Protein powders and shakes contain high amounts of lead, new report says – a pharmacologist explains the data

Source: The Conversation – USA (3) – By C. Michael White, Distinguished Professor of Pharmacy Practice, University of Connecticut

If consumed in high doses, lead and other heavy metals have serious, well-documented health risks. whitebalance.space/E+ via Getty Images

Powder and ready-to-drink protein sales have exploded, reaching over US$32 billion globally from 2024 to 2025. Increasingly, consumers are using these protein sources daily.

A new study by Consumer Reports, published on Oct. 14, 2025, claims that some such protein products contain dangerously high levels of lead, as well as other heavy metals such as cadmium and arsenic. At high levels, these substances have serious, well-documented health risks.

I am a clinical pharmacologist who has evaluated the heavy metal content of baby food, calcium supplements and kratom products. Lead and other heavy metals occur naturally in soil and water, so achieving zero-level exposure would be impossible. Additionally, the level of lead exposure that Consumer Reports deems safe is significantly lower than those set by the Food and Drug Administration.

However, regardless of the safety cutoff, the study does show that a few products are delivering a concerningly high dose of heavy metals per serving.

How Consumer Reports did the study

The new study assessed 23 powder and ready-to-drink protein products from popular brands by sending three samples of each product to an independent commercial laboratory.

Consumer Reports considered anything over 0.5 micrograms per day from any single source to be above recommended maximum lead levels. That number comes from the California Office of Environmental Health Hazard Assessment, which established recommended maximum levels for a variety of substances that could cause cancer or fetal harm.

It is significantly more conservative than the safety standard for lead exposure used by the FDA for drugs and supplements. The discrepancy is driven by Consumer Reports’ aspirational goals of very low exposure versus the more realistic but actionable requirements from the FDA.

According to the FDA, the limit for the amount of lead that a person should consume from any single dietary supplement product is 5 micrograms per day. That number is 10 times higher than the Consumer Report limit.

The FDA has another standard for the total daily amount of lead a person can safely consume from food, drugs and supplements combined. This number, called the Interim Reference Level, or IRL, for lead is based on concentrations of lead in the blood that are associated with negative health effects in different populations.

For people who could become pregnant, that level is 8.8 micrograms per day, and for children it’s 2.2 micrograms per day. For everyone else, it’s 12.5 micrograms per day. Every food, drug and dietary supplement that contains lead contributes to the total daily exposure, which should be less than this amount.

Bodybuilder at the gym drinking a protein shake
In assessing lead levels, Consumer Reports used a more conservative safety standard than the one used by the FDA for drugs and supplements.
lakshmiprasad S/iStock via Getty Images Plus

What the report found

The nonprofit advocacy group found that 16 of the 23 products it tested exceeded 0.5 micrograms, the level of lead in a standard serving that the organization deems safe.

Four of the 23 products exceeded 2.2 micrograms, the FDA’s cutoff for the total daily amount of lead children should consume. Two products contained 72% and 88%, respectively, of the total daily amount of lead that the FDA deems safe for pregnant women.

In addition, Consumer Reports found that two of the 23 products delivered more than what it considers a safe amount of cadmium per serving, and one had more arsenic than was recommended.

The organization’s safety cutoff for cadmium is 4.1 micrograms per day, and for arsenic it is 7 micrograms per day. These numbers align fairly closely with the FDA’s recommended exposure limit for cadmium and arsenic from a single product. For cadmium, the FDA’s limit is set at 5 micrograms per day for a given dietary supplement product and 15 micrograms per day for arsenic.

The study found that the source of protein was key: Plant-derived protein products had nine times the lead found in dairy proteins like whey, and twice as much as beef-based protein.

Where are these heavy metals coming from?

Lead and other heavy metals are present in high amounts in volcanic rock, which comes from molten rock called magma beneath the Earth’s surface. When volcanic rock is eroded, the heavy metals contaminate the local soil and water supply. What’s more, some crop plants are especially efficient at extracting heavy metals from the soil and placing them in the parts of the plants that consumers ingest.

Fossil fuels, which come from deep within the Earth, also billow heavy metals into the air when they are burned. These substances then settle out into the soil and water. Finally, some fertilizers, herbicides and pesticides also contain heavy metals that can further contaminate soil and local water.

High levels of heavy metals have been found in plant-based protein powder, spices like cinnamon, dark chocolate, root vegetables like carrots and sweet potatoes, rice, legumes such as pea pods and many herbal supplements.

A cast iron pot of cubed sweet potatoes
Root vegetables such as sweet potatoes can absorb heavy metals from the soil.
Virginia State Parks, CC BY

Should consumers be concerned? And what can they do?

Occasionally exceeding the daily recommended heavy metal doses is unlikely to result in serious health issues.

Repeated, heavy exposure to heavy metals can cause harm, however. When they accumulate in the blood, these substances can delay or impair mental functioning, damage nerves, soften bones and raise blood pressure – which in turn increases the risk of strokes and heart attacks. Heavy metals can also increase the risk of developing cancer.

It’s important to note that all the products Consumer Reports flagged have lead levels significantly lower than the maximum daily exposure levels established by the FDA.

Consumers can limit exposure by choosing dairy- or animal-based sources of protein products, since they generally seemed to have less heavy metal contamination than plant-based ones. However, some plant-based protein products in the study did not have high levels of heavy metals. Heavy metal levels vary widely in the environment, so the results from the Consumer Reports study show a snapshot in time. They might not be consistently accurate across batches if, for example, a manufacturer changes the source of its raw ingredients.

For protein products that do show an especially high heavy metal content, using them more sporadically, rather than daily, can reduce exposure. Studies suggest that organic plant-based products generally yield less heavy metal content than traditionally farmed ones.

Finally, the Consumer Reports study measured heavy metals in a single serving of protein products, so it’s helpful to understand what constitutes a serving for specific products and to avoid sharply increasing daily consumption.

Overall, the wide variation in lead levels across different protein powders and ready-made protein products highlights the need for manufacturers to tighten product testing and good manufacturing practices.

The Conversation

C. Michael White does not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and has disclosed no relevant affiliations beyond their academic appointment.

ref. Protein powders and shakes contain high amounts of lead, new report says – a pharmacologist explains the data – https://theconversation.com/protein-powders-and-shakes-contain-high-amounts-of-lead-new-report-says-a-pharmacologist-explains-the-data-267591

Antioxidants help stave off a host of health problems – but figuring out how much you’re getting can be tricky

Source: The Conversation – USA (3) – By Nathaniel Johnson, Assistant Professor of Nutrition and Dietetics, University of North Dakota

Many fruits and vegetables are high in antioxidants. istetiana/Moment via Getty Images

When it comes to describing what an antioxidant is, it’s all in the name: Antioxidants counter oxidants.

And that’s a good thing. Oxidants can damage the structure and function of the chemicals in your body critical to life – like the proteins and lipids within your cells, and your DNA, which stores genetic information. A special class of oxidants, free radicals, are even more reactive and dangerous.

As an assistant professor of nutrition, I’ve studied the long-standing research showing how the imbalances in antioxidants and oxidants lead to oxidative stress, which is linked to cancer, diabetes, cardiovascular disease and dementia and Alzheimer’s disease. In fact, a primary cause of aging is the damage accumulated across of a lifetime of oxidative stress.

Simply put: To help prevent oxidative stress, people need to eat foods with antioxidants and limit their exposure to oxidants, particularly free radicals.

The research: Food, not supplements

There’s no way for any of us to avoid some oxidative stress. Just metabolism – the processes in your body that keep you alive, such as breathing, digestion and maintaining body temperature – are a source of oxidants and free radicals.
Inflammation, pollution and radiation are other sources.

As a result, everyone needs antioxidants. There are many different types: enzymes, minerals, vitamins and phytochemicals.

Two types of phytochemicals deserve special mention: carotenoids and flavonoids. Carotenoids are pigments, with the colors yellow, orange and red; they contain the antioxidants beta-carotene, lycopene and lutein. Some flavonoids, called anthocyanins, are pigments that give foods a blue, red or purple color.

Although your body produces some of these antioxidants, you can get them from the foods you eat, and they’re better for you than supplements.

In fact, researchers found that antioxidant supplements did not reduce deaths, and some supplements in excessive amounts contribute to oxidative stress, and may even increase the risk of dying.

