Such a beautiful week with the girls. I moved them in a larger tent(120x120x200), they deserve it :) The buds are taking nice shape, it felt like it took for ages since I flipped them. The Criticals were more vigorous, but now the GZs seem to be catching up :D They turned a bit dark green, so I will go back to 750ppm. Next week I will focus the time-lapse on the GZs, as I feel they are more trendy.

Dolato is finishing up nicely and bulking up pretty well, buds are falling over so I tied most of them to hold them up right but there were a few I couldn’t reach which are still down. Scent on her is very Gelato like but not as fruity or creamy nor is she very strong scented. Calyx swelled up but some pistils seem to have more time to darken and recede. Been flushing for a week now just waiting for more trichomes to get cloudy before harvesting!

Приветствую всех, кто следить за мной. Ваша поддержка очень важна для меня. На следующий день после того как я обновил прошлую неделю дневника наступило время пересадить растения в более крупное ведро. Я покажу вам как использовать дешовые пивные стаканы для пересадки ваших растений. Вы можете посмотреть это на первом видео. Когда я пересаживал растения я дополнительно добавил микоризу в большое ведро. Одно из растений "ЛСД -феминизированное" всё ещё показывает замедленный рост, несмотря на то, что я решил подсветить его LED полный спектр. Так же я внёс базовое питание, корневые стимуляторы и стимуляторы роста, в добавок с гуминовыми кислотами. Я планирую сделать из эти растений много клонов и запустить новый дневник в другой палатке, а эти растения потом переставить в маленькую палатку. Если вам интересно следить за приключениями травки в России, подписывайтесь на мой дневник -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Greetings to all who follow me. Your support is very important to me. The day after I updated the last week of the diary, it was time to transplant the plants into a larger bucket. I will show you how to use cheap beer glasses to transplant your plants. You can watch it on the first video. When I transplanted plants, I additionally added mycorrhiza to a large bucket. One of the "LSD-feminized" plants still shows slow growth, despite the fact that I decided to highlight its full spectrum LED. I also added basic nutrition, root stimulators and growth stimulators, in addition to humic acids. I plan to make many clones of these plants and start a new diary in another tent, and then move these plants to a small tent. If you are interested in following the adventures of weed in Russia, subscribe to my diary.

Do you have the Xs Factor? email [email protected] for open apprenticeship spots. Open to Canada and USA (no cost) MARS HYDRO LIGHTS: https://www.mars-hydro.com/mars-tsw-2000-led-full-spectrum-hydroponic-led-grow-light DISCOUNT CODE FOR LIGHT: BudXs CULTIVAR: BudXs2 GROWER: @PsGrowers ________________________________________________________________________________________________________________________________________________________ Notes: @PsGrowers - Well, well, well. This tent continues to impress. The XL's are really starting to stand out and take over the tent. This is a good lesson in auto seed buying and planning your grow. A regular auto will tend to stay short and bushy. An XL will grow tall. Which one will yield more???? Thats subjective. Which one will have less issues with humidity and bud rot? Certainly the xl. IT is my preference, hence why the trait is bred into BudXs2. You will get a kick out of how potent this flower is. Lets see some close up crystal shots next week, see if you can get a few natural daytime light photos:)

While I was away in Mallorca, enjoying the sun and smoking some Sativa Landrace, the girls were given a more simple feed to make things easier for my friend whilst he was taking care of the garden. The feedings came to around 700ppm (Including 150-190ppm tap water). As you can see in the video I've been bending her down for a couple of days instead of tying a string to her. It's just a lazy LST that should basically do the same thing. This girl has really bounced back and shown great growth since increasing the feed strength. She's keeping a good structure and should make a nice bush. Every second feed from here on out will also contain Mammoth P for the first time in my garden! 🐺

Hi guys So we are on day 42 from switch so going into week 7 now, these are a 45-50 day flowering plant, I will be using a ripner for the next 10 days then give it a final flush of just water at ph 6.2. So there starting there fade now on some of the leaves and the buds are are fattening up. There really really sticky and covered in trichomes. I'm really looking forward to the end result. Temps and humidity are all good I took a few leafs off that was blocking buds but other than that its been a normal week. Happy growing guys and keep it up 💚💚💚 Day 44 on the scrog there fattening up but jeez there's so many white pistils. I'm not sure whether to just flush with alternating water and molasses or to use a ripner on it???? Any suggestions🤔 Thanks guys 💚💚💚 Day 47, started feeding bio heaven, bloom and topmax again for the next 2 weeks after a discussion about the organic range im using. Buds are swealing and really sticky, smell really sweet now. Humidity and room temps are consistent to where I want them, no signs of powdery mildew or rot of any sort. Stacking on the trichomes now too I cant wait to see the final finished plant in her glory. Happy growing guys I thanks for looking 💚👌

