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This Nonprofit Health System Cuts Off Patients With Medical Debt

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This Nonprofit Health System Cuts Off Patients With Medical Debt

Many hospitals in the United States use aggressive tactics to collect medical debt. They flood local courts with collections lawsuits. They garnish patients’ wages. They seize their tax refunds.

But a wealthy nonprofit health system in the Midwest is among those taking things a step further: withholding care from patients who have unpaid medical bills.

Allina Health System, which runs more than 100 hospitals and clinics in Minnesota and Wisconsin and brings in $4 billion a year in revenue, sometimes rejects patients who are deep in debt, according to internal documents and interviews with doctors, nurses and patients.

Although Allina’s hospitals will treat anyone in emergency rooms, other services can be cut off for indebted patients, including children and those with chronic illnesses like diabetes and depression. Patients aren’t allowed back until they pay off their debt entirely.

Nonprofit hospitals like Allina get enormous tax breaks in exchange for providing care for the poorest people in their communities. But a New York Times investigation last year found that over the past several decades, nonprofits have fallen short of their charitable missions, with few consequences.

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Allina has an explicit policy for cutting off patients who owe money for services they received at the health system’s 90 clinics. A 12-page document reviewed by The Times instructs Allina’s staff on how to cancel appointments for patients with at least $4,500 of unpaid debt. The policy walks through how to lock their electronic health records so that staffers cannot schedule future appointments.

“These are the poorest patients who have the most severe medical problems,” said Matt Hoffman, an Allina primary care doctor in Vadnais Heights, Minn. “These are the patients that need our care the most.”

Allina Health said it has a robust financial assistance program that in an average year helps over 12,000 of its 1.9 million patients with medical bills. The hospital system cuts off patients only if they have racked up at least $1,500 of unpaid debt three separate times. It contacts them by phone and with repeated letters that include information about applying for financial help, said Conny Bergerson, a hospital spokeswoman.

“Allina Health’s goal is, and will always be, to have zero patients go without services for financial reasons,” Ms. Bergerson said. She said that cutting off services was “rare” but declined to provide information on how often it happens.

Allina suspended its policy of cutting off patients in March 2020, at the onset of the coronavirus pandemic, before reinstating it in April 2021.

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An estimated 100 million Americans have medical debts. Their bills make up about half of all outstanding debt in the country.

About 20 percent of hospitals nationwide have debt-collection policies that allow them to cancel care, according to an investigation last year by KFF Health News. Many of those are nonprofits. The government does not track how often hospitals withhold care.

Under federal law, hospitals are required to treat everyone who comes to the emergency room, regardless of their ability to pay. But the law — called the Emergency Medical Treatment and Labor Act — is silent on how health systems should treat patients who need other kinds of lifesaving care, like those with aggressive cancers or diabetes.

In 2020, thanks to its nonprofit status, Allina avoided roughly $266 million in state, local and federal taxes, according to the Lown Institute, a think tank that studies health care.

In exchange, the Internal Revenue Service requires Allina and thousands of other nonprofit hospital systems to benefit their local communities, including by providing free or reduced-cost care to patients with low incomes.

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But the federal rules do not dictate how poor a patient needs to be to qualify for free care. In 2020, Allina spent less than half of 1 percent of its expenses on charity care, well below the nationwide average of about 2 percent for nonprofit hospitals, according to an analysis of hospital financial filings by Ge Bai, a professor at the Johns Hopkins Bloomberg School of Public Health.

Allina is one of Minnesota’s largest health systems, having largely grown through acquisitions. Since 2013, its annual profits have ranged from $30 million to $380 million. Last year was the first in the past decade when it lost money, largely owing to investment losses.

The financial success has paid dividends. Allina’s president earned $3.5 million in 2021, the most recent year for which data is available. The health system recently built a $12 million conference center.

Yet Allina sometimes plays hardball with patients. Doctors have become accustomed to seeing messages in the electronic medical record notifying them that a patient “will no longer be eligible to receive care” because of “unpaid medical balances.”

Dr. Rita Raverty, a primary care doctor who works at an Allina clinic, said the notifications were alarming because they meant she could not provide continuous care for some of her patients facing a number of health risks.

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“Nobody wins when patients can’t get preventive care,” Dr. Raverty said. “It creates worse disease outcomes when you’re not catching things early.”

Doctors and patients described being unable to complete medical forms that children needed to enroll in day care or show proof of vaccination for school.

