think my net is pretty useless other than a visual to plan nodes. i guess the real support will come from placing more plastic rods around the colas and fastening them. hope Christmas was kind to everyone. this oncoming week will be the last week of veg i think for tent two and we flip to flower. thanks for looking.

Hey everyone 😊. The last 2 weeks of flowering have come and I can't wait to harvest them 🤗. The Ec is turned down a little every week, and next week the water is completely changed again to rinse 👍. They have developed very well, are just getting their full load of resin, and smell exactly as they should smell . Otherwise there is nothing to report this week. I wish you a lot of fun with the update, stay healthy 🙏🏻 and let it grow 🍀 You can buy This Strain at : www.Zamnesia.com ☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼☝️🏼 Strain Gelato clone from mother (Zamnesia ) ☝️ Genetics: Wedding Cake x Gelato x Gelato 33 👍 Vega lamp: 2 x Todogrow LED CXB3590 COB 55 W 1 x Sanlight S2W 62 W 💡 Flower lamp : 2 x Todogrow LED CXB3590 COB 55 W 1 x Sanlight S2W 62 W 💡 ☝️ Grow Aero System : Growtool 0.8 ☝️ Fertilizer: Canna Aqua Vega A + B , Canna Aqua Flores A + B , Rizotonic, Cannazym, CANNA Boost, Pk 13/14, Canna Cal / Mag, Canna Ph - Grow, Canna Ph-Bloom ☝️🌱 Water: Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EG. Add Cal / Mag to 0.4 Ec Ph with ph- to 5.5 - 5.8 💦 💧

An Tag 23 habe ich das LST neu angepasst um die kleine niedrig und buschig zu halten. An Tag 24 habe ich fast alle großen Fächerblätter entfernt und das LST erneut angepasst. An Tag 25 erneut LST angepasst. An Tag 27 wurden zu viele der unteren Triebe mit Schatten bedeckt, so dass ich einiger der Blätter wegnehmen musste.