(biologist - artist - queer)

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You’re the only magician that could make a falling horse turn into thirteen gerbils

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Joined 1 year ago
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Cake day: June 10th, 2023

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  • Disclaimer: I am not an expert in this and this is just my understanding of how to answer this question

    You may or may not realize that most voters don’t usually go out well in advance and research all potential candidates, selecting the one they feel represents their values the best. Many of them don’t even check in to the conversation until the primaries are over and they can make a simple red vs. blue choice. Among voters that do participate in primaries, they mostly rely on information they learn about those potential candidates by watching advertisements, endorsements from other well known politicians, clips from debates, news and social media coverage, etc.

    Creating that information (ads, debates, news coverage, social media, etc.) requires two things: money and momentum. Money comes first, and is disbursed according to the process the other commenter described-- the party talks with its donors and collectively they decide who to fund.

    In Bernie’s case, he was systematically deprived of money by the DNC as described above, in addition to his moral philosophy of not taking money from big donors. Instead, he funded his campaign through small donations-- which he earned a LOT of-- but he still had fewer funds to generate advertisements, to host events, to “get the word out”.

    Without this funding and support, Bernie couldn’t generate momentum as effectively. The fact that he is as popular as he is despite the lack of support from the party illustrates how popular his platform is, but that isn’t enough to get disengaged voters interested. Further, in his case, other party members actively wanted him to NOT be the nominee, so there were fewer endorsements, more intentional maneuvering by the party to convince voters to vote for other candidates, etc.

    In essence, the idea that having the purest moral and policy philosophy is the most important element to winning the nomination is naive: it takes money and support from institutions, or else no one will ever even know what that pure philosophy is.




  • The point this guy is trying to make is that people are conflating Israel, Judaism, and Zionism in ways that don’t always make sense

    Like, the polls you’re quoting are sentiments of Israelis, so this guy (and the vast majority of Jewish people in the world) are not included in those polls.

    Even within Israel, that’s, what, 3-4 million people that disagree with that sentiment? And Israelis are only ~73% Jewish anyway?

    On top of that, tons of zionists arent even Jewish, they are even likely to be antisemitic tbh.

    So… what you said sounds a lot like “I don’t have anything against one particular group, but the sentiment of the citizens of this one country makes me second guess the perspective of a person in a totally different country just because they share one dimension of identity”… In essence, it sounds a lot like prejudice

    (free palestine, in case that isn’t obvious)


  • because the very first thing you say in this post basically amounts to “I think I have the authority to decide the basis on which we determine who deserves to vote”

    like, yeah, most people can navigate to their secretary of state websites. And it’s not really your responsibility to have to link the pages anyway.

    But doing it for that reason aligns you philosophically with people who think that the illiterate, the elderly, the poor, the disabled, the critically ill, etc. somehow don’t deserve to vote. It aligns you ideologically with other people who think they can decide who deserves to vote, with people who want to disenfranchise others-- in essence, it aligns you ideologically with many Republicans




  • As an education professional: what the hell, dude? It’s not unfortunate that we aren’t just dropping struggling students without first carefully examining why they’re not succeeding.

    You might be right that you can’t let some students detract from the class for other students, but the solution there is advocating for better funding and more staff to be able to give every student what they need, whether they’re above or below the expectation for their age.

    Saying it’s “unfortunate” that students don’t fail (read: ruin their whole god damn lives) as often anymore is blaming our most vulnerable YOUTH for the systemic problems of our society. It’s not their job to be what the school environment wants them to be, they don’t even have a choice about whether or not they are there. It’s our (as educators, and as tax paying and voting community members) responsibility to make sure they get the education they need to be functional members of our society.

    We even have huge bodies of research to reinforce this. It’s not a secret that the school environment excels at making nice workers, not critical-thinking and well-adjusted adult humans.

    Take it up with the school board! Take it up with the local, state, and federal government! Take it up with the voters!





  • Oooh it’s even cooler than that!! You’re spot on, acid is the problem. And acid from food, candy, coffee, etc. is harmful for enamel for sure.