Serena Gragert, who worked as a scheduler at an Allina clinic in Minneapolis until 2021, said the computer system simply wouldn’t let her book future appointments for some patients with outstanding balances.

Ms. Gragert and other Allina employees said some of the patients who were kicked out had incomes low enough to qualify for Medicaid, the federal-state insurance program for poor people. That also means those patients would be eligible for free care under Allina’s own financial assistance policy — something many patients are unaware exists when they seek treatment.

Ms. Bergerson, the Allina spokeswoman, did not dispute that but said the health system goes “to tremendous lengths to assist patients with their financial obligations for medical care.”

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Allina employees said the policy has forced them to ration care.

Beth Gunhus, a pediatric nurse practitioner, recalled a case in which a mother brought in her three children. One had scabies, an intensely itchy skin condition caused by mites burrowing into the body. She wanted to follow best practices and treat the entire family, who were sharing one bed in a single room they rented, to ensure it didn’t spread further. But she could write a prescription for only two of the children. The third’s account was locked because of unpaid bills.

“There are so many better ways of saving money than what we’re doing,” Ms. Gunhus said.

Allina says the policy applies only to debts related to care provided by its clinics, not its hospitals. But patients said in interviews that they got cut off after falling into debt for services they received at Allina’s hospitals.

Because Allina is the dominant health system in some rural parts of Minnesota, getting kicked out can leave patients with few options.

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Jennifer Blaido lives in Isanti, a small town outside Minneapolis, and Allina owns the only hospital there. Ms. Blaido, a mechanic, said she racked up nearly $200,000 in bills from a two-week stay at Allina’s Mercy Hospital in 2009 for complications from pneumonia, along with several visits to the emergency department for asthma flare-ups. Ms. Blaido, a mother of four, said most of the hospital stay was not covered by her health insurance and she was unable to scrounge together enough money to make a dent in the debt.

Last year, Ms. Blaido had a cancer scare and said she couldn’t get an appointment with a doctor at Mercy Hospital. She had to drive more than an hour to get examined at a health system unconnected to Allina.

Allina does not make this policy explicit to patients. It is not mentioned in the health system’s list of “frequently asked questions” about billing practices. In at least one case, Allina has denied that it even existed.

In a lawsuit filed last year in state court in Minnesota, Allina sued a couple, Jordan and JoLynda Anderson, for nearly $10,000 in unpaid medical bills.

In court filings, the couple described how Allina canceled Ms. Anderson’s appointments and told her that she could not book new ones until she had set up three separate payment plans — one with the health system and two with its debt collectors.

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Even after setting up those payment plans, which totaled $580 a month, the canceled appointments were never restored. Allina allows patients to come back only after they have paid the entire debt.

Ms. Anderson recalls being devastated about losing her visit to an endocrinologist that specialized in a chronic condition she has. She had already been waiting four months for the appointment, and was unable to get a new one.

“It felt like I was being punished, and the punishment was you get to stay ill,” she said.

Ms. Bergerson declined to comment on these cases, citing patient privacy.

When the Andersons asked in court for a copy of Allina’s policy of barring patients with unpaid bills, the hospital’s lawyers responded: “Allina does not have a written policy regarding the canceling of services or termination of scheduled and/or physician referral services or appointments for unpaid debts.”

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In fact, Allina’s policy, which was created in 2006, instructs employees on how to do exactly that. Among other things, it tells staff to “cancel any future appointments the patient has scheduled at any clinic.”

It does provide a few ways for patients to continue being seen despite their unpaid bills. One is by getting approved for a loan through the hospital. Another is by filing for bankruptcy.

Susan C. Beachy contributed research.

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Column: Right-wing judges are on a mission to stop the FDA from warning consumers about snake oil

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Column: Right-wing judges are on a mission to stop the FDA from warning consumers about snake oil

To anyone who has paid even a modicum of serious attention to COVID-19 and its treatment, ivermectin is the zombiest of zombie drugs.

Used to treat parasitic diseases in animals and humans, the drug became a darling of anti-vaccination activists and conspiracy-mongers, who pushed it as a treatment for the pandemic disease and claimed it was being suppressed by Big Pharma, among other sinister forces.

Contrary to its continued promotion by quacks such as Florida Surgeon General Joseph Ladapo, the drug has been conclusively shown to be utterly useless against COVID.

You are not a horse. Stop it with the #ivermectin. It’s not authorized for treating #COVID.

