Start of Week 9 🙌 I plan to use fertilizer for bud growth from day 64 to day 70+... depending on when the harvest time occurs 😉😄👍 Started working with fertilizer today, every 2 days a mixture of 10ml per liter as long as the buds have not properly developed trichomes 😵 I hope this works 😵😲😱 Day 68 with fertilizer again

They are growing nicely, i forgot to upload for some time and now they are finally fully flowering, i pretty much fertilze them with everything.

Loving the tight bud structure on this plus size gurl.. she greasy, drinkin like a fish and F U N K Y fuely ppfd ranging 800-1100 check and adjust every few days.

2 more weeks a d she should be ready to harvest

The buds are getting fat and now all cover in crystals

She receive the final part this week and nest week she will be flushed and harvested

The buds are getting heavier and the stems want to bend. Two more weeks and she will be ready for harvest

As to the number 144 it totals nine. Nine is the end of all numerical integers. No higher number is available. Out of the One(1) come all other numerical values, which show by the four elemental qualities(4), the dual polarity(44), in this case, as matter and antimatter - the visible revealing the invisible. the physical polarity of the metaphysical. The mind grows from observing failed attempts, The body grows from observing failed attempts, One set, fail. Note: As gibberellic acid is not soluble in water you need to dissolve in alcohol. 75% Ethanol or rubbing alcohol can be used. Dispense 100 mg of Gibberellic Acid 3 into a 250 mL container. Create a solution by mixing 90 ml of distilled water with 10 ml of ethanol (Ethyl Alcohol). Introduce 100 ml of the water-ethanol mix and agitate until complete dissolution, achieving a final concentration of 1 mg/ml (1000 ppm). Tailor the concentration of GA3 to your experiment, varying from 0.1 mg/ml to 1 mg/ml based on specific requirements. Gibberellic acid + Diethyl aminoethyl hexanoate 10% SG Gibberellic acid A4, A7 + 6-benzylamino-purine p.6% EC Gibberellic acid + Paclobutrazol 3.2% WP Gibberellic acid + Forchlorfenuron 0.3% SL Gibberellic acid + Brassinolide 0.4% SL Nutrients for the week are recipe foliar application. The boombox (containing a 3 KHz signal and nature sounds) is played at high volume with high treble and medium bass for 10 minutes before spraying the plants. The plants are then sprayed while its playing and the sound is continued for another 20 minutes after spraying. Both sides of the leaves should be saturated. Treatment is best performed early in the morning/daylight, preferably in foggy 65%rh+ dew. On cold mornings, spraying should be delayed until late afternoon if outdoors. Do not spray plants when the temperature falls below 50o F. The formula also can be administered in the regular weather supply, by drip-feeding, hydroponics, etc.. The nutrient solution should be applied once somewhere in first 4 weeks, then twice weekly thereafter. The sound ought to be played daily for at least 30 minutes during daylight hours no more than 3 hours. https://biologydictionary.net/gibberellin/ Often through our various senses, we receive impressions that bring the pleasure of nature's harmony into our thoughts. At other times we are aware that man has intervened in nature's processes to produce something by art, which to our highly evolved senses seems to rival even the best nature can display of beauty and harmony. We become aware at such times of man's wonderful ability to bring seemingly unrelated elements into harmonic balance, and receive a glimpse into a world where everything exists in conscious sympathetic attunement to everything else. When we listen to a piece of music that seems to strike a beautiful chord somewhere inside us, or view a painting that simply glows with harmonic awareness well executed, we probably do not spare much time to contemplate the wonderfully intricate combination of vibrations that our sensors make it possible for us to perceive. We tend to appreciate the relationship between the parts of something, by an awareness of the harmony or dissonance of the whole. This ability enables us to say "what a beautiful house!" instead of "analysis has proven that this collection of building materials exhibits certain elements of harmonic proportion." While this ability to instinctively appreciate the beauty of true harmony has an important role to play in evolution, a more analytical understanding of the laws involved can be most useful. This is especially so if we wish to create works of art where each part exists in true harmony, not only with the other part of that particular whole, but with the universe within which the creator and the created exist. Everything vibrates. From the most dense matter to the most subtle cosmic rays, everything which our senses allow our thoughts to become aware of, can be specified in terms of wavelength or frequency of vibration. These two terms define the same thing, but from different points of view. (See Illustration 1) The following are the approximate wavelengths of various energy carriers: Cosmic rays 0.000,000,001 mm Gamma rays 0.000,000,1 mm X rays 0.000,500 mm Ultraviolet rays 0.003 mm Visible light 0.006 mm Infrared 0.01 mm Sound waves 1 meter Radio waves 300 meters Violet light 400 nm to 450 nm Blue light 450 nm to 500 nm Green light 500 nm to 570 nm Yellow light 570 nm to 590 nm Orange light 590 nm to 610 nm Red light 610 to 700 nm 1 nanometer (nm) = 0.000,000,1 cm = 1/10,000,000 cm If a guitar string is plucked and we hear a sound, it is not too difficult for the human mind to associate this sound with the vibration of the guitar string. With color it is quite different. It is difficult for us to conceive that the color of a substance is not an inherent property of the substance itself, but an indication picked up by our senses of that substance's ability to absorb or reflect the light which happens to be shining on it at that moment. Neither the matter nor the light is colored. What happens is that the brain learns to differentiate between the frequencies reflected or transmitted by the substance the eyes are focused on. The same thing happens with sound. When we say "Oh! Listen, they're playing my favorite song," what we really mean is: "My brain has stored within it a particular pattern of frequencies. I have compared the new information being received with this stored pattern and have deduced the answer that the two patterns are similar within certain specified tolerances." The 'pleasure' involved could have something to do with our running the pre-recorded pattern at the same time, in 'sympathy' with the new pattern as it is received. The word sympathy describes very well our ability to appreciate color and sound. It also describes the reason behind certain elements of harmony. For instance, if a substance vibrating at 100 cycles per second (tone 1) is in the proximity of another substance vibrating at 200 cycles per second (tone 2), we could perceive, if we had the right equipment, a certain sympathetic relationship between the two. If our equipment was a wave form plotter, we may have a drawing like illustration 2. Illust 2 We will see from this that there is a uniform doubling of the first tone seen in the second. At various points along the waves, the two are the same in amplitude. At other points, they are at opposite poles to each other. This doubled frequency has more points of similarity to the original than any other frequency except the original itself. If the equipment we had available for measuring these two frequencies was a soundboard amplifier and a pair of ears, then we would hear what would sound to us like one tone. If we had the opportunity to hear one at a time, we would hear that although they sound the same, one is higher in pitch than the other. This characteristic of 'the same but different in pitch', musicians have called the octave. Any two tones produced where one has exactly doubled the frequency of the other is called an octave. Speaking in ratios, an octave would appear then as the ratio 2:1 