Lemon pie 2weeks and OG auto 1 weeks

September 4th dropped em in the shotglass

Esta preciosa cepa ha crecido bastante rápido llegando a ser la más alta del armario, durante la floración ha creado unas increíbles flores llenas de resina que poco a poco se caían del peso de las mismas. Una locura de genética que todos deberíamos de cultivar al menos una vez. Espero que os guste estas bonitas fotos.

here they are! 2 beauties. I plan to apply all existing stress techniques to them. topping LST HST Mainlining and so on. Most likely I hang them in one pot. I have experience growing 2 plants in 1 pot and it works great.

This is going very well, the buds have grown in abundance and there are still new flowers sprouting, there are still a couple of weeks imag

03/12/2019 Day 81 The Dr seems to be concentrating in forming buds but I think she's grown some half centimeter, is she going to touch the ceiling? She has to know that is is confined and the sky is not the limit, at least in her condition. Day 82 (04-12-2019) The shoot at the rear left is almost touching the celiling of the grow tent😨 and i keep on tying other shoots and keeping them the farthest from the burning lights (many leaves' tips are scorched, but fortunately it's just the tip and the bud is still far from that hot point. Other leaves that are close to the lights, well, I took scissors and there's no need to speak further. Look the hard work I'm having with this plant height's issue. Goddammit why can't I have a normal grow like everyone? Day 83 just looking the video and the pics is self explanatory. No further comments 😒 Day 84 Ithe tallest shoot has reached the ceiling and seems to try to keep on growing so she needed to start bending at the very top because she wouldn't get past the tent fabric. Regarding EC, I am using a fertigation solution about 1,3 mS/cm and the runoff EC at 1.5 mS/cm. EC has been kept controlled since I raised fertigation volume to 6 L per fertigation event (1/day), unfortunately this solution containing nutrients goes to waste :( Day 85 07/12 I'lllst the tops that get to touch the ceiling and keep observing and acting as needed. I fear she'll stilll keep going up for a while. Fertigations as usual, got runoff EC 650 ppm today (1.3 ms/cm) which I think it's very good of a value. Day 86 (08/12/2019) Following advice I defoliated and even cut some thin and improductive shoots. Removed a lot of foliage and even supercropped a long tall shoot, I want to see how this high stress technique affects her. Because I plan to keep it doing if other shoots decided to continue growing. I wonder why do shoots continue growing vertical after having passed the light's level. Is it the glow coming from the reflective walls perhaps? Many questions. I decided to take down some tall shoots by suspending little weights near the tip, it seems to work more or less fine. Day 87 luckily the HST seems to have worked fine, the shoots are recovering and point upwards again. The main tip is quite unruly, today I supercropped that tip. Runoff EC is 650 ppm, perfect. Day 92 /14-12-2019) I think that despite her exaggerate growth she's managing to thrive fine with some limitations, buds seems going well. Shoots are still growing vertical but supercropping and resistance seems to have hampered her a while, but now I see she engaged on growing some centimeters more :/ Day 93 two days from starting the 14th week, despite the lights and the heat of this season (added to the lights I had to keep the tent door open for there was 32 ºC inside) the Dr is taking it well, I see the buds foxtailing as I expected, and I'm positive this grow will get to a good end. I'll work day by day to achieve that. Regarding fertigation, I gave her a solution half concentrated (relative to the solutions that I had given her the preceding days) because I noticed salt build-up by the EC measurements. I left run off EC at 800 ppm which is still a bit high for my liking but not excessively. For the amount of runoff I collected today, I see she seems to be drinking a little more.

Giorno 1 bene le ragazze si sono riprese bene dal trapianto e stanno sviluppando bene le radici e iniziano a bere più acqua. Giorno 2 LST e verrà già pulita con una leggera defogliazione e più che altro lollipopping( solamente 1 nodo in meno per ogni ramo e 2 nei più sviluppati) perché è già più grande della compagna e ha i rami troppo cespugliosi che rovinano il flusso di aria e il loro corretto sviluppo. Giorno 3 annaffiata con 1L di acqua Giorno 7 defogliazione e lollipopping

This beautiful girl turned out to be a real strong queen who withstood very strong stresses, she is very persuasive for ScrOG, in 2-3 days when she comes out of the stresses I will switch the light cycle to 12/12.💚💚💚

Hi again I'm into the last couple weeks of nutrients and then the final part ripen. Before I then flush them 14days . They are smelling amazing fruits and cream all in the grow room its lovely... Back next week my growmies...