— Food and Drug Administration counsels against a useless COVID treatment

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One would have hoped that hard scientific evidence and a stern advisory by the Food and Drug Administration against its use would have been enough to kill the ivermectin craze, but it lives on. Last year, three doctors sued the FDA, claiming that its public warning harmed their practices and cost them their jobs at hospitals and medical schools.

A few months later, a federal judge in Galveston threw out their case, ruling in effect that they didn’t come close to having a leg to stand on. That should have been an end to it. But earlier this month, the case was revived by the U.S. 5th Circuit Court of Appeals, which takes cases from Texas, Louisiana and Mississippi and is, by many measures, the hackiest of hack-ridden federal courts.

The three judges hearing this appeal — two appointed by George W. Bush and one (the opinion’s author) by Donald Trump — found that the FDA had exceeded its authority in advising against the use of ivermectin against COVID. “The FDA can inform,” the court said, “but it has identified no authority allowing it to recommend consumers ‘stop’ taking medicine.” (Emphasis in the original.)

That’s absurd, says Dorit Rubinstein Reiss, an expert on vaccine policy at University of California College of the Law, San Francisco, and the author of a withering analysis of the 5th Circuit opinion.

The FDA’s job, Reiss told me, is to “balance the need for treatment with safety concerns. If the FDA can’t translate what it’s finding into plain language — ‘do this, don’t do that’ — then it can’t do its job. That undermines the whole regulatory scheme.”

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More on that in a moment. First, some context.

Undermining the FDA’s authority has been a right-wing project for years. That’s because the agency’s duty is to stand in the way of businesses desiring to push unsafe and ineffective nostrums at unwary consumers, and also in the way of a perverse idea that personal freedom includes the freedom to be gulled by charlatans.

This campaign got pumped up during the Trump administration. Trump in 2018 signed a federal “right-to-try” law that masqueraded as a compassionate path giving sufferers of intractable, incurable diseases access to experimental treatments. In fact, as I wrote, it was a cynical ploy backed by the Koch brothers’ network aimed at emasculating the FDA in a way that would undermine public health.

Trump subsequently browbeat his maladroit FDA chairman, Stephen Hahn, into issuing an emergency authorization for the use of convalescent plasma to treat COVID-19 patients. Like ivermectin, that was another utterly ineffective treatment.

In announcing his decision while Trump stood glaring at him, Hahn grossly misrepresented the results of a medical trial conducted by the Mayo Clinic, which failed to demonstrate any effectiveness for the treatment. In the run-up to the announcement, Trump issued a tweet accusing “the deep state … at the FDA” of deliberately delaying effective COVID treatments until after the upcoming Nov. 3, 2020, election, which Trump lost. Hahn didn’t respond to that frontal attack on his agency’s integrity.

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The FDA is under more solid management now, but the malign influence of judges Trump installed in the federal judiciary lives on. That brings us to the 5th Circuit, on which 12 of the 16 currently active judges were appointed by Republican presidents — six by Trump.

The court has received appeals of some of the loopiest district court rulings of recent memory, largely because conservative litigants in Texas have the ability to hand-pick judges who see things their way.

Among the recent rulings those judges have issued that swear at precedent and common sense are those outlawing the use of the medication mifepristone for abortion (another case aimed at undermining FDA authority) and barring agencies of the federal government from communicating with social media companies, which was brought by right-wing litigants hoping to hobble the government’s battle against medical misinformation.

The 5th Circuit judges have frequently matched the district court rulings they’re reviewing with loopy opinions of their own.

Trump appointee James Ho issued a partial concurrence in the mifepristone case in which he asserted that an “unborn child” was “killed by mifepristone,” and justified outlawing use of the drug by stating that “unborn babies are a source of profound joy for those who view them. Expectant parents eagerly share ultrasound photos with loved ones. Friends and family cheer at the sight of an unborn child. Doctors delight in working with their unborn patients — and experience an aesthetic injury when they are aborted.”

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(The court narrowed the FDA’s authority to approve the drug, but its ruling is under review by the Supreme Court.)

In a 2019 case, a three-judge panel voted 2-1 to find that a key provision of the Affordable Care Act, and possibly the entire law, was unconstitutional. In her concurrence, Jennifer Walker Elrod, a George W. Bush appointee in the majority, approvingly repeated a right-wing congressman’s claim that the act was “a fraud on the American people.”