or 1:2, depending on whether we are talking of an octave up or down. A single note produced by almost any instrument will contain more than one wavelength or frequency. It will have a dominant frequency, the wavelength of which we would call the note's 'fundamental' or 1st harmonic. It will also have a varying number of upper harmonics, gradually fading in intensity into infinity or silence. Natural harmonics always have the same pattern of intervals between them. The interval between the 1st and 2nd harmonic is a perfect octave; between the 2nd and 3rd a perfect fifth; between the 3rd and 4th a perfect 4th; and so on, the intervals becoming smaller and smaller until they lose any relationship with the western 12 tone scale as it exists at the moment. Just as an octave has certain elements of sympathy with its fundamental, so some intervals have been noted to be more perfectly in sympathy with the fundamental than others. The ratio of the 'perfect 5th' or interval of 7 semitones, as it occurs in the harmonic series, is 3:2 or 2:3, while that of the 'perfect fourth" is 4:3 or 3:4. All the tones in the western 12 tone scale can be expressed in terms of the ratio between the upper tone and its fundamental. This would seem to be an ideal way of generating a scale from any given fundamental and several attempts have been made to do this, the Pythagorean system being probably the most well known. Although when working with a single tone instrument playing on its own, the Pythagorean formula works wonderfully well, if we had several instruments tuned this way together and asked them to play almost any western music, we would find that at times they sounded quite out of tune to each other. The lack of flexibility of the various scale systems based on the harmonic series has led to what is known as the 'tempered' scale. This uses as its primary unit of interval the ratio of the octave or 2:1. It then proceeds to divide the interval between any fundamental and its upper octave into 12 smaller intervals by applying the ratio: two to the one-twelfth power, to one (21/12:1). This equals 1.059463094, so by multiplying any frequency by this number, we will obtain the tempered semitone next up from our fundamental. We will also find that any tone twelve semitones up from any other tone, in a scale generated in this way, will have exactly double the frequency. If we took the note middle C on a piano and halved the wavelength, we would have the note C one octave above. If we halved this, we would have the C above, and so on. However, within about 6 octaves, we would find that although a 'sound' was being produced, no human ear could perceive it. If we kept on going, halving and producing upper octaves of our fundamental C, we would proceed through the infrared band, into the visible light spectrum. If we happened to be outside during the day, we would, for one octave only, see the note C with our eyes. The next octave above would already be in the ultraviolet band, and outside the eye's sensitivity range. If we can think of color as being an indication of a substance's vibratory rate or wavelength, we may begin to see a relationship that could exist between the color and sound spectrums. The logical extension of what has so far been said is that there exists a scale in the color spectrum that coresponds exactly to the scale in the sound spectrum, each color tone being an octave of the equivalent note in the sound range. This is not the end of the story but only the beginning. If we can for the moment accept that any wavelength in one band has upper and lower octave stretching out to infinity, then tne next question is 'fine, but what shall we use as our fundamental? A particular color? A particular sound frequency?' The musicians among us will probably say 'A 440'. This means that the note A should vibrate at 440 Hertz, or 440 times per second. They would tell us that this is standard pitch has been adopted by most orchestras around the world; pianos are tuned to it, instruments are constructed to formulas based on it, and so to them it would probably seem the most appropriate place to begin. Some of these musicians may know of the battle that is still raging with regards to this being the standard, but few would know why A = 440 Hz was chosen except that it werned when it was set to be a suitable compromise between the many different pitches in use at the time. There is also a scientific standard of pitch of C= 512 Hz which, although not in common use in nusic, has a lot of theoretical followers, as it is generated from the lower octave of C = 1 cycle per second and has certain advantages of numerical simplicity in mathematical research. A scale built upon either of these standards will yield an upper octave scale in the color spectrum. However, with the A = 440 Hz scale, we end up with a color series which, although interesting, is hard to relate to any color system or set of values in current use. The C = 512 Hz system, on the other hand, seems a more obvious choice at first sight, having 12 definite color tones and containing the strongest and most pure colors in the spectrum. Further research showed that there were still things not quite right with this system, and has led to a modified version in which correspondences with other systems seemed to fit into place. Of course the proof of the pudding is in the eating and before being accepted this system will need further research to substantiate the correspondences and prove its value to mankind. What follows is a summary of the process used in drawing up this modified scale. The upper octave color of a fundamental of one cycle per second is found to be exactly emerald green, which is recognized as having a wavelength of 511 nanometers (this is at 20o in air). 511 nm is also the color of malachite, or hydrous carbonate of copper occurring as a mineral. It would seem reasonable, given the teachings in the QBL, to associate this with the planet Venus. If we take 1 Hz or its upper octave 512 Hz as our fundamental, then build a scale upon it using our tempered scale 'formula', we will have the following 12 color tones: 723 nm = infrared 682 nm = deep red 644 nm = orange red 608 nm = orange 574 nm = yellow 541 nm = yellow green 511 nm = emerald green 482 rim = green blue 455 nm = royal blue 430 nm = indigo 406 nm = violet 383 nm = ultraviolet There are certain immediate correspondences that become apparent between some of these colors and our teachings in Parachemistry. The yellow here is the color of chromate lead and zinc yellow, the most 'yellow yellow', for want of a better description, to be found in the spectrum. It seems rather logical, if we follow the Queen scale of color, to call this the Sun, or Vulcan, depending on which system we choose to look at. The orange here is exactly the frequency of sulphide of mercury or cinnabar. It would seem appropriate to relate this to the planet Mercury on the tree of life. If we then call the deepest red in our scale Mars and the Royal Blue Jupiter we find a pattern beginning to form. The ultraviolet here is outside our range of color vision and would appear black to us. If we call this Saturn, as Saturn is described as either black or violet, then we have six tones out of the twelve named. There is in natural things a certain truth which cannot be seen with the outward eye, but is perceived by the mind alone. The philosophers have known it, and they have found that its power is so great as to work miracles. This miracle, we suggest, is at work in the observation of a rose in your garden. This miracle is at work in the observation of a friend in your heart as well as your eyes. The mysterium coniunctionis of the alchemists, that mysterious marriage of the Sun and the Moon, is a conjunction of the most extraordinary scope, because it is a conjunction of physical fact with metaphysical reality. This unique vision is not the result of a tersely factual pouring of acetic acid onto calcined stibium. nor is it the result of a mere figurative allusion that one given substance is the Sun