Va muy bien, ya alcanzo su altura máxima al parecer, está mostrando sus colores, muy bonitos 🌈🌱🔥 ahora solo a engordar esos cogollos, huele delicioso a frutos cítricos 😋

the girl went to the tent on the 69th, they predict very bad weather, which would probably cause her to rot, I will try to finish the growth in the tent, she has 14 days left and will be cut, I am going on vacation, so I am forced to do it a little earlier... In general, the girl is very it's healthy, it barely fit in the tent, so a fair amount of leaves were stuck to the edges of the tent, I've never seen anything like it, that people carry from nature to the tent - and not from it to nature :D it will be interesting to see how it all ends :) good luck:)

Friday, Feb. 19th. Today Iam going to make a Grow just for me I bought in November the 25 Years Anniversary Box from T.H. -Seeds Today ive chosen the Bubblegum Its just because ive grown it once and only had 1 Plant ( clone) and it was soooo delicious We will see if i can repeat that Taste with the " Legendary Bubblegum" from T.H.-Seeds As I have a bigger Growspace, these Girls are going to start under 12/12 Lightschedule Starting in 3l Airpots and then transplanting into 11l Amended Soilmix ( RQS Easy Boost Organic Nutrient) I took 3 Seeds, they were looking quite lightgreen--------and put them into a Glass of lukewarm Water for a few Hours Tomorrow i am going to make Further Germination under a wet Kitchensponge Saturday Feb. 27th. Those seeds took longer to Germinate than the other Strains But on saturday Roots were long enough to Plant them Monday Plants show barely up... still in Shell... one looking like wilted yeah we will see in the next 2 days who made it Girls are growing under 12/12 in the Big Tent. its quite dry here ( RH 40 or less) and they have to fight more, than in the other Tents But in the End.... Cannabis grows under nearly every Condition... its just the Question how good so stay tuned for the next update.... in week 1 Stay Tuned Saturday Feb.20th After a few Hours sokaing into Water, they moved under a wet Kitchensponge for further Germination Then they are covered and placed on a warm Spot. Breeders Information: Bubblegum is one of the first strain in T.H. Seeds collection. It was created in 1993. Today Bubblegum is an outstanding and famous cannabis variety with a big amount of awards. The plant demonstrates a good stabillity. It has a quite short size and reaches to 120-160 cm tall. The harvest comes after 55-60 days of the flowering and produces yields of 350-500 gr/m2. The smoke provides an intense fruity flavor and a mostly indica effect.

Day 58 FLOWER and this girls keep surprising me every day, they keep on getting bigger 🤷‍♂️🙌💚💚💚 the trichomes and smell department is doing the same 😂 they are definitely showing me the reason why i have to always make clones 🤦‍♂️🤦‍♂️🤦‍♂️ my bad 😆💚💚💚 As always thanks guys for checking and reading my diaries, I truly appreciate the love and it all 💚💚💚🙏🙏🙏 growers love and keep on groweing 💨💨💨💚💚💚 PPFD - 1000 Umol/m2 DLI - 40.0 mol/m2d VPD - 1.72 kPa Girls: Gelato OG @Seedsman Light Lumatek Zeus 465W compact pro at 100% More info and updates @ https://growdiaries.com/grower/dogdoctor https://instagram.com/dogdoctorofficial https://youtube.com/channel/UCR7ta4DKLFMg2xxTMr2cpIg All i grow is medecine for myself, nothing to sell, dont even ask !!!! Stay safe and do it with love for the love ❤️ 🙏 💚Growers Love to you all 💚

Ripening in progress. The buds smell good.

EMERALD TRIANGLE SEEDS ROYAL PURPLE KUSH AUTO Genetics - Black Afghani x Bubba Kush Yield - Medium Indica/Sativa/Ruderalis - 75/15/10 Height - Medium Pathogen Resistance - Pests Harvest - 55 days Flavor - Fruity, Peppery, Sweet Great auto strain.. Grew very well through veg and bloom.. Had no problems with her at all, she produced some very nice flowers and yielded the most out of all 4 strains..lovely classic kush taste and smell to her with a good initial kick from the smoke following a relaxing more couched feeling.. Great for relaxing.. My first strain from Emerald and im very happy with the results from her.. https://www.viparspectra.com/?aff=454&utm_source=affiliate https://partners.viparspectra.com/create-account?ref=454 Coupons - code: Itxsgdvip code: JEF https://www.amazon.com/dp/B08CHCFCG1?ref_=ast_sto_dp

Que pasa familia, vamos con la cosecha de estas Lemonpaya de FastBuds. Por dónde empiezo, fue una variedad que me resultó complicada cultivar y a nada que alimentada lo marcaba las flores son bien compactas y van llenas de resina, tienen tonos verdes bonitos, y tiene unos aromas afrutados bastante marcados con toques citricos. Es muy complicada a mi parecer, es de ciclo de 2 meses y medio, pero bien agradecida aún así. Hasta aquí todo, Buenos humos 💨💨💨

Hallo zusammen 🤙 Sie wächst sehr schön und macht keine Probleme

Es Fehlen noch paar Wochen zwischen drine wenn ich mal dazu komme wird es noch aktualisiert. Leider ist mein 80x80 zelt deutlich zu klein. die Linke Pflanze 94cm wurde absichtlich um 0.2 mS überdüngt und ist doppelt so groß wie die Rechte.