It should be pointed out that in most of these studies, only one or two antioxidants were given, and often in amounts far greater than the recommended daily value. One study, for example, gave participants only vitamin A, and at an amount more than 60 times an adult’s recommended intake.

A synopsis of the study that measured the antioxidant content of more than 3,000 foods.

Foods rich in antioxidants

In contrast, increased antioxidant intake from whole foods is related to decreased risk of death. And although antioxidant supplementation didn’t reduce cancer rates in smokers, the antioxidants in whole foods did.

But measuring antioxidants in foods is complicated. Extensive laboratory testing is required, and too many foods exist to test them all anyway. Even individual food items that are the same exact variety of food – such as two Gala apples – can have different amounts of antioxidants. Where the food was grown and harvested, how it was processed and how it was stored during transportation and while in the supermarket are factors. The variety of the food also matters – the many different types of apples, for instance, can have different amounts of antioxidants.

Nonetheless, in 2018, researchers quantified the antioxidant content of more than 3,100 foods – the first antioxidant database. Each food’s antioxidant capacity was determined by the amount of oxidants neutralized by a given amount of food. The researchers measured this capacity in millimoles per 100 grams, or about 4 ounces.

For fruits easily found in the grocery store, the database shows blueberries have the most antioxidants – just over 9 millimoles per 4 ounces. The same serving of pomegranates and blackberries each have about 6.5 millimoles.

For common vegetables, cooked artichoke has 4.54 millimoles per 4 ounces; red kale, 4.09 millimoles; cooked red cabbage, 2.15; and orange bell pepper, 1.94.

Coffee has 2.5 millimoles per 4 ounces; green tea has 1.5; whole walnuts, just over 13; whole pecans, about 9.7; and sunflower seeds, just over 5. Herbs and spices have a lot: clove has 465 millimoles per 4 ounces; rosemary has 67; and thyme, about 64. But keep in mind that those enormous numbers are based on a quarter-pound. Still, just a normal sprinkle packs a powerful nutritional punch.

A young woman picks up a package of fresh produce at the supermarket.
The antioxidant levels of a food can be affected by its storage time in the supermarket.
d3sign/Moment via Getty Images

Other tips

Other ways to choose antioxidant-rich foods: Read the nutrition facts label and look for antioxidant vitamins and minerals – vitamins A, C, E, D, B2, B3 and B9, and the minerals selenium, zinc and manganese.

Just know the label has a drawback. Food producers and manufacturers are not required to list every nutrient of the food on the label. In fact, the only vitamins and minerals required by law are sodium, potassium, calcium, iron and vitamin D.

Also, focus on eating the rainbow. Colorful foods are often higher in antioxidants, like blue corn. Many darker foods are rich in antioxidants, too, like dark chocolate, black barley and dark leafy vegetables, such as kale and Swiss chard.

Although heat can degrade oxidants, that mostly occurs during the storage and transportation of the food. In some cases, cooking may increase the food’s antioxidant capacity, as with leafy green vegetables.

Keep in mind that while blueberries, red kale and pecans are great, their antioxidant profile will be different than that of other fruits, vegetables and nuts. That’s why diversity is the key: To increase the power of antioxidants, choose a variety of fresh, flavorful, colorful and, ideally, local foods.

The Conversation

Nathaniel Johnson does not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and has disclosed no relevant affiliations beyond their academic appointment.

ref. Antioxidants help stave off a host of health problems – but figuring out how much you’re getting can be tricky – https://theconversation.com/antioxidants-help-stave-off-a-host-of-health-problems-but-figuring-out-how-much-youre-getting-can-be-tricky-256974

How new foreign worker visa fees might worsen doctor shortages in rural America

Source: The Conversation – USA (3) – By Patrick Aguilar, Managing Director of Health, Washington University in St. Louis

Many physicians who aren’t U.S. citizens come to the U.S. to do medical residency programs. SDI Productions/E+ via Getty Images

There are almost 1.1 million licensed physicians in the United States. That may sound like a lot, but the country has struggled for decades to train enough physicians to meet its needs – and, in particular, to provide care in rural and underserved communities.

Foreign-born physicians have long filled that gap, reducing the overall national shortage and signing up to practice in often overlooked regions and specialties. Today, 1 in 5 doctors licensed to practice in the U.S. were born and trained in another country.

But the ability of physicians from other countries to obtain work in the U.S. may be threatened by the Trump administration’s aims of limiting foreign workers. In September, Trump issued a proclamation requiring employers sponsoring foreign-born workers through a type of work visa called an H-1B to pay a fee of US$100,000 to the government. The White House has signaled doctors may be exempt but has not clarified its position.

As a physician and professor who studies the intersection of business and medicine, I believe increasing restrictions on H-1B visas for physicians may exacerbate the physician shortage. To grasp why that is, it’s important to understand how foreign-trained doctors became such an integral part of U.S. health care – and the role they play today.

The roots of today’s physician shortage

The Association of American Medical Colleges, a trade association representing U.S. medical schools, estimates there will be a deficit of about 86,000 physicians in the country by 2036.

The roots of this shortage stretch back more than a century. In 1910, a landmark study called the Flexner Report detailed significant inconsistencies in the quality of education at American medical schools. The report resulted in the closure of over half the country’s medical schools, winnowing their numbers down from 148 to 66 over two decades.

As a result, the number of doctors in the U.S. declined until new training programs emerged. Between 1960 and 1980, 40 new medical schools launched with the help of federal funding. In 1980, a congressionally mandated assessment deemed the problem solved, but by the early 2000s, a physician shortage emerged once more. In 2006, the American Association of Medical Colleges called for raising medical school enrollment by 30%.

Doctor looking at x-rays
Foreign-born doctors have helped the U.S. bridge a physician shortage for decades.
stevecoleimages/E+ via Getty Images

Growth in medical school enrollment hit that target in the late 2010s, but even so, the U.S. still lacks enough medical graduates to fill yearslong training programs, called residencies, that early-career physicians must complete to become fully qualified to practice.

Especially lacking are primary care physicians – particularly in rural areas, where there are one-third as many physicians per capita as in urban areas.

Opportunities for foreign-born doctors

Even as the U.S. built up medical school enrollment in the 1960s and 1970s, the government joined other countries such as the U.K. and Canada in creating immigration policies that drew physicians from developing countries to practice in underserved areas. Between 1970 and 1980, their numbers grew sharply, from 57,000 to 97,000.

Foreign-born and -trained physicians have remained a key pillar of the U.S. medical system. In recent years, the majority of those physicians have come from India and Pakistan. Citizens of Canada and Middle Eastern countries have added significantly to that count, as well. Most arrive in the U.S. as trainees in residency programs through one of two main visa programs.

The majority come on J-1 visas, which allow physicians to enter the U.S. for training but require them to return to their home country for at least two years when their training is complete. Those who wish to remain in the U.S. to practice must transition to an H-1B visa.

A small percentage of physicians come to the U.S. on H-1Bs from the start.

H-1B visas are employer-sponsored temporary work permits that allow foreign-born, highly skilled workers to obtain U.S. employment. Employers directly petition the government on behalf of visa applicants, certifying that a foreign worker will be paid a similar wage to U.S. workers and will not adversely affect the working conditions of Americans.

Several programs sponsor H-1B visas for physicians, though the most common requires a three-year commitment to work in an underserved area after completing their training.

Foreign physicians fill a crucial need

In 2025, foreign-trained medical graduates filled 9,700 of the nearly 40,000 training positions. Of those, roughly one-third were actually U.S. citizens who attended medical schools in other countries, with the remainder being foreign citizens seeking more training in the U.S.

After residency, these doctors frequently practice in precisely the geographic areas where the physician shortage is most severe. A nationwide survey of international medical graduates found that two-thirds practice in regions that the federal government has designated as lacking sufficient access to health care.

These doctors also occupy a disproportionate number of primary care positions. In a sample of 15,000 physicians who accepted new jobs in one year, foreign-born doctors were nine times more likely to enter primary care specialties. In 2025, 33.3% of internal medicine, 20.4% of pediatric and 17.6% of family medicine training positions were filled by physicians trained in other countries.

Who will pay?