and another, the Moon. Just as with physical facts, the quality of the ingredients has an important influence on the result, so in mental terms, the quality of the thought put into the work has a bearing on its ultimate success or failure. In this truth lies the whole art of freeing the spirit from its fetters, in the same way that, as we have said, the mind can be freed from the body. This last phrase-"the mind can be freed from the body"-is, as we see it, a direct reference to the meditative technique of the alchemist. But perhaps our word "technique" is not quite the correct one, for it seems to imply a formula of sorts, a preconceived set of ideas, whereas in truth, spontaneity is of the essence in meditation as it is in alchemy. Meditation is, after all, a kind of fishing into the subconscious for the wellspring of a truth. The conscious mind, selecting its subject or question (the 'bait') dips like a fishhook into the water. But the bait does not seek the fish. The fish seeks the bait. And this is one of the most commonly misunderstood principles in all of metaphysics. We do not meditate. We are 'meditated.' To achieve this, we must be receptive. Who among us is receptive? Even in the privacy of our laboratory, don't we often tend to adjust flasks, measure substances, think in the jargon of the alchemical work as though we were really performing it? After all, 'I have studied for years; I have read the texts. I direct the course of this work.' Only God directs the work. And not one among us has access to the wellsprings of that wisdom unless we are receptive. That is why alchemy is an art as well as a science. It is not only the art of directing the work as we understand it after being instructed by a book or a teacher. it is also the art of receiving the work, i.e., being receptive to it in our hearts, and letting the work refine us, even as we refine our work. That is the confluence of two worlds that the true alchemist experiences. We can, and must, strive for that through years of intellectual, physical and emotional effort, but in the end, we do not make it happen-we let it happen. And only through meditation is this "letting go possible. Thou wilt never make the One which thou seekest, except first there be made one thing of thyself. This "one thing" is the one-pointed concentration and subsequent meditation of the devoted student. It involves and utilizes every level of his being. It brings those levels to a pitch of alertness previously unknown, and then, once attained, it lets go of them. The technique is familiar to readers acquainted with Zen, with Yoga, with Taoism, and with many other religious disciplines. But it has not been consciously identified with alchemy for the simple reason that alchemy is so widely misunderstood or even ignored, its terminology and methods being so notoriously obscure and complex. Martin Ruland's Lexicon of Alchemy defines meditatio as follows: The word MEDITATIO is used when a man has an inner dialogue with someone unseen. It may be with God, when He is invoked, or with himself, or with his good angel. Clearly, then, the meditative aspect of the alchemical work is not merely cogitation, or simply sitting down and thinking about the work. To be sure, preliminary organization of the theory of a given procedure is essential; master the theory before the praxis. But meditation goes deeper than this, and involves a much more complex process. The point to be emphasized is that meditation is an inner dialogue. We must select our terms for it with care, in attempting to describe it. The occultist will see it as a profound revelation from the Higher Self. the ceremonial magician, as the Knowledge and Conversation of the Holy Guardian Angel. the religionist as a form of prayer; the skeptic as an hypnotic trance; and the psychologist as a means of coming to terms with the contents of the unconscious. ' Little wonder that the alchemist is said to begin his work with a massa confusa! Both in his mind and in his physIcal labors, he must sort out of the primal chaos a goodly order. If his thoughts are not in order, his substances will not be properly handled. And even at best, if both are in order, he must have the courage to dive deeper into his inner resources to understand the relationship between his own soul and that "soul" of matter with which he works. He can still expect to be attacked on the one hand by skeptical occultists for being too "literal" in using laboratory methods; and on the other by scientifically learned friends for being a religious sentimentalist over a few flasks and retorts. So the alchemist, even today, has his own razor's edge to walk. But the challenge of the work goes beyond trite dismissals and defies the easy categories of those who try to explain it away. The man or woman who enters it with a prayerful and meditative heart can only benefit by its pursuit. Not one writer in this century or in those past can tell us the path is an easy one. Yet as Michael Maler has said: There is in our chemistry a certain noble substance over whose beginning, affliction rules with vinegar, but over whose end, joy rules with mirth. Finally, we draw from the wisdom of Morienus in instructing Khalid: This thing for which you have sought so long is not to be acquired or accomplished by force or passion. It is only to be won by patience and humility and by a determined and most perfect love. For God bestows this divine and immaculate science on his faithful servants, namely those on whom he resolved to bestow it from the original nature of things.... Nor were they able to hold anything back save through the strength granted to them by God, and they themselves could no longer direct their minds save toward the goal appointed for them by God. For God charges those of his servants whom he has purposely chosen that they seek this divine science which is hidden from men, and that they keep it to themselves. This is the science that draws its master away from the suffering of this world and leads to the knowledge of future good. The following short poem was dated December, 1633, and signed only with the initials W.B. It later appeared (in 1651) in a collection of alchemical works compiled by Elias Ashmole titled THEATRUM CHEMICUM BRITANNICUM, Still considered one of the finest collections of alchemical works in English. This short poem exemplifies the efforts of early writers not only to summarize their work but to meditate on it-a point dealt with in another article in this issue-and to direct the reader to meditate as well on the alchemical message implicit in the ancient myths. The fifth stanza urges the student to a careful consideration of the myths of Cadmus and Jason, advice both given and followed three hundred years later by Fulcanelli in his famous work, LE MYSTERE DES CATHEDRALES. We have modernized the poet's spelling. -Editor Through want of skill and reason's light Men stumble at noon day; Whilst busily our Stone they seek, That lieth in the way. Who thus do seek they know not what Is it likely they should find? Or hit the mark whereat they aim Better than can the blind? No, Hermes' sons for Wisdom ask, Your footsteps she'll direct: She'll Nature's way and secret cave And Tree of Life detect. Son and Moon in Hermes' vessel Learn how the colors show; The nature of the elements, And how the daisies grow. Great Python how Apollo slew, Cadmus his hollow oak: His new raised army, and Jason how The fiery steers did yoke. The eagle which aloft doth fly See that thou bring to ground, And give unto the snake some wings, Which in the earth is found. Then in one room sure bind them both, To fight till they be dead, And that a Prince of Kingdoms three Of both them shall be bred. Which from the cradle to his crown Is fed with his own blood; And though to some it seems strange, He hath no other food. Into his virgin mother's womb Again he enter must; So shall the King by his new birth, Be ten times stronger just. And able is his foes to foil, The dead he will revive: Oh, happy man that understands This medicine to achieve!

