Amazing plant to grow, very easy! The smell is strong, really strong and the buds are super fluffy, fat and sticky...love love love!!! Now I just have to dry and cure! Thumbs up for fast buds genetics and Hesi nutrients

14.04.25 VD#35 Guten Abend zusammen ✌️ Der Caramba geht es wunderbar man sieht direkt das sie richtig bock hat. Heute gab es wieder ne Ladung Nährstoffe von Hesi TNT Complex 4ml/L Hesi PowerZyme 2ml/L Hesi Wurzel Complex 5ml/L Hesi SuperVit 0,2ml/L Jetzt darf sie noch 2 Wochen in der Vegiphase verbringen dann noch neue Schuhe 30L dann erholen und ab in die Blüte. Bin gespannt was Sie uns noch zeigen wird es kann nur schön werden. Bis nächste Woche mit neuen Updates bis dahin bleibt Sauber and Stay High. Mögen all eure Ladys Gesund und prächtig wachsen und euch mit schmackhaften Stuff versorgen😁 ■■■■■■■■■■■■■■■■■■■■■■■■■■■■■ 14.04.25 VD#35 Good evening everyone ✌️ The Caramba is doing wonderfully, you can see straight away that it is really keen. Today I gave it another load of nutrients from Hesi TNT Complex 4ml/L Hesi PowerZyme 2ml/L Hesi Root Complex 5ml/L Hesi SuperVit 0.2ml/L Now it can spend another 2 weeks in the veg phase, then new shoes 30L, then recover and off into flowering. I can't wait to see what else she will show us - it can only be good. See you next week with new updates until then stay clean and stay high. May all your ladies grow healthy and splendid and provide you with tasty stuff😁

Week #10 Gnomo Auto By Kannabia Week#10 Dec.30th-Jan.6th Gnomo Auto had stayed true to the indica genetics she has she's a shorter plant that's stocky with tight dense buds that are covered in trichomes. She's been a easy grow due to her genetics No real issues. I highly recommend if you like to grow indica or have limited space!

D63 - 26/11 - Lowered EC as I see some signs of burn D64 - 27/11 - Nothing D65 - 28/11 - Added pure water to lowered EC again to 1.5 D66 - 29/11 - Nothing D67 - 30/11 - Fungus gnat infestation, I added some protections and ordered the neem oil spray. D68 - 01/12 - Some supercropping on a bud. D69 - 02/12 - Neem Oil used against fungus gnat

Etapa final de engorde, me está sorprendiendo el engorde final. Olor muy tenue pero delicioso a limon dulce y un fondo a pino. En 1 semanas más calculo estar cosechando

Plant is showing signs of possible nitrogen and phosphorus deficiency with brown curling leaves and purple tipped leaves, but not too worried about it seeing as there's only about a few weeks left of growth. Removing smaller fan leaves to uncover bud sites. Heavy smells of pine and berries 😁

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.

I'm very happy with this weeks progress. They transitioned very well to the garden, which I'm chocking up to the row cover. They didn't need any water due to the thunderstorm we had last night, but I did make a ring around the base of each plant and gave them about 1-2 TBSP of the Coast of Maine Stonington Blend fertilizer. They also got their tomato cages.

Week3

Start Flush

Day 78: This week I only gave them water with regulator, humic-blast and ezymen because they where ready to harvest. Those others from last week where kept inside a dark room for some days before cutting them down. By doing this, your plants will increase making thc. In the middle of this week i also putted some plants inside the dark/drying room to make them ready to harvest. These will also be in the dark for a few days before I harvest them. At the end of this week all other plants are in the dark as well for a couple of days, i will keep them in the grow room because there is no point to move them to the other room lol. Because i put them into the dark for days instead of cutting them down, I can cut them fresh and put them in drying nets instead of putting the full plant upside down on ropes. I will use a cutting machine for this.

