Recently posted benchmarks have revealed how capable the brand-new Apple M4 chip is in terms of single-core performance, outpacing even the best processors on the market.
As spotted by Tom’s Hardware, there’s a new champion in the Geekbench 6 CPU benchmarks as the iPad Pro line featuring the M4 chip actually beat out the previously leading Intel Core i9-14900KS in single-core benchmarks. Apple’s latest silicon scored confident averages of around 3,800 in comparison to Team Blue’s average of 3,100.
While things aren’t quite as exciting in terms of multi-core performance, this marks an incredibly rare occassion where mobile hardware can not only stand in league with desktop, but surpass it. It’s due in part to the new 10-core (4P + 6E) processor of the M4 chip which is bolstered by 10-core GPU, and a larger 16-core Neural Engine weighing in at 38 TOPS.
Apple claims that the M4 chip is roughly 50% faster than the M2 processor that you’ll find in the incoming Apple iPad Air models as well as older MacBooks and iMacs from 2022. The M4 silicon’s specs confidently tout improved branch prediction, next-gen ML accelerators, and a deeper execution engine according to Apple.
It’s still early days for the new iPad Pro lineup which also feature what the company describes as a “Tandem OLED” display, and appear to be pushing the form factor in new directions. That means we can’t quite draw a definitive line on Apple’s tablets beating out leading desktop models across the board, even if the early reports are encouraging.
These strong figures are due in part to the newly revised Neural Engine which is the largest on Apple Silicon yet. Considering many manufacturers such as AMD and Intel are going all-in on AI computing with their incoming CPU generations, it’s good to see Apple make a statement here, as the fourth-generation in-house chip makes a strong impression.
The start of what’s to come from the AI revolution
It’s still early days for AI computing regardless of form factor and time will tell exactly how well-optimized iPad OS software is to the new M4 chipset and more advanced Neural Engine. AMD has thrown its hat into the ring with the upcoming AMD Ryzen AI 9 HX 170 flagship with an NPU of up to 77 TOPS according to a recent Asus leak.
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Meanwhile, Intel already has a piece on the board with the Core Ultra 100 chips as Meteor Lake debuted in laptops last year. The real test for what the M4 chip is able to do will emerge when the playing ground is levelled. We’re expecting Intel Arrow Lake later this year, so Team Red and Team Blue could widen the gap again. Until then, however, Apple’s proven its tablets can hold their own against x86 confidently.
A nanopore sequencing device is typically used for sequencing DNA and RNA.Credit: Anthony Kwan/Bloomberg/Getty
With its fast analyses and ultra-long reads, nanopore sequencing has transformed genomics, transcriptomics and epigenomics. Now, thanks to advances in nanopore design and protein engineering, protein analysis using the technique might be catching up.
“All the pieces are there to start with to do single-molecule proteomics and identify proteins and their modifications using nanopores,” says chemical biologist Giovanni Maglia at the University of Groningen, the Netherlands. That’s not precisely sequencing, but it could help to work out which proteins are present. “There are many different ways you can identify proteins which doesn’t really require the exact identification of all 20 amino acids,” he says, referring to the usual number found in proteins.
In nanopore DNA sequencing, single-stranded DNA is driven through a protein pore by an electrical current. As a DNA residue traverses the pore, it disrupts the current to produce a characteristic signal that can be decoded into a sequence of DNA bases.
Proteins, however, are harder to crack. They cannot be consistently unfolded and moved by a voltage gradient because, unlike DNA, proteins don’t carry a uniform charge. They might also be adorned with post-translational modifications (PTMs) that alter the amino acids’ size and chemistry — and the signals that they produce. Still, researchers are making progress.
Water power
One way to push proteins through a pore is to make them hitch a ride on flowing water, like logs in a flume. Maglia and his team engineered a nanopore1 with charges positioned so that the pore could create an electro-osmotic flow that was strong enough to unfold a full-length protein and carry it through the pore. The team tested its design with a polypeptide containing negatively charged amino acids, including up to 19 in a row, says Maglia. This concentrated charge created a strong pull against the electric field, but the force of the moving water kept the protein moving in the right direction. “That was really amazing,” he says. “We really did not expect it would work so well.”
Super-speedy sequencing puts genomic diagnosis in the fast lane
Chemists Hagan Bayley and Yujia Qing at the University of Oxford, UK, and their colleagues have also exploited electro-osmotic force, this time to distinguish between PTMs2. The team synthesized a long polypeptide with a central modification site. Addition of any of three distinct PTMs to that site changed how much the current through the pore was altered relative to the unmodified residues. The change was also characteristic of the modifying group. Initially, “we’re going for polypeptide modifications, because we think that’s where the important biology lies”, explains Qing.
And, because nanopore sequencing leaves the peptide chain intact, researchers can use it to determine which PTMs coexist in the same molecule — a detail that can be difficult to establish using proteomics methods, such as ‘bottom up’ mass spectrometry, because proteins are cut into small fragments. Bayley and Qing have used their method to scan artificial polypeptides longer than 1,000 amino acids, identifying and localizing PTMs deep in the sequence. “I think mass spec is fantastic and provides a lot of amazing information that we didn’t have 10 or 20 years ago, but what we’d like to do is make an inventory of the modifications in individual polypeptide chains,” Bayley says — that is, identifying individual protein isoforms, or ‘proteoforms’.
Molecular ratchets
Another approach to nanopore protein analysis uses molecular motors to ratchet a polypeptide through the pore one residue at a time. This can be done by attaching a polypeptide to a leader strand of DNA and using a DNA helicase enzyme to pull the molecule through. But that limits how much of the protein the method can read, says synthetic biologist Jeff Nivala at the University of Washington, Seattle. “As soon as the DNA motor would hit the protein strand, it would fall off.”