After my 2 month coma stone we are back at it. New digs too. The ancient tradition of Sacred Geometry is still alive and well in the person of Frank Chester. He has discovered a new geometric form that unites the five Platonic solids and provides some startling indications about the form and function of the human heart. This new form, called the Chestahedron, was discovered in 2000, and is a seven-sided polyhedron with surfaces of equal area. Frank has been exploring the form and its significance for over a decade, His work has potential implications across a number of areas, from physiology to architecture, sculpture, geology, and beyond. Organic cotton stands out with a frequency of 100, mirroring the human body's frequency. *burp* It's all bout the salt Water is stirred counterclockwise while being oxygenated. Plants need 17 elements for normal growth. Three of them--carbon, hydrogen, and oxygen--are found in air and water. The rest are found in the soil. Six soil elements are called macronutrients because they are used in relatively large amounts by plants. They are nitrogen, potassium, magnesium, calcium, phosphorus, and sulfur. Eight other soil elements are used in much smaller amounts and are called micronutrients or trace elements. They are iron, zinc, molybdenum, manganese, boron, copper, cobalt, and chlorine. They make up less than 1% of the total but are nonetheless vital. Most of the nutrients a plant needs are dissolved in water and then absorbed by its roots. In fact, 98 percent are absorbed from the soil-water solution, and only about 2 percent are actually extracted from soil particles. on that note, some points of interest regarding Boron. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073895/ Boron (B) is an essential trace element required for the physiological functioning of higher plants. B deficiency is considered as a nutritional disorder that adversely affects the metabolism and growth of plants. B is involved in the structural and functional integrity of the cell wall and membranes, ion fluxes (H+, K+, PO43−, Rb+, Ca2+) across the membranes, cell division and elongation, nitrogen and carbohydrate metabolism, sugar transport, cytoskeletal proteins, and plasmalemma-bound enzymes, nucleic acid, indoleacetic acid, polyamines, ascorbic acid, and phenol metabolism and transport. This review critically examines the functions of B in plants, deficiency symptoms, and the mechanism of B uptake and transport under limited B conditions. B deficiency can be mitigated by inorganic fertilizer supplementation, but the deleterious impact of frequent fertilizer application disrupts soil fertility and creates environmental pollution. Considering this, we have summarized the available information regarding alternative approaches, such as root structural modification, grafting, application of biostimulators (mycorrhizal fungi (MF) and rhizobacteria), and nanotechnology, that can be effectively utilized for B acquisition, leading to resource conservation. Additionally, we have discussed several new aspects, such as the combination of grafting or MF with nanotechnology, combined inoculation of arbuscular MF and rhizobacteria, melatonin application, and the use of natural and synthetic chelators, that possibly play a role in B uptake and translocation under B stress conditions. Apart from the data obtained from agricultural reports that prove the involvement of B in plant growth and development, B often results in deficiency or toxicity because it is a unique micronutrient for which the threshold levels of deficiency and toxicity are very narrow [12]. B deficiency and excess are both widespread agricultural problems for higher plants in arid and semi-arid conditions. B deficiency was primarily observed in apples growing in Australia in the 1930s and subsequently reported in more than 132 field crops grown in sandy soils with low pH and organic matter from 80 different countries [28]. Depending on the age and species, plants manifest a wide range of deficiency symptoms, including stunted root growth, restricted apical meristem growth, brittle leaves, reduced chlorophyll content and photosynthetic activity, disruption in ion transport, increased phenolic and lignin contents, and reduced crop yield [1,8,20]. The prevalence of symptoms depends on the severity of the B-deficiency condition because plants show uniform deficiency symptoms on entire leaves but sometimes in the form of isolated patches. Given the immobile nature of B, it usually accumulates in mature leaves, whereas young leaves do not receive sufficient B for proper growth. Thus, the deficiency symptoms first appear on young leaves, including thick, curled, and brittle leaves with reduced leaf expansion; corky veins; interveinal chlorosis; yellow water-soaked spots on lamina; and a short internodal distance, resulting in a bushy plant appearance [14,29,30]. In severe cases, leaf apex necrosis and leaf dieback occur [12]. The expansion of stems and petioles leads to hollow stem disorder in broccoli and stem crack symptoms in celery [1]. However, in tomato, cauliflower, apple, and citrus, scaly surface development with internal and external corking of fruits is a typical feature associated with B deficiency [13,28]. Amino acids improve plant nutrition by affecting soil microbial activity through the production of a beneficial microbial community and nutrient mineralization in the soil solution, thus enhancing micronutrient mobility [84]. Seaweed extract contains several ions, growth regulators, carbohydrates, proteins, vitamins, and polyuronides, including alginates and fucoidans. These polyuronides can form highly cross-linked polymers and condition the soil, thereby improving the water retention and ion uptake capacity within the soil [89]. Kahydrin, a commercial seaweed component, acidifies the rhizosphere by altering the plasma membrane proton pump and secretes H+ ions that change the soil redox condition and make the metal ions available to plants, leading to improved crop production [90]. Turan and Kose [91] applied three seaweed extracts, including Maxicrop, Algipower, and Proton, on grapevine (Vitis vinifera L. cv. Karaerik) to check the ion uptake efficacy under optimal and deficient ion availability. Maximum micronutrient uptake under optimal conditions were observed with no significant difference among the three kinds of extracts. The alteration in uptake of one ion influences the availability of another ion [85], supporting the idea of B uptake through biostimulator application, but this requires further investigation. The application of biofertilizers opens new routes of ion acquisition by increasing nutrient use efficiency in plants. In this regard, mycorrhizal and non-mycorrhizal fungi, endosymbiotic bacteria, and plant-growth-promoting rhizobacteria are important because of their dual function as microbial biostimulants and biocontrol agents. We explain the functions of these biostimulators and their possible relationship with ion acquisition in plants. Indeed, grafting and AMF inoculation improve plant physiological and nutritional aspects and a number of studies have proved their pivotal role in B uptake [74,75,79,105]. Additionally, nanotechnology is an emerging technique to solve plant-nutrition-related problems. The combination of these techniques may improve B uptake. For instance, a combination of grafting and Cu NPs improved growth and development of watermelon by increasing ion uptake [129]. Melatonin application improves plant performance by inducing resistance against stress conditions. According to a report, melatonin application reversed the toxic effect of B by moderating B accumulation in leaf and fruit, increasing photosynthetic activity, and improving dry weight that ultimately enhanced plant growth of Capsicum annuum [138]. Similarly, in watermelon, melatonin application enhanced the N concentration in roots by improving root elongation, root diameter, and root surface area under limited N availability [61]. However, no evidence for B uptake under deficient conditions has been found yet, and that requires further investigation. https://pubmed.ncbi.nlm.nih.gov/8508192/ https://pubmed.ncbi.nlm.nih.gov/34988929/

