When I was writing Faith Versus Fact, I sometimes visited professors in our Divinity School, located right across the Quad. I discovered that the faculty was divided neatly into two parts. There were the Biblical scholars, who addressed themselves wholly to figuring out how the Bible was made, the chronology of its writing, comparisons of different religions, and so on. Their questions were basically historical and sociological, and I found that, as far as I could tell, most of this group were atheists.
Then there were the real theologians: the believers who engaged in prizing truth out of the Bible, and taking for granted that yes, there was a god and somehow the Bible had something to tell us about him. These I had little use for. Indeed, if you look up “theology” in the Oxford English Dictionary, you find this as the relevant definition. It describes the second class of academics who inhabit the Div School—the ones who accept that there is a god:
After writing my book, and having to plow through volume after volume of theology, including theological luminaries like Langdon Gilkey, Martin Marty, Alvin Plantinga, William Lane Craig, John Polkinghorne, Edward Feser, C. S. Lewis (cough) and Karen Armstrong, I finished my two years’ of reading realizing that I had learned nothing about the “nature and attributes of God and His relations with man and the universe.” That, of course, is because there is no evidence for god, and the Bible, insofar as it treats of things divine, is fictional. Yes, there is anthropology in the Bible, as Richard Dawkins notes below, but it tells us absolutely nothing about god, his plan, or how he works. If you don’t believe me, consult the theologians of other faiths: Hindus, Muslims, and yes, Scientologists. They find a whole different set of “truths”! There is no empirical truth that adds to what humanists have found (as Dawkins notes below “moral truths” are not empirical truths), but only assertions that can’t be tested. (Well, a few facts are correct, but many, like the Exodus of the Jews from Egypt and the census that drove the Jesus Family to Bethlehem, are flatly wrong.)
The discipline of theology as described by the OED is a scam, and I’m amazed that people get paid to do it. The atheist Thomas Jefferson (perhaps he was a deist) realized this, and, when he founded the University of Virginia, prohibited any religious instruction. But pressure grew over the centuries, and I see that U. VA. now has a Department of Religious Studies, founded in 1967. So much the worse for them.
In the end, the only value I see in theology comprises the anthropological, sociological, and psychological aspects: what can we discern about what people thought and how they behaved in the past, and how the book was cobbled together. I see no value in its exegesis of God’s ways and thoughts.
And so I agree with what Richard says in the video below. Here he discusses the “value” of theology, but the only value he sees is as “form of anthropology. . . the only form of theology that is a subject is historical scholarship, literary scholarship. . . that kind of thing.” (“Clip taken from the Cosmic Skeptic Podcast #10.”)
I just wrote a piece for another venue that partly involves theology (stay tuned), and once again I was struck by the intellectual vacuity and weaselly nature of traditional theologians. And so I ask readers a question:
What is the value of theology? Has its endless delving into the nature of God and his ways yielded anything of value?
And I still don’t think that divinity schools are of any value, even though we have one at Chicago. After all, concerning their concentration on Christianity and Judaism, they are entire schools devoted to a single work of fiction. Granted, it’s an influential work of fiction, and deserves extra attention for that, but trying to pry truth out if it. . . well, it’s wasted effort and money.
I asked this question five years ago, noting that Dan Barker defined theology as “a subject without an object.”
A few kindly readers, such as ecologist Susan Harrison of UC Davis, have sent in photos, so the feature is not yet moribund. Susan’s narrative and IDs are indented, and you can enlarge the owl photos by clicking on them.
A winter visit to the owls of Bob Dylan Country
Many North American owls are not regularly migratory like songbirds, but will shift many miles to the north or south depending on yearly weather conditions and prey availability. Once every five or more years, the northernmost Midwest receives a winter influx of Boreal Owls (Aegolius funereus). The arrival of this handsome little raptor is so exciting that some birders will travel from as far away as (say) California for a weekend to see it.
Having heard about the Boreal Owls in January, I reached out to a local guide and arranged a late February trip to Two Harbors, Minnesota on the north shore of Lake Superior. On our first day it seemed I might have waited too long. The weather had warmed and no owls had been reported for a few days. We spent 10 fruitless hours cruising the roads and staring obsessively into the willows, alders, and small spruce along the verges. Had the owls moved back north?
Our second day dawned as clear and cold as a proper Minnesota winter morning. Not half an hour into our renewed search, a teardrop-shaped gray bundle stared back at us from the roadside shrubbery. With a nod to Bob Dylan, “Highway 61 Revisited” describes exactly how we found this owl!
Our first Boreal Owl:
Later that day we saw another one at Sax-Zim Bog, a famous destination for seeking overwintering owls of multiple species.
Our second Boreal Owl:
We were greatly helped by the close-knit network of regional owlers who share sightings with one another over an app. They guard information closely to spare owls from excessive attention.
Owlers at our second Boreal Owl sighting:
Having achieved success with the elusive Boreal Owl, we cruised around Sax-Zim Bog looking for the magnificent and more regularly occurring Great Gray Owl (Strix nebulosa). These are similar to Boreal Owls in being boreal forest inhabitants, nonmigratory, and shifting farther south in some years. We found a very sleepy owl perched along a roadside.
Great Gray Owl:
Finally we looked for Snowy Owls (Bubo scandiacus), which unlike the other two, undergo a regular winter migration to this area from their breeding grounds in the high Arctic. In most years they reach only the northern tier of US states, but they wander much farther south every now and then. They seem to be highly adaptable; one reliable place to see them, in fact, is the industrial district of Superior, Wisconsin. I think Bob Dylan would approve of their taste in gritty, down-to-earth surroundings.
Snowy Owl:
As part of my post last week about measurement and measurement devices, I provided a very simple example of a measuring device. It consists of a ball sitting in a dip on a hill (Fig. 1a), or, as a microscopic version of the same, a microsopic ball, made out of only a small number of atoms, in a magnetic trap (Fig. 1b). Either object, if struck hard by an incoming projectile, can escape and never return, and so the absence of the ball from the dip (or trap) serves to confirm that a projectile has come by. The measurement is crude — it only tells us whether there was a projectile or not — but it is reasonably definitive.
Fig. 1a: A ball in a dimple on the side of the hill will be easily and permanently removed from its perch if struck by a passing object. Fig. 1b: Similarly to Fig. 1a, a microscopic ball in a trap made from electric and/or magnetic field may easily escape the trap if struck.In fact, we could learn more about the projectile with a bit more work. If we measured the ball’s position and speed (approximately, to the degree allowed by the quantum uncertainty principle), we would get an estimate of the energy carried by the projectile and the time when the collision occurred. But how definitive would these measurements be?
With a macroscopic ball, we’d be pretty safe in drawing conclusions. However, if the objects being measured and the measurement device are ultra-microscopic — something approaching atomic size or even smaller — then the measurement evidence is fragile. Our efforts to learn something from the microscopic ball will be in vain if the ball suffers additional collisions before we get to study it. Indeed, if a tiny ball interacts with any other object, microscopic or macroscopic, there is a risk that the detailed information about its collision with the projectile will be lost, long before we are able to obtain it.
Amplify QuicklyThe best way to keep this from happening is to quickly translate the information from the collision, as captured in the microscopic ball’s behavior, into some kind of macroscopic effect. Once the information is stored macroscopically, it is far harder to erase.
For instance, while a large meteor striking the Earth might leave a pond-sized crater, a subatomic particle striking a metal table might leave a hole only an atom wide. It doesn’t take much to fill in an atom-sized hole in the blink of an eye, but a crater that you could swim in isn’t going to disappear overnight. So if we want to know about the subatomic particle’s arrival, it would be good if we could quickly cause the hole to grow much larger.