The 5th Circuit judges combine their clownish approach to the law with a clownish confusion over the federal rules of procedure they are bound to apply. As recently as Tuesday, the appeals court had to withdraw an order it had issued the day before, granting red state plaintiffs a rehearing in the case involving government contacts with social media companies.

The court had originally allowed four government agencies to continue interacting with the companies; the red states wanted the judges to withdraw their permission. But the court’s granting of a rehearing so flagrantly violated procedural rules governing cases, like this one, that are already under consideration by the Supreme Court, that it had to immediately backtrack. (The circuit’s clerk of the court obligingly accepted the blame, attributing Monday’s grant to a “clerical error.”

The judges who made this blunder — Elrod, Edith Brown Clement and Don R. Willett — are the same ones who ruled in the ivermectin case. Let’s take another gander at that ruling.

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Reiss terms the ruling “problematic on legal and policy grounds” by “undercutting the FDA’s ability to offer expertise-based guidance about products they regulate.”

The judges were particularly exercised by an FDA Twitter campaign that aimed to dissuade consumers from taking the veterinary preparation of ivermectin commonly administered to horses.

“You are not a horse,” the agency tweeted. “Stop it with the #ivermectin. It’s not authorized for treating #COVID.” The agency also issued a general warning headlined “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19,” explaining that the drug has not been shown to be effective for the purpose and is dangerous in high doses.

The three plaintiff doctors — one from Virginia, one from Texas, and one practicing in Washington and Arizona — had lost their hospital privileges or other professional positions for promoting the drug. The latter plaintiff is under investigation by medical regulators in the two states where he’s licensed. All three blamed the FDA.

The 5th Circuit judges agreed that even though the agency pointed out that it has no power to order patients to do or not do anything and no authority over physicians — who have the legal right to prescribe medications approved by the FDA for “off-label” uses — it had exceeded its authority by using “imperative” language (i.e., “Stop it”) instead of merely declaring that the drug wasn’t approved for COVID.

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Yet as Reiss points out, the FDA frequently couches its advisories in such straightforward terms, and has done so virtually since its creation in its present form in 1930. The agency’s warning against unproven stem cell treatments — a dark and dangerous hive of medical charlatans — advises patients, “Don’t believe the hype” and adds that it’s “increasing its oversight and enforcement to protect people from dishonest and unscrupulous stem cell clinics.”

Carrying the 5th Circuit’s ruling to its logical extreme, the agency’s stem cell warning would exacerbate the vulnerability of disease sufferers to quacks hawking expensive and ineffective treatments.

Thanks to its promotion by anti-vaxxers and conspiracy-mongers, ivermectin prescriptions in the U.S. spiked to 88,000 in mid-August 2021 from 3,600 per week prior to the pandemic, despite a lack of any evidence that it is useful against COVID.

(Centers for Disease Control and Prevention)

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Despite the judges’ contention that it has no authority to offer recommendations to the public, Reiss notes that such authority is actually embedded in federal law, which gives the FDA the right to undertake “collecting, reporting, and illustrating the results of [its] investigations.”

“That certainly seems to include conclusions based on the data collected,” Reiss wrote: “Reporting on the result of an investigation that showed ivermectin is not effective for COVID-19 would naturally include a comment that it should not be used.”

In any event, there’s no case to be made that the FDA warnings caused the doctors’ professional troubles. Several professional organizations have warned of the ineffectiveness of ivermectin for COVID, including the American Medical Assn. No medical board needed the FDA to tell it that doctors prescribing this modern snake oil deserved scrutiny.

It’s possible that the appellate judges themselves had an inkling that they were on thin ice in their ruling. They didn’t rule conclusively that the FDA was wrong, but rather sent the case back to the trial court judge for further pondering on technical grounds, such as whether the FDA’s advisories amount to “final agency actions” subject to court review or whether the doctors even had standing to bring the lawsuit in the first case.

“They seem to be trying to hedge,” Reiss says. On the other hand, they didn’t dismiss the case outright, as they should have. The judges cast a shadow over the FDA, at a time when its crucial, lifesaving campaign against medical misinformation doesn’t need any more head winds.

