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gemini 2.0 on a p5.js challenge prompt: Write a p5.js script that simulates 25 particles in a vacuum space of a cylindrical container, bouncing within its boundaries. Use different colors for each ball and ensure they leave a trail showing their movement. Add a slow rotation of the container...

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AK

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28,538 görüntüleme • 1 yıl önce •via X (Twitter)

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app:

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zooming in and out is not a good effect, it makes people sick.

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claude 3.7 sonnet same prompt Write a p5.js script that simulates 100 colorful balls bouncing inside a sphere. Each ball should leave behind a fading trail showing its recent path. The container sphere should rotate slowly. Make sure to implement proper collision detection so the balls stay within the sphere.

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🇺🇸 GROK 3: NEXT-LEVEL PHYSICS VISUALIZATION IN MOTION 25 particles, each a different color, bounce inside a vacuum-sealed cylindrical container, leaving behind glowing trails. The container rotates slowly, shifting perspectives, while an outer spherical boundary adds complexity. Physics-driven collisions keep everything in motion, and a subtle zoom effect pulls viewers in and out, enhancing the experience. This isn’t just code—it’s a visual experiment in dynamic movement, space, and interaction. Source: AK
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🇺🇸 GROK 3: NEXT-LEVEL PHYSICS VISUALIZATION IN MOTION 25 particles, each a different color, bounce inside a vacuum-sealed cylindrical container, leaving behind glowing trails. The container rotates slowly, shifting perspectives, while an outer spherical boundary adds complexity. Physics-driven collisions keep everything in motion, and a subtle zoom effect pulls viewers in and out, enhancing the experience. This isn’t just code—it’s a visual experiment in dynamic movement, space, and interaction. Source: AK

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“Senator RENNICK: In TGA FOI 3390-11 there were 67 particles greater than 10 microns in a particular batch. That's about 1000 times greater than what the FDA recommended. Do you know what those 67 particles were? Dr Kerr: I have a bit to say to that. We have actually responded to that question before in SQ-24000188. The particles question we've also answered before. The particles in that particular document are not DNA, and we've responded to that question before. The particles. Senator RENNICK: So what are they? That's my question. Dr Kerr: They're normally particles in injectables. There are limits on them. Companies are supposed to check for those in their batch release process. But, ultimately, those particles are not DNA. Senator RENNICK: I'm not saying they are. I'm just asking: what are they? Dr Kerr: It's not related to the 10 nanograms per dose. Senator RENNICK: But is it a contaminant? If it's not DNA and it is not mRNA or a lipid, what is it? Dr Kerr: It's acceptable for pharmaceutical preparations to have a small number of particles present. Senator RENNICK: But my question is: what is the particle? That's a big particle, 10 microns. I mean, the lipids were like - Dr Kerr: I think l'd have to go back and have a look at that FOl to make sure it actually was 10 microns. Senator RENNICK: I can give it to you, if you like. Dr Kerr: Perhaps we could go back and have a look at it and take that on notice. Senator RENNICK: Okay. l'd like to know exactly what it was, if that's okay.” ••••••••••••••••••••••••••••••••• And the answer is: “The specification for the particulates test in the European Pharmacopoeia is: The preparation complies with the test if the average number of particles present in the units tested does not exceed 6000 per container equal to or greater than 10 um and does not exceed 600 per container equal to or greater than 25 um. Therefore, the results for particulates shown in FOl 3390-11 are well within the pharmacopoeial requirements. The particles are not DNA. DNA is highly soluble in aqueous solution, so any DNA present in the vaccines would not appear as micron scale particles. Batch release testing includes residual DNA quantitation on every batch, and this ensures DNA (above trace amounts) would be detected. mRNA vaccines may contain trace amounts of residual DNA at no more than 10 nanograms (ng) of DNA per dose ( The limit of 10 ng per dose prevents the formation of particles large enough to be detected in the micron scale. All injectable or infusion products, including vaccines, are permitted to contain subvisible particles if they comply with the US FDA and European Pharmacopeia 2.9.19 specification for particulate matter. These limits were established after a long history of use of injectables without adverse events occurring in the presence of particulates within this specification. There is no requirement to identify subvisible particles counted in injectable or infusion products, however these particles are likely to consist of extraneous undissolved particulates from the manufacturing process (e.g. trace amounts of dust or fibres) and not DNA.” •••••••••••••••••••••••••••••• And there you have it. The TGA don’t know what are they putting into your bodies. 10 microns is a big particle when you’re talking in biochemistry terms. It’s a third of a dose size of the lipids. Rather than actually answer my question as to what the particles are they skirt the answer by claiming they fall within European guidelines. The same as when they use the WHO guidelines to ignore autopsy reports about reported deaths. Furthermore, what does 6,000 per container mean? How big is the container? How many batches does a container hold? And does this apply to DNA? What this answer tells us is the TGA don’t know what is in the Covid-19 batches and they have misled the Senate by providing a misleading answer. #auspol
2:19