This is why almost all microscopic measurements include a step of amplification — the conversion of a microscopic effect into a macroscopic one. Finding new, clever and precise ways of doing this is part of the creativity and artistry of experimental physicists who study atoms, atomic nuclei, or elementary particles.
There are various methods of amplification, but most methods can be thought of, in a sort of cartoon view, as a chain of ever more stable measurements, such as this:
A classic and simple device that uses amplification is a Geiger counter (or Geiger-Müller counter). (Hans Geiger, while a postdoctoral researcher for Ernest Rutherford, performed a key set of experiments that Rutherford eventually interpreted as evidence that atoms have tiny nuclei.) This counter, like our microscopic ball in Fig. 1b, simply records the arrival of high-energy subatomic projectiles. It does so by turning the passage of a single ultra-microscopic object into a measurable electric current. (Often it is designed to make a concurrent audible electronic “click” for ease of use.)
How does this device turn a single particle, with a lot of energy relative to a typical atomic energy level but very little relative to human activity, into something powerful enough to create a substantial, measurable electric current? The trick is to use the electric field to create a chain reaction.
The Electric FieldThe electric field is present throughout the universe (like all cosmic fields). But usually, between the molecules of air or out in deep space, it is zero or quite small. However, when it is strong, as when you have just taken off a wool hat in winter, or just before a lightning strike, it can make your hair stand on end.
More generally, a strong electric field exerts a powerful pull on electrically charged objects, such as electrons or atomic nuclei. Positively charged objects will accelerate in one direction, while negatively charged objects will accelerate in the other. That means that a strong electric field will
Meanwhile electrically neutral objects are largely left alone.
The StrategySo here’s the strategy behind the Geiger-Müller counter. Start with a gas of atoms, sitting inside of a closed tube in a region with a strong electric field. Atoms are electrically neutral, so they aren’t much affected by the electric field.
But the atoms will serve as our initial measurement devices. If a high-energy subatomic particle comes flying through the gas, it will strike some of the gas atoms and “ionize” them — that is, it will strip an electron off the atom. In doing so it breaks the electrically neutral atom into a negatively charged electron and a positively charged leftover, called an “ion.”
If it weren’t for the strong electric field, the story would remain microscopic; the relatively few ions and electrons would quickly find their way back together, and all evidence of the atomic-scale measurements would be lost. But instead, the powerful electric field causes the ions to move in one direction and the electrons to move in the opposite direction, so that they cannot simply rejoin each other. Not only that, the field causes these subatomic objects to speed up as they separate.
This is especially significant for the electrons, which pick up so much speed that they are able to ionize even more atoms — our secondary measurement devices. Now the number of electrons freed from their atoms has become much larger.
The effect is an chain reaction, with more and more electrons stripped off their atoms, accelerated by the electric field to high speed, allowing them in their turn to ionize yet more atoms. The resulting cascade, or “avalanche,” is called a Townsend discharge; it was discovered in the late 1890s. In a tiny fraction of a second, the small number of electrons liberated by the passage of a single subatomic particle has been multiplied exceedingly, and a crowd of electrons now moves through the gas.
The chain reaction continues until this electron mob arrives at a wire in the center of the counter — the final measurement device in the long chain from microscopic to macroscopic. The inflow of a huge number of the electrons onto the wire, combined with the flow of the ions onto the wall of the device, causes an electrical current to flow. Thanks to the amplification, this current is large enough to be easily detected, and in response a separate signal is sent to the device’s sound speaker, causing it to make a “click!”
Broader LessonsIt’s worth noting that the strategy behind the Geiger-Müller counter requires an input of energy from outside the device, supplied by a battery or the electrical grid. When you think about it, this is not surprising. After the initial step there are rather few moving electrons, and their total motion-energy is still rather low; but by the end of the avalanche, the motion-energy of the tremendous number of moving electrons is far greater. Since energy is conserved, that energy has to have come from somewhere.
Said another way, to keep the electric field strong amid all these charged particles, which would tend to cancel the field out, requires the maintenance of high voltage between the outer wall and inner wire of the counter. Doing so requires a powerful source of energy.
Without this added energy and the resulting amplification, the current from the few initially ionized atoms would be extremely small, and the information about the passing high-energy particle could easily be lost due to ordinary microscopic processes. But the chain reaction’s amplification of the number of electrons and their total amount of energy dramatically increases the current and reduces the risk of losing the information.
Many devices, such as the photomultiplier tube for the detection of photons [particles of light], are like the Geiger-Müller counter in using an external source of energy to boost a microscopic effect. Other devices (like the cloud chamber) use natural forms of amplification that can occur in unstable systems. (The basic principle is similar to what happens with unstable snow on a steep slope: as any off-piste skier will warn you, under the correct circumstances a minor disturbance can cause a mountain-wide snow avalanche.) If these issues interest you, I suggest you read more about the various detectors and subdetectors at ongoing particle experiments, such as those at the Large Hadron Collider.
Amplification in a Simplified SettingI’ve described the Geiger-Müller counter without any explicit reference to quantum physics. Is there any hope that we could understand how this process really takes place using quantum language, complete with a wave function?
Not in practice: the chain reaction is far, far too complicated. A quantum system’s wave function does not exist in the physical space we live in; it exists in the space of possibilities. Amplification involving hordes of electrons and ions forces us to consider a gigantic space of possibilities; for instance, a million particles moving in our familiar three spatial dimensions would correspond to a space of possibilities that has three million dimensions. Neither you nor I nor the world’s most expert mathematical physicist can visualize that.
Nevertheless, we can gain intuition about the basic idea behind this device by simplifying the chain reaction into a minimal form, one that involves just three objects moving in one dimension, and three stages:
You can think of these as the first steps of a chain reaction.
So let’s explore this simplified idea. As I often do, I’ll start with a pre-quantum viewpoint, and use that to understand what is happening in a corresponding quantum wave function.
The Pre-Quantum ViewThe pre-quantum viewpoint differs from that in my last post (which you should read if you haven’t already) in that we have two steps in the measurement rather than just one:
The projectile, microball and macroball will be colored purple, blue and orange, and their positions along the x-axis of physical space will be referred to as x1, x2 and x3. Our space of possibilities then is a three-dimensional space consisting of all possible values of x1, x2 and x3.
The two-step measurement process really involves four stages:
The view of this process in physical space is shown on the left side of Fig 2. Notice the acceleration of the microball between the two collisions.
Figure 2: (Left) In physical space, the projectile travels to the right and strikes the stationary microball, causing the latter to move; the microball is then accelerated to high speed and strikes the macroball, which recoils in response. The information from the initial collision has been transferred to the more stable macroball. (Right) The same process seen in the space of possibilities; note the labels on the axes. The system is marked by a red dot, with a gray trail showing its history. Note the two collisions and the acceleration between them. At the end, the system’s x3 is increasing, reflecting the macroball’s motionOn the right side of Fig. 2, the motion of the three-object system within the space of possibilities is shown by the moving red dot. To make it easier to see how the red dot moves acrossthe space of possibilities, I’ve plotted its trail across that space as a gray line. Notice there are two collisions, the first one when the projectile and microball collide (x1=x2) and the second where the two balls collide (x2=x3), resulting in two sudden changes in the motion of the dot. Notice also the rapid acceleration between the first collision and the second, as the microball gains sufficient energy to give the macroball appreciable speed.
The Quantum ViewIn quantum physics, the idea is the same, where the dot representing the system’s value of (x1, x2, x3) is replaced by the peak of a spread-out wave function. It’s difficult to plot a wave function in three dimensions, but I can at least mark out the region where its absolute value is large — where the probability to find the system is highest. I’ve sketched this in Fig. 3. Not surprisingly if follows the same path as the system in Fig. 2.