Nivala developed a different technique, using an enzyme called ClpX (see ‘Read and repeat’). In the cell, ClpX unfolds proteins for degradation; in Nivala’s method, it pulls proteins back through the pore. The protein to be sequenced is modified at either end. A negatively charged sequence at one end allows the electric field to drive the protein through the pore until it encounters a stably folded ‘blocking’ domain that is too large to pass through. ClpX then grabs that folded end and pulls the protein in the other direction, at which point the sequence is read. “Much like you would pull a rope hand over hand, the enzyme has these little hooks and it’s just dragging the protein back up through the pore,” Nivala says.
Source: Ref. 3
Nivala’s approach has another advantage: when ClpX reaches the end of the protein, a special ‘slip sequence’ causes it to let go so that the current can pull the protein through the pore for a second time. As ClpX reels it back out again and again, the system gets multiple peeks at the same sequence, improving accuracy.
Last October3, Nivala and his colleagues showed that their method can read synthetic protein strands of hundreds of amino acids in length, as well as an 89-amino-acid piece of the protein titin. The read data not only allowed them to distinguish between sequences, but also provided unambiguous identification of amino acids in some contexts. Still, it can be difficult to deduce the amino-acid sequence of a completely unknown protein, because an amino acid’s electrical signature varies on the basis of both its surrounding sequence and its modifications. Nivala predicts that the method will have a ‘fingerprinting’ application, in which an unknown protein is matched to a database of reference nanopore signals. “We just need more data to be able to feed these machine-learning algorithms to make them robust to many different sequences,” he says.
NatureTech hub
Stefan Howorka, a chemical biologist at University College London, says that nanopore protein sequencing could boost a range of disciplines. But the technology isn’t quite ready for prime time. “A couple of very promising proof-of-concept papers have been published. That’s wonderful, but it’s not the end.” The accuracy of reads needs to improve, he says, and better methods will be needed to handle larger PTMs, such as bulky carbohydrate groups, that can impede the peptide’s movement through the pore.
How easy it will be to extend the technology to the proteome level is also unclear, he says, given the vast number and wide dynamic range of proteins in the cell. But he is optimistic. “Progress in the field is moving extremely fast.”
Upgraded versions of Logic Pro for iPad and Mac will give musicians and music producers new tools for crafting killer tracks.
New features in Apple’s pro audio software — Logic Pro for iPad 2 and Logic Pro for Mac 11 — include:
Session Players, which puts virtual musicians in the mix.
Stem Splitter, which producers extract drums, bass, vocals and other instruments from audio files.
ChromaGlow, a processing tool designed to bring analog “warmth” to digital tracks.
“Logic Pro for iPad turns things up for music producers,” said Will Hui, Apple’s product manager for creative apps, in a prerecorded video Tuesday. “Designed for everyone from emerging to established artists, Logic Pro for iPad has delivered the entire studio experience with the simplicity of touch. Logic Pro 2 is so exciting — and it’s smarter than ever.”
Logic Pro 2 for iPad and Logic Pro 11 for Mac
The announcement came during Apple’s iPad-focused “Let Loose” event. During the streamed product launch, which the company touted as “the biggest day for iPad since its introduction,” Apple unveiled next-gen iPad Pros powered by a new M4 chip as well as new iPad Air models, an updated Magic Keyboard for iPad Pro and an all-new Apple Pencil Pro stylus.
Logic Pro for iPad 2 and Logic Pro for Mac 11 build on Apple’s foundation of pro-level software for creatives. And, like everything Apple announces these days, they emphasize the power of AI that’s built into the company’s hardware and software.
“Logic Pro gives creatives everything they need to write, produce, and mix a great song, and our latest features take that creativity to a whole new level,” said Brent Chiu-Watson, Apple’s senior director of apps worldwide product marketing, in a press release Tuesday. “Logic Pro’s new AI-backed updates, combined with the unparalleled performance of iPad, Mac, and M-series Apple silicon, provide creative pros with the best music creation experience in the industry.”
The new features in Logic Pro aren’t exactly groundbreaking. Other software tools and plugins offer similar functionality. But by baking these into its music-making software, Apple adds even more functionality to an already-capable app.
Session Players
Apple calls Session Players “a personalized AI-driven backing band.” The feature builds on Drummer, a longstanding feature of Logic Pro, adding a virtual Bass Player and Keyboard Player to the mix.
“Session Players augment the live-playing experience while ensuring artists maintain full agency during any phase of their music-making process,” the company said.
Here’s more on the specifics of Apple’s new virtual musicians:
Bass Player was trained in collaboration with today’s best bass players using advanced AI and sampling technologies. Users can choose from eight different Bass Players and guide their performance with controls for complexity and intensity, while leveraging advanced parameters for slides, mutes, dead notes, and pickup hits. Bass Player can jam along with chord progressions, or users can choose from 100 Bass Player loops to draw new inspiration. With Chord Track, users can define and edit the chord progressions to a song, and the virtual Bass Player will follow along perfectly. Plus, with Studio Bass plug-in, users gain access to six new, meticulously recorded instruments, from acoustic to electric — all inspired by the sounds of today’s most popular bass tones and genres.
With Keyboard Player, users can choose from four different styles, designed in cooperation with top studio musicians and made to accompany a wide variety of music genres. Keyboard Player can play everything from simple block chords to chord voicing with extended harmony — with nearly endless variations. Like Bass Player, Chord Track adds and edits the chord progression of the song, so Keyboard Player follows along. Using Studio Piano plug-in, users can select additional sound-shaping options, with the ability to adjust three mic positions, pedal noise, key noise, release samples, and sympathetic resonance.