Es ist super heiß Sommer 2024. Nachtphase ist Tags und umgekehrt. Ich benutze eine Klimaanlagen.

🤤

Start of Week 9 🙌 I plan to use fertilizer for bud growth from day 64 to day 70+... depending on when the harvest time occurs 😉😄👍 Started working with fertilizer today, every 2 days a mixture of 10ml per liter as long as the buds have not properly developed trichomes 😵 I hope this works 😵😲😱 Day 68 with fertilizer again

This week, I had to cut three leaves—two smaller ones that looked like some kind of insect had laid eggs on them, and one of the big sun leaves. Finally, I can see some brown trichomes on the B-grade buds. I thought about harvesting soon, but it will probably take another two weeks or so... Or I may have to harvest her week by week. I haven't decided yet. What I can say is that increasing the amount of fertilizer has helped improve the health of the leaves. I should have increased it sooner; it seems that autos need more nutrients earlier than photoperiod plants.

After my 2 month coma stone we are back at it. New digs too. The ancient tradition of Sacred Geometry is still alive and well in the person of Frank Chester. He has discovered a new geometric form that unites the five Platonic solids and provides some startling indications about the form and function of the human heart. This new form, called the Chestahedron, was discovered in 2000, and is a seven-sided polyhedron with surfaces of equal area. Frank has been exploring the form and its significance for over a decade, His work has potential implications across a number of areas, from physiology to architecture, sculpture, geology, and beyond. Organic cotton stands out with a frequency of 100, mirroring the human body's frequency. *burp* It's all bout the salt Water is stirred counterclockwise while being oxygenated. Plants need 17 elements for normal growth. Three of them--carbon, hydrogen, and oxygen--are found in air and water. The rest are found in the soil. Six soil elements are called macronutrients because they are used in relatively large amounts by plants. They are nitrogen, potassium, magnesium, calcium, phosphorus, and sulfur. Eight other soil elements are used in much smaller amounts and are called micronutrients or trace elements. They are iron, zinc, molybdenum, manganese, boron, copper, cobalt, and chlorine. They make up less than 1% of the total but are nonetheless vital. Most of the nutrients a plant needs are dissolved in water and then absorbed by its roots. In fact, 98 percent are absorbed from the soil-water solution, and only about 2 percent are actually extracted from soil particles. on that note, some points of interest regarding Boron. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073895/ Boron (B) is an essential trace element required for the physiological functioning of higher plants. B deficiency is considered as a nutritional disorder that adversely affects the metabolism and growth of plants. B is involved in the structural and functional integrity of the cell wall and membranes, ion fluxes (H+, K+, PO43−, Rb+, Ca2+) across the membranes, cell division and elongation, nitrogen and carbohydrate metabolism, sugar transport, cytoskeletal proteins, and plasmalemma-bound enzymes, nucleic acid, indoleacetic acid, polyamines, ascorbic acid, and phenol metabolism and transport. This review critically examines the functions of B in plants, deficiency symptoms, and the mechanism of B uptake and transport under limited B conditions. B deficiency can be mitigated by inorganic fertilizer supplementation, but the deleterious impact of frequent fertilizer application disrupts soil fertility and creates environmental pollution. Considering this, we have summarized the available information regarding alternative approaches, such as root structural modification, grafting, application of biostimulators (mycorrhizal fungi (MF) and rhizobacteria), and nanotechnology, that can be effectively utilized for B acquisition, leading to resource conservation. Additionally, we have discussed several new aspects, such as the combination of grafting or MF with nanotechnology, combined inoculation of arbuscular MF and rhizobacteria, melatonin application, and the use of natural and synthetic chelators, that possibly play a role in B uptake and translocation under B stress conditions. Apart from the data obtained from agricultural reports that prove the involvement of B in plant growth and development, B often results in deficiency or toxicity because it is a unique micronutrient for which the threshold levels of deficiency and toxicity are very narrow [12]. B deficiency and excess are both widespread agricultural problems for higher plants in arid and semi-arid conditions. B deficiency was primarily observed in apples growing in Australia in the 1930s and subsequently reported in more than 132 field crops grown in sandy soils with low pH and organic matter from 80 different countries [28]. Depending on the age and species, plants manifest a wide range of deficiency symptoms, including stunted root growth, restricted apical meristem growth, brittle leaves, reduced chlorophyll content and photosynthetic activity, disruption in ion transport, increased phenolic and lignin contents, and reduced crop yield [1,8,20]. The prevalence of symptoms depends on the severity of the B-deficiency condition because plants show uniform deficiency symptoms on entire leaves but sometimes in the form of isolated patches. Given the immobile nature of B, it usually accumulates in mature leaves, whereas young leaves do not receive sufficient B for proper growth. Thus, the deficiency symptoms first appear on young leaves, including thick, curled, and brittle leaves with reduced leaf expansion; corky veins; interveinal chlorosis; yellow water-soaked spots on lamina; and a short internodal distance, resulting in a bushy plant appearance [14,29,30]. In severe cases, leaf apex necrosis and leaf dieback occur [12]. The expansion of stems and petioles leads to hollow stem disorder in broccoli and stem crack symptoms in celery [1]. However, in tomato, cauliflower, apple, and citrus, scaly surface development with internal and external corking of fruits is a typical feature associated with B deficiency [13,28]. Amino acids improve plant nutrition by affecting soil microbial activity through the production of a beneficial microbial community and nutrient mineralization in the soil solution, thus enhancing micronutrient mobility [84]. Seaweed extract contains several ions, growth regulators, carbohydrates, proteins, vitamins, and polyuronides, including alginates and fucoidans. These polyuronides can form highly cross-linked polymers and condition the soil, thereby improving the water retention and ion uptake capacity within the soil [89]. Kahydrin, a commercial seaweed component, acidifies the rhizosphere by altering the plasma membrane proton pump and secretes H+ ions that change the soil redox condition and make the metal ions available to plants, leading to improved crop production [90]. Turan and Kose [91] applied three seaweed extracts, including Maxicrop, Algipower, and Proton, on grapevine (Vitis vinifera L. cv. Karaerik) to check the ion uptake efficacy under optimal and deficient ion availability. Maximum micronutrient uptake under optimal conditions were observed with no significant difference among the three kinds of extracts. The alteration in uptake of one ion influences the availability of another ion [85], supporting the idea of B uptake through biostimulator application, but this requires further investigation. The application of biofertilizers opens new routes of ion acquisition by increasing nutrient use efficiency in plants. In this regard, mycorrhizal and non-mycorrhizal fungi, endosymbiotic bacteria, and plant-growth-promoting rhizobacteria are important because of their dual function as microbial biostimulants and biocontrol agents. We explain the functions of these biostimulators and their possible relationship with ion acquisition in plants. Indeed, grafting and AMF inoculation improve plant physiological and nutritional aspects and a number of studies have proved their pivotal role in B uptake [74,75,79,105]. Additionally, nanotechnology is an emerging technique to solve plant-nutrition-related problems. The combination of these techniques may improve B uptake. For instance, a combination of grafting and Cu NPs improved growth and development of watermelon by increasing ion uptake [129]. Melatonin application improves plant performance by inducing resistance against stress conditions. According to a report, melatonin application reversed the toxic effect of B by moderating B accumulation in leaf and fruit, increasing photosynthetic activity, and improving dry weight that ultimately enhanced plant growth of Capsicum annuum [138]. Similarly, in watermelon, melatonin application enhanced the N concentration in roots by improving root elongation, root diameter, and root surface area under limited N availability [61]. However, no evidence for B uptake under deficient conditions has been found yet, and that requires further investigation. https://pubmed.ncbi.nlm.nih.gov/8508192/ https://pubmed.ncbi.nlm.nih.gov/34988929/

Hbss is 27in tall ABxRKO is 38.5in tall I'm starting to run out of height because of the ABxRKO as it finally flowers. Still slight nute issues with the HBSS, but nothing too tough to handle for now. The smells the HBSS give off are absolutely crazy. Just letting them grow, and watering every day seems to work. Will upgrade to earth boxes for this tent since a little autonomy is nice