Figure 3: Sketch of the wave function for this system (compare to Fig. 2a), showing only the location of the highest peak of the wave function (the region where we are most likely to find the system.)In the pre-quantum case of Fig. 2, the red dot asserts certainty; if we were to measure x1, x2 and/or x3, we would find exactly the values of these quantities corresponding to the location of the dot. In quantum physics of Fig. 3, the peak of the wave function asserts high probability but not certainty. The wave function is spread out; we don’t know exactly what we would find if we directly measured x1, x2 and x3 at any particular moment.
Still, the path of the wave function’s peak is very similar to the path of the red dot, as was also true in the previous post. Generally, in the examples we’ve looked at so far, we haven’t shown much difference between the pre-quantum viewpoint and the quantum viewpoint. You might even be wondering if they’re more similar than people say. But there can be big differences, as we will see very soon.
The Wider ViewIf I could draw something with more than three dimensions, we could add another stage to our microball and macroball; we could accelerate the macroball and cause it to collide with something even larger, perhaps visible to the naked eye. Or instead of one macroball, we could amplify and transfer the microball’s energy to ten microballs, which in turn could have their energy amplified and transferred to a hundred microballs… and then we would have something akin to a Townsend discharge avalanche and a Geiger-Müller counter. Both in pre-quantum and in quantum physics, this would be impossible to draw; the space of possibilities is far too large. Nevertheless, the simple example in Figs. 2 and 3 provides some intuition for how a longer chain of amplification would work. It shows the basic steps needed to turn a fragile microscopic measurement into a robust macroscopic one, suitable for human scientific research or for our sense perceptions in daily living.
In the articles that will follow, I will generally assume (unless specified otherwise) that each microscopic measurement that I describe is followed by this kind of amplification and conversion to something macroscopic. I won’t be able to draw it, but as we can see in this example, the fundamental underlying idea isn’t that hard to understand.
Remember CRISPR (clustered regularly interspaced short palindromic repeats) – that new gene-editing system which is faster and cheaper than anything that came before it? CRISPR is derived from bacterial systems which uses guide RNA to target a specific sequence on a DNA strand. It is coupled with a Cas (CRISPR Associated) protein which can do things like cleave the DNA at the targeted location. We are really just at the beginning of exploring the potential of this new system, in both research and therapeutics.
Well – we may already have something better than CSRISP: TIGR-Tas. This is also an RNA-based system for targeting specific sequences of DNA and delivering a TIGR associated protein to perform a specific function. TIGR (Tandem Interspaced Guide RNA) may have some useful advantages of CRISPR.
As presented in a new paper, TIGR is actually a family of gene editing systems. It was discovered not by happy accident, but by specifically looking for it. As the paper details: “through iterative structural and sequence homology-based mining starting with a guide RNA-interaction domain of Cas9”. This means they started with Cas9 and then trolled through the vast database of phage and parasitic bacteria for similar sequences. They found what they were looking for – another family of RNA-guided gene editing systems.
Like CRISPR, TIGR is an RNA guided system, and has a modular structure. Different Tas proteins can be coupled with the TIGR to perform different actions at the targeted site. But there are several potential advantages for TIGR over CRISPR. Like CRISPR it is RNA guided, but TIGR uses both strands of the DNA to find its target sequence. This “dual guided” approach may lead to fewer off-target errors. While CRISPR works very well, there is a trade-off in CRISPR systems between speed and precision. The faster it works, the greater the number of off-target actions – like cleaving the DNA in the wrong place. The hope is that TIGR will make fewer off-target mistakes because of better targeting.
TIGR also has “PAM-Independent targeting”. What does that mean? PAM stands for protospacer adjacent motifs – these are short DNA sequences, about 6 base pairs, that exist next to the sequence that his being targeted by CRISPR. The Cas9 protease will not function without the PAM. It appears to have evolved so that the bacteria using CRISPR as an adaptive immune system can tell self from non-self, as invading bacteria or viruses will have the PAM sequences, but the native DNA will not. The end result is that CRISPR needs PAM sequences in order to function, but the TIGR system does not. This makes the TIGR system much more versatile.
I saved what is potentially the best advantage for last – Tas proteins are much smaller than Cas proteins, about a quarter of the size. At first this might not seem like a huge advantage, but for some applications it is. One of the main limiting factors for using CRISPR therapeutically is getting the CRISPR-Cas complex into human cells. There are several available approaches – physical methods like direct injection, chemical methods, and viral vectors. Specific methods, however, generally have a size limit on the package they can deliver into a cell. Adeno-associated vectors (AAVs) for example have lots of advantaged but only can deliver relatively small payloads. Having a much more compact gene-editing system, therefore, is a huge potential advantage.
When it comes to therapeutics, the delivery system is perhaps the greater limiting factor than the gene targeting and editing system itself. There are currently two FDA indications for CRISPR-based therapies, both for blood disorders (sickle cell and thalassemia). For these disorders bone marrow can be removed from the patient, CRISPR is then applied to make the desired genetic changes, and then the bone marrow is transplanted back into the patient. In essence, we bring the cells to the CRISPR rather than the CRISPR to the cells. But how do we deliver CRISPR to a cell population within a living adult human?
We use the methods I listed above, such as the AAVs, but these all have limitations. Having a smaller package to deliver, however, will greatly expand our options.
The world of genetic engineering is moving incredibly fast. We are taking advantage of the fact that nature has already tinkered with these systems for hundreds of millions of years. There are likely more systems and variations out there for us to find. But already we have powerful tools to make precise edits of DNA at targeted locations, and TIGR just adds to our toolkit.
The post The New TIGR-Tas Gene Editing System first appeared on NeuroLogica Blog.
Measles is back, and so are all the old antivax tropes about the disease and the vaccine. Unfortunately, there's an antivaxxer in charge.
The post Measles is back, and so are all the old antivax tropes about it first appeared on Science-Based Medicine.There are several well-documented health risks that come from spending extended periods in microgravity, including muscle atrophy, bone density loss, and changes to organ function and health. In addition, astronauts have reported symptoms of immune dysfunction, including skin rashes and other inflammatory conditions. According to a new study, these issues could be due to the extremely sterile environment inside spacecraft and the International Space Station (ISS). Their results suggest that more microbes could help improve human health in space.
The study was led by Rodolfo A. Salido and Haoqi Nina Zhao, a bioengineer and an environmental analytical chemist at the University of California San Diego (UCSD), respectively. They were joined by researchers from multiple UCSD programs and centers, the University of Denver, the Chiba University-UC San Diego Center for Mucosal Immunology Allergy and Vaccines (cMAV), Space Research Within Reach, the Baylor College Center for Space Medicine, the Blue Marble Space Institute of Science (BMSIS), the Biotechnology and Planetary Protection Group at NASA JPL, and the Astronaut Office at NASA Johnson.
The study was a collaborative effort with astronauts aboard the ISS, who swabbed 803 different surfaces – 100 times that of previous surveys – to get a census of microbes aboard the station. The researchers identified which bacterial species and chemicals were present in each sample and created three-dimensional maps to illustrate where each of them was found and how they might be interacting. Their results indicate that the ISS has a much lower diversity of microbes compared to human-built environments on Earth.
NASA astronaut Catherine (Cady) Coleman, Expedition 26 flight engineer, is pictured with a stowage container and its contents in the Harmony node of the International Space Station. Credit: NASAOverall, the team found that chemicals from cleaning products and disinfectants were ubiquitously throughout the station and that astronauts mostly introduce microbes aboard the ISS through shed human skin cells. They also found that different modules hosted different microbial communities and chemical signatures based on the module’s use. For example, dining and food preparation areas contained more food-related microbes, whereas the ISS’s space toilet contained more urine- and fecal matter-related microbes and bioproducts of metabolism (metabolites).