Stem Splitter
The new Stem Splitter feature in Logic Pro 2 for iPad and Logic Pro 11 for Mac give musicians and music producers a way to separate existing recordings into four basic elements: drums, bass, vocals and other instruments.
Apple describes the feature as a way to work with your own recordings. However, it should come in handy for anybody wanting to disassemble hit songs into their component parts.
Here’s Apple’s description of the feature:
Most musicians perform their best without the pressure of a formal studio session. These moments are often found in Voice Memos recordings, an old demo cassette tape, or are captured from a live show. Listening back, these recordings can reveal magical performances that are nearly impossible to re-create, making them lost to time. Now, with Stem Splitter, an artist can recover moments of inspiration from any audio file and separate nearly any mixed audio recording into four distinct parts: Drums, Bass, Vocals, and Other instruments, right on the device. With these tracks separated, it’s easy to apply effects, add new parts, or change the mix. Powered by AI and M-series Apple silicon, Stem Splitter is lightning fast.
ChromaGlow: Dial in the Perfect Tone
Apple pitches the new ChromaGlow feature in Logic Pro 2 for iPad and Logic Pro 11 for Mac as a way to “dial in the perfect tone.”
The feature attempts to make up for one of the major shortcomings of digital recording: a lack of analog “warmth” achieved by recording on actual tape and using analog equipment like tube amps.
The new Logic Pro feature will use digital models of classic music gear to produce the effect, Apple says:
ChromaGlow models the sounds produced by a blend of the world’s most revered studio hardware by leveraging AI and the power of M-series Apple silicon. Users can dial in the perfect tone with five different saturation styles to add ultrarealistic warmth, presence, and punch to any track. They can also choose from modern clean sounds, nostalgic vintage warmth, or more extreme styles that can be shaped and molded to taste.
Logic Pro 2 for iPad and Logic Pro 11 for Mac: Pricing and availability.
The new versions of Logic Pro will hit the App Store on May 13 as free updates for existing users, Apple said.
Logic Pro for Mac 11 will cost $199.99 for new users on the Mac App Store. It requires macOS Ventura 13.5 or later.
Logic Pro for iPad 2 will cost $4.99 per month or $49 per year, with a one-month free trial for new users. It requires iPadOS 17.4 or later.
The Cheyenne supercomputer, based at the NCAR-Wyoming Supercomputing Center (NWSC) in Cheyenne, Wyoming, was ranked as the 20th most powerful computer in the world in 2016 – but now it’s up for sale through the US General Services Administration (GSA).
By November 2023, the 5.34-petaflops system’s ranking had slipped to 160th in the world, but it’s still a monster, able to carry out 5.34 quadrillion calculations per second. It has been put to a number of noteworthy purposes in the past, including studying weather phenomena and predicting natural disasters.
The Cheyenne Supercomputer is a monster installation made up of SGI ICE XA modules which comprises of 14 E-Cells, weighing 1,500 lbs each, and 28 water-cooled E-Racks. There are 8,064 Intel “Broadwell” Xeon processors (18-core 2.3GHz E5-2697v4) with a total count of 145,152 cores. In terms of memory, it has 313,344GB of DDR4-2400 ECC single-rank memory and 224 IB Switches. The supercomputer also comes with two air-cooled management racks, each featuring 26 1U servers.
“Repairable”
Howeer, potential buyers do need to be aware of a few issues. Firstly, the unit doesn’t come with fiber optic and CAT5/6 cabling, although the internal DAC cables within each cell are provided and will be “meticulously labeled and packaged in boxes”, and it comes with previously used PGW coolant fluid (around10 gallons per E-cell). It will need to be collected by a professional moving company and the purchaser “assumes responsibility for transferring the racks from the facility onto trucks using their equipment.”
A major red flag is that the supercomputer is worryingly listed as “repairable”. The auction page states “the system is currently experiencing maintenance limitations due to faulty quick disconnects causing water spray. Given the expense and downtime associated with rectifying this issue in the last six months of operation, it’s deemed more detrimental than the anticipated failure rate of compute nodes.
Approximately 1% of nodes experienced failure during this period, primarily attributed to DIMMs with ECC errors, which will remain unrepaired. Additionally, the system will undergo coolant drainage.”
With a couple of days to go before the auction ends, bidding currently stands at $50,085 with the reserve not yet met. Should you wish to buy a piece of supercomputer history, and have the deep pockets required to get it up and running, and the space to house it, you can put in a bid here.
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Hisense just announced its new Hisense U9N series mini-LED TVs, and as part of that announcement, the company invited reviewers, myself included, to spend quality hands-on time with a pre-production 75-inch version of the U9N at a launch event in New York.
The Hisense U9N series TVs slot between the company’s flagship ULED X series and the new U8N series (review coming soon) TVs, and incorporate technology from the ULED X lineup. Specifically, they use Hisense’s Hi-View Engine X picture processing and a mini-LED backlight with up to 5,300 local dimming zones. That’s a strikingly high number, even among the best TVs that use mini-LED – the Hisense U8K, in contrast, topped out at around 1,000 local dimming zones.
As you might expect, the premium tech packaged in the U9N series comes with a price boost over the U8N series, with the 75-inch version selling for $2,999 (around £2,400 / AU$ 4,530) and $3,999 (around £3,200 / AU$ 6,050) for the 85-inch version. (Compare that to the $1,999 pricing for the 75-inch Hisense U8N.) Hisense plans to ship both models this summer, and they will be sold at Best Buy and Amazon.
The Hisense U9N features substantial side-firing speakers, as shown here. (Image credit: Future)
The U9N series also has a premium design that aligns closely with the ULED X series TVs. That includes an aluminum bezel and side-mounted speakers, with the latter providing the left and right channels for the TV’s built-in 4.1.2 Dolby Atmos speaker system, which gets up to 82 watts of power (on the 85-inch model).
