Let´s get this going asap 😎 See you again very soon 😍

Phenotipos muy similares pero con problemas de Hermafroditismo, tuvimos que cortar los bajos para que no se polenize lo demas.. Producto final increíble! Terpenos a auténtico Gelato dulce y cremoso con toques Gassy que la hace casi perfecta en mi paladar! Planta pequeña con pocas ramas y cosecha poca-media de calidad top!

Week is looking good so far. Kaya's Coffee is a taller plant with less leaves than other strains. Where it lacks in leaves it adds in height. I have been removing damaged leaves from light burn slowly but surly. day 13 have leaves getting yellow on the ends... Adjusted my PH down from 6.0 to 5.5. I was keeping the PH high for the plants to take up more Cal-Mag. So I'm thinking the PH is keeping them from taking up Nitrogen causing the plant to take it from other leaves.

Eccoci qui... Non ho più parole per giudicare questa meraviglia!!! Strain 1 è la migliore varietà che io abbia mai coltivato, nel processo di maturazione delle cime ho visto qualcosa di assurdo in quanto questa piccola ha una maturazione totalmente diversa rispetto a tutte le altre erbe!!! Sono davvero soddisfatto, peccato che Strain 2 sia cresciuta storta, ma poco importa anche essa ha cime che sono dure come sassi, e sono solo 4 settimane di’ fioritura, NE VEDREMO DELLE BELLE!!! Grazie a @KhalifaGenetics e @xpertnutrients per la collab e a tutti per il supporto🔥🌲❤️

Week 4 done and in the books. I tried to limit growth of the side shoots during the week by pinching & crushing the stems. I will monitor the effect this has. Last week with her as main focus as there are some photo seeds growing alongside. I will veg them at 20h light hoping this blackberry is done before I have to flip those girls to flower. If this blackberry has to do a week or two on 12/12 so be it I'm afraid.

They just get recover so fast and build new leafs

Pretty normal week, lots of flushing and smell definitely increased Managed to control temps a little better

Buds are really coming on now. Stretch is slowing. Very happy with the new lights and fan. Not sure I'll do scrog next time as its hard to keep up with all the grow and pruning/defoliation required. Adjusted my lights to get everyone even coverage. Light meter would be nice at some point!

Esta semana todo tranquilo, en un par de días más haré poda de bajos y defoliación . También se colocaran tutores de vara a cada planta

La canopée est couverte a 90%

Day 78 - pheno 1 was cut down, id normally hang dry the whole plant but decided to do it in branches instead. Second pheno has been left in darkness as i haven't had the time to cut. Pheno one is hung up and drying.. Room Humidity 60/60. As soon as she's dry enough I'll finish trimming her up. Then put them into jars. Might use boveda 60% packs but I'll see. Smells strong! Will post a harvest when both plants have been dried fully an in jars. Hope you enjoy the videos and pictures. Stay tuned.

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.

Plant 1: 2.40 Oz dry (chopped day 84) Plant 2: 4.85 Oz dry (chopped day 88) Happy with them so far. Will update post cure and smoke report.