“We noticed that the abundance of disinfectant on the surface of the International Space Station is highly correlated with the microbiome diversity at different locations on the space station,” said Zhao in a Cell Press release. These results suggest that more microbes from Earth could help improve astronaut health. Said Salido:
“Future built environments, including space stations, could benefit from intentionally fostering diverse microbial communities that better mimic the natural microbial exposures experienced on Earth, rather than relying on highly sanitized spaces. If we really want life to thrive outside Earth, we can’t just take a small branch of the tree of life and launch it into space and hope that it will work out. We need to start thinking about what other beneficial companions we should be sending with these astronauts to help them develop ecosystems that will be sustainable and beneficial for all.”
The team found that microbial communities were less diverse aboard the ISS than most places on Earth, except where urban, industrialized, and isolated environments (i.e., hospitals) were concerned. They further found that ISS surfaces lacked free-living environmental microbes usually found in soil and water. Similar to the well-documented benefits gardening has for the human immune system, the researchers conclude that incorporating these microbes and their substrates into the ISS could improve astronaut health without sacrificing hygiene.
Astronauts on the International Space Station experience an orbital reboost. Credit: NASA/ESA“There’s a big difference between exposure to healthy soil from gardening versus stewing in our own filth, which is kind of what happens if we’re in a strictly enclosed environment with no ongoing input of those healthy sources of microbes from the outside,” said co-author Robin Knight, a computational microbiologist and professor at UCSD and leader of the Knight Lab.
Looking to the future, the researchers hope to refine their analyses to detect potentially pathogenic microbes and how environmental metabolites could be used as indicators for astronaut health. The team claims that these methods could also help improve the health of people living and working in similarly sterile environments on Earth.
This research was supported by the National Institute of Health (NIH), the Alfred P. Sloan Foundation, UCSD, the Center for the Advancement of Science in Space (CASIS), and the ISS National Laboratory. The paper detailing their findings, “The International Space Station has a unique and extreme microbial and chemical environment driven by use patterns,” was published on February 27th in the journal Cell.
Further Reading: EurekAlert!
The post For the Sake of Astronaut Health, Should we Make the ISS Dirtier? appeared first on Universe Today.
I guess the number of papers and articles people send me about the definition of sex is one sign that it remains an important issue for the populace. Indeed, I think that in future decades people will see the kerfuffle about a simple and widely accepted definition (the gametic one) as a tempest in a teapot, stirred up by activists who demand that nature conform to their own ideology.
Philosopher Alex Byrne of MIT, whose recent book Trouble with Gender: Sex Facts, Gender Fictions I recommend, has also written a short and useful article on the site Fairer Disputations (“Sex-Realist Feminism for the 21st Century”) that covers a lot of ground, including the recent definition of sex given by the Department of Health and Human Services, the history of the definition that was used (the gametic one), the opposition to that definition, and “the British gender wars”, which are particularly nasty but have some smart combatants, like Helen Joyce, Emma Hilton, and J. K. Rowling, to defend those women who lose their jobs or get demonized for speaking the truth.
You can (and should) read Alex’s article by clicking below (it’s free), and I’ll give a few quotes (indented)
The beginning of understanding the nature of biological sex. Nobody really knew about gametes until 1677, when the Dutch scientist Antonie van Leeuwenhoek found little wiggly “animalcules” in his sperm. Over the years since then, biologists began to realize that all animals and plants have two sexes with different gametes, and those gametes must usually unite to produce to produce a new offspring. Further, regardless of whether the sexes are produced by chromosomes, the environment, genes, or social interactions, they are always two, and this condition has evolved independently nearly a dozen times. Here’s Alex’s description of the beginning, and how the definition continues–up to this day:
Sexual reproduction remained something of a mystery for the next five millennia, until the German physician Theodor von Bischoff hypothesized in the mid-nineteenth century that it involved the fusion of (in the EO’s language) two “reproductive cells”—one sperm and one ovum, or egg. The sperm is small and relatively simple, the egg large and much more complicated. When von Bischoff’s theory was later confirmed, it was a short step to uncovering the deep distinction between females and males: females produce large reproductive cells (or gametes), males produce small ones. What about producing both? Some animals (and many plants) do just that: they are hermaphrodites—female and male.
Here’s Robert Payne Bigelow, a biology professor from my own university, writing in 1903:
The ability to produce a macro- or microgamete constitutes the essential distinction of sex. The individual which produces the latter is said to be of the male sex, the individual producing the former is said to be of the female sex. In most of the higher plants and in a few of the lower animals both sexes are included in a single individual, which is then said to be hermaphrodite.
The French philosopher Simone de Beauvoir noted that the sexes are “defined primarily … by the gametes which they produce—sperms and eggs respectively” in The Second Sex, published in 1949. Yet in her 2023 book Beyond the Binary: Thinking About Sex and Gender, the feminist philosopher Shannon Dea tells us that “papaya trees come in three sexes—male, female, and hermaphroditic.” That is wrong, as Bigelow made clear 120 years earlier. Hermaphroditic papaya trees are both male and female, not a third sex.
The misguided critics. I can’t resist quoting this part, but the article has far more stuff in it:
In short, the EO’s [Executive Order’s] definitions of “female” and “male” are right, or at least substantially on the right lines. (On February 19, the Department of Health and Human Services issued a memo with improved versions.) So why the furor? What were the experts’ main complaints?
Some struggled with reading comprehension. The Director of the Centre for Indigenous Initiatives at Carleton University criticized the claim that there are “two genders” as “ignorant,” evidently thinking of so-called “third genders” in some traditional North American societies. But the EO pronounces on the number of sexes, not on the special cultural arrangements that have sometimes been made to accommodate homosexual men. In any case, even if the EO had said there were only two “genders,” it would have used the word as a synonym for “sex.”
Others were just painfully muddled. A biological anthropologist at the University of Urbana-Champaign declared that sex has multiple definitions, each valid for different purposes. One definition “is around typical hormone ranges. [For instance, people with] polycystic ovary syndrome end up having androgen levels that are very different from those of most people that we might put in the sex category of female.” The suggestion seemed to be that on one acceptable definition of “female,” people with polycystic ovary syndrome aren’t female because they have (relatively) high androgen levels. (The clue is in the name: polycystic ovary syndrome.)
Any acceptable definition of sex needs to get the right results for cats, ibises, and date palms, and one based on circulating hormones won’t. A definition based on chromosomes works for cats and date palms: they both employ the XX/XY sex determination system, with the males being XY. But ibises have it the other way round: the lady ibis is the one with different sex chromosomes. And what about other animals known to the ancient Egyptians, such as the Nile crocodile and the honeybee? The sex of a baby croc is determined not by chromosomes, but by the temperature of the nest, and male bees develop from unfertilized eggs, with half a set of chromosomes.
There is no definition of sex other than the standard gamete one that classifies female humans, cats, ibises, date palms, crocodiles, and bees correctly. That did not stop the anthropologist from saying that the EO “misunderstand[s] basic human biology.”
Anthropologists can be flaky. Still, one might have expected the Presidents of the Society for the Study of Evolution, the American Society of Naturalists, and the Society of Systematic Biologists to get basic biology right. However, according to them, in a letter to Trump and members of Congress, sex is a spectrum, a “continuum of male to female.” This “continuum” apparently has something to do with “chromosomes, hormonal balances, … gonads, external genitalia,” although the three presidents declined to spell out the details. Presumably, on this account, women with polycystic ovary syndrome are mostly-but-not-entirely female—perhaps a slight improvement on the anthropologist’s position. The biologist Jerry Coyne dissected the letter on his blog, writing in an email, “I used to be President of the Society for the Study of Evolution. Now it embarrasses me.”