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An Ancient Whale Named for King Tut, but Moby-Dinky in Size

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An Ancient Whale Named for King Tut, but Moby-Dinky in Size

In 1842, a vast, nearly intact skeleton was unearthed on a plantation in Alabama; it was soon identified as a member of Basilosaurus, a recently named genus of prehistoric sea serpent. But when some of its enormous bones were shipped to England, Richard Owen, an anatomist, noted that its molars had two roots, not one, a dental morphology unknown in any reptile. He determined that the fossil was actually a marine mammal: a primitive whale. Herman Melville name-drops the behemoth — Mr. Owen called it Zeuglodon — in Chapter 104 of “Moby-Dick,” and Mr. Owen, in a paper that he read to the London Geological Society, pronounced it “one of the most extraordinary creatures which the mutations of the globe have blotted out of existence.”

In August, a team of paleontologists announced the discovery of another extraordinary creature that was blotted out of existence. Eleven years ago, while working in the Fayum Depression of the Western Desert in Egypt, the team excavated the fossil of what they initially thought was a small amphibian. But closer inspection revealed that the bones belonged to a previously unknown species of miniature whale that existed during the late middle Eocene, in a period called the Bartonian Age, which lasted from about 48 million to 38 million years ago. The species, described in a paper in the journal Communications Biology, inhabited the Tethys Sea, the tropical precursor of the Mediterranean, which covered about a third of what is now northern Africa.

Ishmael, the protagonist of “Moby-Dick,” asserts somewhat disingenuously that a whale is a “spouting fish with a horizontal tail.” The newly documented specimen looked less like a fish than a bottlenose dolphin, with a less-bulbous forehead and a more elongated body and tail. Based on a skull, jaw, teeth and vertebrae fragments embedded in compacted limestone, researchers inferred that the wee whale, which dates back some 41 million years, was about eight feet long and weighed roughly 400 pounds, making it the tiniest known member of the basilosaurid family.

All whales are descended from terrestrial animals that ventured into the sea. Some early whales evolved into forms that ventured back onto land; basilosaurids are thought to be the first widespread group to have stuck with the sea life. They were also the last to have hind limbs that were still recognizable as legs, which were probably used less for locomotion than as reproductive guides to help orient the whales during sex.

Melville dismissed whale taxonomy as “mere sounds, full of Leviathanism, but signifying nothing.” He likely would have had little use for Tutcetus rayanensis, the official name of the small-scale whale ancestor. Tutcetus combines Tut — recalling the pharaoh Tutankhamen — and cetus, Greek for whale. The designation also follows the centenary of the discovery of King Tut’s tomb, and coincides with the impending opening of the Grand Egyptian Museum in Giza, Egypt. The “rayan” part of the name derives from the Wadi El-Rayan Protected Area, which sits about 25 miles northeast of a site so rich in fossil whales that it has been called Wadi Al-Hitan, or Valley of the Whales.

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Like Tut, who died in the Valley of the Kings at age 18, the whale is believed to have been a juvenile nearing adulthood. The research team used CT scanning to analyze Tutcetus’s teeth and bones, reconstructing its growth patterns. The bones of the skull had fused, as had parts of the first vertebrae, and while some of the teeth had emerged, some were still in transition. The rapid dental development and small bone size of Tutcetus suggest a short, fast life compared with larger and later basilosaurids, said Hesham Sallam, a paleontologist at the American University of Cairo and leader of the project.

The whale may have been able to feed itself and move independently almost from birth, researchers said. The soft enamel and configuration of its teeth suggest that it was a meat-eater, with a diet of aquatic animals.

The discovery challenges some conventional assumptions about the life history of primitive whales. “The geological age of Tutcetus is a bit older than other closely related fossil whales, which hints that some evolutionary changes in whale anatomy happened a bit earlier than we suspected,” said Nicholas Pyenson, curator of fossil marine mammals at the Smithsonian’s National Museum of Natural History, who was not involved in the work. “The fossil pushes back the timing of how the earliest whales changed from foot- to tail-propelled movement in the water.”

Whales have an unexpected past. Genetically they are closely related to hoofed mammals, called ungulates, and within that group they are most similar to the artiodactyls, such as camels, pigs, giraffes and hippos, all of which have an even number of toes. One of the best-known early forebears of whales was a 50-million-year-old quadruped called Pakicetus that waded in the estuaries of southern Asia, ate meat and, by some accounts, might have resembled a large house cat with hoof-like claws.

Scientists were able to link Pakicetus to the evolutionary lineage of whales because it had an ear bone with a feature unique to those modern-day giants of the deep. “Importantly, its ankle bones look like those of artiodactyls and helped to support the link of whales to artiodactyls that had previously been suggested by DNA,” said Erik Seiffert, an anatomist at the University of Southern California who collaborated on the paper.