***** Week 12 growth - February 20 to 26, 2021 - Week 3 Flower ***** This girl has been happy all week and praying hard.....she’s just a shorter girl😂 However, she had a god growth week and her top cola is reaching up tall and proud! Another sign that she just needed more Veg time for consistency across the canopy is all. She was fed some fulvic acid on Monday to encourage stretch through Gold Storm at 5ml/L🤞 Her tricombs have come on strong as well at the end of the week. Her buds are not that large yet but she seems to feel to almost be 5 or 7 days behind the other girls??? She was stripped of a number of leaves, a couple of lower branches and bud sites this week. She has some good internode spacing and it’s allowing some more light down lower. Thinking she is going to be more of nugs rather than colas? Here leaves are up hard so hard that the increase in light intensity at the end of the week will only benefit this girl given her distance from the light. Light is at 20” and pulling 480 watts at the end of the week. Stated off with 400 watts at the start of the week but keep pushing it up this week. I don’t want to break 1,000 to 1,100 PAR by very much as I am not supplementing with true CO2. I have an Exhale bag to raise it a couple hundred ppm. Feel the need to keep the intensity high for penetration lower in the canopy. Will lower the amount of time in daylight if stress gets too high. Push to 11/13???? Nutrients are following IPP HOG 3 Part pretty closely. Just playing with macro nutrient ratios but otherwise supplements are at full week dosages following week 3. Have been seeing great resin production last runs so staying with Rezin as part of their feed schedule in flower. Terpinator......I think I see a lot of sulfer benefit here so it stays in the grows as well. Recharge seems to be working out well but we did the change mid grow from Microbial Mass. Since in coco have to feed the microbes so they reproduce and really dig Nature’s Candy with Remos additives in there👍 To help keep the root zone clean we add Enzymes😃 I have been debating a lot lately about the addition of CalMag to these nutrient lines and it’s necessity but since in coco I keep adding some......noticed a couple of spots on MM2 so have added it back in a bit more this week. Little more detail....... Feb 20/21 - Day 15 - Full feed today.....it’s been five days. - tap water with Silica @ 1.5ml, IPP line at full strength. - 1400ppm and 6.1pH - This girl was given some fulvic acid in Gold Storm. Help with giving her a chance to reach higher. - 5ml/L added to feed for 1490ppm and 6.1pH - help her grow taller. Feb 21/21 - Day16 - Dry out day Feb 22/21 - Day 17 - watering with supplements and light feed today. We are in mid flower now.....need to keep the macro nutrients up. - Epsom salts @ 1 Tbsp in 20L. Purple on stems is getting prominent......could be cold temps but also giving magnesium. - Terpinator @ 3ml, Rezin @ 1.5ml, Nature’s Candy @ 1ml, grow @ 1ml, micro @ 2ml, bloom @ 2.5ml, Recharge @ 1 Tbsp in 20L. - 1400ppm and 6.0pH. - 4L Feb 23/21 - Day 18 - keeping up the silica this watering - silica @ 1ml, CalMag @ 1ml, Ultimate B+ @ 1ml - 600ppm and 6.0pH - 3L Little to no runoff this watering. Feb 24/21 - Day 19 - full feed again today.....girls are big and growing hard......keep it going💪 - IPP line as listed for full line. - Terpinator @ 3ml, Rezin @ 1.5ml - 1425ppm and 6.0pH - they are taking the high ppm feeding well. Feb 25/21 - Day 20 - Had some feed water left from yesterday. Added plain tap water to get 20L. - 810ppm and 6.1pH - 1.5L......don’t want to over saturate the medium. Feb 26/21 - Day 21 - Nothing today. - Will feed early tomorrow as it’s Saturday. - Let the root zone get some oxygen is my thought and water to nice runoff first thing in morning. Week 3 behind us and going into 4.....middle of flower and girls are feeding hard. Pushing the lights hard now as well so need to keep the ppm up👍 Looking good ETS....she has reached up there and doing very well😎

