Hello guys😍😍 We have reached the 5th week of flowering. The plants are almost done with their longitudinal growth and most of the plant is focused on buds. I used overdrive fertilizer this week. The smell of the buds has increased a lot. And the buds have a stronger smell than the mother (cakes n cream) and give off a stronger OG smell😍 Because I increased the temperature difference between night and day, the color of the buds started to change. Thanks for commenting🙏 "farah4weed"

8/27 needs to hurry up lol I’m ready to start a new grow buds not really forming thing just getting frosty

Things have been a bit slower with the triple gs but I'm not in any rush bt yeah looking good that big chem is a strong looking girly 😁

Tag 68: Noch eine Woche bis zur Ernte. Zum Glück. Die Blätter sehen auch echt nicht mehr gut aus. Vermutlich war ich beim ph wert einstellen noch zur vorsichtig, und er war noch etwas zu hoch?!? Ich traue mich immer nicht soviel von Säure zum senken rein zu machen 😬

The pistils are still white Shes very fat now and i think 2 weeks before harvest, i feed less now at 400ppm and starting ripen feed when half of her pustils turned brown August 18 (mid this week) I flushed her completely and fed ripen untill runoff got in the 200ppm. Now she is ready to finish Harvest will be at august 28th

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.

Al corte ✂️✂️✂️

Great growth so far, for autos these are very uniform I’m impressed compared to other genetics I’ve grown for autos piña takes the cake already. So far very happy with them. 2.5 inches at the start of week 3

This weeks been strong switched the nutrients on em! They’ve been getting use to them and starting to stretch!! Been defoliating when I can I’m nervous to do too much! But there’s good air flow in the tent! 🔥 it’s been hot out here in the desert so I might get another bag for co2 read that will help the plants deal with the heat!

Esta semana apesar de tener temp Máxima de 28... se va recuperando bien de las podas, el led de TodoGrowled funciona perfectamente para sus 55w farmers!🍁

Hey Friends, end of Week 10 from seed Colas are looking Very nice Noticed some orange color on some leaf tips so I lowered the amount nutrition when feeding I used a magnifier to have a closer look at the colas, trichomes used to looked like little crystals, now they are bigger and cloudy. So far no amber coloring on trichomes I need some advice as to when I should begin flushing and harvest Smell is slowly getting stronger, like a muffin with a small touch of gas ⛽️ Looking Forward in seeing some bud growth in the following week, will keep you guys posted!

Start of week 5 - days 9 to 15 April 9/4/2020 - She's reacting better to LST 12/4/2020 - After 6 days I gave her 1L RO water with: GHE Terra Aquatics Cal -Mag - 60 PPM Biobizz Acti-Vera - 30 PPM Biobizz Heaven - 30 PPM Biobizz Top-Max - 10 PPM Biobizz Grow - 10 PPM Biobizz Bloom - 10 PPM Biobizz PH Up RO Water - 4 PPM About 154 PPM PH 6.6 15/4/2020 - Raised the Light to 60cm she reacted positively, also turned on the oscilating fan.

WOW that was a much needed week of plumping up. What a wonderful difference 1 week made in the tent. The ladies are really looking healthy and beautiful. Absolutely caked in crystals. My guess/hope is another 4-7 days of plumping up, then a week to mature and ripen up before harvest. Hoping to see some color soon but the smell is wonderful. Smells creamy. 😍😍 Hopefully what I've learned and changed from the previous grows is paying off, they are nice and short, fairly level. Most of the flowers are in direct light. Was pretty worried and thankfully for no reason. Cheers to another week of plumping up 🙏🙏🙏

Cut down on day 110, after 30 hours of darkness.. Added ice blocks to the substrate over the last couple days and got some lovely red and purple notes from it... Found one more spot of mould in a main cola, total loss of 40 grams of wet flower. Not a huge problem seeing as I still have colas the size of my forearm. Half wet trimmed on the large colas to reduce risk of mould, left less dense and smaller nugs with most leaves on to aid a slow dry. Hung in as little light possible in ~19°c at ~55%RH with filtered air from outside and extract system, dehumidifier circulating air in the room. Air refresh rate is ~90 seconds.

Chopped on day 80, hanging in 65F and 62 H. Hoping to slow this dry down to 10 days so wish me luck.

Everything is going fine...🍃🍃🍃 girls switched to 12/12 on the 40th day of vegetation... 🍃🍃🍃Good luck with the flowering stage girls🍃🍃🍃 Happy growing 🍃🍃🍃

Plants are now what appears in Week 4 of flower, even though the natural light cycle is still above 14 hours per day. It’s likely that the streak of cloudy mornings over the past couple of weeks has contributed to the transition by simulating shorter effective light periods.. that in addition to going from indoor to outdoor Nutrient Activity: • Started the week with a cap mag-only feeding to address ongoing signs of magnesium deficiency. • Later in the week, applied a strict Epsom salt feeding at 1 tsp per gallon, one dose per plant. I also moved my watering schedule from late in the evenings too early morning and midday to address a potential cold shock. Observations: • Minor yellowing remains present, particularly in the older leaves. Still leaning toward a magnesium deficiency as the primary cause. • Toward the end of the week, tip burn began to appear, likely due to nutrient buildup from trying to aggressively correct the deficiency. It’s a delicate line right now between resolving deficiencies and avoiding overfeeding. ⸻ Next Steps / Adjustments: • Reduce feedings to no more than twice per week going forward to minimize the risk of nutrient burn. • Monitor new growth and bud development closely for any signs of stress or improvement. • If tip burn continues or worsens, consider a mild flush to rebalance the root zone. If the yellowing stabilizes and tip burn is contained, I’ll resume light feeding adjustments in the following week.

Mit einem Blick auf die fünfte Blütewoche der Permanent Marker von Traphouse Genetics präsentiert sich die Pflanze in absoluter Bestform, wobei die generative Entwicklung exakt nach Plan verläuft. Das dichte, tiefgrüne Blätterdach zeugt von einer optimalen Nährstoffversorgung, während sich die Blütenkelche ungestört differenzieren und bereits deutlich an Masse zulegen. Die kompakten Internodienabstände, ein Resultat des erfolgreichen Lollipopping und Toppings, führen nun zur Ausbildung mehrerer ausgeprägter, langer Colas. Mit dieser Bilderbuch-Entwicklung sind alle anatomischen und physiologischen Voraussetzungen für eine ertragreiche finale Phase dieser vielversprechenden Genetik geschaffen.