Picture-enhancing features of the U9N series include Dolby Vision IQ and HDR10+ high dynamic range support, and IMAX Enhanced and Filmmaker Mode presets. An ultra-wide viewing angle feature ensures that picture quality is maintained when viewing from off-center seats and the screen also has an anti-glare coating to reduce reflections.
On the gaming front, the U9N series supports a 144Hz refresh rate, VRR with AMD FreeSync Premium Pro, and Dolby Vision gaming.
The Google TV platform handles smart features and streaming and there’s an ATSC 3.0 tuner for receiving next-gen digital TV broadcasts.
The U9N’s off-axis viewing performance is excellent as demonstrated by this color test pattern shown straight on and at an extreme angle. (Image credit: Future)
Picture Performance
Along with its massive dimming zone count, Hisense has made dramatic brightness claims for its U9N series and the other new Hisense TVs announced for 2024. With the TV in its Filmmaker Mode picture preset, I measured around 3,000 nits peak brightness on a 10% white window pattern – a result that bests even the new Samsung QN900D flagship 8K TV, which measured around 2,400 nits on the same test. Dramatically high brightness confirmed!
Brightness with a fullscreen white test pattern in the same mode was 600 nits, a result that also bests Samsung’s flagship TV. On other tests, the 75-inch U9N managed a very impressive 99.3% coverage of the UHDA-P3 color gamut and 82% of the BT.2020 color gamut, and a measured input lag of 15.2ms when in Game mode. That level of input lag isn’t the best we’ve measured – some of the best gaming TVs clock in under 10ms – but it’s still considered good enough.
Along with its stellar measured performance, the QN9 has excellent off-axis uniformity. Looking at a pattern from the Spears & Munsil Ultra HD Benchmark4K Blu-ray disc designed to test off-axis performance, the TV’s ultra-wide viewing angle feature ensured that color and contrast were perfectly uniform even at a far off-center viewing position.
Although this picture exaggerates the effect, screen reflections could be seen on the U9N with overhead lights on. (Image credit: Future)
With 5,300 local dimming zones, you’d expect to see detailed reproduction of shadows in dark scenes, and the UN9 didn’t disappoint. Watching the scene in Dune: Part One where Paul Atreides is tested by the Reverend Mother (Question: “What’s in the box?” Answer: “Pain”), backgrounds in the dim environment had a high level of clarity, and the mesh covering her face was a deep, solid black tone.
While I didn’t notice anything off with movies, I did note some “black blotching’ effects on a starfield test pattern on the Spears & Munsil disc designed to test local dimming performance. Basically, with local dimming switched off, I could see plenty of stars in the pattern, and when switched to the Filmmaker Mode’s default High setting, large patches of stars disappeared. Hisense told me the issue is something they had also noted, however, and it will be fixed before the UN9 ships this summer.
Turning to No Time to Die, another demo 4K Blu-ray and one that I use to test motion handling, there was a high level of motion judder in a shot where the camera pans across a cemetery on a craggy hillside. Adjusting both the Custom Judder and Blur settings in the Motion Clarity menu to +4 remedied the issue, and it only added a very slight amount of “motion smoothing” to the image.
Although the U9N is touted as having an anti-glare screen, I could see a fair amount of screen reflections when I turned on the overhead lights in the room I tested it in. It certainly wasn’t the worst instance of this I’ve encountered, but having seen the new Samsung S95D OLED TV’s Glare-Free technology in action, which proved completely immune to room lighting, I’m starting to have higher expectations for glare-reduction tech.
Sound performance
Most high-end TVs now arrive with built-in 4.1.2 Dolby Atmos speaker systems, which use actual upfiring speaker drivers on the TV’s top edge rather than virtual processing to deliver Dolby Atmos soundtracks. Hisense’s U9N managed to play loud during the action scenes in both Dune and No Time to Die without sounding overly strained and there was good bass and dialogue clarity. Built-in TV speakers typically aren’t a match for the best soundbars, but anyone wanting spacious Dolby Atmos sound from a TV alone will not be disappointed with the U9N’s performance.
The Hisense U9N comes with a much improved new remote control with a backlit keypad. (Image credit: Future)
Mini-LED to the max
The Hisense U9N’s high brightness and impressive local dimming make it a hot prospect to land among the best TVs of 2024. And even though the 75-inch model’s $2,999 price could be considered high for a TV, it’s still quite reasonable compared to the mini-LED competition – it’s lower than the 75-inch Samsung QN90D, for example, which costs $3,299.
Does the Hisense U9N leave room for improvement? Its motion handling isn’t the best, and when I measured it in Filmmaker Mode, both gamma and white balance were less accurate than what I usually expect from a premium TV. Even so, I walked away from my encounter with the U9N impressed, and could see it making serious waves this summer once it arrives.
Female animals and women have been ignored or actively excluded in clinical and laboratory-based biomedical research since such research began. This was especially true until the US Congress passed the National Institutes of Health (NIH) Revitalization Act in 1993, which directed the NIH to establish guidelines on the inclusion of women and members of under-represented racial and ethnic groups in clinical trials.
By 2009, a review of 10 fields in biology found that more than 60% of studies with human participants reported on both sexes. For studies using non-human animals, however, only 26% included both male and female subjects1.
To try to correct this persistent imbalance, the NIH implemented extra guidelines in 2016 — this time, on the inclusion of sex as a biological variable in all preclinical research2. At least with respect to the inclusion of female individuals in basic research, this funding-agency mandate and others like it have been effective. Another bibliometric analysis found that 49% of 720 studies on animals published in 2019 used both males and females3.