Bud forming so fast!!!!!! Comparing to previous plants I growth in witch I used biobizz light soil I changed kind of soil in this one I’m using canna professional and the different is quite noticeable I’m really satisfied. I was worried that the small box I’m growing in would eventually make the plant suffer but it’s totally not, the plant is responding well!! Started with the maximum dose of bud ignitor by advanced nutrient. I’m really exited for this lady can’t wait to se the beautiful complete resinous buds.. keeping growing with LOVE 💚

Привет садоводы Началась новая неделя и я решил перевести ее на цветение хотел подержать еще неделю на вегетации , но надоело сегодня я заправил ее по полной удобрениями и стимуляторами так что остается ей пожелать доброго пути и следить как пойдут у нее дела всем удачи и красивых цветов !

Chugging along. Much better fertilization rate than expected. All looking good up and down each branch. Almost all budsites are stacked with seeds even the lower ones Moved to different tent cuz original one was a damn mess with plant matter and whatnot on the floor. Only one that looks possibly behind us the PotG. I just think it’s a matter of not having seeds busting out the bracts quite like the others. Very happy with the results Check out previous weeks for procedure information. I’ll add them to each with soon. If not showing now go back to first couple weeks of the diary to see specifics on what I used, and how.

Ela segue crescendo bem após a cobertura, devo fazer alguma defolhação? Segue crescendo bem. 04.03 os galhos começaram a pegar força de crescimento, vou fazer umas amarras em breve, mas não sei se devo fazer desfolhação, se alguém puder ajudar nos comentários? Obrigado

Wow I can say she is doing great have done a lot of defoliation on her also have done lolipoping to get more energy to the top buds this my 1st time trying it let see how she does. Feed 8th week chart mix with my fox farm will continue on the chart schedule haven’t tried the sledgehammer yet but before the end of flower I will. Will start to post videos of the grow from now on also of course tons of more pics. Day time temp 74-76 and RH is around 50-56%.

Background Fingers crossed that these Spicy Bitch regs provide at least one male so that we can back build some stock of it. In the event that does take place we’ve got a single clone of each strain from the previous pollen chuck to sit in the tent with them so they can make babies for the next few months. The whole point of the last year was to start making some foundational genetics for a third generational cross we could call our own. If you’ve been following along than you’ll know that it’s been anything but easy. Our previous pollen picks didn’t pan out at all so we’re back to the drawing board with a new option from ExoticSeeds. This’ll be a 10 plant run with 5 regs and 6 strains for pollination including the strain itself. We’re running in a 2x4 MarsHydro grow tent all powered by a Mars Sp6500. That’s a little more than 600w packed into half the recommended footprint😳. Why? you ask - because we like our buds big and overcompensatory😂. Really, I’m just of the mind that we can pack more light into this space than recommended and get much better results. The math doesn’t lie. At least not as long as I wasn’t high when using the calculator again….. Many thanks to @MarsHydroLED for the opportunity to test run the equipment👊. In addition, we’ve also moved to a new nutrient system - Druid Nutrients out of the Netherlands. They don’t really have a presence on GD yet but you’ll be hearing about them very soon I’m sure. The beauty of this system is that it’s literally a 1 (one) component system for the entirety of the plants grow cycle. It really has changed the game in terms of ease of feeding and maintenance. It’s also very versatile and seems to provide everything needed across multiple different strains in the same ratios. Keep your eyes peeled for these folks. Pretty much a guarantee that they absolutely blow up once more people know about them👍👌😎. Strain Background Spicy Bitch: predominantly sativa, heavy yielder with a daytime kinda trip profile. It’s a cross of Queen Mother and a Pre-2000 AK47. We’ll pull what pollen we can and hope to have a female run out a larger supply of seed for the future. Many thanks to @Exoticseeds for the chance to give these beans a go👍👊. Pollination Strains: Holy Surfer S1 - this is one of the focal points for this cycle. A fellow growmie was kind enough to ship over some S1 genetics I took an interest in. The only ask back was that if I did cross it to send a few his way for testing👍. Shoutout and cheers to @blendmedmedman. Hoping to have something back to ya in short order. For full details on this alluring hybrid option check my buddies link at seedfinder - https://en.seedfinder.eu/strain-info/Holy_Surfer/Smiling_Tiger/ Northern Lights - this came from a particularly interesting batch of seeds that have shown a very dependable variegation trait. It’s a compact and squat plant requiring very little maintenance. Typical for the strain really. It’s been chosen as an option to potentially mellow out the high , shorten the stature of the resulting hybrid and inject it with some of that mellow indica effect. Boogie Nights - total shot in the dark. Still haven’t even tried the strain myself yet but it was available at the right time and interesting enough to make a salad with. Big thanks to AMS who’ve been nothing short of an excellent seedbank to collaborate with. Expect similar growth characteristics to that of the Northern Lights. Better resilience however. Blueberry - this particular clone is from extremely strong stock. Spliff seeds broke the mold with this strain. She’s lower maintenance than the NL, more resilient than anything else we’ve got on the menu and the terp. Profile on this girl is out of this world. If we can bring any of these qualities to the cross, then it could be magic👌. White Widow - garrghh, I just can’t get away from this particular plant. Again, still haven’t even tested the buds yet and all I can say is that the growth characteristics are extremely vigorous and desirable. This plant is one of 3 unicorns that I have yet to tame due to a combo of extremely bad luck and circumstance. All told, it’s still the same story: a VERY experimental breeding project designed to shotgun a broad swath of genetics against a reliable and dependable Breeder who’s put out proven fire 🔥🤟😎👍.