“Senator RENNICK: In TGA FOI 3390-11 there were 67 particles greater than 10 microns in a particular batch. That's about 1000 times greater than what the FDA recommended. Do you know what those 67 particles were? Dr Kerr: I have a bit to say to that. We have actually responded to that question before in SQ-24000188. The particles question we've also answered before. The particles in that particular document are not DNA, and we've responded to that question before. The particles. Senator RENNICK: So what are they? That's my question. Dr Kerr: They're normally particles in injectables. There are limits on them. Companies are supposed to check for those in their batch release process. But, ultimately, those particles are not DNA. Senator RENNICK: I'm not saying they are. I'm just asking: what are they? Dr Kerr: It's not related to the 10 nanograms per dose. Senator RENNICK: But is it a contaminant? If it's not DNA and it is not mRNA or a lipid, what is it? Dr Kerr: It's acceptable for pharmaceutical preparations to have a small number of particles present. Senator RENNICK: But my question is: what is the particle? That's a big particle, 10 microns. I mean, the lipids were like - Dr Kerr: I think l'd have to go back and have a look at that FOl to make sure it actually was 10 microns. Senator RENNICK: I can give it to you, if you like. Dr Kerr: Perhaps we could go back and have a look at it and take that on notice. Senator RENNICK: Okay. l'd like to know exactly what it was, if that's okay.” ••••••••••••••••••••••••••••••••• And the answer is: “The specification for the particulates test in the European Pharmacopoeia is: The preparation complies with the test if the average number of particles present in the units tested does not exceed 6000 per container equal to or greater than 10 um and does not exceed 600 per container equal to or greater than 25 um. Therefore, the results for particulates shown in FOl 3390-11 are well within the pharmacopoeial requirements. The particles are not DNA. DNA is highly soluble in aqueous solution, so any DNA present in the vaccines would not appear as micron scale particles. Batch release testing includes residual DNA quantitation on every batch, and this ensures DNA (above trace amounts) would be detected. mRNA vaccines may contain trace amounts of residual DNA at no more than 10 nanograms (ng) of DNA per dose ( The limit of 10 ng per dose prevents the formation of particles large enough to be detected in the micron scale. All injectable or infusion products, including vaccines, are permitted to contain subvisible particles if they comply with the US FDA and European Pharmacopeia 2.9.19 specification for particulate matter. These limits were established after a long history of use of injectables without adverse events occurring in the presence of particulates within this specification. There is no requirement to identify subvisible particles counted in injectable or infusion products, however these particles are likely to consist of extraneous undissolved particulates from the manufacturing process (e.g. trace amounts of dust or fibres) and not DNA.” •••••••••••••••••••••••••••••• And there you have it. The TGA don’t know what are they putting into your bodies. 10 microns is a big particle when you’re talking in biochemistry terms. It’s a third of a dose size of the lipids. Rather than actually answer my question as to what the particles are they skirt the answer by claiming they fall within European guidelines. The same as when they use the WHO guidelines to ignore autopsy reports about reported deaths. Furthermore, what does 6,000 per container mean? How big is the container? How many batches does a container hold? And does this apply to DNA? What this answer tells us is the TGA don’t know what is in the Covid-19 batches and they have misled the Senate by providing a misleading answer. #auspol

Senator Gerard Rennick

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