Hallo liebe Growfreunde, Diese Woche verläuft sehr angenehm, keine Mängel oder sonstige Beschwerden 😁. Die automatische Bewässerung wurde angeschaltet nachdem ich erstmal von oben gegossen habe. 1l Wasser pro Pflanze mit dem Enhancer von Greenhouse. Werde dass alle 2 Wochen so machen aber sonst gibt's nur PH korrigiertes Wasser. Dünger wurde ja der Erde untergemischt. Ach ja, CalMag kommt immer mit ins Wasser bei mir. Wie man gut sehen kann entwickeln sie sich toll soweit. Die Peyote Critical ist um einiges langsamer im Wachstum als die anderen, aber sie sieht sehr gesund aus. Die Gorilla Zkittlez entwickelt sich auch gut, aber liegt eben fast 10 Tage hinterher. Aber was solls, dann bleibt sie eben etwas kleiner wie die anderen😅. Ich denke am Sonntag nächste Woche geht's für alle in die Blütephase. Naja, mal schauen... mach am Sonntag nochmal ein Update.😉 Bis dahin euch allen einen guten Zeit. Ciaoiiiii

First week of flower and the plants seem to be doing alright still … remember this is my first time planting indoor

Not much this week except watering every 2 days with 1/4 gallon to each. Day 51 - rain water pH 6.4 Day 53 - rain water w/ Recharge @ 1 tsp per gallon & Natural Wet @ 1 tbsp per gallon pH 6.9 Day 55 - rain water pH 6.4 StayWeeded ✌️

Yeet yeeet! Everything's looking great! Still trying to use up this Nitrogen in this soil b4 I flip... Bc I haven't fed ANYTHING other than plain distilled water... I need to flush and re water with correct nutes b4 flipping to flower

Nueva poda de apicales y una de silicio. Con 26 dias Harto de los plomos me deshice de ellos y así seguiran creciendo , tal cual quedaron. No pretendo hacerles mucho más, más adelante igual doblamos alguna rama para guiarla y quitar algun chupóptero. A los 26 dias también se subió la potencia del lumatek al 75%. unos 220 W. áprox. y así pasaran hasta que se cambie el fotoperiodo.

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.

💩Holy Crap We Are Back At It And Loving It💩 Growmies we are at DAY 21 and she's just killing💀it👌 So Shit , I gave them just a tad to much nutes 👈 But I have since fixed it So I'm starting to pull her over and do some low stress training 🙃 Lights being readjusted and chart updated .........👍rain water to be used entire growth👈 👉I used NutriNPK for nutrients for my grows and welcome anyone to give them a try .👈 👉 www.nutrinpk.com 👈 NutriNPK Cal MAG 14-0-14 NutriNPK Grow 28-14-14 NutriNPK Bloom 8-20-30 NutriNPK Bloom Booster 0-52-34 I GOT MULTIPLE DIARIES ON THE GO 😱 please check them out 😎 👉THANKS FOR TAKING THE TIME TO GO OVER MY DIARIES 👈

The smell is strong, healthy and fast growing.

Info: Unfortunately, I had to find out that my account is used for fake pages in social media. I am only active here on growdiaries. I am not on facebook instagram twitter etc All accounts except this one are fake. Have fun with the update. Hey everyone :-). This week the baby saw the light :). She came out 2 days ago. It is sprayed into the main area every day so that the humidity stays at the upper level :-). Until the main comes down next week, it does not have to be poured but only sprayed :-). I am very curious how it will develop in the coming week and until then I wish you a lot of fun with the update 😊. Stay healthy 🙏🏻 and let it grow 🍀👍 You can buy this Strain at : https://originalsensible.com/original-sensible-seeds-zkittlez~20503 Type: Zkittlez ☝️🏼 Genetics: Afghan Kush Indica x Grandaddy Purple x Grapefruit hybrid 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Fertilizer: Green House Powder Feeding ☝️🏼🌱 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 5.5 - 5.8 .