And I’ll add that while most of the evolutionists I know agree about the gametic definition of sex, there is of course still debate about how that definition will be used on documents, driver’s licenses, and the like. Alex recognizes that these issues are far more contentious—at least to biologists:
Trump’s EO does not rest with the biological facts; it also sets a raft of policies. Among other things, government officials are directed “to require that government-issued identification documents, including passports, visas, and Global Entry cards, accurately reflect the holder’s sex.” It is understandable that someone seeking peace of mind by living as a member of the other sex would want a sex marker to match, especially when traveling to the less tolerant parts of the world. We should hope that the EO does not make life more difficult for such people than it already is. That hope is undoubtedly in vain, but the problem with pushing the pendulum too far in one direction is that it will tend to swing too far in the other. The activists who—predictably—have produced an equal and opposite reaction have only themselves to blame.
Here we have a new paper in Nature Scientific Reports, accompanied by a news piece in Science, that sends a misleading message to the public, both about “inheritance of trauma” and the effects of epigenetic changes. Both pieces are free to access; click on the first headline below to go to the news piece, and the second to go to the scientific report (its pdf is here).
I must add that most of the “misleading” appears not in the paper but in the News piece by Andrew Curry, who suggests that trauma is inherited when in fact there’s not a scintilla of evidence for that. But the authors of the real paper don’t go to any great lengths to dispel that notion, either, and this suggestion is undoubtedly why Nature Scientific Reports found the piece clickbaity and publishable.
Note that the news piece suggests that what is inherited across three generations is trauma. That is false. What the researchers shows is that Syrian women exposed to trauma during their country’s wars have offspring and grand-offspring that inherited certain epigenetic markers in the DNA: methyl groups affixed to consistent positions in the offspring DNA. This “epigenetic inheritance” may indeed be caused by maternal trauma, for trauma messes up the fetal environment, and since female fetuses already carry their own eggs after a few months, it could affect grandchildren at all.
But inheritance of trauma itself? NO EVIDENCE. They have no idea what the DNA positions that are methylated even do, much less that they’re in genes that affect trauma.
The situation described in both the news puffery and the paper resembles the “epigenetic” inheritance associated with the Dutch “Hunger Winter” of 1944-1945, during which a German blockade of food killed around 20,000 people in the Netherlands. It turns out that the children of survivors who were pregnant during the famine had a higher frequency obesity, higher cholesterol, as well as higher incidences of diabetes and schizophrenia, than did children of survivors who were not pregnant. The former also lived less long, but what they inherited as not “famine”, but a panoply of diseases and conditions that may well have been the result of biochemical changes in a pregnant mother experiencing famine. These changes were certainly not adaptive, either! However, the inheritance lasted only one generation (grandchildren of pregnant survivors were normal). PLUS, what was inherited in the famous Dutch case were conditions and behaviors, while in the present case the “trauma” appears to have caused only slight changes in the DNA sequence that had an unknown effect. There was no inheritance of trauma described at all. But look at the headline below!
The news piece:
It summarizes the scientific report this way:
Rana Dajani, a biologist at Hashemite University in Amman, Jordan, wondered whether the recent conflicts in neighboring Syria might have left traces in the epigenomes of people in the country—with implications for the health of future generations. “I wanted to ask if environmental exposure was impacting different genes,” Dajani says. “Can those changes be transferred across three generations, or more?”
To answer that, Dajani, a Jordanian researcher of Palestinian and Syrian descent, teamed up with researchers in the United States and Jordan, leveraging her family contacts to assemble a cohort of Syrian women living in Jordan. In one group were women and girls who were either pregnant or in utero themselves during the Syrian civil war that began in 2011 and had fled to Jordan. Another group included someone who was pregnant during a government-orchestrated massacre in the city of Hama in the early 1980s, her daughter and grandchildren, and other unrelated female descendants of survivors. As a control group, Dajani included Syrian families who emigrated to Jordan almost a century ago, sharing a culture with the rest of the participants but with no direct experience of violent conflict.
Biologist Dima Hamadmad, a co-author and a descendant of survivors of the Hama violence, spent hundreds of hours over the course of 5 years contacting potential participants and listening to their stories. Many of them had experienced trauma such as being severely beaten, witnessing wounded or dead bodies, or seeing someone being shot or killed. “It’s a lot of work, and the victims also deserve a lot of credit,” says Isabelle Mansuy, an epigeneticist at ETH Zürich who was not part of the research. “What they’ve done is remarkable.”
After using cheek swabs to collect DNA from more than 130 women, the team looked for patterns in DNA methylation, a process in which responses to environmental circumstances—such as trauma—add or subtract to genes chemical tags known as methyl groups that alter the gene’s function. DNA methylation is among the most studied examples of epigenetic change.
The team found that women who experienced wartime trauma directly shared such changes in 21 different spots in their genome; grandchildren in the study showed alterations in a different set of 14 sites. “We discovered a number of genes with signatures of trauma transferred across generations compared to the control group,” Dajani says. The function of the genes and proteins associated with the sites isn’t known.
Comparing those results with the surveys and interviews revealed the more wartime horrors someone experienced, the more methylation changes they seemed to have. “It doesn’t look random,” says Mulligan, who co-led the study with Dajani.
I’m prepared to believe all that, though I’m disturbed by the important control group, which is described as “Syrian families who emigrated to Jordan almost a century ago, sharing a culture with the rest of the participants but with no direct experience of violent conflict.” Well, one can debate whether a group that has been in non-warring Jordan for a century has experienced the same “culture” as Syrians who emigrated in 1980 and 2011. But others who know more about epigenetics than I have weighed in with other criticisms (see below). What was affected may not have been trauma, but just gum disease!
Click the article to read. I can’t find any description of the control group in the paper except for this—”In the control group, Syrian grandmothers and mothers lived in Jordan prior to 1980″, and it adds they were “unexposed to war,” but it doesn’t say that not that the ancestors of the control individuals been in Jordan for a century. Oh well, we’ll let that slide.
The paper:
Here’s a diagram of the experimental setup from the paper; the caption is also from the paper. Click to enlarge.
There are three groups: the control (right), consisting of pregnant women unexposed to war; the 1980 group, which included women who experienced violence when the fetuses had eggs (about 12 weeks into pregnancy); and the 2011 group, which included women who experienced violence in the early stages of pregnancy, before the (female) fetus developed eggs. Click diagram to enlarge:
(From paper): Our research strategy was designed to test contrasting exposures to violence (direct, prenatal, germline) for changes in DNAm in three groups of three-generation Syrian families. The violence exposures of three generations (F1, F2, F3) for each group are indicated—the 1980 group was directly, prenatally, and germline exposed in the F1 generation, the 2011 group was directly and prenatally exposed in the F2 generation, and the Control group was unexposed. Exposure types are color coded: red = direct exposure, green = prenatal exposure, blue = germline exposure, and yellow = no exposure.Note the very small sample size of both women exposed to trauma and their children and grandchildren. Here is the violence the authors describe what was experienced by pregnant women:
“. . . . violent traumatic experiences that included being severely beaten, being persecuted (by the authorities/militia), seeing a wounded or dead body, and seeing someone else severely beaten, shot or killed.”