Why it’s essential to study sex and gender, even as tensions rise
Although it is still early days and there is much room for improvement, the inclusion of female participants and animal subjects is already having a revolutionary impact on numerous areas of study — from chronic pain to mental health. Yet we see an impending collision between research policies and societal changes regarding ideas and attitudes around sex and gender that threatens this nascent enterprise. We also see the threat of lobbyists, legislators and others in the United States and elsewhere weaponizing research on sex differences — either to marginalize individuals or groups that they deem to be outside a narrowly defined norm, or to reinforce derogatory ideas about people who identify as divergent4. (In this article, sex refers to differences between females and males caused by biological factors, whereas gender refers to differences caused by social factors, including gender roles, expectations and identity.)
Our concern is that various critiques of research on sex differences from scholars approaching sex and gender from different viewpoints — in combination with valid concerns around the misinterpretation or misuse of findings — could undermine an approach that has proved both practical and powerful. As a counterweight to this possibility, here we argue for the ongoing value of comparing female and male individuals in biomedical research.
Mammalian biology
Several scholars have argued in recent years that an overemphasis on biological sex will distract investigators from the effects of gendered environments and of non-sex-related variables, such as age, ethnicity or socio-economic status, on many traits. Another common criticism is that comparing female and male participants ignores transgender people and other individuals who do not fall within these binary categories, leading to their further marginalization in society5. Others have argued that a focus on the difference between the mean values of male and female individuals distracts researchers from considering the variability around those means — the implication being that variability within a sex is more important than variability between sexes. Some even question whether sex is a viable concept6.
Before addressing these specific complaints, it is worth briefly reviewing the current understanding of mammalian biology as it relates to sex — as well as some of the diverse and surprising findings that have already emerged from research comparing two sexes.
We need more-nuanced approaches to exploring sex and gender in research
Sex has been with us since our species originated as a result of sexual reproduction. The division of humans and other mammals into two sexes, female and male, derives from the fact that each individual is created by the union of a sperm and an egg. On the basis of the type of germ cell (gamete) that reproducing individuals are able to produce, there are only two sex categories in mammals. (Intersex is not a third category with respect to the type of gamete individuals can produce.) Indeed, understanding of how the mammalian genome evolved and how it functions is based on the foundation of sexual reproduction.
In mammals, as in many other taxa, the biological difference between sexes starts with the genetic difference encoded by the sex chromosomes — typically XX and XY in mammals — which are the only features that differ in female and male zygotes at the beginning of life. The salient role of the sex chromosomes is determining whether the embryo will develop ovaries or testes, because this specifies the type of germ cell that will be made, and the level and secretory patterns of testicular or ovarian hormones. Sex-chromosome genes and gonadal hormones influence almost every tissue in the body. The result might be sex differences in tissue development and function, or similar phenotypes based on different underlying mechanisms7.
Sex differences in immune function might have arisen from the need for female organisms to transfer immunity to the next generation.Credit: Klein & Hubert/Nature Picture Library
As in all things in biology, in humans and other mammals there are variations in the number and type of sex chromosomes and in the downstream mechanisms determining the phenotypic features associated with sex. This leads to variability among individuals in diverse sex-related traits, such as genital anatomy, body size and some behaviours. Also, particularly in humans, biological factors that drive sex differences in cells and tissues are confounded by social and environmental factors that also cause differences between individuals.
To serve all individuals equitably — including those who experience an incongruency between the sex they were assigned at birth and their current gender identity, and those who do not find that they align with either the male or female sex category — the medical profession and biomedical community must identify and interrogate these variations in biological attributes and in lived experiences, all of which can influence people’s physiology, risk of developing disease and prognosis8. This includes carefully attending to the distinctions between cisgender, transgender and non-binary individuals when reporting findings.
Yet we maintain that, in humans and other mammals, the comparison of individuals who have XX chromosomes and ovaries with individuals who have XY chromosomes and testes is a necessary component of basic and clinical research that seeks to improve human health.
Rich pickings
Male and female individuals represent most of the mammalian population. And research regarding biological sex differences has focused first on the largest groups, but in a manner that provides insights about variation within and beyond the binary.
For example, investigators have manipulated factors such as gonadal hormones and sex-chromosome genes to test their effects on sexual differentiation and their role in sex differences in disease. These manipulations, which mimic numerous intersex variations, such as the presence of ovarian hormonal secretions in an individual with XY chromosomes, have shed light on the effects of hormones, sex-chromosome genes and other factors in everyone. Studies of people with a variety of naturally occurring hormonal and chromosomal differences, for instance, are consistent with the interpretation that prenatal exposure to androgens, such as testosterone, is an important component of male psychosocial development9.
Nature journals raise the bar on sex and gender reporting in research
Importantly, the study of female and male individuals, as defined here, establishes a baseline measurement against which to compare findings from those who do not fit into a binary categorization scheme.
Understanding the effects of sex also anchors discussions about how different gendered environments intersect with biological differences, to amplify or mitigate their effects. More than half a century of animal research has been key to developing concepts of mammalian sexual differentiation, because in animals, unlike in humans, researchers can manipulate single genes or molecules to observe their effects on phenotypes. Moreover, although numerous environmental or social effects can be manipulated and studied in animals, such as diet, stress and levels of interaction with other individuals, animals provide useful models of the biological effects of sex in the absence of hard-to-control human gendered variables, such as cultural norms and expectations around child care and work.
The power of comparing female and male individuals in biomedical research is demonstrated most convincingly, however, by the data themselves — as illustrated by four examples from our fields of expertise.