    But sugary stuff that isn’t acidic also rots teeth. Why? Because the bacteria in your mouth do what’s called lactic acid fermentation. Basically, when they take a sugar molecule and want to make “usable” energy out of it (in the form of something called ATP, or adenosine triphosphate), they end up creating lactic acid as a byproduct. In essence, the stuff living in your mouth makes acid out of sugar.

    We also need to break sugar down into ATP, but we do something called cellular respiration instead. It uses oxygen and creates CO2 as a byproduct! That’s why we need oxygen to breathe, and why we breathe out carbon dioxide. But, when you work your muscles hard (lifting weights, sprinting), you might use the ATP in your muscles faster than your body can make it with cellular respiration. In that case, your cells will also do lactic acid fermentation! That’s what we’re feeling when we “feel the burn” (well, that and micro-tears in the muscle, in some cases).

    Source: I’m a biologist! And I love sharing weird facts like this! Thank you for the excuse to write this out :-)


  • Other commenters have good suggestions also, but one option I haven’t seen mentioned would be to buy a powdered acid and make your own dilutions

    It’s easy to get citric acid in a dry form (like the crystal coating on sour candy), you can get 10 lbs (enough to make many gallons) of it for like $30-50 online. I put a small scoop in my dishwasher to keep my cups from getting foggy from our hard water, and I use it to descale our kettle and in our laundry, too.

    Just be careful, acid dilutions are no joke. Whether you get the cleaning vinegar or make a citric acid solution for yourself:

    • use nitrile or latex gloves when working with the acid solutions

    • wear something to protect your eyes, glasses are probably good enough but goggles are better

    • if you have an acid solution and want to dilute it, pour the acid into the water, not the water into the acid!!!

    • flush your skin or eyes with water immediately if the acid gets on you or your clothes

    These rules might seem like overkill but better safe than sorry!

    Citric acid is slightly stronger than acetic acid so if I were you I’d make like a 20% solution to have a similar effect to the cleaning vinegar (so like 100 g powdered acid to 400 mL water). You might have to mix it on the stove so that the water is simmering to get the acid to dissolve.

    Again, be careful! But as long as you’re smart about it, take your time, and prioritize safety, you can definitely use this for descaling and cleaning (and cooking!)


  • When I say “the cell isn’t a machine”, it is in specific reference to the machine model of the cell, which is a previously established conceptual framework in the field of molecular biology. If you want to understand why that model is falling out of favor today, you’re invited to read the article linked by OP and/or the articles I have linked in other comments.

    The gist is that the cell is more complicated, flexible, and emergent than any machine has ever been and will be for the foreseeable future, and the idea that we can simply map the functions of each molecule in the cell to get a perfect “circuit diagram” of how everything plays together is defunct.

    I don’t have time to mess with this thread any more. You can either accept what myself (an expert in this field), the author of this publication (which happens to be one of the most prestigious journals in the world), and others who do this research daily are saying about this, or you can not. Frankly, if you are an expert also, the field, the research, and the truth barely cares about our opinion-- it certainly doesn’t care about non-expert opinions on the internet.


  • Junk DNA is repeating codons, or codons that occur in areas that are outside of the “start/stop” codon triplicate pairs.

    Those sequences do things and have effects. In fact, the coding regions are often less functional than the non-coding ones.

    They aren’t there for structural reasons, all DNA is the same 4 codons linked together over and over, all the different chromosomes are different sizes.

    Sometimes they ARE there for structural reasons? Read: enhancers, or CTCF binding sites? Among many other myriad examples of functional noncoding regions? Also, nucleotides =/= codons. There are 64 codons.

    All of this DNA is reported when the cells divide, that’s the only time those regions between the stops and starts actually come into play. This is very easily proven, we know the structure of the reading proteins down to the molecule (indeed there are starts and stops and triplicate base pairs that design these transcribing proteins).