They then did DNA sequencing of all individuals using a sampling system that identified 850,000 nucleotide bases (SNPs). Out of these, they found 21 sites that were methylated in a pretty consistent way among those who experienced violence; these were in the pregnant women’s non-germline DNA, so could not be passed on. However, they found another 14 sites methylated in the germline (mother’s or fetus’s eggs), and were inherited across not just one generation, but across two (this might be expected since fetal eggs can also be exposed to grandmother’s physiological conditions). But in no case did they know which genes were involved in the changes, though they speculate that some regions could be involved in “gene regulation”.
The authors conclude this:
There is strong scientific evidence indicating that impacts of stress and trauma can reverberate far into the future, possibly through epigenetic mechanisms.
Well, that’s true if “far into the future” means “three generations,” but epigenetic marks are usually wiped clean from the DNA when gametes (sperm and eggs) are made, and four generations is about as far as any environmental alterations of mammalian DNA have persisted. What we do not have here is either inheritance of trauma or any kind of permanent evolutionary change produced by the environment. This is manifestly not “Lamarckian inheritance“!
The news piece does proffer some mild criticism:
These results are consistent with research in mice and other organisms that shows trauma can be passed down across generations. But other researchers note that the sample size isn’t big enough to confidently conclude that trauma passes from generation to generation through the germline—in this case via egg cells. “It’s important to do studies like this, and we need more of them, and with larger samples,” says Michael Pluess, a psychologist at the University of Surrey who was not involved in this study but whose own work with Syrian refugee children has found similar violence-related methylation changes in different places of the genome. “We also need to replicate the findings to know if they’re real or just chance.”
If you click on the first link in the preceding paragraph, you’ll find changes in biomarkers that may be associated with trauma in humans and mice, but not evidence for the inheritance of trauma itself.
But there is even stronger criticism of the methods and conclusions posted on Bluesky by John Greally, a professor of genetics at Albert Einstein College of Medicine, and he has the chops to criticize. Here’s his post thread in its entirety. One of his important criticisms appears to be that they got the Syrian DNA by using buccal (cheek) swabs, and, as Greally notes, “This could be a very expensive study of gingivitis.” Also, note the penultimate post in which Greally says that there’s not any convincing evidence (including this paper) for transmission of acquired characteristics in mammals.” Just remember that when you hear about this study or the famous but misleading Dutch famine study.
As I wrote on February 13, three important societies representing evolutionary biology, ecology, and systematics issued a grossly misleading statement aimed at the government. (It is dated February 5, but I don’t think it’s yet been sent):
As I reported recently, the Presidents of three organismal-biology societies, the Society for the Study of Evolution (SSE), the American Society of Naturalists (ASN) and the Society of Systematic Biologists (SSB) sent a declaration addressed to President Trump and all the members of Congress. (declaration archived here) Implicitly claiming that its sentiments were endorsed by the 3500 members of the societies, the declaration also declared that there is a scientific consensus on the definition of sex, and the consensus is that sex is not binary but rather some unspecified but multivariate combination of different traits, a definition that makes sex a continuum or spectrum—and in all species! The bolding below is Jerry’s:
Scientific consensus defines sex in humans as a biological construct that relies on a combination of chromosomes, hormonal balances, and the resulting expression of gonads, external genitalia and secondary sex characteristics. There is variation in all these biological attributes that make up sex. Accordingly, sex (and gendered expression) is not a binary trait. While some aspects of sex are bimodal, variation along the continuum of male to female is well documented in humans through hundreds of scientific articles. Such variation is observed at both the genetic level and at the individual level (including hormone levels, secondary sexual characteristics, as well as genital morphology). Beyond the incorrect claim that science backs up a simple binary definition of sex, the lived experience of people clearly demonstrates that the genetic composition at conception does not define one’s identity. Rather, sex and gender result from the interplay of genetics and environment. Such diversity is a hallmark of biological species, including humans.
And as I write this today, I am still baffled how the different traits are supposed to be combined to determine one’s sex. I’d also like to ask the three societies exactly how many human sexes there are. As I’ve said before, I’m embarrassed to have been associated with the SSE since it’s now rejecting science in favor of currying favor with “progressive” ideology. It’s okay for societies to respond to situations that fall within their ambit, as this case does, but it’s not okay for them to purvey bogus science to buttress a political position.
Our original letter included 23 signers, most of whom are included in this second and final version of the letter. The first letter never received a response (I find that rather rude), but we’re hoping for a response to this one.
The list of signers has now grown to 125, whose names are placed below the fold to keep this post shorter. If we’ve counted correctly, the signers come from nineteen countries. (We have omitted the names of five medical doctors and a nurse who also signed.) Every signer was willing to make their names public—a condition for signing the group letter. Others I know of have written privately to the Presidents of the Societies—and received a response, so the Societies clearly didn’t think they had to respond to our first letter.
The point of this letter is not to show that our view is a “consensus” (the Societies did not poll their members, either), but simply to affirm that a variety of people in biology or adjacent areas reject the Societies’ construal of sex as both a “construct” and a “spectrum”. The letter below speaks for itself.
By the way, the driving force for writing the letter and collecting the signatures was Luana Maroja, Professor of Biology at Williams College, so kudos to her. And below this line is our letter, which was sent to the societies four minutes before this posting.
Dear presidents of the Tri-societies: ASN, SSB and SSE,
We, Tri-society members and/or biologists, are deeply disappointed by your recent letter “Letter to the US President and Congress on the Scientific Understanding of Sex and Gender” issued last Wednesday, Feb 5, 2025, in response to Trump’s executive order “Defending Women From Gender Ideology Extremism And Restoring Biological Truth To The Federal Government”.
While we agree that Trump’s executive orders are misleading, we disagree with your statements about the sex binary and its definition. In animals and plants, binary sex is universally defined by gamete type, even though sexes vary in how they are developmentally determined and phenotypically identified across taxa. Thus, your letter misrepresents the scientific understanding of many members of the Tri-societies.
You state that: “Scientific consensus defines sex in humans as a biological construct that relies on a combination of chromosomes, hormonal balances, and the resulting expression of gonads, external genitalia, and secondary sex characteristics.”
However, we do not see sex as a “construct” and we do not see other mentioned human-specific characteristics, such as “lived experiences” or “[phenotypic] variation along the continuum of male to female”, as having anything to do with the biological definition of sex. While we humans might be unique in having gender identities and certain types of sexual dimorphism, sex applies to us just as it applies to dragonflies, butterflies, or fish – there is no human exceptionalism. Yes, there are developmental pathologies that cause sterility and there are variations in phenotypic traits related to sexual dimorphism. However, the existence of this variation does not make sex any less binary or more complex, because what defines sex is not a combination of chromosomes or hormonal balances or external genitalia and secondary sex characteristics. The universal biological definition of sex is gamete size.
If you and the signers of this letter do not agree on these points, then the Tri-societies were wrong to speak in our names and claim that there is a scientific consensus without even conducting a survey of society members to see if such a consensus exists. Distorting reality to comply with ideology and using a misleading claim of consensus to give a veneer of scientific authority to your statement does more harm than just misrepresenting our views: it also weakens public trust in science, which has declined rapidly in the last few years. Because of this, scientific societies should stay away from politics as much as possible, except for political issues that directly affect the mission of the society.
Respectfully,
NAMES OF 125 SIGNERS ARE BELOW THE FOLD
[Click “continue reading” to see the names.]