Sex chromosomes versus hormones. Until recently, all of the biological hypotheses proposed to explain the significant sex differences in body weight and metabolism found in humans and animals (including birds and other mammals) were centred on the action of hormones. And extensive research during the twentieth century supported the idea that, in mammals, almost all sex differences in tissues other than the gonads (the organs that produce the gametes) result from the effects of ovarian and testicular hormones.
By the early 2000s, researchers studying gonadal development had created mouse models in which the complement of sex chromosomes could be manipulated in individuals with the same type of gonad10. This meant that investigators could assess whether the sex chromosomes cause differences in phenotypes, even when levels of gonadal hormones are similar7. Studies using the modified mice, while confirming the importance of gonadal hormones in influencing body weight and metabolism, uncovered the effects of sex chromosomes11. Comparable studies have also shown that sex chromosomes have much broader effects on physiology and behaviour than was originally thought10.
Accounting for sex and gender makes for better science
The copy number of an X-linked gene called Kdm5c, for example, contributes to a sex difference found in mice in the metabolism of adipose cells12. Mice with XY chromosomes have one copy of Kdm5c. They also have less body fat than do mice with XX chromosomes, which have two copies of the Kdm5c gene.
Over the past two decades, investigators have found that similar sex-chromosome effects contribute to sex differences in many other physiological systems in mice. And these sex differences, in turn, affect individuals’ likelihood of developing autoimmune conditions, cardiovascular diseases, cancer and developmental defects in the neural tube, the embryonic precursor to the central nervous system. The X-linked gene Kdm6a, for instance, increases the severity of autoimmune disease, and protects against bladder cancer and an Alzheimer’s-like disease in XX mice7. Similarly, the Y-linked gene Uty protects against pulmonary hypertension in mice13. Sex-chromosome genes also affect mouse behaviour, from the social behaviour of juveniles to responses to pain, as well as the size of certain brain regions7,10.
All of this work in mice provides investigators with clues about where to look for potential therapeutic targets in the human genome, for diseases that tend to affect women and men differently.
Pain. It is well established that among people with chronic pain, women far outnumber men14. Also, in experimental settings, women tend to be more sensitive than men are to pain — induced, for instance, by the application of heat, cold or pressure.
Pain researchers have proposed various gender-based and sex-based explanations for these differences14, such as that women are more likely than men to go to the doctor, as shown by usage rates for health-care services. However, investigations in male and female mice have suggested that, at least in rodents, different mechanisms are responsible for the processing of persistent pain in females and males.
Why the sexes don’t feel pain the same way
A 2015 study in mice15, for example, and follow-up findings demonstrated that a well-studied mechanism for the processing of persistent pain — involving immune cells called microglia — operates only in male rodents. (It is well studied in males, at least.) In males, the microglia release a factor that causes neurons in the spinal cord to increase their firing, which sustains chronic pain. Although female mice have just as many microglia as male mice do, their microglia don’t seem to be involved in the pain circuit — or, if they are involved, it is in a more complicated way. In fact, in females, T cells might play a similar part to microglia in males.
Whether the microglial or T-cell mechanism for the processing of persistent pain is engaged in any one individual seems to be due to testosterone levels being above or below a certain threshold. This dimorphism suggests that different physiological mechanisms could contribute to some of the differences observed in men and women in relation to chronic pain.
Immune function. Numerous studies that involve comparing immune responses in female and male organisms — whether they are fruit flies, fish, lizards, birds or mammals — have shown that females often generate more robust immune responses to antigens than do their male counterparts16. This suggests that sex differences in immune function are evolutionarily conserved, perhaps because of a common need for female individuals to transfer immunity to the next generation (whether through breast milk or a yolk sac), or because of some other sex-specific selective pressure.
In humans, these immunological stimuli can be self-antigens (proteins made by our own cells), allergens, cancerous cells or pathogenic microbes. Because women have larger immune responses than men, they are more likely to develop autoimmune diseases and allergies, but less likely to be diagnosed with non-reproductive cancers, such as skin or colon cancer17, and certain infectious diseases, such as tuberculosis16 and COVID-1918.
Some studies suggest that women generate a greater immune response to certain vaccines than do men.Credit: Patrick Meinhardt/Bloomberg/Getty
The difference between female and male organisms in the amount of antibodies produced in response to immunological stimuli changes across the life course, being most robust during the reproductive years19. This could explain why females of reproductive age often generate more antibodies in response to vaccines and microbes than males do20, and why female antibody responses are more durable and cross-reactive against diverse variants, such as different strains of influenza virus.
Mouse models have shown that gonadal hormones contribute more to mammalian sex differences in vaccine-induced immunity than do genes linked to sex chromosomes, at least against influenza viruses21. In both mice and humans, concentrations of estradiol (a hormone that is typically produced at higher levels in female organisms) are positively associated with greater antibody responses to influenza vaccines22. In short, a wealth of insights about the benefits (and downsides) of a bolstered immune response have emerged only because researchers have compared immune responses in male and female organisms.
Mental health. Sex and gender differences in the prevalence of mental-health disorders in humans span the life course. Prepubescent boys are significantly more likely than prepubescent girls to be diagnosed with autism spectrum disorder or attention deficit and hyperactivity disorder23. In their late teens or early 20s, men are more likely to be diagnosed with early-life schizophrenia. They are also more likely to experience a brain injury caused by a lack of oxygen at birth, and to have neurological conditions, such as Tourette’s syndrome. After puberty, however, disorders involving depression, anxiety, compulsion and obsession are more frequent in women23.
Sociocultural factors probably contribute to the differences in the prevalence of many of these conditions, including biases around the criteria used to diagnose early-life disorders by clinicians. Similarly, by the time a woman is diagnosed with a mood or affective disorder, she has often lived for decades in a gendered environment, making it hard for researchers to separate the effects of biology during development from those of life experience. Studies conducted over the past two decades in male and female rodents, however, have revealed an integral role for the immune system — specifically microglial cells — in affecting how testosterone acts on the brain and alters the structure and function of certain regions.