Approximately 8,000 foreign-born physicians received H-1B visas in 2024. The new requirement of a $100,000 sponsorship fee would hit hardest for hospitals, health systems and clinics in areas of the country most significantly affected by the physician shortage.

These organizations are already under economic strain due to increasing labor costs and Medicare payments that have not kept pace with inflation. Dozens of these hospitals have closed in recent years, and many currently do not make enough money to support their operations.

On Sept. 25, 2025, 57 physician organizations cosigned a letter petitioning Homeland Security Secretary Kristi Noem to waive the new application fee for physicians.

Already, however, the new rule may be having a chilling effect. Despite years of annual growth in the number of foreign-born applicants to U.S. physician training programs, 2025 has seen a nearly 10% drop. If the new H-1B fee is applied to physicians, the number is likely to keep falling.

The Conversation

Patrick Aguilar Washington University, an employer of physicians.

ref. How new foreign worker visa fees might worsen doctor shortages in rural America – https://theconversation.com/how-new-foreign-worker-visa-fees-might-worsen-doctor-shortages-in-rural-america-266544

Madagascar’s military power grab shows Africa’s coup problem isn’t restricted to the Sahel region

Source: The Conversation – Global Perspectives – By John Joseph Chin, Assistant Teaching Professor of Strategy and Technology, Carnegie Mellon University

Military Col. Michael Randrianirina joins protesters as he announces that the armed forces are taking control of Madagascar on Oct. 14, 2025.
AP Photo/Brian Ingang

Those who rise to power through a coup often fall by the same means.

That is one of the takeaways from events in Madagascar, where on Oct. 14, 2025, the military seized power after weeks of protests largely driven by Gen Z. Ironically, it was the same elite military unit that helped bring Andry Rajoelina, former mayor of the capital Antananarivo, to power in a March 2009 coup that now supported anti-government protesters and ultimately forced the president to flee.

I lead a research team that compiles the Colpus Dataset of coup types and characteristics and have written on the history of coups d’état from 1946 through 2025.

Our data suggests that even as coups have declined globally overall, coup risk remains comparatively high in Africa. Since 2020, the continent has now seen 10 successful coups across eight countries.

But the military takeover in Madagascar marks only the second coup in that period to take place outside of the Sahel region, stretching from the Atlantic to the Horn of Africa – a signal that Africa’s coup problem is becoming a continental one.

But why do some coups succeed and others fail? And why do Madagascar and various states in Africa have trouble escaping so-called coup traps?

Our data provides some answers. But first it is worth exploring what we mean when we use the term coup.

What is a coup?

A coup d’état is a seizure of executive power involving one or more concrete, observable and illegal actions by security personnel or civilian officials.

Here, Madagascar’s military takeover appears to qualify. Despite claims by the country’s new military leader, Col. Michael Randrianirina, that he had an order from the High Constitutional Court legitimizing his seizure of power, this seemed to be contradicted by statements a day earlier that Randrianirina’s military council had suspended the high court’s powers.

That’s not to say that every political event that smells like a coup is, in fact, a coup.

Many coup plots never come to fruition. A bona fide plot may be preempted and the plotters arrested, or plotters may abandon their plan before taking any concrete action. Moreover, sometimes a leader falsely alleges a coup plot to purge members of the government suspected of disloyalty.

A plot without an attempt to oust the leader is not, in our book, a coup.

Conversely, attempts to target a leader without a plan to seize power are not coups. This includes leader assassination attempts by political opponents or lone wolves or mutinies by disgruntled soldiers who might even march on the presidential palace to demand higher pay, promotions or other policy concessions.

Nor do most civilian-led mass uprisings entail coups, even if they are successful in toppling the government. Take Nepal, where in September a Gen Z-led protest turned violent and ousted the government. But there was no coup insofar as the military remained quartered rather than actively joining the protests or issuing a threat to compel the prime minister to resign.

However, some revolutions and coups do co-occur, resulting in a “coupvolution” or “endgame coup.”

Determining whether a coup accompanies anti-government protests depends on how elites and the military behave, not on how violent protesters may be.

In Madagascar, mostly peaceful civilian protests turned into a coup attempt once troops actively joined the demonstrations. That attempt succeeded when Randrianirina, commander of the elite CAPSAT force, claimed the interim presidency and insisted a military council would rule for the time being.

Why do coups succeed?

There have been 601 coup attempts since 1946, according to our database, with 299 being successful – or about 50%. In Africa during that period, 111 out of 225 coup attempts were successful.

Coups come in a variety of forms, with different causes and outcomes, and not all are equally likely to succeed. The events in Madagascar, however, tick many of the boxes associated with determining coup success.

Coups depend on coordinating a lot of people, while simultaneously preventing the leader from finding out about the plot. Mass protests of the kind that rocked Madagascar in recent weeks provide cover – as well as motive and opportunity – for coup plotters.

Counterintuitively, military force is rarely decisive. In a typical coup attempt, much of the military remains neutral, biding its time to see whether the leader or coupists will prevail. Consequently, the perceived momentum of events influences how the military rank and file react: If they think the coupmakers will succeed, they typically join; if they think the coup will fail, they generally oppose it.

A coup’s momentum depends on a variety of factors, including the identity, location and strategy of coup leaders, as well as domestic and international reactions to the coup.

Coups that are launched by government insiders and senior military officers in the capital and are nonviolent and result in pro-coup mass mobilization are the most likely to succeed. By contrast, coups that are launched by government outsiders and junior officers outside the capital and are bloody and generate fierce anti-coup mass mobilization are the most likely to fail.

Coup violence is inversely correlated with success. When no force is threatened – usually because the security forces remain united under a senior command – coups succeed 85% of the time.

By contrast, less than 40% of coups that escalate into civil-war levels of violence – that is, resulting in over 1,000 fatalities – succeed.

In Madagascar, we saw the involvement of government elites and senior officers in the capital, mass pro-coup mobilization, low levels of coup violence and a history of prior successful coups – all of which make coup success likely.

A crowd of protesters.
Coup supporters cheer police officers in Gabon in August 2023.
AP Photo/Betiness Mackosso

Madagascar is not alone

Since 2020, military actors have also taken power in coups in Burkina Faso, Chad, Gabon, Guinea, Mali, Niger and Sudan.

So why are so many African countries prone to falling into a coup trap?

Scholars have asked this question for decades. Development economist Paul Collier suggests that Africa is the most coup-prone region because it is the poorest region of the world, and it is poverty and low growth – and associated political violence – that drive coups.

Others have pointed to high levels of ethnic diversity, and a history of ethnic exclusion and ethnic militaries, as long-standing drivers of coups on the continent.

But since 2020, a number of other factors also appear to be driving up structural coup risk on the continent. Many African countries have seen declining trust in public institutions and leaders and a rise of terrorist violence, which have generated mass popularity for recent coups on the continent.

Anti-coup norms have also weakened in recent years. International pressure to restore civilian rule was quite strong in the 1990s and 2000s, contributing to the decline of African military coups. But new post-coup African governments appear more resilient to sanctions, are cooperating more with each other and are able to draw on the support of authoritarian “patrons,” notably Russia and China.

As a result, African post-coup governments are staying in power longer, which in turn emboldens coup plotters elsewhere who see a more permissive environment.

So even if there are limits to Africa’s “coup contagion,” Madagascar likely won’t be the last domino to fall, given structural conditions on the continent.

The Conversation

John Joseph Chin does not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and has disclosed no relevant affiliations beyond their academic appointment.

ref. Madagascar’s military power grab shows Africa’s coup problem isn’t restricted to the Sahel region – https://theconversation.com/madagascars-military-power-grab-shows-africas-coup-problem-isnt-restricted-to-the-sahel-region-267581

Academic freedom: how to defend ‘the very condition of a living democracy’ in France and worldwide

Source: The Conversation – France – By Stéphanie Balme, Director, CERI (Centre de recherches internationales), Sciences Po

Director of the CERI at SciencesPo, Stéphanie Balme conducted a study for France Universités, an organisation whose members are presidents of universities, titled “Defending and promoting academic freedom. A global issue, an urgent matter for France and Europe. Findings and proposals for action.” She shares some of her insights here.