    That’s bull. You’re out of your depth. A contemporary college molecular biology course would show your examples to the contrary.

    The “important” junk DNA that has significance while not being in a “start->stop” zone are the codons that occur before the first start codon on either side of a DNA strand, when DNA is replicated the protein that starts replicating it has to start at 1 end of 1 side of the DNA in order to be able to read it

    I feel like a broken record but Enhancers! lncRNAs! siRNAs! Binding sites! Other gene regulatory regions! Epigenetic nucleosome modifications! Chromatin remodeler sites!

    except it needs to find the end first, and to make sure it’s all the end it “clips” the first 6 (? Maybe more maybe less, it’s been decades since I’ve studied this)

    Oh, there’s your problem. A lot has changed. You refuse to see the sea change happening around you because it means you’re out of date.

    Sorry for the wall of text, but there’s plenty of examples of blatantly junk DNA, and there are known methods of how it occurs. Anyone who says every codon pair has a purpose has a screw loose and is ignorant to the mechanics of evolution.

    I was happy to reply to you and engage pleasantly originally but you are only engaging with people that know less about biology than you do. You are not an expert if you last studied biology decades ago and can’t remember the details. You certainly aren’t enough of an authority on the subject to question a contemporary article published in Science or the work of other researchers currently in the field.

    I really, really encourage you to read these papers thoroughly. You are the target audience-- people who learned the machine model of the cell and who are gripping it so tightly that they are blind to the nuance that we’ve uncovered. I also encourage you to not write insults about people who disagree with you, especially people with more domain knowledge than you have.


  • This is a funny comment though, because “junk” DNA is involved with epigenetic regulation and cellular behavior.

    “It’s there so it must have function”, “it’s still in the genetic code so it must have been selected for” is the least nuanced take,

    “It’s there just randomly and therefore is junk”, and “evolution does not select for efficiency” is an improvement,

    But “it’s there and it’s doing something despite not having a bespoke, prescribed function” and “evolution is a cascade of emergent effects and random chance, none of our genome is non-functional even though it is random” is the most up to date take

    You seem like a biologist, why not go read some of these papers? Like the one I linked by Dan Nichols? Most people don’t have the background necessary to understand the language (no shade) but you seem to!


  • I would encourage you to read the linked Science paper and Dan Nichol’s paper, Is the Cell Really a Machine?

    You feel that if a codon isn’t meant for something, if it doesn’t have a purpose– then it is junk. This is a mindset that is reflective of the machine model of the cell. We used to expect that each protein was bespoke for a function, each transcript necessary.

    The whole paradigm shift at hand is this model falls flat, even for coding regions. I think you’re actually very spot in here with the prokaryotic DNA or the plant genomes (love me some violets for their weird genomes). Some parts of a genome will rapidly change and appear to serve no real purpose, but the next bite is the important one: even if it seems like there isn’t a purpose, like a top-down prescription for functionality, those regions are still doing something while they are present.

    For example, some long non-coding regions affect the likelihood that a person will develop Parkinson’s disease, or in the case of plants with various polyploidies, the relative expression of their genes won’t necessarily change, but the absolute expression may.

    Basically, you aren’t wrong that these regions dont have a purpose, because no genes have a purpose. The cell isn’t a machine.



  • So I think I can make the claim that I am an expert in this, at least compared to 95%+ of biological researchers. My research foci include epigenetic and emergent interactions like the ones discussed in the article, and although I am not going to back this up by identifying myself, please believe me when I say I’ve written some papers on the topic.

    The concept of junk DNA is perhaps the problem here. Obviously there are large swaths of our genome that do not encode anything or have instructions for proteins. However, dismissing all non-coding DNA as “junk” is a critical error.

    Your telomeres are a great example. They don’t contain vital information so much as they serve a specific function-- providing a buffer region to be consumed during replication in place of DNA that does contain vital information. Your cells would work less well without telomeres, so calling them junk is inaccurate.