The fraught quest to account for sex in biology research
For instance, experiments measuring cellular activity in post-mortem animals have shown that during development, male rodents have a greater number of activated microglia in certain regions of their brains than do female rodents. These activated microglia release more of the signalling molecules that are crucial to forming synapses and controlling cell numbers. Many of the brain regions affected by the selective elimination of cells are also those implicated in mental-health disorders in humans (in both sexes) that originate during development24.
These findings could offer clues as to why messenger RNAs obtained from the cortex of human male fetuses indicate higher expression levels of genes involved in inflammation than do those obtained from human female fetuses. Post-mortem, higher levels of inflammation have even been found in the cortices of men who had been diagnosed with autism than in those of men who had not received a mental-health diagnosis25.
All of this suggests that, in mammals, greater activity of the neuroimmune system is somehow involved in the process of brain masculinization — which means that various mental-health disorders that affect boys more than girls could involve disruptions to immune-system processes.
Early days
Ultimately, we support efforts to interrogate both biological and social determinants of disease. Indeed, having more information is always preferable to having less. It is crucial to consider how biological factors linked to sex interact with each other and with other biological factors, such as age and genetic background, as well as with sociocultural or environmental influences. But whether the variables that have the most impact on physiology and disease are sex-based, gender-based or unrelated to either is a question that must be answered by research.
Sex and gender analysis improves science and engineering
Related to this, although there is always a danger of scientists and journalists oversimplifying things — particularly in relation to sex and gender — any rigorous analysis requires the consideration of averages as well as measures of variation. Just as with the importance of sex-related variables compared to other variables, it is an empirical question whether within-sex variation has more or less impact on a trait of interest than between-sex variation does.
When it comes to the threat of people misusing statements about an inherent difference between female and male individuals to rationalize continuing the historical subordination of women, transgender people and others, we agree that this danger is real and urgent. Since September 2023, for instance, health-care providers in Texas have been prohibited from giving gender-transition surgeries, puberty-blocking medication or hormone therapies to people under 18. This was decided on the basis of claims that everyone belongs to one of two groups, and that this reality is settled by science. The solution, however, is not to deny a priori the importance of sex differences, but rather to improve understanding of variation in human populations and how it relates to biological and social factors. Similarly, whereas we recognize the importance of studying intersex, non-binary, transgender and other individuals whose biology or life experiences are not encompassed by a simplistic binary, the neglect of such individuals should not be addressed by abandoning female–male comparisons.
Because female organisms have for so long been left out of investigations in many biomedical fields, researchers are still surprisingly ignorant of their fundamental biology across numerous taxa, and how it does or does not differ from that of males. There is also much room for improvement in research on sex differences — in terms of statistical and reporting practices26, researchers actually splitting their data by sex and analysing those data appropriately3, and journals improving their policies around sex and gender. The highly fruitful approach of comparing female and male organisms should not be abandoned just as investigators are starting to make progress.
A prominent hardware leaker has uncovered new patch notes revealing that the now-allegedly canceled AMD Navi 4X / 4C graphics cards would have been significantly more powerful than the current AMD flagship RX 7900 XTX.
Uncovered by Kepler_L2 (via Tweaktown), new patch notes for AMD GFX12 supposedly showcase Navi 4X die models, the newer equivalent of the Radeon RX 7900 XTX, which would feature up to 50% more shader engines, however, it’s not looking likely that anything from RDNA 4 will be as quick as has been touted here.
Specifically, the patch notes reveal that Navi 4X / 4C die GPUs would have featured nine shading engines which is a significant upgrade over the six available from Navi 31 for a significant boost. RNDA 4 appears to be targeting the value crowd, so while the tech could have technically rivaled leading models from Intel, it’s likely the top-end was cut due to wanting to keep the prices competitive.
It calls back to an earlier leak at the end of last year as the supposed RX 8900 XTX design had reportedly leaked. Documentation from Moore’s Law is Dead showcased the Navi 4C config overview with an alleged patent for complex GPU architecture revealing up to 12 dies in parallel without a central or master die.
According to Videocardz, AMD decided to cancel the highest-end RDNA 4 GPU but no reason was offered. To speculate, this could have all come down to pricing. We’ve seen Nvidia‘s mid-range and top-end cards explode in MSRP in the generational gap between Ampere and Ada, so it’s possible that Team Red wanted to avoid this from happening.
Cost is king in the new GPU market
While we’re champions of bleeding-edge hardware, it’s important to remember that the top-end will always be a luxury few can afford. There’s no question that the RTX 4090 is the best graphics card from a raw technical perspective, but it outprices the RX 7900 XTX by nearly $600 at MSRP.
For AMD to compete at the top-end, as it sounds like the 4C GPU could have, we would likely have seen prices creeping up past the $1,000 mark, which its RX 7900 XTX avoided. Until the release of the RTX 4080 Super, AMD had cornered the mid-range market with its line of 1440p and 4K graphics cards for gamers, and losing that edge to compete on a power front likely would have done more harm than good.
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New information on Fujifilm’s next camera, the X-T50, has recently leaked providing some insight into its performance. According to Fuji Rumors, the device will sport in-body image stabilization (IBIS). This feature will reduce the amount of camera shake to ensure crystal-clear photographs. It’s a piece of tech that can also be found on the higher-end Fujifilm X-T5. What’s more, the X-T50 is said to house a 40 MP X-Trans V image sensor just like its counterpart
This could mean the new camera might perform just as well as the X-T5, capable of taking the same level of high-quality photographs. However, as NotebookCheck points out, this is unlikely since the X-T50 is supposed to be a budget model. Fujifilm won’t want to cannibalize sales of the X-T5 so the publication theorizes that the company will hold back their new device in some way.
