So as you can see I now have four flowering which I guess were the autos and I have one gelato that is still vegging and is doing damn good. There are two that have lighter color leaves, I’m trying to focus on on these and see if I can get better production. As for the tall GG in the back, leaves are waxy and have resin production starting. A lot better, overall I’m learning more and more every week! Hope everyone is enjoying my grow and stick around, ask questions. Happy New Year!

It’s bern roughly two months these guys have been growing! Lst’d Both but untied the gg because I wasn’t sure she was benefiting from it so I’m going to do it over. These ladies (I hope) will start their flower journey next week when I revive my new flower tent 😎..stay tuned for some epic buds..I hope!!

Happy new year everyone! I hope everyone had some amazing festivities! 😃 Regarding my babies I think I might be underfeeding them and one might be shocked thanks to the heat and the lack of nutrients I gave them, last week's runoff water scared me and the plants might be suffering because of that! Most of the issues starts to get more noticeable later during the week! 😖 I started giving them few nutrients to see how they would react and at the end of the week it's clear that I had to give them waaaaay more 😵 Besides that I also moved them to their final pots and I topped Pistachio, out of the two she's the one that looks the best. I also defoliated them a little. I also believe they didn't get a transplant shock (I mean, they would've been worse if that was the case haha) and I added more mycorrhizas during the transplant (I heard they help a lot with hot climates and I need help with that badly) Anyway, thanks for reading! Stay tuned for the next update! 😉

Started the final week of nutrients. Then ill be switching to flawless finish and pure water the last week. The blue gelato big cola is finally starting to stack up. It has only one more week of nutrients, so hopefully it stacks quick.. Then a 1week flawless finish and a week of straight 100ppm water.

She is alot different than last week shi is so bushy and she is indica for sure Day 49 I find her even more bigger I upload video too she is way wider than door 🚪 and she grow in 6L I'm shock she is too big

Gorilla Jealousy F1 is growing great. She has loads if med sized frost colas developed. She is actively working on bulking now. Ever since she got hungry and started a early fade. I increased her feed to stop it. Looks like she took to it well. She did get a bit tall for my liking in this tent. So I am not running the light at 100 percent. It gets too warm when the tent is really full and it being Sumner. Everything is looking great. Thank you Spider Farmer, and Seedsman. 🤜🏻🤛🏻🌱❄️🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 https://www.seedsman.com/?a_aid=Mrsour420. This is my affiliate link to seedsman. Thank you Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

8e Semaine de floraison impeccable grossi bien chargé en résine irrigation a l'eau uniquement durant les 2 dernières semaines. J'ai vérifié les colas es celle-ci c'est fait polinisé par le male Sour tangie dawg mais rien de grave quelques graines, cela me permettra d'avoir une nouvelle génétique issue de ces deux plantes donc a voir ne pas ce précipiter. Elle dégage une plus douce odeur durant ces derniers jours.

💩Holy Crap Growmies , we are outdoors and in the Ground and there Doing Great💩 👉It's been another full week 42 days from seed and she's doing great , very nice Growth, considering shes been up against the wind and rain 👈 No problems 😊 so far so good 👍And she's now in full on flowering 😁👈 DO TO THE AMOUNT OF RAIN , IVE ONLY BEEN ABLE TO TOP DRESS HER😎 I GOT MULTIPLE DIARIES ON THE GO 😱 please check them out 😎 👉THANKS FOR TAKING THE TIME TO GO OVER MY DIARIES 👈 👉NutriNPK NUTRIENTS USED FOR FEEDING 👈rain water to be used entire growth👈 👉www.nutrinpk.com right now get 10% off using SPRING2022 as the coupon code👈

Feeding was through water , with the exception of barrier as dosed as spray as flowering hasnt boomed yet and the auto one one is quite coordinated on time with this ones on the bright side. Controlled height through intention is more for damage control became a closer purpose like scrog net and clips to give branch directions easier, that use make me now that understand how optimize better with them at future , and truly purposed as getting all the ladies good illuminated : how much good are really doing the side lights , as the net itself marks the lack of penetration of the top lights my niggas. :)

My Purple Star Killer girl looks great. I am doing a lot of LST to try to keep her spread out and not get too tall. She's drinking 5 gallons a day now and I think I'll have move that up to 10 gallons soon.