As to the number 144 it totals nine. Nine is the end of all numerical integers. No higher number is available. Out of the One(1) come all other numerical values, which show by the four elemental qualities(4), the dual polarity(44), in this case, as matter and antimatter - the visible revealing the invisible. the physical polarity of the metaphysical. The mind grows from observing failed attempts, The body grows from observing failed attempts, One set, fail. Note: As gibberellic acid is not soluble in water you need to dissolve in alcohol. 75% Ethanol or rubbing alcohol can be used. Dispense 100 mg of Gibberellic Acid 3 into a 250 mL container. Create a solution by mixing 90 ml of distilled water with 10 ml of ethanol (Ethyl Alcohol). Introduce 100 ml of the water-ethanol mix and agitate until complete dissolution, achieving a final concentration of 1 mg/ml (1000 ppm). Tailor the concentration of GA3 to your experiment, varying from 0.1 mg/ml to 1 mg/ml based on specific requirements. Gibberellic acid + Diethyl aminoethyl hexanoate 10% SG Gibberellic acid A4, A7 + 6-benzylamino-purine p.6% EC Gibberellic acid + Paclobutrazol 3.2% WP Gibberellic acid + Forchlorfenuron 0.3% SL Gibberellic acid + Brassinolide 0.4% SL Nutrients for the week are recipe foliar application. The boombox (containing a 3 KHz signal and nature sounds) is played at high volume with high treble and medium bass for 10 minutes before spraying the plants. The plants are then sprayed while its playing and the sound is continued for another 20 minutes after spraying. Both sides of the leaves should be saturated. Treatment is best performed early in the morning/daylight, preferably in foggy 65%rh+ dew. On cold mornings, spraying should be delayed until late afternoon if outdoors. Do not spray plants when the temperature falls below 50o F. The formula also can be administered in the regular weather supply, by drip-feeding, hydroponics, etc.. The nutrient solution should be applied once somewhere in first 4 weeks, then twice weekly thereafter. The sound ought to be played daily for at least 30 minutes during daylight hours no more than 3 hours. https://biologydictionary.net/gibberellin/ Often through our various senses, we receive impressions that bring the pleasure of nature's harmony into our thoughts. At other times we are aware that man has intervened in nature's processes to produce something by art, which to our highly evolved senses seems to rival even the best nature can display of beauty and harmony. We become aware at such times of man's wonderful ability to bring seemingly unrelated elements into harmonic balance, and receive a glimpse into a world where everything exists in conscious sympathetic attunement to everything else. When we listen to a piece of music that seems to strike a beautiful chord somewhere inside us, or view a painting that simply glows with harmonic awareness well executed, we probably do not spare much time to contemplate the wonderfully intricate combination of vibrations that our sensors make it possible for us to perceive. We tend to appreciate the relationship between the parts of something, by an awareness of the harmony or dissonance of the whole. This ability enables us to say "what a beautiful house!" instead of "analysis has proven that this collection of building materials exhibits certain elements of harmonic proportion." While this ability to instinctively appreciate the beauty of true harmony has an important role to play in evolution, a more analytical understanding of the laws involved can be most useful. This is especially so if we wish to create works of art where each part exists in true harmony, not only with the other part of that particular whole, but with the universe within which the creator and the created exist. Everything vibrates. From the most dense matter to the most subtle cosmic rays, everything which our senses allow our thoughts to become aware of, can be specified in terms of wavelength or frequency of vibration. These two terms define the same thing, but from different points of view. (See Illustration 1) The following are the approximate wavelengths of various energy carriers: Cosmic rays 0.000,000,001 mm Gamma rays 0.000,000,1 mm X rays 0.000,500 mm Ultraviolet rays 0.003 mm Visible light 0.006 mm Infrared 0.01 mm Sound waves 1 meter Radio waves 300 meters Violet light 400 nm to 450 nm Blue light 450 nm to 500 nm Green light 500 nm to 570 nm Yellow light 570 nm to 590 nm Orange light 590 nm to 610 nm Red light 610 to 700 nm 1 nanometer (nm) = 0.000,000,1 cm = 1/10,000,000 cm If a guitar string is plucked and we hear a sound, it is not too difficult for the human mind to associate this sound with the vibration of the guitar string. With color it is quite different. It is difficult for us to conceive that the color of a substance is not an inherent property of the substance itself, but an indication picked up by our senses of that substance's ability to absorb or reflect the light which happens to be shining on it at that moment. Neither the matter nor the light is colored. What happens is that the brain learns to differentiate between the frequencies reflected or transmitted by the substance the eyes are focused on. The same thing happens with sound. When we say "Oh! Listen, they're playing my favorite song," what we really mean is: "My brain has stored within it a particular pattern of frequencies. I have compared the new information being received with this stored pattern and have deduced the answer that the two patterns are similar within certain specified tolerances." The 'pleasure' involved could have something to do with our running the pre-recorded pattern at the same time, in 'sympathy' with the new pattern as it is received. The word sympathy describes very well our ability to appreciate color and sound. It also describes the reason behind certain elements of harmony. For instance, if a substance vibrating at 100 cycles per second (tone 1) is in the proximity of another substance vibrating at 200 cycles per second (tone 2), we could perceive, if we had the right equipment, a certain sympathetic relationship between the two. If our equipment was a wave form plotter, we may have a drawing like illustration 2. Illust 2 We will see from this that there is a uniform doubling of the first tone seen in the second. At various points along the waves, the two are the same in amplitude. At other points, they are at opposite poles to each other. This doubled frequency has more points of similarity to the original than any other frequency except the original itself. If the equipment we had available for measuring these two frequencies was a soundboard amplifier and a pair of ears, then we would hear what would sound to us like one tone. If we had the opportunity to hear one at a time, we would hear that although they sound the same, one is higher in pitch than the other. This characteristic of 'the same but different in pitch', musicians have called the octave. Any two tones produced where one has exactly doubled the frequency of the other is called an octave. Speaking in ratios, an octave would appear then as the ratio 2:1 or 1:2, depending on whether we are talking of an octave up or down. A single note produced by almost any instrument will contain more than one wavelength or frequency. It will have a dominant frequency, the wavelength of which we would call the note's 'fundamental' or 1st harmonic. It will also have a varying number of upper harmonics, gradually fading in intensity into infinity or silence. Natural harmonics always have the same pattern of intervals between them. The interval between the 1st and 2nd harmonic is a perfect octave; between the 2nd and 3rd a perfect fifth; between the 3rd and 4th a perfect 4th; and so on, the intervals becoming smaller and smaller until they lose any relationship with the western 12 tone scale as it exists at the moment. Just as an octave has certain elements of sympathy with its fundamental, so some intervals have been noted to be more perfectly in sympathy with the fundamental than others. The ratio of the 'perfect 5th' or interval of 7 semitones, as it occurs in the harmonic series, is 3:2 or 2:3, while that of the 'perfect fourth" is 4:3 or 3:4. All the tones in the western 12 tone scale can be expressed in terms of the ratio between the upper tone and its fundamental. This would seem to be an ideal way of generating a scale from any given fundamental and several attempts have been made to do this, the Pythagorean system being probably the most well known. Although when working with a single tone instrument playing on its own, the Pythagorean formula works wonderfully well, if we had several instruments tuned this way together and asked them to play almost any western music, we would find that at times they sounded quite out of tune to each other. The lack of flexibility of the various scale systems based on the harmonic series has led to what is known as the 'tempered' scale. This uses as its primary unit of interval the ratio of the octave or 2:1. It then proceeds to divide the interval between any fundamental and its upper octave into 12 smaller intervals by applying the ratio: two to the one-twelfth power, to one (21/12:1). This equals 1.059463094, so by multiplying any frequency by this number, we will obtain the tempered semitone next up from our fundamental. We will also find that any tone twelve semitones up from any other tone, in a scale generated in this way, will have exactly double the frequency. If we took the note middle C on a piano and halved the wavelength, we would have the note C one octave above. If we halved this, we would have the C above, and so on. However, within about 6 octaves, we would find that although a 'sound' was being produced, no human ear could perceive it. If we kept on going, halving and producing upper octaves of our fundamental C, we would proceed through the infrared band, into the visible light spectrum. If we happened to be outside during the day, we would, for one octave only, see the note C with our eyes. The next octave above would already be in the ultraviolet band, and outside the eye's sensitivity range. If we can think of color as being an indication of a substance's vibratory rate or wavelength, we may begin to see a relationship that could exist between the color and sound spectrums. The logical extension of what has so far been said is that there exists a scale in the color spectrum that coresponds exactly to the scale in the sound spectrum, each color tone being an octave of the equivalent note in the sound range. This is not the end of the story but only the beginning. If we can for the moment accept that any wavelength in one band has upper and lower octave stretching out to infinity, then tne next question is 'fine, but what shall we use as our fundamental? A particular color? A particular sound frequency?' The musicians among us will probably say 'A 440'. This means that the note A should vibrate at 440 Hertz, or 440 times per second. They would tell us that this is standard pitch has been adopted by most orchestras around the world; pianos are tuned to it, instruments are constructed to formulas based on it, and so to them it would probably seem the most appropriate place to begin. Some of these musicians may know of the battle that is still raging with regards to this being the standard, but few would know why A = 440 Hz was chosen except that it werned when it was set to be a suitable compromise between the many different pitches in use at the time. There is also a scientific standard of pitch of C= 512 Hz which, although not in common use in nusic, has a lot of theoretical followers, as it is generated from the lower octave of C = 1 cycle per second and has certain advantages of numerical simplicity in mathematical research. A scale built upon either of these standards will yield an upper octave scale in the color spectrum. However, with the A = 440 Hz scale, we end up with a color series which, although interesting, is hard to relate to any color system or set of values in current use. The C = 512 Hz system, on the other hand, seems a more obvious choice at first sight, having 12 definite color tones and containing the strongest and most pure colors in the spectrum. Further research showed that there were still things not quite right with this system, and has led to a modified version in which correspondences with other systems seemed to fit into place. Of course the proof of the pudding is in the eating and before being accepted this system will need further research to substantiate the correspondences and prove its value to mankind. What follows is a summary of the process used in drawing up this modified scale. The upper octave color of a fundamental of one cycle per second is found to be exactly emerald green, which is recognized as having a wavelength of 511 nanometers (this is at 20o in air). 