Day 43 let's start week 7! the plants grow and continue to stretch. unfortunately two weeks ago my ph meter broke. last week I started giving 1ml / l of green sensation and the plants seem to have lightened a lot. these days i should have the ph meter back so i can check. all in all they seem to grow well apart from this "yellowing". Day 44 the pH pen arrived and I discovered the cause of the yellowing. the ph was about 5 😭😭😭 now I let it dry well and brought the ph back to 6.7 and given 0.5 l and I wait for it to dry again keep following me to see my progress. it is my first growth and I make many mistakes, leave a like and give me an opinion or advice to improve. good luck and happy day!🌱💚

Flowering day 15 since time change to 12 / 12 h Hey guys :-) This week the ladies developed beautifully 👍. The stretch has started very strongly :-) . Watering was done twice this week with 1.2 l (see table above for nutrients). The heating mat does exactly what it is supposed to do, you can see that the ladies are doing perfectly again 😃. Fresh osmosis water was mixed with tap water in a 100 liter tank so that I would have enough stale water for the coming week 👍. Otherwise everything was cleaned and checked. During the check, I noticed that after spraying neem oil 3 times, there were still a few damn trips to see. I have ordered nematodes for leaf and substrate against tripse. Then they should finally be gone again 🙏🏻 have fun and stay healthy 💚 👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼 You can buy this Nutrients at : https://greenbuzzliquids.com/en/shop/ With the discount code: Made_in_Germany you get a discount of 15% on all products from an order value of 100 euros. 👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼 You can buy this strain at : https://gardenofgreenseedbank.com/candyland/ 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 5.8 - 6.5 MadeInGermany

Hi guys This week I been tucking and pulling off selective leafs. The stretch is still real the blue cheese has exploded In growth and absolutely stink. I will be doing a major end of the week and removing little nodes that didn't make it. I finished a week flush as I did burn them, but now there back on the nutes, 2ml per litre of bloom and 1ml per litre of top max. I put 25l In the resivour so will see how long that lasts. Both plants are showing calyx and pistils. Looking forward to this one hopefully the nutes will kick in and the dark phoenix will be healthier green again. I will keep you updated thru the week as I expect a few changes in thru the week. Happy growing guys 👌💪💚 Day 16 12-12 So I done a little defoliation, I will be doing final one one day 21. So on there back on nutrients now at half dose. Autopot system is working brilliant. Felling good for this run. I'll keep you all updated if any major changes occur. 💚👊💪

Flowering is obvious on both plants. for this week I´m going to switch to Flowering HPS bulb. Keeping the day room temperature around 22-23°C while night temperatures are around 18-19°C. Plants looks happy, however I´ll have to add net to support branches in near future. Also, I will start to use some potassium fertilizer to keep incoming buds big and juicy. I did a little bit of defoliation too to keep the bottom of the plant clean so air can flow easily there. You can see on the video two fans which are working 24/7.

Día 8: 🔹Descanso 😴 Día 9: 🔹Trasplante a macetas de 1litro (en los siguientes cultivos pondré directamente en macetas de 1litro). 🔹 Riego con una solución de 2ml/l de acti-vera de BioBizz Ec: 600 y pH a 5.9. Siempre en base a un Ec de agua de 400 🔹Abono foliarmente con una solución de acti-vera de Bio Buzz unas 2, 3 veces al día. 🔹 Aplico tierra de Diatomeas sobre el sustrato, media cucharadita de café por cada maceta de 1litro para el control de plagas. Día 10: 🔹Abono foliarmente 2,3 veces al día con acti-vera de Bio Bizz Día 11:. 🔹Abono foliarmente 2,3 veces al día con Rootbastic 1ml/l. Día 12: 🔹 Aplico foliarmente 1ml/l Acti-vera BioBizz + 0.1ml/l y pH a 6.0. 🔹Remuevo la tierra para por encima con unas pinzas para airear el sustrato. Día 13: 🔹Riego con 0.2ml/l Acti-vera y 0.01 Rootbastic, Ec 1000 y PH 5.9 🔹Pongo unas guías de madera para una mejor estabilidad y desarrollo de la planta. Día 14: 🔹Aplico foliarmente 1ml/l Acti-vera BioBizz + 0.1ml/l y pH a 6.0.