In alphabetical order:
Charleen Adams, Lead Statistical Geneticist, Beth Israel Deaconess Medical Center
Eli Vieira Araujo-Jnr, biologist and independent journalist, Brazil
John Avise, Emeritus Professor, Univ, of California, Irvine
Nick Bailey, Research Fellow in Bioinformatics
Daniel A. Barbash, Professor, Molecular Biology and Genetics, Cornell University
Alexander T. Baugh, Associate Professor, Department of Biology, Swarthmore College
David Bertioli, Distinguished Investigator and Professor, College of Agricultural and Environmental Sciences, University of Georgia, USA
Andreas Bikfalvi, Professor MD PhD, University of Bordeaux, France
Franco Biondi, Professor of Natural Resources and Environmental Science
Ranieri Bizzarri, Professor of Biochemistry, University of Pisa, Italy
William J. Boecklen, Professor, Department of Biology, New Mexico State University
Jacobus (Koos) Boomsma, Emeritus Professor, University of Copenhagen Department of Biology
Glenn Borchardt, Director, Progressive Science Institute
Gary Bowering, Member, Royal Society of New Zealand
Gordon M. Burghardt, Professor of Psychology and Ecology & Evolutionary Biology (Emeritus), University of Tennessee
Chris Campbell, Research Assistant Professor (retired)/ University at Buffalo
Joseph Ciccolini, Professor/University Hospital of Marseille France
Kendall Clements, Professor, School of Biological Sciences, University of Auckland
Mark Collard, Chair in Human Evolutionary Studies, Simon Fraser University
Michael Coon, Scientist/Biopharma (cell therapy)
Athel Cornish-Bowden, Directeur de Recherche Émérite au CNRS (retired)
Richard Cowling, Emeritus Professor of Botany, Nelson Mandela University
Jerry Coyne, Professor Emeritus, Ecology and Evolution, University of Chicago
David Curtis, Honorary Professor, Genetics Institute, University College London, UK
Richard Dawkins, Emeritus Professor, University of Oxford
Robert O. Deaner, Professor, Department of Psychology, Grand Valley State University; PhD Biological Anthropology & Anatomy, Duke University
Gilly Denham, SSE member, Williams College
Lynn Devenport, Professor Emeritus of Psychology, University of Oklahoma
Chet Dickson, Secondary Education (retired)
Paul Doerder, Professor Emeritus Cleveland State University
Gavin Douglas, Postdoctoral Researcher, North Carolina State University
Janet Roman Dreyer, Retired PhD Research Fellow Caltech
Joan Edwards, Samuel Fessenden Clarke Professor of Biology, Williams College
Nelson Jurandi Rosa Fagundes, Associate Professor, Department of Genetics, Federal University of Rio Grande do Sul
Lars Figenschou, PhD. The Arctic University of Norway
David Frayer, Prof. Emeritus – Anthropology, University of Kansas
Steven M. Fredman, Associate Professor of Physiology & Neuroscience (retired)
Jonathan Gallant, Professor Emeritus of Genome Sciences, University of Washington
Constantino Macías Garcia, Full-time researcher (professor), Instituto de Ecología, Universidad Nacional Autónoma de México (UNAM)
Brian Gill, retired natural history curator from Auckland Museum, New Zealand
David Greene, Professor, California State Polytechnic University, Humboldt
Christy Hammer, Associate Professor of Education, Sociology, and Women and Gender Studies, University of Southern Maine
Brian Hanley, Biologist, PhD. UC Davis
Sheila Rutledge Harding, Professor (ret’d), College of Medicine, University of Saskatchewan
Michael Hart, Professor, Simon Fraser University
Wesley Hawthornthwaite, BSc Neuroscience and Mental Health, Carleton University
James Heard, MS Biology, San Francisco State, SF, California, Retired
Jody Hey, Professor, Temple University
Emma Hilton, Developmental Biology, University of Manchester, U.K.
Susan Hoffman, Associate Professor of Biology, Miami University and 40 year member of SSE
Carole Kennedy Hooven, Senior Fellow, AEI; Affiliate, Harvard Psychology.
David Hughes, Teaching Fellow in Marine Biology (retired), Scottish Association for Marine Science
Peter M. Hurley, PHD Widlife Biologist, currently GIS Analyst, Grant County, NM
Christine Janis, Professor Emerita, Ecology, Evolution, and Organismal Biology, Brown University
Maria Garza Jinich, Retired CS professor. National University of Mexico.
Brian Jones, Retired Principal Fish Pathologist, Government of Western Australia
Robert King, Dr, University College Cork, Ireland
Anatoly Kolomeisky, Professor of Chemistry, Rice University
Shawn R. Kuchta, Professor, Biological Sciences, Ohio University
Michael Lattorff, Associate Professor (Parasitology) / University of KwaZulu-Natal, School of Life Sciences, Durban, South Africa
Benoît Leblanc, Lecturer, Sherbrooke University
Edward Lee, SSE member, Williams College
Harry Lusic, Associate Professor of Chemistry, William Peace University
Dan Lynch, Professor of Biology, Emeritus, Williams College
Maya Dyankova Markova, Associate Professor of Biology at the Medical University of Sofia, Bulgaria
Luana S. Maroja, Professor of Biology, Williams College
Edward Matalka, SSE member, Adjunct Professor of Biology, Worcester State University
Nicholas J. Matzke, Senior Lecturer, School of Biological Sciences, University of Auckland
Gregory C. Mayer, Professor of Biological Sciences, University of Wisconsin-Parkside
Stephanie Mayer, Senior Instructor Emerita, Department of Ecology and Evolutionary Biology, University of Colorado, Boulder
Marcella McClure, Microbiology retired from Montana State University
Richard J. McNally, Professor of Psychology, Harvard University
Axel Meyer, Lehrstuhl für Zoologie und Evolutionsbiologie, University of Konstanz
William Meyer, Educator, General Science, Mokena Junior High School, Illinois
Neil Millar, Biology textbook author and retired biology teacher
Michael Mills, Associate Professor of Psychology, Loyola Marymount University
Graeme Minto, Biologist, Πανεπεστιμιο Κριτις
Robert Montgomerie, Professor Emeritus of Biology Queen’s University
Greg Murray, Professor Emeritus of Biology, Hope College
Paulo Nadanovsky, Professor of Epidemiology, Universidade do Estado do Rio de Janeiro
Raymond Nelson, Biology Educator/North Thurston Public Schools
Howard S. Neufeld, Professor of Biology, Appalachian State University
Judith Totman Parrish, Professor and Dean Emerita/University of Idaho
Laurent Penet, PI in Agricultural Science, INRAe, Guadeloupe
Charles C. Peterson, Ph.D., Retired biologist Copper Mountain College
Steven Pinker, Johnstone Family Professor of Psychology, Harvard University
David Policansky, PhD, Scholar, US National Research Council, retired.