511 nm is also the color of malachite, or hydrous carbonate of copper occurring as a mineral. It would seem reasonable, given the teachings in the QBL, to associate this with the planet Venus. If we take 1 Hz or its upper octave 512 Hz as our fundamental, then build a scale upon it using our tempered scale 'formula', we will have the following 12 color tones: 723 nm = infrared 682 nm = deep red 644 nm = orange red 608 nm = orange 574 nm = yellow 541 nm = yellow green 511 nm = emerald green 482 rim = green blue 455 nm = royal blue 430 nm = indigo 406 nm = violet 383 nm = ultraviolet There are certain immediate correspondences that become apparent between some of these colors and our teachings in Parachemistry. The yellow here is the color of chromate lead and zinc yellow, the most 'yellow yellow', for want of a better description, to be found in the spectrum. It seems rather logical, if we follow the Queen scale of color, to call this the Sun, or Vulcan, depending on which system we choose to look at. The orange here is exactly the frequency of sulphide of mercury or cinnabar. It would seem appropriate to relate this to the planet Mercury on the tree of life. If we then call the deepest red in our scale Mars and the Royal Blue Jupiter we find a pattern beginning to form. The ultraviolet here is outside our range of color vision and would appear black to us. If we call this Saturn, as Saturn is described as either black or violet, then we have six tones out of the twelve named. There is in natural things a certain truth which cannot be seen with the outward eye, but is perceived by the mind alone. The philosophers have known it, and they have found that its power is so great as to work miracles. This miracle, we suggest, is at work in the observation of a rose in your garden. This miracle is at work in the observation of a friend in your heart as well as your eyes. The mysterium coniunctionis of the alchemists, that mysterious marriage of the Sun and the Moon, is a conjunction of the most extraordinary scope, because it is a conjunction of physical fact with metaphysical reality. This unique vision is not the result of a tersely factual pouring of acetic acid onto calcined stibium. nor is it the result of a mere figurative allusion that one given substance is the Sun and another, the Moon. Just as with physical facts, the quality of the ingredients has an important influence on the result, so in mental terms, the quality of the thought put into the work has a bearing on its ultimate success or failure. In this truth lies the whole art of freeing the spirit from its fetters, in the same way that, as we have said, the mind can be freed from the body. This last phrase-"the mind can be freed from the body"-is, as we see it, a direct reference to the meditative technique of the alchemist. But perhaps our word "technique" is not quite the correct one, for it seems to imply a formula of sorts, a preconceived set of ideas, whereas in truth, spontaneity is of the essence in meditation as it is in alchemy. Meditation is, after all, a kind of fishing into the subconscious for the wellspring of a truth. The conscious mind, selecting its subject or question (the 'bait') dips like a fishhook into the water. But the bait does not seek the fish. The fish seeks the bait. And this is one of the most commonly misunderstood principles in all of metaphysics. We do not meditate. We are 'meditated.' To achieve this, we must be receptive. Who among us is receptive? Even in the privacy of our laboratory, don't we often tend to adjust flasks, measure substances, think in the jargon of the alchemical work as though we were really performing it? After all, 'I have studied for years; I have read the texts. I direct the course of this work.' Only God directs the work. And not one among us has access to the wellsprings of that wisdom unless we are receptive. That is why alchemy is an art as well as a science. It is not only the art of directing the work as we understand it after being instructed by a book or a teacher. it is also the art of receiving the work, i.e., being receptive to it in our hearts, and letting the work refine us, even as we refine our work. That is the confluence of two worlds that the true alchemist experiences. We can, and must, strive for that through years of intellectual, physical and emotional effort, but in the end, we do not make it happen-we let it happen. And only through meditation is this "letting go possible. Thou wilt never make the One which thou seekest, except first there be made one thing of thyself. This "one thing" is the one-pointed concentration and subsequent meditation of the devoted student. It involves and utilizes every level of his being. It brings those levels to a pitch of alertness previously unknown, and then, once attained, it lets go of them. The technique is familiar to readers acquainted with Zen, with Yoga, with Taoism, and with many other religious disciplines. But it has not been consciously identified with alchemy for the simple reason that alchemy is so widely misunderstood or even ignored, its terminology and methods being so notoriously obscure and complex. Martin Ruland's Lexicon of Alchemy defines meditatio as follows: The word MEDITATIO is used when a man has an inner dialogue with someone unseen. It may be with God, when He is invoked, or with himself, or with his good angel. Clearly, then, the meditative aspect of the alchemical work is not merely cogitation, or simply sitting down and thinking about the work. To be sure, preliminary organization of the theory of a given procedure is essential; master the theory before the praxis. But meditation goes deeper than this, and involves a much more complex process. The point to be emphasized is that meditation is an inner dialogue. We must select our terms for it with care, in attempting to describe it. The occultist will see it as a profound revelation from the Higher Self. the ceremonial magician, as the Knowledge and Conversation of the Holy Guardian Angel. the religionist as a form of prayer; the skeptic as an hypnotic trance; and the psychologist as a means of coming to terms with the contents of the unconscious. ' Little wonder that the alchemist is said to begin his work with a massa confusa! Both in his mind and in his physIcal labors, he must sort out of the primal chaos a goodly order. If his thoughts are not in order, his substances will not be properly handled. And even at best, if both are in order, he must have the courage to dive deeper into his inner resources to understand the relationship between his own soul and that "soul" of matter with which he works. He can still expect to be attacked on the one hand by skeptical occultists for being too "literal" in using laboratory methods; and on the other by scientifically learned friends for being a religious sentimentalist over a few flasks and retorts. So the alchemist, even today, has his own razor's edge to walk. But the challenge of the work goes beyond trite dismissals and defies the easy categories of those who try to explain it away. The man or woman who enters it with a prayerful and meditative heart can only benefit by its pursuit. Not one writer in this century or in those past can tell us the path is an easy one. Yet as Michael Maler has said: There is in our chemistry a certain noble substance over whose beginning, affliction rules with vinegar, but over whose end, joy rules with mirth. Finally, we draw from the wisdom of Morienus in instructing Khalid: This thing for which you have sought so long is not to be acquired or accomplished by force or passion. It is only to be won by patience and humility and by a determined and most perfect love. For God bestows this divine and immaculate science on his faithful servants, namely those on whom he resolved to bestow it from the original nature of things.... Nor were they able to hold anything back save through the strength granted to them by God, and they themselves could no longer direct their minds save toward the goal appointed for them by God. For God charges those of his servants whom he has purposely chosen that they seek this divine science which is hidden from men, and that they keep it to themselves. This is the science that draws its master away from the suffering of this world and leads to the knowledge of future good. The following short poem was dated December, 1633, and signed only with the initials W.B. It later appeared (in 1651) in a collection of alchemical works compiled by Elias Ashmole titled THEATRUM CHEMICUM BRITANNICUM, Still considered one of the finest collections of alchemical works in English. This short poem exemplifies the efforts of early writers not only to summarize their work but to meditate on it-a point dealt with in another article in this issue-and to direct the reader to meditate as well on the alchemical message implicit in the ancient myths. The fifth stanza urges the student to a careful consideration of the myths of Cadmus and Jason, advice both given and followed three hundred years later by Fulcanelli in his famous work, LE MYSTERE DES CATHEDRALES. We have modernized the poet's spelling. -Editor Through want of skill and reason's light Men stumble at noon day; Whilst busily our Stone they seek, That lieth in the way. Who thus do seek they know not what Is it likely they should find? Or hit the mark whereat they aim Better than can the blind? No, Hermes' sons for Wisdom ask, Your footsteps she'll direct: She'll Nature's way and secret cave And Tree of Life detect. Son and Moon in Hermes' vessel Learn how the colors show; The nature of the elements, And how the daisies grow. Great Python how Apollo slew, Cadmus his hollow oak: His new raised army, and Jason how The fiery steers did yoke. The eagle which aloft doth fly See that thou bring to ground, And give unto the snake some wings, Which in the earth is found. Then in one room sure bind them both, To fight till they be dead, And that a Prince of Kingdoms three Of both them shall be bred. Which from the cradle to his crown Is fed with his own blood; And though to some it seems strange, He hath no other food. Into his virgin mother's womb Again he enter must; So shall the King by his new birth, Be ten times stronger just. And able is his foes to foil, The dead he will revive: Oh, happy man that understands This medicine to achieve!