GOOD MORNING VIETNAM😈💚 Week 6 Day 35: Pics from this noon. Mutants main cola is strecthing like crazy😁 like 30 cm in a week. Not as many white pistils as the other 2 girls. Tb; i topped the 2 other ones. I'm lil worried mutant cola will continue streching till it hits light😁 they continue drinking lots of nute water and no complaints yet😎 One love 💚 Day 37: no nute burn!! I was fully expectin bad nute burn when i fed them on 1600ppm😁 but they seemed to be ok with it ä, although i gave them ph water the next day (36). I might be dumb but seeing the girls are not showing any sings of slowing down or nute burning and all checks out, i gave 900ppm feeding. ( All cal w 0.5 ). Colas have starting to see first snow💚 Day 38: Morning fellow greenthumbs💚 Today i defoliated #3 mutant, did some lst aswell. Gave feeding of 1.9 ec ph 5.7. checked runoff and came as 6.3 and ec 1.9 (might be high from 1600ppm feed😂) no signs of lockout or burns👌👌snapped brach yesterday cos forgot not to train after watering🙁 but got it taped up really quickly and seems like it has maked a recovery😇 Day 39: Had quite busy day as i germinated 2 other strains so no pics. Gave girls ph water of 5.9, 1.8L per gal. No news, mutant is streching but 1 and 2 are full flower and fattening sites😎💚 Day 40: gave #3 and #1 feeding and ph 6.3. skipped plant 2 cos pot was heavy and had still lil bit of runoff. Amazing budsite and frostness development! Even the fan leaves are getting real frosty❄️😎 Day 43: All good , giving 5.9ph 900ppm feedings and check runoff. Beatiful snowy tops😍

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! Things get a little more calculated from here on in, the countdown of flowering has begun, although not my first "day of flower", it will be this week I will be able to see the first flowers. Lowered light to maximize growth across the space and really try and push on. BP4000 is recommended for a 6x6 space, it's in a 4x4, so even the edges of the growing space have good coverage. Raised canopy temperature to ambient 84% (Daytime), maximum photosynthesis occurs at 87% LST (leaf surface temperature). 73% Night Added supplemental Co2 Sugar/Yeast to raise ambient co2 levels above optimal 1200ppm. Added 30min Far-red LED 660, 850 nm to both sunrise and sunset. Added 4 hours 280nm UVB (Activating UVR8 photosynthesis) To this point I haven't really applied a day/night cycle to temperature, as we head into flower I will add a generous day-night cycle 84-73, I want to keep it as large as possible but still nice and cozy, keeping temperatures optimal for growth, this is in my opinion important to establish a cycle of large difference as it may help later with "purpling". Cannabis plants are creatures of habit and plan ahead accordingly for different stages of the day/night cycle based on their "history" Photosynthesis ramping up, humidity levels really starting to increase as we build towards the stretch, massive self topping taking place all over the plants. 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.

Hola que tal? yo me he levantado en domingo a las 08:30 me he tomado un café y me pegado un bongazo de aúpa jaja después, musica y hacerles una sesión de fotos a las plantitas 😇👌🏽 Pues hoy es el último día de la 7ª semana de floración, veo a 3-4 plantas listas para cosecha. Esta semana en los directos de twitch usaremos la lupa para ver el punto de maduracion de los tricomas. Deciros que estoy muy sorprendido con las Harlequin CBD ya que están sacando unas porras muy interesantes con aromas súper inciensados, son plantas mega compactas ideales para espacios pequeños y súper productivas!! vaya tela! Una de ellas está súper oscura y tiene mitad planta color verde mitad morada/negra de locos. Sobre las mimosa pues más de lo mismo, más resina, más cogollos, más aroma y plantas muy fáciles de llevar sinceramente... Los colores morados rojizos y naranjas que están sacando me encantan Que deciros de la Mimosa GB que mutó y desarrolló Fasciacion en una de sus ramas satélite. Da cierto miedo ver el cogollo parece que me vaya a engullir jjajjjaja 90 dias desde que se empezaron a germinar son semillas de gbstrains bajo los leds de gblightning y abonadas con boom nutrients todo gracias a @gbthegreenbrand @growbarato