Unofficially unveiled on October 2, 2025, US President Donald Trump’s Compact for Academic Excellence in Higher Education is a striking illustration of the politicisation of knowledge and the desire for ideological control over scientific output in the United States. Behind the rhetoric of “restoring excellence” lies a new stage in the institutionalisation of “sciento-populism”: mistrust of science is being strategically exploited to flatter populist sentiments and turn academics into scapegoats, held responsible for the “decline” of US civilisational hegemony.

This phenomenon, although exaggerated, is not isolated. At the same time as Trump’s announcement, the 2025 edition of the Global Innovation Index (GII) revealed that China had entered the top 10 most innovative nations for the first time, while the US, still in third place, showed signs of structural weakness. Eight European countries, a little-known fact, are among the top 15. France has been downgraded to 13th place, the position occupied by China three years ago.

The GII’s 80 indicators, covering nearly 140 countries, are not limited to measuring technological or scientific performance: they also assess the ability of states to guarantee a comprehensive, free and secure political-institutional, economic and financial environment. By cross-referencing these data with those of the Academic Freedom Index, the main reference tool developed since 2019, we can see that academic freedom is no longer solely threatened in authoritarian regimes. It is now being undermined at the very heart of democracies, affecting the humanities and social sciences as much as the experimental sciences.

The awarding of the 2025 Nobel prize in economics to Philippe Aghion, Peter Howitt and Joel Mokyr is a timely reminder that growth and innovation depend on an ecosystem based on freedom of research and the free flow of ideas. Their work on the historical and structural conditions of technological progress shows that no economy can prosper sustainably when knowledge is constrained or subject to ideological control.

Authoritarian regimes and ‘techno-nationalism’

Paradoxically, authoritarian regimes are now among the main investors in research, although they strictly control its objectives in line with their political priorities. Engaged in a phase of rapid “techno-nationalist” development, they are investing heavily in science and technology as instruments of power, without yet suffering the corrosive effects of mistrust of knowledge.

Democracies, on the other hand, struggle to fund research while maintaining their defence spending and must contend with the rise of movements that challenge the very legitimacy of science as it is practiced. In order to better understand these dynamics, I conducted a study for France Universités titled “Defending and promoting academic freedom. A global issue, an urgent matter for France and Europe. Findings and proposals for action”.

Multiple violations in France

France is a particularly striking example of the vulnerabilities described above. In 2024–2025, attacks on academic freedom took many forms: increased foreign interference, regional public funding made conditional on charters with vague criteria, ideological pressure on teaching and research content, conference cancellations, campaigns to stigmatise teachers and researchers on social media, interventions by politicians even in university boards of governors, restrictions on access to research sites or grants, and finally, an increase in gag orders.

Unlike other fundamental rights, academic freedom in France is distinguished by the absence of a firmly rooted political, professional and civic culture. Academics who are victims of attacks on their freedom to practice their profession often find themselves isolated, while the institutional capacity of universities to act as a counterweight remains limited.

This vulnerability is exacerbated by dependence on public funding, career insecurity, administrative overload and a lack of real institutional autonomy. Nevertheless, the current fragility could be transformed into a lever for renewal, promoting the emergence of a strong culture of academic freedom and, in so doing, strengthening France’s position in global science geopolitics.

A multidimensional strategy

The study for France Universités proposes a proactive strategy based on several complementary areas, targeting four categories of stakeholders: the state, the universities, civil society, and those at the European level.

The first area concerns strengthening the legal foundation: constitutionalising academic freedom, reaffirming the autonomy of institutions and the independence of staff, and finally, recognising the principle of source confidentiality (as for journalists) and incorporating a specific regime into the French research code for sensitive data. It is also proposed to extend the system for protecting the nation’s scientific and technical potential (PPST) to the humanities and social sciences, incorporating risks of interference to reconcile scientific security and freedom.

The second area focuses on action by universities: coordinating initiatives at the national level via an independent body, rolling out academic freedom charters across all institutions and research organisations, strengthening the protection of teachers through a dedicated national fund, and establishing rapid assistance protocols. It also provides for the creation of an independent observatory to monitor violations of academic freedom, training for management and advisers on these issues, and the coordination of legal, psychological and digital support for academics who are targeted. Finally, this area aims to promote cross-collaboration between security or defence officials and researchers and teacher-researchers.

The third area aims to promote a genuine culture of academic freedom in the public sphere: launching a national awareness campaign, encouraging student initiatives, transforming France’s Fête de la science (Science Festival) into a Festival of Science and Academic Freedom, organising a national conference to define a participatory action plan, and rolling out a wide-ranging campaign to promote research in partnership with all operators, starting with the National Centre for Scientific Research (CNRS). This campaign, supported by visual aids, posters, drawings and a unifying hashtag, should celebrate research in all media and highlight its essential role in serving a democratic society.

The fourth and final priority aims to incorporate these measures into European science diplomacy by re-establishing a European ranking of universities worldwide that includes an academic freedom index, and by working to have that included in major international rankings. It also aims to strengthen cooperation between the European University Association and European university alliances, establish a European observatory on academic freedom, create a European talent passport for refugee researchers, and make Europe a safe haven for scientists in danger, with the ultimate goal of obtaining recognition in the form of a Nobel Peace Prize dedicated to academic freedom.

A precious common good

Defending academic freedom is not a corporatist reflex: on the contrary, it means protecting a precious common good and the very condition of a living democracy. Of course, this right belongs to only a small number of people, but it benefits everyone, just like freedom of the press, which in France is guaranteed by the law of 1881. Contrary to popular belief, academics are often the last to defend their professional rights, while journalists, quite rightly, actively protect theirs.

The French university system, as it has been constructed since 1945, and even more so after 1968, was not designed to confront authoritarianism. Today, French institutions would not be able to resist systematic attacks for very long if a populist and/or authoritarian regime came to power. Powerful, wealthy and autonomous, the Ivy League universities themselves faltered in the face of the MAGA movement and are still struggling to recover. Many US scientists are now moving to Europe, Japan or South Korea.

How, then, could French universities, which are both financially and institutionally dependent and have only recently established alumni associations, cope with such an onslaught? Not to mention that this would ultimately spell the end of the ambition behind the EU’s Choose Europe for Science programme.

Despite the gravity of the situation, it opens up unprecedented opportunities for collective action, democratic innovation and the development of concrete solutions. Now is the time to act collectively, coordinate stakeholders and launch a broad French and European campaign in support of academic freedom: this is the purpose of the study I conducted.


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Stéphanie Balme ne travaille pas, ne conseille pas, ne possède pas de parts, ne reçoit pas de fonds d’une organisation qui pourrait tirer profit de cet article, et n’a déclaré aucune autre affiliation que son organisme de recherche.

ref. Academic freedom: how to defend ‘the very condition of a living democracy’ in France and worldwide – https://theconversation.com/academic-freedom-how-to-defend-the-very-condition-of-a-living-democracy-in-france-and-worldwide-267689

The Life of Violet: three unearthed early stories where Virginia Woolf’s genius first sparks to life

Source: The Conversation – UK – By Jade French, Postdoctoral Researcher , Loughborough University

BotaniHue/Shutterstock/Wikimedia

Few feelings are more thrilling for a literature scholar than unearthing an archival gem. Urmila Seshagiri, professor of English at the University of Tennessee, got to experience such a jolt when she was told about previously unseen typescripts of three short stories by Virginia Woolf.

These interconnected tales, written in 1907, comprise a mock biography of Woolf’s friend Mary Violet Dickinson, an independent woman who moved in aristocratic circles and who would be crucial to the development of Woolf’s early writing.

In 2022, Seshagiri was finally able to make the trip to Longleat House, a stately home in south-west England, and open up a cream-coloured case containing a polished version of the stories. Another set exists in the US at the New York Public Library, catalogued as Friendships Gallery (the title of the first story). However, to see these drafts reworked by Seshagiri gives them fresh editorial impetus.

It had previously been presumed these stories were a lighthearted footnote to Woolf’s canon in draft form, written as a joke for a friend rather than work to be taken seriously. But now they have been published, bound and critically contextualised for the first time as The Life of Violet: Three Early Stories.

In contextualising these stories, Seshagiri introduces us to a young Virginia Stephen’s “first fully realised literary experiment”, written as she stood on the precipice of Bloomsbury Group-inflected fame.

Juvenilia – work produced when an artist is still young – often isn’t taken seriously. Woolf was even quoted as saying: “I don’t want immaturities, things torn out of time, preserved.”