Chris Pook, Senior Research Fellow; Lead Technologist, The Liggins Institute, The University of Auckland
Anthony M. Poole, Professor, School of Biological Sciences, University of Auckland
Jorge Octavio Juarez Ramirez, PhD Candidate (Biological Sciences, Evolution and Genetics)/Universidad Nacional Autonoma de Mexico
Mary Rasmussen, Professor Emerita, Biomedical and Health Information Sciences, University of Illinois Chicago
Michel Raymond, Evolutionary Anthropology, Institute of Evolutionary Studies, Montpellier, France
Jaime Renart, Retired researcher, molecular and cellular biology, CSIC. Spain
Jacques Robert, Emeritus professor of cancer biology, University of Bordeaux, France
Mel Robertson, Professor Emeritus of Biology, Queen’s University at Kingston, ON, Canada
Rafael L. Rodriguez, Professor, Biological Sciences, University of Wisconsin-Milwaukee
James J. Roper, Professor (retired), ecology, evolution, ornithology, Institute for Tropical Ecology, Panama
Callum Ross, Professor of Organismal Biology and Anatomy, University of Chicago
Claudio Rubiliani, Docteur d’Etat. Honorary MCF Biologie des Organismes. Univ. Aix-Marseille (France)Visiting Professor Duke
Bjørn Ove Sætre, Developmental biology University of Bergen, Norway retired teacher
Lisa Sanders, Ph.D., Genetics, North Carolina State University
David Scadden, Professor, Stem Cell and Regenerative Biology and of Medicine, Harvard University
Julia Schaletzky, Professor of Molecular Therapeutics (Adj.), Dept. of Molecular and Cell Biology, University of California, Berkeley
Brandon Schmit, Wildlife Disease Biologist, USDA
Corrie Schoeman, Associate Professor, School of Life Sciences, University of KwaZulu Natal
Garvin Schulz, Dr., Department of Sociobiology/Anthropology, University of Göttingen
Elizabeth Sherman, Professor of Biology, Emerita, Bennington College
David Smith, Emeritus, Department of Biology, Williams College
Flavio S.J, de Souza, Group leader in Developmental Biology, IFIBYNE-CONICET, University of Buenos Aires, Argentina
Robert Paul Spence, Biotechnology company Chief Scientist
Steve Stewart-Williams, Professor of Psychology, University of Nottingham Malaysia
Malcolm Storey, PhD, naturalist retired
Mark Sturtevant, Associate Professor of Practice, Biological Sciences, Oakland University
John P. Sullivan, SSB member, PhD in Zoology, Duke University
Douglas Swartzendruber, Professor Emeritus, Biology, University of Colorado
Costas A. Thanos, Prof. Emer., Dept Biology, National and Kapodistrian University of Athens, Greece
Keith M. Vogelsang, Professor of Biology, Ivy Tech Community College
Schulte von Drach, Biologist (PhD). Journalist
Graham Wallis, Emeritus Professor, Population genetics and molecular evolution, University of Otago
Philip Ward, Professor Entomology, University of California Davis
Bob Warneke, Jr., BA (’73) and MS (’76) – Biology; Trinity University
Randy Wayne, Associate professor of plant biology, Cornell University
Marcelo Weksler, Professor, Museu Nacional, Universidade Federal do Rio de Janeiro, Brazil
Landon Whitby, Chemical Biologist, PhD, The Scripps Research Institute
Mike Zenanko, Director Emeritus, Jacksonville State University
Because it’s Sunday, we get another dollop of photos from John Avise, who continues his series on North American butterflies. John’s captions and IDs are indented, and you can enlarge the photos by clicking on them.
Butterflies in North America, Part 12
This week continues my 18-part series on butterflies that I’ve photographed in North America. I’m continuing to go down my list of species in alphabetical order by common name.
Mourning Cloak (Nymphalis antiopa), topwing:
Mourning Cloak, underwing:
Mourning Cloak, larvae on a host plant Arroyo Willow (Salix lasiolepis):
Mylitta Crescent (Phyciodes mylitta):
Northern Crescent (Phyciodes cocyta), topwing:
Northern Crescent, underwing:
Northern Pearly-eye (Lethe anthedon), underwing:
Northern White Skipper (Heliopetes ericetorum), topwing:
Northern White Skipper, underwing:
Ocola Skipper (Panoquina ocola) underwing:
Orange Sulphur (Colias eurytheme) underwing:
Orange-barred Sulphur (Phoebis philea), underwing:
On December 27th, 2024, the Chilean station of the Asteroid Terrestrial-impact Last Alert System (ATLAS) detected 2024 YR4. This Near-Earth Asteroid (NEA) belongs to the Apollo group, which orbits the Sun with a period of approximately four years. For most of its orbit, 2024 YR4 orbits far from Earth, but sometimes, it crosses Earth’s orbit. The asteroid was spotted shortly after it made a close approach to Earth on Christmas Day 2024 and is now moving away. Additional observations determined it had a 1% probability of hitting Earth when it makes its next close pass in December 2032.
This led the International Asteroid Warning Network (IAWN) – overseen by the United Nations Office for Outer Space Affairs (UNOOSA) – to issue the first-ever official impact risk notification for 2024 YR4. The possibility of an impact also prompted several major telescopes to gather additional data on the asteroid. This included the Subaru Telescope at the Mauna Kea Observatory in Hawaii, which captured images of the asteroid on February 20th, 2025. Thanks to the updated positional data from these observations, astronomers have refined the asteroid’s orbit and determined that it will not hit Earth.
This is not the first time the odds of the asteroid hitting Earth have been reevaluated. Throughout February, refined measurements of the asteroid altered the estimated likelihood multiple times, first to 2.3% and then to 3.1%, before dropping significantly to 0.28%. Thanks to the observations of the Subaru Telescope, which were conducted at the request of the JAXA Planetary Defense Team and in response to the IAWN’s call for improved orbital tracking, the chance of impact has been downgraded to 0.004%.
Monte Carlo modeling of 2024 YR4’s swath of possible locations as of February 23rd, 2025 – 0.004% probability of impact. Credit: iawn.netThe updated estimate was calculated by NASA’s Center for NEO Studies (CNEOS), the ESA’s Near-Earth Objects Coordination Centre (NEOCC), and the NEO Dynamic Site (NEODyS). The Subaru observations were conducted using the telescope’s Hyper Suprime-Cam (HSC), a wide-field prime-focus camera that captured images of 2024 YR4 as it grew dimmer. The observations have since been forwarded to the Minor Planet Center (MPC) of the International Astronomical Union (IAU). Dr. Tsuyoshi Terai of the National Astronomical Observatory of Japan (NAOJ), who led the observations, explained:
“Although 2024 YR4 appeared relatively bright at the time of its discovery, it has been steadily fading as it moves away from the Earth. By late February, observations would have been extremely challenging without a large telescope. This mission was successfully accomplished thanks to the Subaru Telescope’s powerful light-gathering capability and HSC’s high imaging performance.”
Based on these latest observations, the IAWN reports that 2020 YR4 will “pass at a distance beyond the geosynchronous satellites and possibly beyond the Moon.” They also indicate that there is no significant potential that the asteroid will impact Earth in the next century. The IAWN also states that it will continue to track 2024 YR4 through early April. At this point, it will be too faint to image and won’t be observable from Earth again until 2028.
Further Reading: NAOJ
The post Good News! The Subaru Telescope Confirms that Asteroid 2024 YR4 Will Not Hit Earth. appeared first on Universe Today.
There are several well-documented health risks that come from spending extended periods in microgravity, including muscle atrophy, bone density loss, and changes to organ function and health. In addition, astronauts have reported symptoms of immune dysfunction, including skin rashes and other inflammatory conditions. According to a new study, these issues could be due to the extremely sterile environment inside spacecraft and the International Space Station (ISS). Their results suggest that more microbes could help improve human health in space.
by Greg Mayer
As someone interested in history, I am both interested and wary when analogies are drawn among different periods and events in history, especially applying the past to the present day. And, as another prelude, I should note that I have said here before at WEIT that Bret Stephens is wrong about most things. But when he’s right, he’s right, and he’s right about yesterday’s cringe-inducing display of depravity by the erstwhile leaders of the free world, the President and Vice President of the United States. [JAC: You can find Stephens’s piece archived here.] I found Stephens’ historical analogy to the pre-Pearl Harbor meeting between Franklin D. Roosevelt and Winston Churchill, which led to the Atlantic Charter, whose principles include that there should be “no aggrandizement, territorial or other” and that “sovereign rights and self-government [shall be] restored to those who have been forcibly deprived of them”, very clarifying. Money quote:
If Roosevelt had told Churchill to sue for peace on any terms with Adolf Hitler and to fork over Britain’s coal reserves to the United States in exchange for no American security guarantees, it might have approximated what Trump did to Zelensky.