Hola que tal? yo me he levantado en domingo a las 08:30 me he tomado un café y me pegado un bongazo de aúpa jaja después, musica y hacerles una sesión de fotos a las plantitas 😇👌🏽 Pues hoy es el último día de la 7ª semana de floración, veo a 3-4 plantas listas para cosecha. Esta semana en los directos de twitch usaremos la lupa para ver el punto de maduracion de los tricomas. Deciros que estoy muy sorprendido con las Harlequin CBD ya que están sacando unas porras muy interesantes con aromas súper inciensados, son plantas mega compactas ideales para espacios pequeños y súper productivas!! vaya tela! Una de ellas está súper oscura y tiene mitad planta color verde mitad morada/negra de locos. Sobre las mimosa pues más de lo mismo, más resina, más cogollos, más aroma y plantas muy fáciles de llevar sinceramente... Los colores morados rojizos y naranjas que están sacando me encantan Que deciros de la Mimosa GB que mutó y desarrolló Fasciacion en una de sus ramas satélite. Da cierto miedo ver el cogollo parece que me vaya a engullir jjajjjaja 90 dias desde que se empezaron a germinar son semillas de gbstrains bajo los leds de gblightning y abonadas con boom nutrients todo gracias a @gbthegreenbrand @growbarato

Hola que tal? yo me he levantado en domingo a las 08:30 me he tomado un café y me pegado un bongazo de aúpa jaja después, musica y hacerles una sesión de fotos a las plantitas 😇👌🏽 Pues hoy es el último día de la 7ª semana de floración, veo a 3-4 plantas listas para cosecha. Esta semana en los directos de twitch usaremos la lupa para ver el punto de maduracion de los tricomas. Deciros que estoy muy sorprendido con las Harlequin CBD ya que están sacando unas porras muy interesantes con aromas súper inciensados, son plantas mega compactas ideales para espacios pequeños y súper productivas!! vaya tela! Una de ellas está súper oscura y tiene mitad planta color verde mitad morada/negra de locos. Sobre las mimosa pues más de lo mismo, más resina, más cogollos, más aroma y plantas muy fáciles de llevar sinceramente... Los colores morados rojizos y naranjas que están sacando me encantan Que deciros de la Mimosa GB que mutó y desarrolló Fasciacion en una de sus ramas satélite. Da cierto miedo ver el cogollo parece que me vaya a engullir jjajjjaja 90 dias desde que se empezaron a germinar son semillas de gbstrains bajo los leds de gblightning y abonadas con boom nutrients todo gracias a @gbthegreenbrand @growbarato

Die Autopots sind im Einsatz, nach anfänglichem zögern wegen dem ph-Wert. Der sich durchgehend verändert hat, von 5,6 bis zu 6,8. Habe ich mich dann erstmal durch etliche Foren gelesen. Es gibt die Möglichkeit das Wasser zu demineralisieren. Allerdings halte ich das für sinnlos, da die Minerale ja durch den Dünger wieder zugegeben werden. Bisher haben sich diese ph-Wert Schwankungen nicht bei den Pflanzen bemerkbar gemacht. Eher im Gegenteil, das Wachstum ist beachtlich. Zum Ende der Woche habe ich das Wasser im Reservoir ausgetauscht. Noch einmal ein paar Blätter rausgeschnitten und angefangen die Triebe mit den Hanfseilen herunter zu binden. Bei der einen Pflanze ist aus dem topping eher ein Fimming geworden, finde ich jetzt nicht weiter schlimm aber seht selbst. 😉 Grow on!

Day 99 - Ripening week in DWC a. pumped out the Flowering blend, and installed the Ripen b. this plant is certainly a small bush like FastBuds claimed c. I can see how this would be perfect for SOG d. Her pistils are all almost colored, and the trichomes are milky Day 100 a. I always love using Ripen, it works so well b. first day, already notice the top of the buds filling out more c. her life is coming to an end. she will get this week to ripen, then next week we will flush/chop d. growing in DWC makes the ripening and flushing mush faster than other substrates Day 101 - the purple is setting in a. looks like they are ripening up fast, the purple is getting darker and the buds harder Day 102 - ripening really nice, the smell is quite intense a. she is smelling up our barn, we dont have a filter b. Ripen always makes the buds very hard, she is drinking a L a day right now in the end. Day 104 - incredible smell a. this is finally smelling pungent like kush, well kushy haze b. sampled a small top bud, its killer c. Will be cutting down in a few days Day 105 - ripe a. the buds are ripe, I will gradually start the flush before harvest b. will give them 1 or 2 more days of ripen formula, then flush with Florakleen for a day