But the typescripts stored at Longleat House suggest otherwise. Woolf had made amendments and opinions were sought from her sister Vanessa Bell, who thought the work was “very witty and brilliant”.

Seshagiri writes about the seemingly minor changes made by Woolf in detail, with “each clause balanced and weighted for impact”, as well as her overall compositional vision. And she explains how Woolf wove in Dickinson’s own pencilled edits.

Despite such attention to detail, the stories are short – unlike Dickinson, who stood at six feet two inches. Woolf conceptualises her friend as a giant, both literally and figuratively.




Read more:
How Virginia Woolf’s work was shaped by music


Together, Friendships Gallery, The Magic Garden and A Story to Make You Sleep can be read as a manifesto on female friendship and the importance of intergenerational exchange (Woolf was 20 and Dickinson 37 at their first meeting).

These were not merely society ties – their friendship ran deep: Dickinson cared for Woolf during a mental health crisis in 1904 at her home in Welwyn in Hertfordshire. Dickinson is also credited with enabling Woolf’s early literary ambitions as she took steps toward her inimitable style.

In Friendships Gallery, we meet Violet as a child and follow her to middle age, although Woolf’s narrator refuses to fill in the blanks that “yawn like awful caverns”. Instead of facts, we find anecdotes woven into an elevated mediation on biography.

Woolf asks: “Where does care for others become care for oneself?” Individual care is extended collectively outwards, as Violet’s bold laughter and antics slough off Victorian values. Through her friend’s example, Woolf maps out a route towards independence for a new generation of women.

In The Magic Garden, Violet takes tea in an aristocratic home, fielding information on gardening and plumbing. Such information fuels her quest for autonomy, as she cries out with joy about the benefits of having “a cottage of one’s own”. Such calls for creative independence preempt Woolf’s later manifesto, A Room Of One’s Own (1929).

While the first two stories are anchored in an insider’s perspective of English class dynamics, skewering prevailing social norms, the last, A Story to Make You Sleep, takes inspiration from Dickinson’s visit to Japan and the letters she wrote to Woolf.

Turning from mock biography to ancient myth, the story follows a giant princess who saves a village through laughter, before riding a sea monster into an unknown destiny. Unmoored from a context Woolf knew, the use of made-up words and faux Japanese customs stand out – a point Seshagiri reflects on with nuance in the Afterword.

These fantastical, farcical, anti-fairytales offer a glimpse into the early friendships that underpinned Woolf’s world in the years after her parents passed away. They also hint at the playfulness to come in Flush: A Biography (1933) – a social commentary told from the perspective of poet Elizabeth Barrett Browning’s cocker spaniel. They equally foreshadow the tale of queer love and time travel in Orlando: A Biography (1928), based on Woolf’s relationship with the writer and gardener Vita Sackville-West.

Beyond Woolf’s own canon of experimental biography, they also connect her to a tradition of surreal, feminist fabulists. In them, she finds odd kinship with the likes of Leonora Carrington and Angela Carter.




Read more:
Virginia Woolf on the magic of going to the cinema


In bringing together these stories under the title The Life of Violet, the edition charts a literary turning point in the Woolf’s life. The stories are filled with recurring subjects found in her writing: of women’s history and education, of egalitarianism, of experimenting, and of blending biographical fact with fiction.

They remind us that Woolf had a playful, sardonic side and used comedy, as much as highbrow literary experiments, to push beyond the boundaries of tradition. Discoveries such as this also show that the steady image of literary figures (especially those with a booming industry behind them) is never fixed – but rather, reshaped through new readers and ongoing interpretation.

This article features references to books that have been included for editorial reasons, and may contain links to bookshop.org. If you click on one of the links and go on to buy something from bookshop.org The Conversation UK may earn a commission.


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The Conversation

Jade French receives funding from The Leverhulme Trust.

ref. The Life of Violet: three unearthed early stories where Virginia Woolf’s genius first sparks to life – https://theconversation.com/the-life-of-violet-three-unearthed-early-stories-where-virginia-woolfs-genius-first-sparks-to-life-266005

Should the UK introduce targeted prostate cancer screening? The case for and against

Source: The Conversation – UK – By Pinar Uysal-Onganer, Reader in Molecular Biology, University of Westminster

StanislavSukhin/Shutterstock.com

Former UK prime minister Rishi Sunak has called for a targeted prostate cancer screening programme for men most at high risk of the disease, reviving a national debate on how to save more lives and tackle health inequalities among men.

The plan, supported by Prostate Cancer Research, would provide regular screening for men aged 45 to 69, particularly those of African-Caribbean descent or with a family history of the disease.

The case for prostate cancer screening

Pinar Uysal-Onganer, Reader in Molecular Biology, University of Westminster

Prostate cancer is the most common cancer in men in the UK, with more than 63,000 new cases each year. But big gaps remain in who gets diagnosed, how early it’s caught and who survives, reflecting differences in race, region and access to healthcare.

African-Caribbean men are twice as likely to develop the disease and are more likely to die from it than white men. The risk is also higher for those with a father or brother who has had prostate cancer. These differences are not purely biological – they also reflect gaps in awareness, access to care and trust in the health system. A targeted screening programme could begin to close that gap.

The screening process would begin with a PSA (prostate-specific antigen) test, which detects the concentration of a protein produced by the prostate gland. If the PSA level is higher than expected, this would trigger a step-by-step diagnostic process, including MRI scans to improve accuracy and, when necessary, a biopsy to confirm the diagnosis.

Recent improvements in imaging technology help doctors to differentiate aggressive prostate cancers from less aggressive ones with much greater accuracy, making modern screening considerably more precise than it was ten years ago.

Early detection is vital in prostate cancer, as it is with many other cancers. Prostate cancer often develops silently for years before any symptoms appear. By the time it is noticed, it may already have spread beyond the prostate gland.

At that stage, treatments such as hormone therapy or chemotherapy can help control the cancer, although rarely cure it. Detecting prostate cancer earlier through targeted screening would enable less invasive and more effective treatment, offering a far greater chance of full recovery.

Importantly, this proposal recognises the need for greater inclusivity in men’s health. African-Caribbean men and those living in deprived areas are often underrepresented in clinical research, which contributes to gaps in understanding and poorer outcomes.

A screening model based on scientific evidence and community engagement could help close that gap. It would also encourage younger men, particularly those in their 40s, to take a more active interest in preventive health, replacing fear and stigma with informed confidence.

The proposed programme, estimated to cost £25 million annually (approximately £18 per patient, would be less expensive than many current national screening initiatives while offering potentially transformative benefits.

Notably, men in Scotland, as well as the north-west, West Midlands and Wales, have significantly lower survival rates, indicating persistent geographical inequalities in prostate cancer prognosis. Beyond early diagnosis, the proposal could foster trust and participation among underrepresented groups, stimulate biobank research to better understand ethnic and genetic risk and ultimately set a precedent for equity-driven preventive healthcare.

A national targeted PSA screening programme would save lives and demonstrate that all men, regardless of background or postcode, deserve the same chance of early detection.

Rishi Sunak.
Rishi Sunak is a patron of Prostate Cancer Research.
Sussex Photographer/Shutterstock.com

The case against prostate cancer screening

Alwyn Dart, Lecturer, Cancer Institute, UCL

Men should see their doctor regularly to look after their health and spot problems early. Serious illnesses like heart disease, diabetes and some cancers can be controlled or stopped altogether if caught in time. But men don’t always look after their health as well as women do.

One in five men put off going to the doctor or having tests. This is often because they feel embarrassed, awkward, or worried about what other people might think, especially when it comes to intimate health issues. When men finally do get help, their problems are often more serious and harder to fix by then. This is particularly true for prostate problems and prostate cancer.

A test called the PSA test has been suggested as a simple way to screen for prostate cancer. A single blood test could easily be added to routine health checks. Women already have screening programmes for breast and cervical cancer that have been running for years and save thousands of lives every year by catching cancer early. So on the face of it, having a similar blood test for prostate cancer in men seems like an obvious good idea.

But here’s the problem. The PSA test isn’t nearly as reliable as the tests for breast and cervical cancer. While breast cancer tests have a “sensitivity” (ability to accurately detect cancer) of between 50-91%, the PSA test has a sensitivity of around 20% – at the standard PSA cut-off of 4ng/mL. Things like an enlarged prostate, infections, or even recent exercise can give false results and make it look like someone has cancer when they don’t.