Hello All. I took a lot of pictures. Hope you don't mine, but I had fun. I think everyone likes to see large harvest pictures. It all started back in early January when I took clones of my favorite plants. It was a cold winter here this year, for these parts. So it was mid March when I got the plants out in the greenhouse. The spring was damp and cold too. I found powdery mildew in the garden about 2 weeks before I found it in the greenhouse. I got it on the Skunkberry and the Burmberry, But not on either Amnesia Lemon or the Sister Amnesia Lemon. I was very pleased about that :) I found some spider mites in the last week and a half. I decided to turn up the fans instead of spray. Yes they still spread but very slowly when they can't spin their webs. I didn't find many when I harvested. Everything else went well this season. I found a male Dr. Atomic Northern Lights that I liked. So I'll try to make some seeds with the Amnesia Lemon, Skunkberry and the Burmberry. I'm trying to fatten up the Burmberry. I'm interested to see if the Amnesia Lemon gets fatter buds and carries the P.M. resistance to the seeds, I'm hoping. The tall Sister Amnesia lemon in the middle did cause a drop of production from the plants on either side of it. They were in more shade. Something to work on for next year :) The Skunkberry had the most P.M. I used a new produce that I'm pleased with, it's White Wash frequency altered water. Knocks the P.M. right out. I found that if you put a large tray under where you are spraying you can catch the run off. I could use it a couple of times with no change in effectiveness. It must be the Scottish in me. I try to reuse or recycle as much as possible. Cuts costs, and help make me feel like I'm doing good and helping the planet. My feeding schedule was: I had a 15 gallon half barrel and pump with hoses and nozzles. I filled the barrel with nutrient solution and watered by minuets, 15 for clod days and 25 or 30 minuets on hot days. After 3 or4 days I added water when the solution got low. Mixed new solution once a week, and cleaned the barrel and pump. I also took the hose in the greenhouse and soaked them till run off once a week and measured the ph. I saw a few fungus gnats, but the spiders and nematodes (from my compost I added when I mixed soil) sure help to keep the numbers down. I like to put my buds in a paper bag to dry and cure. Inside I hang the buds for 3 days before putting the buds in paper bags. But it was so hot in the green house that 2 days was more that enough before putting the buds in the paper bags. The bags sat in the greenhouse for 3 days and then went in to the basement to finish. The old hippies told me that they use to put their buds to cure in the middle of a bushel of straw. I seems that the drying buds gives off a gas, that when trapped around the buds helps to take away the bitterness and raunchiness' of the uncured buds. The bags also help in wicking away the moisture of the drying buds, just like the straw did. After a week I check to see if it is dry enough. If the buds are dense the bag might need to be rehung for a few days to finish. I prefer a dryer bud. I like to hear a light crunch when I put a bud in my pipe. I like to hear a light crunch when I put the bud in a grinder. > Amnesia Lemon- Plant #1 North plant=343 g. >Amnesia Lemon - Plant #2 South plant=397 g. > Sister Amnesia Lemon - Middle Tall Plant=401 g. Winner :) > Skunkberry - Southern Middle Plant=316 g. > Burmberry - Plant #1 North Plant=239 g. > Burmberry - Plant #2 South Plant=294 g. > Total= 1990 g. or 71 oz. or 4.4 lbs. In Conclusion: This was my best grow ever! Big thanks to Barneys farm, for great seeds. I've got LSD started and I will try that in the greenhouse next year, 5/5 for mold and pest resistance. I'm very happy with the results. I was concerned because I have 2 rental houses behind me and one of them had a big backyard party at my week 5 of flowering. You could smell the grow by then and I was hoping I wasn't going to get ripped off. I looked through the fence a few days later and saw about 12 large plant pots, growing cannabis. I'm very happy. Cheers Chuck. > November 3 Added pictures of the seeds I made this summer.

Blütetag 21. VPD kann ich mit meinem Luftentfeuchter und einer aktuellen RLF von ca. 56% auf 1,5 in der Lichtphase halten und 1,2 in der Dunkelphase. Wenn es weiter so feucht/regnerisch hier bei mir bleibt, wird es schwer die RLF selbst mit Luftentfeuchter unter 40% zu bekommen. Mal gucken. Der Grow sollte insgesamt dann noch 5-7 Wochen gehen.

Week 8

Day 78, I switched plant #2 to an all PK diet with FloraFlex Full Tilt. She’ll take up the whole 3.5 gals of nutes by Wednesday. I’m then going to begin my 3 day flush Wednesday evening. And I will chop her on Saturday evening. I also took a little sample nug off plant #2 just want to compare non-flushed to flushed weed. Also see how much they shrink in size. Day 79, Plant #2 is on schedule to start flush in 2 days. And I will give her the chop this coming weekend. Going to try a ice flush using frozen water bottles to see if I can help bring out more color. The other plants #1 and #3 are still a two weeks or so away from being chopped. Day 81, started the 3 day flush on Plant #2. And took some more photo shots of her buds and a 360° view video. Day 84, Plant #2 got the chop. Wet weight, before light trim and removing large stems is 760 grams!!! I will update once they finish drying, and then again once I finish the trim and about to jar them for cure. Plants #1 & #3 are still flowering, probably another week or two before they are ready to be chopped.

Day 54 and as you can see guys she is finally producing trichomes and starting to look like blueberry if that makes sense.. if you look up close the buds have almost a bluish tint so I'm super excited and very pleased with Sensible Seeds so far.. they are two for two obviously I have not harvested or smoked this yet but this has been a breeze to grow from beginning to end or up until now anyway all I do is top dress every week and a half to two weeks and go between silica and recharge in between.. as you can see nitrogen levels are low but that is okay I'm used to synthetics so I'm very excited to see the fade I hope it looks like fall in my tent ... Big shout out to Sensible Seeds they are your place for bulk seeds I think they are the world's biggest Warehouse don't mark my words but they have a massive selection.. I hope everybody is doing well God bless and happy growing ✌️😎

Same as there big sister, 54th day of flower.. These plants haven’t had any work done what so ever, not one leaf has been removed from the start, no folding of leaves, literally just left to flourish in there “natural” environment, and I couldn’t be more happier with what’s inbetween the “mess”😂.. buds are swollen and ❄️, stinking of 🍋.