Die Blüten haben leicht zugenommen...aber eben nur leicht

Gute ( 160 Tag -1 woche blüte)

Flower kicked

2024-08-31 One more Week and she will be harvested too, this is around her 5th. week in Flower, and she buddes up very well, as long as it stays hot and dry she can stand, but if it starts to rain for days, iam going to cut her. BREEDERS INFO What exactly are the genetics in Auto Critical Orange Punch? Auto Critical Orange Punch is a feminized autoflowering seed variety, the first Dutch Passion auto to use Critical genetics. The genetic base was Grandaddy Purple (Purps) x Orange Bud. This was called Orange Punch, and gave great potency and flavor. But yields were below average until she was crossed with an elite XXL Auto Kritical Bilbo. Auto Critical Orange Punch is one of our strongest strains with abundant yields and white buds that are completely covered with a thick layer of resin and beautiful orange flower hairs. Auto Critical Orange Punch has thick compact buds that will provide a good yield in a relatively short period of time Auto Critical Orange Punch is the autoflower seed version of our photoperiod Critical Orange Punch. This stable hybrid cannabis plant has roughly the same Indica and Sativa genetic content and can be regarded as a 50/50 variety. In this autoflower version, ruderalis genes (autoflower genetics) have of course also been crossed to make this strain flower automatically. This results in slightly more phenotype differences between the different plants than in the photoperiod version. This strain can grow quite fast during the first 5-7 weeks of its life cycle. She grows strong branches that can bear long flowers. Blooms of 30-50 cm are no exception. She is classified as an XXL autoflower for all the right reasons! Her leaf structure is also that of a hybrid, she can grow very large fan leaves that convert a lot of light into energy. By the end of the flowering phase, the thickest branches with the heaviest flowers will need some support. By the 9th - 10th week, the buds will become so heavy that the branches can collapse under the weight.