This unreliability causes a lot of problems. A high PSA result triggers a whole chain of tests and investigations into the prostate, some of which can be invasive, uncomfortable and painful. These investigations themselves can cause unnecessary worry and put men at risk of harm. Men might end up anxious and stressed for no good reason.

The other issue is that some prostate cancers grow very slowly and might never actually harm a person during their lifetime. They might just need careful watching rather than aggressive treatment. But when tests give “false positives” – saying someone has cancer when they don’t – each one means more investigations that need to happen. This piles pressure on doctors, radiologists and other specialists who are already stretched thin.

If someone is diagnosed with prostate cancer and gets surgery or radiation treatment, it can lead to serious side-effects like loss of bladder control, erectile dysfunction and serious psychological stress. Research shows that most prostate cancers tend to grow slowly and are not be life-threatening.

The PSA test is also unreliable in the other direction. Some men who actually do have prostate cancer may get a normal result and don’t get checked properly when they should have been.

Looking at the bigger picture, studies show that PSA screening only prevents three deaths from prostate cancer out of every 1,000 men tested. But it leads to unnecessary diagnoses and interventions in up to 60 out of 1,000 men. That’s far more harm than good.

From the NHS’s point of view, setting up a nationwide PSA screening programme would be hugely expensive and disruptive. Experts estimate it would increase the number of tests and scans needed by approximately 23%.

This would mean thousands more appointments, more specialist doctors and staff, and lots of money spent on scanners and lab work – all things the NHS is already stretched thin trying to provide. This extra workload could mean less time and money for patients who urgently need help with other cancers or serious illnesses.

The real answer isn’t just to test more men for prostate cancer; it’s to find a better test. Men should definitely pay more attention to their own health, but until we have a test that can tell the difference between prostate cancers that will genuinely threaten someone’s life and those that won’t, a nationwide PSA screening programme would do more damage than good.

It would turn healthy men into patients, overload hospitals even more, and wouldn’t actually give people clear answers. What we really need is a test that finds the right cancers, at the right time, using the right tool – in other words, a better test.

The Conversation

Pinar Uysal-Onganer receives funding from Prostate Cancer UK.

Alwyn Dart does not work for, consult, own shares in or receive funding from any company or organisation that would benefit from this article, and has disclosed no relevant affiliations beyond their academic appointment.

ref. Should the UK introduce targeted prostate cancer screening? The case for and against – https://theconversation.com/should-the-uk-introduce-targeted-prostate-cancer-screening-the-case-for-and-against-267493

As social media age restrictions spread, is the internet entering its Victorian era?

Source: The Conversation – Global Perspectives – By Alex Beattie, Lecturer, Media and Communication, Te Herenga Waka — Victoria University of Wellington

Getty Images

A wave of proposed social media bans for young people has swept the globe recently, fuelled by mounting concern about the apparent harm the likes of TikTok, Instagram and Snapchat can cause to vulnerable minds.

Australia was the first to announce restrictions on people under 16 having a social media account. New Zealand may soon follow, and Denmark’s prime minister recently declared her country would ban social media for under-15s, accusing mobile phones and social networks of “stealing our children’s childhood”.

The moves are part of a growing international trend: the United Kingdom, France, Norway, Pakistan and the United States are now considering or implementing similar restrictions, often requiring parental consent or digital ID verification.

At first glance, these policies appear to be about protecting young people from mental health harm, explicit content and addictive design. But beneath the language of safety lies something else: a shift in cultural values.

The bans reflect a kind of moral turn, one that risks reviving conservative notions that predate the internet. Might we be entering a new Victorian era of the internet, where the digital lives of young people are reshaped not just by regulation but by a reassertion of moral control?

Policing moral decline

The Victorian era was marked by rigid social codes, modest dress and formal communication. Public behaviour was tightly regulated, and schools were seen as key sites for socialising children into gender and class hierarchies.

Today, we see echoes of this in the way “digital wellness” is framed. Screen-time apps, detox retreats and “dumb” phones are marketed as tools for cultivating a “healthy” digital life – often with moral undertones. The ideal user is calm, focused and restrained. The impulsive, distracted or emotionally expressive user is pathologised.

This framing is especially evident in the work of Jonathan Haidt, psychologist and author of The Anxious Generation, a central text in the age-restriction movement. Haidt argues that social media accelerates performative behaviour and emotional dysregulation in young people.

Viewed this way, youth digital life involves declining psychological resilience, rising polarisation and the erosion of shared civic values, rather than being a symptom of complex developmental or technological shifts. This has helped popularise the idea that social media is not just harmful but corrupting.

Yet the data behind these claims is contested. Critics have pointed out that Haidt’s conclusions often rely on correlational studies and selective interpretations.

For example, while some research links heavy social media use to anxiety and depression, other studies suggest the effects are modest and vary widely depending on context, platform and individual differences.

What’s missing from much of the debate is a recognition of young people’s agency, or their ability to navigate online spaces intelligently, creatively and socially.

Indeed, youth digital life is not just about passive consumption. It’s a site of literacy, expression and connection. Platforms such as TikTok and YouTube have fostered a renaissance of oral and visual communication.

Young people stitch together memes, remix videos and engage in rapid-fire editing to produce new forms of storytelling. These are not signs of decline but evolving literacies. To regulate youth access without acknowledging these skills risks suppressing the new in favour of preserving the familiar.

Regulate platforms, not young people

This is where the Victorian metaphor becomes useful. Just as Victorian norms sought to maintain a particular social order, today’s age restrictions risk enforcing a narrow vision of what digital life should look like.

On the surface, terms such as “brain rot” appear to convey the harm of excessive internet use. But in practice, they’re often used by teenagers to laugh about and resist the pressures of 24/7 hustle culture.

But concerns about young people’s digital habits seem rooted in a fear of cognitive difference – the idea that some users are too impulsive, too irrational, too deviant.

Young people are often cast as unable to communicate properly, hiding behind screens, avoiding phone calls. But these changing habits reflect broader shifts in how we relate to technology. The expectation to be always available, always responsive, ties us to our devices in ways that make switching off genuinely difficult.

Age restrictions may address some symptoms, but they don’t tackle the underlying design of platforms that are built to keep us scrolling, sharing and generating data.

If society and governments are serious about protecting young people, perhaps the better strategy is to regulate the digital platforms. Legal scholar Eric Goldman calls the age-restriction approach a “segregate and suppress” strategy – one that punishes youth rather than holding platforms accountable.

We would never ban children from playgrounds, but we do expect those spaces to be safe. Where are the safety barriers for digital spaces? Where is the duty of care from digital platforms?

The popularity of social media bans suggests a resurgence of conservative values in our digital lives. But protection should not come at the cost of autonomy, creativity or expression.

For many, the internet has become a moral battleground where values around attention, communication and identity are fiercely contested. But it is also a social infrastructure, one that young people are already shaping through new literacies and forms of expression.

Shielding them from it risks suppressing the very skills and voices that could help us build a better digital future.

The Conversation

Alex Beattie receives funding from The Royal Society Te Apārangi. He is a recipient of a Marsden Fast Start Grant.

ref. As social media age restrictions spread, is the internet entering its Victorian era? – https://theconversation.com/as-social-media-age-restrictions-spread-is-the-internet-entering-its-victorian-era-267610

Friday essay: the Nuremberg Trials at 80 – could such a reckoning ever happen again?

Source: The Conversation – Global Perspectives – By Jan Lanicek, Associate Professor in Modern European History and Jewish History, UNSW Sydney

In November 2025, cinemas worldwide will release Nuremberg, a courtroom drama directed by James Vanderbilt. The film focuses on the International Military Tribunal against 24 major Nazi war criminals (though two were ultimately not tried) and seven Nazi organisations – including the SS, the Gestapo and the general staff of the army – at the end of the second world war.

Its release coincides with the 80th anniversary of the Nuremberg Trials, which officially opened on October 18 1945. The film explores our desire to see justice and reckoning for those who committed war crimes against civilian populations in the past and present.

The plot centres on the confrontation between Hermann Göring (played by Russell Crowe), a leading Nazi on trial, and psychiatrist Douglas M. Kelley (played by Rami Malek). Kelley’s task was to examine whether the top Nazis were fit to stand trial.