Update vom Blütetag 39 Ich wünsch euch allen erstmal dicke Buds an den Bäumen und alles gute zum Nikolaus! 🎅💚 Die Woche ging's wieder mit einigen Fragezeichen weiter, aber seht sie euch selber an. Bis jetzt macht mir nur die Blue Cheese n bisschen Sorgen, die braunen spitzen werden schlimmer und die Papaya hat auch angefangen, seit heut macht die Lemon Cherry Gelato noch mit. Erst dacht ich es kommt von Überwässerung, Licht, oder Mangel und mittlerweile denk ich der Booster is schuld. Hatte den letze Woche einmal gegeben und diese Woche auch einmalig, was irgendwie komisch is weil es ja schon davor anfing. Jetzt bekommen sie erstmal nur Wasser, denk das werden wir schon noch zu Ende bringen. Die Erde hat auf jedenfall Power wie das aussieht, oder seht ihr da n Mangel? Schönes Wochenende euch allen! 🤠💚🖖

4 растения радуют, одно набирает и набирает хорошо! 2 растения будут мелкими, но все равно должно получиться круто. Впереди финальные 2 недели

3 março - 9 marco 4 março - Alimentadas pela primeira vez 9 março feeding: Biogrow 1ml; bio heaven 2ml; acti-vera 2ml pH 6.3

Heavy defoliation, and feeding water only from now on

well, that day dawned :) growing in a suitcase was really difficult, temperature, humidity, plant growth, everything was very difficult to control, but I managed something, it was an extremely interesting experience :) 119 gr wet, I think it will be between 25-30 gr dry , which I think is really good from the suitcase :) it was something different than usual, and now I'm going to grow another begina, which is much bigger than this one :) good luck to everyone, and thank you.:)

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.

5/23/2023 Week 7- Day 1 of Flower (Day 110 overall) (Day 49 of Flower) There was a couple of small super small sucker buds on the lower stocks that needed to be cleaned off but that was it. Just watching them Flower!! 5/24/2023 Week 7- Day 2 of Flower (Day 111 overall) Tucked a few fan leaves below lower buds but didn't see any blatant offenders that needed to be removed. I typically do start my checks in Week 8 but since this is a new strain I decided to go ahead and do a Trichome check just to see what was what.. Just as I thought nothing but clear glassy Trichomes. I will check again in one week.... 5/25/2023 Week 7- Day 3 of Flower (Day 112 overall) Just letting them grow today!! Smell is getting stronger I would say it is a hint of Pine and a heavier fruity smell. 5/26/2023 Week 7- Day 4 of Flower (Day 113 overall) I did Nothing but took some pics and I enjoyed it!!!! It is nice to be able to just sit back and watch them on auto pilot.. :-) Tomorrow Water Change Day!! 5/27/2023 Week 7- Day 5 of Flower (Day 114 overall) I admit it.. I had to defoliate a little bit.. I looked in while changing the water today and there were just a couple blatant offenders blocking the light from lower bud sites and those leaves they just had to go. Other than that I changed the water and this week is where I drop everything and start preparing them for this last phase of the grow. Loving a few of these buds they are starting to beef out very nicely. I added 36 gallons Mammoth Silica = .5Mil/Gal= 18Mil Root DRIP = 1Mil/Gal= 36Mil CalMag= .5Mil/Gal= 18Mil FloraMicro = 3.8Mil/Gal= 137Mil FloraGro= 2.8Mil/Gal= 100Mil FLoraBloom= 4.6Mil/Gal= 166Mil LiquidKoolBloom= 2.5Mil/Gal= 90Mil TPS SIGNAL= 4.0Mil/Gal= 144Mil ORCA = .5Mil/Gal= 18Mil Water Temp= 70.1 Tent Temp= 76 Humidity =64 ** I have two dehumidifiers running on Ink bird controllers to try and keep the humidity down, In late in flower I like to keep the humidity above 45 but below 60. 5/28/2023 Week 7- Day 6 of Flower (Day 115 overall) Opened the back of the tent today and boy did she need some defoliation love in the back. Other than that I took off a few little sucker buds trying to form. I did start to setup my Dry space as well as did a Trichome Check today and the brown tips are coming in nicely. 5/29/2023 Week 7- Day 7 of Flower (Day 116 overall) Found a few baby sucker buds trying to form so I removed them. Other than that I am enjoying watching her mature. I also started my Reverse of the Clone I took 6 weeks ago in Apr from #3. I am uploading footage of the reversing process for your viewing pleasure.

Sie haben das Umtopfen ganz gut überstanden. Eine von den dreien macht ganz gut los. Die anderen beiden haben wohl noch etwas Stress durch das Umtopfen. Alle 3 sind Samen der selben Genetik aber selbstverständlich auch verschiedene Phenotypen, sie werden auf jeden Fall unterschiedlich wachsen und aussehen. Ich finde aber No-till besser als Stecklinge und je besser der Züchter um so weniger Phenos 😉 Wir werden sehen... 😎