12/19 - Plants stayed a little too damp, had to let them dry out a bit. 12/20 - RO water only @ 6.1ph 12/21 - Feeding nutrients today @ 6.2ph RO @ 6.1ph 12/22 - Feeding nutrients today @ 6.2ph RO @ 6.3ph Performed a runoff test on the Critical, White Widow, and Wedding Cake 2. I need to bring the ph up. (i had a feeling) 12/23 - Feeding 1 gal of nutrients @ 6.7ph 12/24 - Feeding 2 gal nutrients @6.7/6.8ph and @6.4ph 12/25 -Feeding 2 gal nutrients @ 6.6ph and @6.3ph

Day 1 soaked seeds for 18hrs. Day 2 seeds in dirt two seeds already popped in water and they where the auto's. Day 3 just keeping them moist and warm. Day 4 Northern lights came up and Great white shark came up. Watch these seeds sometimes the shell doesn't come off and you got to help it Northern lights shell was stuck and I took a tooth pick and helped it get it off. Day 5 Acapulco gold came up still waiting on Yumboldt auto and it had a tail on it when put in dirt.. Day 6 planted another Yumboldt auto seed directly in soil the other one was bad. So this one will be 6days behind others.

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.

Easy trim ✂️ The smell is citrus & pine delicious 🍋🎄 Harvest in 2 times first the top buds then 1 week later the lower buds Now 7-10 days in the dry racks then the smoke review in 2025 Take care 😎

Nun, die vergangene Woche ist nicht so gut gelaufen....😞 Ich bin regelrecht in ein Schnippel-wahn verfallen...😱 Dann wollte ich ein Fehler mit dem nächsten ausgleichen, das Ende vom Lied kann man deutlich sehen. Da wollte ich gleich alles richtig machen doch die Pflanze wurde dabei immer weniger.😭 Das dauert bis die Gute sich davon erholt... Gestern habe ich über die verstümmelt Triebe noch Tütchen gefrimelt, um die Luftfeuchtigkeit um die Triebe herum zu erhöhen. Und es hat zum Erfolg geführt! Sie haben sich deutlich innerhalb eines Tages deutlich gestreckt!😃 Allerdings muss ich alles gut im Auge behalten damit es in den Tütchen nicht zu feucht wird, deswegen habe ich heute je ein kleines Belüftungsloch in die Tütchen geschnitten.

El cultivo a sido muy agradecido. Una cepa bastante agradecida y nada dificil de cultivar. La produccion es bastante alta y la calidad fuera de serie si te gusta el sabor caracteristico de la gorila glue esta es tu cepa. Si la cultivas en la fase avanzada de floracion tu indoor sera un mar de colores morados y rosas... Sin ninguna duda de las cepas mas bonitas que e cultivado. Os animo a probarla y uniros a la familia BSF NOS FUIMOS!

D65: Tried taking some pictures with the macro lens. I'd say the majority of the trichromes are cloudy with some still clear and the occasional amber ones. Will keep track of the evolution. D70: Buds keep getting bigger, the main cola is starting to look like one big, consolidated bud. Trichromes remain mainly cloudy, with some still transparent and some amber ones. Also gave her a flush (10l), since I think she'll be ready for harvest in at most 2 weeks. Next watering, I might add molasses a last time. Smell is strong and really sweet, reminds me of vanilla a little.

These lady's have been very good started they flush last Monday they have shown alot of colors one has turned very purply and another has shown its red pheno along with purple I have that just green pheno but are frosty all the lady looking healthy and doing going initially got about a week left before they getting chopped down

Bueno ya empezamos ahora a sumar semanas y ver el gran resultado de este gran banco