Nuremberg is often called “history’s greatest trial”. It was the first international trial that held senior governmental officials accountable for war crimes and crimes against humanity committed across Europe. It also established individual responsibility for committing war crimes, rejecting the defence of following the orders of superiors.

The indictment covered Nazi crimes before and during the war, against both soldiers and civilians. Nuremberg happened in a unique moment in time, when a country that triggered a major war was completely crushed by a military alliance willing to enforce its “unconditional surrender”.

It was also during the short time before the outbreak of the Cold War, when the wartime alliance between the East and West still held together. Such a trial seems unlikely to be repeated in our current historical moment.

What were the Nuremberg trials?

The International Military Tribunal, which held its hearings in Nuremberg, Germany, lasted for almost a year, until October 1946. It was the first in a series of 13 trials that brought to justice representatives of all the Nazi political, military and business elites, as well as mid-ranking representatives of the army, medical professionals and other Nazi agencies.

The reckoning was comprehensive, even though with the developing Cold War, the Western allies soon lost their appetite for further trials.

The Allies chose Nuremberg as the place for the trials for both political and practical reasons. Nuremberg was one of the centres of the Nazi movement. Numerous political rallies and parades took place there during Hitler’s rule. Also, the Palace of Justice in Nuremberg was one of the few suitable buildings that survived the near total destruction of Germany. It had the facilities needed for a major international tribunal.

Besides Göring, the defendants at the first trial included the Nazi foreign minister Joachim von Ribbentrop, military commanders Wilhelm Keitel and Alfred Jodl and armament minister Albert Speer. It also included the vicious antisemite Julius Streicher, and head of the Reich Security Main Office, Ernst Kaltenbrunner – the man in charge of the Nazi policies of persecution.

Several top representatives of Nazi Germany escaped justice: Adolf Hitler, Heinrich Himmler and Joseph Goebbels had died by suicide.

In popular memory, the Holocaust or Shoah, the mass extermination of the European Jews, is now commemorated as the main symbol of Nazi atrocities. But historians offer a mixed assessment of the role the Holocaust played during the Nuremberg trial.

While the persecution of the Jews did not dominate the proceedings, their fate was repeatedly emphasised as one of the Nazi crimes. Three Jewish survivors personally testified in the courtroom, reminding the world about the death of approximately six million Jews and incarceration of hundreds of thousands more who survived the ordeal of the camps.

In the courtroom, the prosecution played the footage from the liberated concentration camps, including Belsen and Buchenwald, which shook the audience – including the defendants. Defence witness Rudolf Höss, former commandant of Auschwitz, described the killing process in the gas chambers and crematoria in detail.

The Nazis’ persecution of other minorities received minimum coverage in the main trial. In addition to Jewish people, they also persecuted the Romani people, disabled people, homosexuals and religious minority groups.

Earlier efforts at international justice

Previous efforts to bring leaders of defeated states to justice and establish their accountability had been relatively unsuccessful. The Versailles Peace Treaty in 1919, for instance, promised to bring German leaders to justice for suspected war crimes during the first world war, though the effort never really materialised.

In the Soviet Union, trials of Nazi war criminals and local collaborators had already begun during the second world war. In 1943, the Krasnodar and Kharkov trials sentenced most defendants to death. In late 1944, a Soviet–Polish court sentenced guards from the Majdanek concentration camp to death. Further local trials continued in the first post-war months by the allied militaries, and new political authorities in the liberated countries.

But Nuremberg was the main piece in the puzzle of a comprehensive, often brutal retribution and cleansing all over Europe that brought tens of thousands of war criminals and collaborators to justice. Not only Germans, but also representatives of occupied nations accused of war crimes and collaboration, sat in the dock. Nazi war crimes trials, on a smaller scale, continued for decades.

In fact, just a few years ago, in 2022, 97-year-old Irmgard Furchner, a former secretary at a Nazi concentration camp, Stutthof, was found guilty of complicity in the murder of more than 10,500 people. She received a two-year suspended sentence.

‘History will judge us’

Nuremberg’s significance was political, legal, moral and historical. The tribunal prosecuting major war criminals “whose offenses have no particular geographical location” was jointly led by the four main Allied powers: the United States, the Soviet Union, Britain and France. Each had representatives among the judges and prosecution teams. The prosecutors also represented the interests of other, minor allies, such as Poland or Czechoslovakia, who could provide evidence for the trial.

The indictment listed four counts: conspiracy to commit crimes, crimes against peace, war crimes and crimes against humanity. In the first trial, 22 Nazis were in the dock.

In his opening speech, US Chief of Counsel for Nuremberg, Justice Robert H. Jackson, stressed:

the wrongs which we seek to condemn and punish have been so calculated, so malignant, and so devastating that civilization cannot tolerate their being ignored because it cannot survive their being repeated.

He continued, “We must never forget that the record on which we judge these defendants today is the record on which history will judge us tomorrow.”

The confirmation of the Nazi crimes that came with the liberation of Europe had shocked the world. When pushing the Wehrmacht (the armed forces of Germany’s Third Reich) from the east and west, seasoned Allied troops liberated destroyed villages and towns, coming across evidence of mass murder of civilians. In 1944 and 1945, the Red Army and western Allies liberated Nazi concentration camps, confirming the mass extermination of Jews and other groups.

At Nuremberg, the charge of “crimes against humanity”, in particular, punished crimes against civilians, such as “murder, extermination, enslavement, deportation, and other inhumane acts”. The promoter of this term was lawyer Hersch Lauterpacht, who was born in Galicia (then part of Austria-Hungary) and lived in the UK.

A competing legal terminology had been developed by another Galician-born lawyer, based in the US, Raphael Lemkin, who coined the term “genocide”. While the concept supported by Lauterpacht focused on the persecution of individuals, Lemkin stressed that the Nazi crimes were committed with the intent to destroy whole groups, particularly the Jews.

Although Nuremberg mentioned genocide on several occasions, the judges preferred “crimes against humanity” when characterising Nazi crimes. This legal concept allowed the Allies to punish German leaders for the persecution of their own citizens, even before the war.

As international lawyer and author Philippe Sands has said, this decision mean that “no longer would a state be free to treat its people entirely as it wished”.

A refined version of Lemkin’s term for genocide was officially enshrined in international law by the United Nations in 1948. It has been criticised for establishing a high threshold of proof. As a result, only a few cases of mass violence against civilians meet the criteria.

There were several notable moments during the trial. Göring, the former head of the Luftwaffe (German airforce), was considered the main defendant, and dominated the trial. Eventually, he had to be isolated from the other defendants, to allow them to speak more freely.

His questioning by Justice Jackson has been characterised as one of the worst cross-examinations in history. US attorney Robert Hedrick said, in 2016, that Göring was a “slippery” witness, who often complained about the translation of questions to buy time to think of an answer – and Jackson “did not control his witness”. But the prosecution had enough evidence to sentence him to death on all four counts, including crimes against humanity.

Rudolf Hess, deputy leader of the Nazi Party, escaped on a plane to Britain in 1941, allegedly with the aim to negotiate peace. He was imprisoned and kept in custody until the end of the war. In Nuremberg, Hess claimed amnesia and mental problems to avoid accountability for his crimes. In the end, he was sentenced to life in prison and died at Spandau prison in Berlin, in 1987.

Architect Albert Speer, who from 1942 became Hitler’s armament minister, cooperated with the court. He expressed remorse for the crimes he committed, though denied any knowledge of the Holocaust. These claims have later been disputed.

For instance, in 1971, Harvard University historian Erich Goldhagen found that Speer had attended a conference of senior Nazis in October 1943, at which SS head Himmler had spoken openly about “the extermination of the Jewish people”. (Though his biographer couldn’t confirm he had heard the speech in person, she concluded “he knew”.) He was sentenced to 20 years and was released in 1966, aged 61.

The judges sentenced 12 defendants to the death penalty. Martin Bormann, the head of the Nazi Party Chancellery and Secretary to Hitler, was sentenced in absentia. Although it was believed he was at large, it was later confirmed he died in the battle of Berlin in early May 1945.