May 02 Entering preflower, I think I don't have much training time ahead but I'm sure I'll be able to get her even and clean. Some small branches are trying to pop out under the already 6-7 ones but I just can't get light on there, we'll see later on if I harvest in sequence! This won't be the most successful grow but it will have been a realllllyyy instructive one. Next one if there is soon will most likely give better result. So far, without being too harsh, I think she's doing great still. Might not be in the most perfect healthy state but it's not a big deal in the sense that she's still pretty happy right now and that's fine with me. From start she has been on 24 hour non stop and I don't see any problem with it. In any case you are sure to not halt her growth by doing so and each one of these led should consume about 6 watts. On 8 we get to a grand total of 48 watts which is very fine. Current light setup might have been upgraded to a potential increase in yield of 25 to 35 % I'd guess. But for the price I paid for all of this, it's very much worth it. Doubling the light setup would raise me to a 100 watts, and light coverage would be sufficient to grow 4 autoflower. Since I only have one plant I'm keeping it on the not too expensive side without sacrificing too much, but a third setup of 4 led with 2 reptile UV led would probably increase significantly the final quality and quantity. In any case, even tho I can say it has pained me to train her since she's so small and bushy, I would probably keep this strain around for sentimental reason, I really see value in life itself and this plant is part of mine, eheh. Good night guys. May 03 I think I can notice 4 pistils growing out of the main head. Magnification from camera. It took me another hour or so to train her but I think it's worth it. I'm at about 9 new heads that are getting a good amount of light, I don't know what will happen to the other smaller ones under these 9s, we'll see if they have time to produce anything ^^. Funny expectation, if the branch don't stretch a good inch from today to 4-5 days in the future, this is gonna be chaotic there xD. Aye aye, I'll be away from pretty girl for roughly 2 day. I gave her about 350 ML of water 2 days ago. Since she has shown minor sign of problems relating to soil ph, I gave her 1 part decarbonated Perrier with about 2.7 part neutral water. Perrier is made from source water which contain macro-nutrient essential to plants. It's PH is also officially cotted at 5.5. There is debates on whether or not carbonated Perrier would be beneficial to a plant, but here I choosed to play narrower. I'm still spraying her with water once in a while. I am progressively lowering the frequency since she is approaching flowering and I don't want the humidity level to raises to much, for any question just message me. Aight, guud night. May 05 Just came back, she need water, it's obvious to me since I know her grow rate which has been slower the past 2 day it seems, pot feel lighter and soil dry ^^. I'm a little bit sick and I just came back so I'll relax a bit and take care of her later tonight. I'll try giving her 600 ml of water this time, she's getting bigger and with flowering approaching I think it's time to look for a increase. Fan leafs did increase in volume from the newly trained branch, but it feel like she has been going at 75% of her speed, but it might also be her entering flowering phase so slowing her vegetative growth, I'll post more picture after training of her later tonight, good night ;) May 07 I have read somewhere that cannabis plant often go for a good stretch before the flowering really kick in and I think that's what she's heading for. I am quite satisfied with the current evenest of each tops, I am expecting the main branch to grow higher even tho she's pretty much equal for now. I think it's normal and as long as possible I'll pull her down from the need of light coverage but everything should be fine, I don't think there will be any problem with the light. I am really looking forward to see how high she will stretch. Ideally, I don't want her to grow too big, but I am very interested in the idea of her being full of tops. The bigger the branch, the better nutrient are delivered and if light is managed correctly, you'll end up with a bigger harvest, bigger colas. So far I gave her nutrient 1 time, she got nitrogen toxicity because the soil is in fact rich enough for pretty much the whole grow, when I bought my fertilizer I thought about the fact that autoflower grow pretty much all in one at the same time but with that soil, I should have gone for something more on the P and K side. I am considering buying a new small amount of fertilizer for cheap, that is better adapted to my need. I do have little worries about micro nutrients but I do believe I am stressing a bit for nothing. In worst case I'll just answer to her need which is totally fine. Have a nice day !

Hello to all you growers!!😁 its fist week of blooming my plants.girls strech very nice.the space is full..im soo exited to see buds in the future.watering every second day .the girls are very thirsty🙂

Day 35 is first Day with 12-12 ger. I get the lights at 60 cm above top of plants with 700 ppfd. About 50% and sprayt them with Neem oil. Placed ScroG net Day 36 lights at 828 PPFD Day 37 lights at 884 PPFD Day 38 lights at 890 PPFD, Distance 66cm Day 39 lights at 890 PPFD Day 40 lights at 890 PPFD One of my females is al little bit smaller. I tryd too feed her with some Alga Grow too see if she becomes more happy. I hope so.

had a lot of issues with my ph and overfeeding so i flushed her the last 2 weeks , overall im happy with the results. Not my best yield but it'll keep improving. She smells great citrus and lemon sense! 🙂