The X-T50 could house older hardware like the X Processor 4 instead of the more recent X Processor 5. Certain functions, like the SD card slot, may be “significantly degraded.” NotebookCheck doesn’t expand on this idea, but it could mean there’ll only be a single SD card slot onboard, for example. Little cuts like these would keep prices low.
Possible pricing
Because the X-T50 is slated to receive a hardware upgrade, there’s a good chance it’ll still cost more than the $900 X-T30 II. No word on how much it’ll cost. That X-Trans sensor and IBIS implementation will bump up the price tag regardless of any cost cutting measures by Fujifilm.
We won’t have to wait long to receive more details. Fuji Rumors claims the X-T50 will be officially announced on May 16 at the company’s X Summit event taking place in Sydney, Australia. Alongside it will be the Fujiflim GFX100SII and the Fujinon XF14-50mm f/2.8-4.8 kit lens. Little is known about either although images for the latter did surface. Sources close to the publication state it’ll receive features normally found on “higher-end lenses” like an internal zoom mechanism.
Sony just revealed its lineup of new TVs for 2024. While many boast interesting features that we’ll get into later, the biggest change is naming conventions. Sony TVs used to be named confusing strings of numbers and letters, but that’s all gone now. The names here are clean and simple. They all use Bravia, a long-time Sony moniker for televisions, and a single digit number.
The Bravia 3 is a standard 4K LED TV with dynamic HDR, upscaling technology and a 60Hz refresh rate. This is the most basic box within Sony’s lineup, but it still looks plenty capable. The company promises that it also uses eight percent less power than last year’s equivalent, which is always nice. The TV is available in sizes ranging from 43-inches all the way up to 85-inches, with prices going from $600 to $1,800.
Sony
Don’t ask what happened to Bravia 4, 5 and 6, because the next TV in the lineup is called the Bravia 7. This is a mini LED box with some neat tech, including a powerful updated processor and Sony’s proprietary Backlight Master Drive local dimming algorithm. The company says this allows it to feature 790 percent more dimming zones compared to last year’s similar X90L. The more dimming zones a TV has, the smaller each one will be. This leads to an increase in precision and a better contrast ratio.
It also uses less power than the X90L, to the tune of 15 percent, and boasts a new calibration mode primarily intended for Prime Video content. The Bravia 7 is available in sizes ranging from 55-inches to 85-inches, with prices fluctuating from $1,900 to $3,500.
The Bravia 8 is the company’s latest OLED model. The OLED panel ensures a “perfect black” response and the box includes the same calibration mode for Prime Video found with the Bravia 7. However, the most interesting aspects of this line have to do with size and form factor. The Bravia 8 is 31 percent thinner than last year’s equivalent model, with a slimmed down bezel. It should really pop when hung on a wall. There are only three sizes in this lineup, and the 55-inch model costs $2,000, the 65-inch version costs $3,400 and the 75-inch box costs a whopping $3,900.
Sony
Finally, there’s the flagship Bravia 9. This is basically a souped-up version of the Bravia 7, as its another mini LED box. Sony says that the display technology is similar to what’s found in a mastering monitor, which is a lofty promise. It’s 50 percent brighter than last year’s X95L, which was already plenty bright, with a 325 percent increase in dimming zones.
There’s also a 20 percent reduction in power consumption when compared to the X95L and new beam tweeters for improved audio. The Bravia 9 features Sony’s proprietary Backlight Master Drive and the new Prime Video calibration feature. The 65-inch version of this TV costs $3,300, while the 85-inch model comes in at a jaw-dropping $5,500.
It’s been a long time since I’ve used a laptop with a screen larger than 13 or 14 inches for any length of time. It’s so refreshing to have the room to spread my apps out … even if the machine no longer fits in my backpack. Maybe being able to fit your bag under the seat in front of you is overrated.
Compared to the cavalcade of 13- and 14-inch laptops that cross my desk, the Samsung Galaxy Book4 Ultra, with its 16-inch touchscreen (2,880 x 1,800 pixels), is a behemoth. Weighing in at 3.9 pounds (but only 19 mm thick), it has a heft that’s backed up by its top-shelf specs, which include 32 GB of RAM, a 1-terabyte SSD, and an Nvidia GeForce RTX 4070 graphics card. The centerpiece is the new Intel Core Ultra 9 185H processor, the current top-of-the-line processor in Intel’s Core Ultra CPU lineup.
Photograph: Samsung
As benchmarks go, the Galaxy Book4 ran rings around all the other Core Ultra laptops I’ve tested in the last few weeks since the new chips launched, though none of those had an Ultra 9 or a discrete graphics processor. On some CPU-based tests, the system doubled up on the performance of the Lenovo X1 Carbon, and on graphics-based tests, I was regularly able to get three to five times the frame rates I saw on machines that used the Core Ultra integrated graphics processor. The Book4 is certainly credible for use as a gaming rig if desired. Plus with 12 hours and 43 minutes of battery life, as tested via my full-screen YouTube rundown test, you need not fret about being away from an outlet all day.
The larger chassis gives Samsung room to squeeze a numeric keypad into the picture, though I longed for full-size arrow keys when working with the device. The responsive keyboard is paired with one of the largest touchpads I’ve ever seen on a laptop. At 6 x 4 inches, it’s considerably bigger than a standard passport—arguably too big, as there’s barely room on the left side of the touchpad for your palms to rest. I generally disliked working with this touchpad, as I found it both missed clicks and inadvertently registered unintended taps much too often.