Three defendants, Hitler’s minister of economics Hjalmar Schacht, propagandist Hans Fritzsche, and Hitler’s erstwhile conservative ally Franz von Papen were acquitted, despite the protest of the Soviet judge. Göring, sentenced to death, escaped justice by dying by suicide the night the execution was ordered.

International war crimes trials since Nuremberg

Nuremberg was the first major international trial for war crimes. It was followed by others. At around the same time, beginning in 1946, the International Military Tribunal for the Far East met in Tokyo, judging Japanese war criminals. The Tokyo Charter closely followed the Nuremberg Charter.

In the 1990s, in the post-Cold War period, the UN Security Council established two more ad hoc international criminal tribunals.

The International Criminal Tribunal for the former Yugoslavia was set up in the Hague, for war criminals from the wars in the former Yugoslavia. Its mandate lasted from 1993 to 2017. The International Criminal Tribunal for Rwanda convened in Arusha, Tanzania, to prosecute persons responsible for genocide and war crimes in the Rwandan civil war, committed in 1994. Both men and women were sentenced to long prison terms at these trials, including for the crime of genocide.

In 2002, the UN General Assembly approved the creation of the permanent International Criminal Court (ICC). Based on the Rome statute, the ICC can judge genocide, war crimes, crimes against humanity and the crime of aggression. However, some of the major world powers, such as the US, Russia, China and India, do not recognise its jurisdiction and do not cooperate with the court.

The ICC is currently investigating several states and their leaders, including Russia, Israel and a Hamas representative. Usually, only heads of smaller states, who lack strong international partners, sit in the dock. More powerful actors ignore the extradition requests, accusing the court of either pro-western bias, “neo-colonialist repression” or antisemitism.

Almost 80% of all indictments issued by the court have been against African leaders. The court has not opened one single case against leaders from the West.

Because of the indictment against Israeli leaders, the US has threatened the court with sanctions, and Hungary has withdrawn from the ICC. The ICC lacks the instruments to enforce extradition and can only rely on members’ cooperation. State leaders sought by the ICC travel relatively freely around the world, visiting major international states including permanent members of the UN Security Council.

Could the Nuremberg trials happen today?

A major trial of international significance – comparable to the Nuremberg Trials – would only be possible in the case of a major military defeat of the investigated government, and its occupation by those willing to bring the leading politicians to justice.

This is unlikely to happen. Countries are unwilling to extradite their leaders to international courts, unless they are coerced by circumstances. Many prefer to settle the scores on their home turf.

The Allies organised the Nuremberg trials with the hope of bringing the horrible chapter of Nazism to an end and sending a clear message for the future. The destruction, war crimes and crimes against humanity revealed at the end of the war truly shocked the world.

Even so, the East and West were only able to meet and sentence the German leaders during this brief historical moment before the outbreak of the Cold War.

With growing divisions in the world today, another Nuremberg is unlikely to happen any time soon.

The Conversation

Jan Lanicek receives funding from the Australian Research Council.

ref. Friday essay: the Nuremberg Trials at 80 – could such a reckoning ever happen again? – https://theconversation.com/friday-essay-the-nuremberg-trials-at-80-could-such-a-reckoning-ever-happen-again-267313

Should I take a magnesium supplement? Will it help me sleep or prevent muscle cramps?

Source: The Conversation – Global Perspectives – By Nial Wheate, Professor, School of Natural Sciences, Macquarie University

Magnesium supplements are everywhere – lined up on pharmacy shelves and promoted on wellness blogs and social media.

Maybe you have a friend or family member who swears a daily tablet will help everything, from better sleep to alleviating muscle cramps.

But do you really need one? Or it is just marketing hype?

What is magnesium and why do we need it?

Magnesium is an essential metal the body needs to make and operate more than 300 different enzymes.

These enzymes build protein, and regulate muscle and nerve function, help in the release of energy from our food, and help to maintain blood function. The body doesn’t produce magnesium so we need to get it from external sources.

The government recommends a daily magnesium dose of 310–420 mg a day for adults and 30–410 mg for children, depending on age and sex.

This is easily met through a good diet. Foods rich in magnesium include nuts and seeds, whole grains, seafood, meat, legumes and green leafy vegetables.

You can even get some of your magnesium needs met through dark chocolate. It has 146 mg per 100 g of chocolate.

How do I know if I’m deficient?

People at risk of experiencing magnesium deficiency include people with restricted diets, gastrointestinal problems such as Crohn’s and coeliac diseases, type 2 diabetes, and alcohol dependence. Older adults are also more likely to be deficient.

You will only need a magnesium supplement if you show signs of low magnesium. One of the most common signs is muscle spasms and twitches. Other symptoms to look out for include low appetite, nausea and vomiting, or your heart beating abnormally.

Magnesium deficiency can be properly diagnosed by a blood test ordered by your doctor. If you need this test, it’s covered by Medicare.

What conditions can it help?

Commercially available magnesium supplements have been promoted to prevent muscle cramps, manage insomnia and help with migraines.

While magnesium deficiency is linked to muscle cramps, the cause of most muscle cramps is unknown.

And the current evidence does not demonstrate that magnesium supplements can prevent muscle cramps in older adults.

Different brands of magnesium supplements
Magnesium supplements come in different brands and doses.
Nial Wheate

There is conflicting data as to whether the use of magnesium helps with sleep. One study reported magnesium was able to reduce the time for a person to fall asleep by 17.4 minutes while others didn’t show an effect.

For migraines, the most recent research suggests taking 122-600 mg of magnesium supplements daily for 4–24 weeks may decrease their frequency and severity.

Are magnesium supplements safe?

Magnesium supplements are generally well tolerated.

However, they can cause gastrointestinal discomfort such as nausea, abdominal cramping and diarrhoea. Magnesium causes diarrhoea by drawing water into the intestine and stimulating movement in the gut.

It is possible to take too much magnesium and you can overdose on it. Very large doses, around 5,000 mg per day, can lead to magnesium toxicity.

Most of the research investigating the clinical use of magnesium focuses on magnesium in oral formulations.

What other formulations are available?

As magnesium is a small metal ion, it can pass through skin – but not easily.

Magnesium bath salts, patches and topical cream-based formulations may be able to raise your blood magnesium levels to some extent.

But due to the amount needed each day, tablets and foods are a better source.

Things to watch out for when taking magnesium

Commercially available magnesium products can vary widely in dose, formulation and cost. Magnesium supplements have between 150 to 350 mg of the metal per tablet. Your required dose will depend on your age and sex, and whether you have any underlying health problems.

Magnesium supplements sometimes contain other vitamins and minerals, such as vitamins C and D, and the metals calcium, chromium and manganese. So it’s important to consider the total quantities if you’re taking other vitamins and supplements.

Many magnesium supplements also include vitamin B6. While this vitamin is important for supporting the immune system, high intakes can it can cause serious health issues. If you’re already taking a B6 supplement, a magnesium supplement that also includes it can put you at risk.

What if you’re considering supplements?

If you think you might be deficient in magnesium, speak to your doctor who can order a blood test.

If you suffer from migraines, cramps, or poor sleep, talk to your doctor or pharmacist who can advise on and monitor the underlying cause. It may be that a change in lifestyle or an alternative treatment may be more appropriate for you.

If you do decide to take a magnesium supplement, check you won’t be taking too much of any other vitamin or mineral. A pharmacist can help select a supplement that suits you best.

The Conversation

Nial Wheate in the past has received funding from the ACT Cancer Council, Tenovus Scotland, Medical Research Scotland, Scottish Crucible, and the Scottish Universities Life Sciences Alliance. He is a fellow of the Royal Australian Chemical Institute. Nial is the chief scientific officer of Vaihea Skincare LLC, a director of SetDose Pty Ltd (a medical device company) and was previously a Standards Australia panel member for sunscreen agents. He is a member of the Haleon Australia Pty Ltd Pain Advisory Board. Nial regularly consults to industry on issues to do with medicine risk assessments, manufacturing, design and testing.

Wai-Jo Jocelin Chan does not work for, consult, own shares in or receive funding from any company or organisation that would benefit from this article, and has disclosed no relevant affiliations beyond their academic appointment.

ref. Should I take a magnesium supplement? Will it help me sleep or prevent muscle cramps? – https://theconversation.com/should-i-take-a-magnesium-supplement-will-it-help-me-sleep-or-prevent-muscle-cramps-267542