    Other examples of important non-coding regions are enhancer and promoter regions. Papers describing the philosophical developments of stochasticity in cellular function note how enhancers are vital for increasing the likelihood of transcription by making it more likely that specific proteins floating in the cellular matrix interact with each other. Promoter regions are something most biologists understand already, so I won’t describe them here (apologies for anyone who needs to go read about them elsewhere!). Some regions also inform the 3D structure of the genome, creating topological associated domains (TADs) that bring regions of interest closer together.

    Even the sequences with less obvious non-coding functions often have some emergent effect on cellular function. Transcription occurs in nonsense regions despite no mRNA being created; instead, tiny, transient non-coding RNAs (ncRNAs) are produced. Because RNA can have functional and catalytic properties like proteins, these small RNAs “do jobs” while they exist. The kinds of things they do before being degraded are less defined than the mechanistic models of proteins, but as we understand more stochastic models, we are beginning to understand how they work.

    One last type of DNA that we used to consider junk: binding sites for transcription factors, nucleosome remodelers, and other DNA binding proteins. Proteins are getting stuck to DNA all the time, and then doing things while they’re stuck there. Sometimes even just being a place where a nucleosome with a epigenetic flag can camp out and direct other cellular processes is enough to invalidate calling that region “junk”.

    Anyway I’m done giving my spiel but the take home message here is that all DNA causes stochastic effects and almost all of it (likely all and we haven’t figured it out yet) serves some function in-context. Calling all DNA that doesn’t encode for a protein “junk” is outdated-- if anything, the protein encoding regions are the boring parts.


  • First, I want to fully admit I didn’t watch the video. Apologies ahead of time if that causes me to be redundant or reductive.

    Second, I’m also a biologist, although a molecular one.

    Third, I agree with almost all of your premise and train of thought. We’re certainly more likely to get the likes of “bacterial mats” than intelligent life anywhere, and especially within a distance that we will ever realistically encounter.

    I do wonder, though, how you (or maybe the video guy, but obviously not enough to watch the source material before making an ass of myself…) conceptually reconcile the small sample number of known planets with life (n=1) with the mindblowingly impossible number of worlds.

    You say that intelligent life evolving only once indicates that it is difficult for evolution to “discover”, which is surely possible to be true. But given that we haven’t seen the evolutionary conditions on other hypothetical worlds, from what we know, the evolution of intelligent life has a perfect 100% success rate of occurring on planets with life.

    In fact, you mention the independent convergent evolution of eyes as an indication that eyes are a “good idea”, and that they must be relatively easy for evolution to discover if they evolve independently, repeatedly. But evolution is subject to the whims of selective forces, so a different world would surely select for different traits. Eyes (or other extremely common evolutionary pathways… looking at you, crab body) might be less frequently selected for or be entirely useless, but intellegent decision making and tool use might evolve in ways we can’t even conceptualize in our context.

    This also extends to the claim of how our world is evolutionarily dynamic (which you point out is hard to quantify in context). We don’t know the dynamics of evolution on other worlds, if it happens at all. Recombination could be a unique characteristic of DNA-based life on Earth or it could be extremely common. Other worlds might have longer or shorter evolutionary time lines, also, since our sun’s “working life” is shorter than average due to its size and density. Without another example for reference, we don’t know whether we’re evolving quickly and with diversity or slowly and conservatively.

    I guess, I don’t think you are wrong, exactly. I just think you are necessarily making assumptions based on how things work here in order to extrapolate how things might work there– one has to! But the whole discussion (which continues, like this, to this day) revolves around just too many unknowns. We just don’t know, and can’t know.

    Climbing down from my high-horse, though, I have to admit I’m biased, since I have a pet-belief that life is basically guaranteed to exist elsewhere (how freakish would it be for it to only happen once out of so, so many chances?). I honestly feel like there’s a good shot that it’s incredibly common, at least in a basic form. In essence, I suspect that if we find bacterial mats (or soup) on Enceladus or Europa then it’s basically certain that life is everywhere. But we won’t even likely know that in my lifetime, so… I keep dreaming!