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The artiodactyls begot the semiaquatic ambulocetus, a so-called walking whale that looked like a crocodile, swam like an otter and waddled on land like a sea lion. “Ambulocetus actually still had fairly well-developed hind limbs, so it wouldn’t have had a hard time getting around on land,” Dr. Seiffert said. Ambulocetus, in turn, begot protocetid, a more streamlined halfway creature that fed in the sea, but may have returned to land to rest. Over evolutionary time, its hind limbs became smaller, and it maneuvered entirely with its tail.

Eventually, these proto-cetaceans gave rise to archaeocet, a fully aquatic basilosaurid. Aided by flippers and paddle-like tails, basilosaurids dispersed through the oceans worldwide. The one that turned up on that Alabama plantation in 1842 may even have crossed the Atlantic.

Mohammed Antar, a paleontologist at Mansoura University who dug up the Tutcetus fossil and was first author of the new paper, said climate and location may have made the Fayum Depression inviting to basilosaurids. “Modern whales migrate to warmer, shallow waters for breeding and reproduction, mirroring the conditions found in Egypt 41 million years ago,” he said.

The setting seems to have provided relatively safe harbor for female whales to give birth in shallow waters. “As far as we can tell from the abundant fossils of tree-living primates found there, the area lining the northern edge of what is now the Sahara was effectively a tropical forest during the middle Eocene,” Dr. Seiffert said. The protected coasts of northern Africa, he added, “might have allowed whale calves time to mature and reach a level of navigational and feeding proficiency before heading out into open water, then very deep water.”

In August, shortly before the diminutive Tutcetus was unveiled in Egypt, paleontologists working in Peru reported the discovery of an extinct whale that may have been the heaviest animal ever. Perucetus colossus swam the oceans 38 million years ago and is estimated to have weighed as much as 200 tons, a figure comparable to the blue whale, the current record-holder.

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Perucetus and Tutcetus were alive just a few million years before primitive whales began their evolutionary split into the two cetacean suborders of today: the toothed whales, dolphins and porpoises known as odontoceti, and the baleen-bearing mysticeti, including blue whales and humpbacks.

“The mysticetes tend to be much larger than the odontocetes,” said Jonathan Geisler, an anatomist at the New York Institute of Technology. “And this difference is related to their different feeding strategies.” Toothed whales hunt individual prey such as fish and squid, while baleen whales filter-feed to gather krill, copepods and tiny schooling fish.

“Understanding the size of the ancestor of all modern whales helps us understand how these feeding behaviors and distinct body size differences evolved,” Dr. Geisler said. “Tutcetus is one data point in the effort, but it supports the hypothesis that the common ancestor of all living cetaceans was fairly small.”

Dr. Sallam said that similar to the way Melville, reflecting on the Basilosaurus skeleton found in 1842, imagines a time when “the whole world was the whale’s,” the discovery underscores the transient nature of existence and provides a tangible connection to a prehistoric past. “The significance of the find, like the fossils described in ‘Moby Dick,’ extends beyond the realm of paleontology,” he said. “It highlights the enduring fascination with Earth’s ancient history.”

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Video: Space Capsule Brings NASA’s First Asteroid Samples to Earth

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Video: Space Capsule Brings NASA’s First Asteroid Samples to Earth

new video loaded: Space Capsule Brings NASA’s First Asteroid Samples to Earth

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Space Capsule Brings NASA’s First Asteroid Samples to Earth

NASA collected a capsule, which contained materials from the asteroid Bennu, after it landed in the Utah desert, concluding a seven-year mission.

“We have confirmed parachute deployment.” “Wow, and after an exhilarating streak across Earth’s atmosphere, we have parachute deployment. You can see just a sigh of relief from the team. I can hear some applause here. You see the reaction there just moments ago as they got that sample back on the ground. The rest of the team members approaching that S.R.C. that has been successfully bagged and prepared to be loaded into the helicopter’s long line. And we have clearance to depart the recovery site. This is a key moment of those recovery operations. We’re already getting that S.R.C out of the landing zone and on its way to the Dugway clean room. In just a few moments, the SR.C. will be back on the ground, its second touchdown of the day, a much calmer one than we had earlier this morning. The doors are now open. We are entering into the clean room and that S.R.C. is about to be moved off onto our clean room fixture. It’s hard to fathom that just a couple of years ago, this sample return capsule that you see here was over 200 million miles away from us on the other side of the solar system.”

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