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.

Hello community, today is day 114 from dry sunflower seeds. Last week before harvest, watering with bottled water all week. The smell of ripe melon, fruity and tart.

smells gut bro...

Got a new light this week, it's basically a HLG 260 R-Spec except locally manufactured using the same Samsung LEDs. Big Mumma got her 60x60cm tent today and will go in there under one Viparspectra 300W blurple (130w from the wall). I trimmed her, super cropped her main stem and added a scrog net in preparation of flowering her in the next couple of days. Because my other plants were getting up past 75cm after 7 days of flower (100cm is my absolute max) , I decided to supercrop the canopy back down to about 60-65cm - it was pretty scary and I definitely broke the outer stem on some of them. Also gave them a good trim. Fortunately most bounced back strong the next day which are the most up-to-date photos you see (17/4/20).

Very easy to grow, this is my second Gorilla Zkittlez and both grew without problems

This week has been hectic ...my gorrila breath mothers started randomly flowering ...i have no idea whats going on ....its not a auto and im pretty sure theres more than 12 hours light a day .....its January in Africa! ! So im gonna take as many cuttings as i can and pollinate them what's left over with ... amnesia zkittlez auto that my girlfriend is growing .....from 420 fast buds.....

Día 87 (26/08) Aplicación foliar de Bacillus thuringiensis a 1 g / litro para evitar a las temidas orugas de los cogollos! Hace un día nublado (29 ºC de maxima) y NO es necesario regar Elimino la malla de sombreado de la cara sur, ya que las temperaturas son más suaves después de la canicula Día 88 (27/08) Riego con 500 ml H2O pH 6,5 Empiezan a bajar las temperaturas a 29 ºC de máxima, y se nota en la demanda de agua por parte de las plantas! OnionOG Se empiezan formar los erizos y se pueden apreciar los primeros tricomas sobre las futuras hojas de azucar 😍💥 Día 89 (28/08) Riego con 500 ml H2O pH 6,5 Cada planta empieza a ir un poco a su marcha en la demanda de riego dependiendo de su tamaño y estado de floración Día 90 (29/08) Riego con 250 / 500 ml H2O pH 6,5 He detectado un gusano de los cogollos muerto sobre una hoja! 💥 Parece que los Bacillus thuringiensis funcionan estupendamente! 😁 Día 91 (30/08) Riego con 250 / 500 ml H2O pH 6,5 Día 92 (31/08) Riego con 1 litro H2O pH 6,5 + 25 ml de Humus de Lombriz Liquido Día 93 (01/09) Aplicación foliar Bacillus Thuringiensis No es necesario regar tras el litro de ayer y dia nublado con pequeños chubascos! 💦Nutrients by Lurpe Solutions - www.lurpenaturalsolutions.com 🌱Substrate PRO-MIX HP BACILLUS + MYCORRHIZAE - www.pthorticulture.com/en/products/pro-mix-hp-biostimulant-plus-mycorrhizae