Month: December 2020

Master Spy Writer John Le Carre Dies at 89, His Agent Says

John le Carre, the spy-turned-novelist whose elegant and intricate narratives defined the Cold War espionage thriller and brought acclaim to a genre critics had once ignored, has died. He was 89.Le Carre died Saturday in Cornwall, southwest England, Saturday after a short illness, his literary agency, Curtis Brown, said Sunday. The death was not related to COVID-19.In such classics as “The Spy Who Came in from the Cold,” “Tinker, Tailor, Soldier Spy” and “The Honorable Schoolboy,” Le Carre combined terse but lyrical prose with the kind of complexity expected in literary fiction. His books grappled with betrayal, moral compromise and the psychological toll of a secret life. In the quiet, watchful spymaster George Smiley, he created one of 20th-century fiction’s iconic characters — a decent man at the heart of a web of deceit.For le Carre, the world of espionage was a “metaphor for the human condition.”Born David Cornwell, le Carre worked for Britain’s intelligence service before turning his experience into fiction in works including “Tinker, Tailor, Soldier Spy” and “The Spy Who Came in from the Cold.””I’m not part of the literary bureaucracy if you like that categorizes everybody: Romantic, Thriller, Serious,” le Carre told The Associated Press in 2008. “I just go with what I want to write about and the characters. I don’t announce this to myself as a thriller or an entertainment.”I think all that is pretty silly stuff. It’s easier for booksellers and critics, but I don’t buy that categorization. I mean, what’s ‘A Tale of Two Cities?’ — a thriller?”His other works included “Smiley’s People,” “The Russia House” and, in 2017, the likely Smiley farewell, “A Legacy of Spies.” Many novels were adapted for film and television, notably the 1965 productions of “Smiley’s People’ and “Tinker, Tailor” featuring Alec Guinness as Smiley.Le Carre was drawn to espionage by an upbringing that was superficially conventional but secretly tumultuous.Born David John Moore Cornwell in Poole, southwest England, on Oct. 19, 1931, he appeared to have a standard upper-middle-class education: the private Sherborne School, a year studying German literature at the University of Bern, compulsory military service in Austria — where his tasks involved interrogating Eastern Bloc defectors — and a degree in modern languages at Oxford University.It was an illusion: his father, Ronnie Cornwell, was a con man who was an associate of gangsters and spent time in jail for insurance fraud. His mother left the family when David was 5; he didn’t meet her again until he was 21.It was a childhood of uncertainty and extremes: one minute limousines and champagne, the next eviction from the family’s latest accommodation. It bred insecurity, an acute awareness of the gap between surface and reality — and a familiarity with secrecy that would serve him well in his future profession.  “These were very early experiences, actually, of clandestine survival,” le Carre said in 1996. “The whole world was enemy territory.”  After university, which was interrupted by his father’s bankruptcy, he taught at the prestigious boarding school Eton before joining the foreign service.  Officially a diplomat, he was in fact an operative with the domestic intelligence service MI5 — he’d started as a student at Oxford — and then its overseas counterpart MI6, serving in Germany, then on the Cold War front line, under the cover of second secretary at the British Embassy.  His first three novels were written while he was a spy, and his employers required him to publish under a pseudonym. He remained “le Carre” for his entire career. He said he chose the name — square in French — simply because he liked the vaguely mysterious, European sound of it.  “Call for the Dead” appeared in 1961 and “A Murder of Quality” in 1962. Then in 1963 came “The Spy Who Came in from the Cold,” a tale of an agent forced to carry out one last, risky operation in divided Berlin. It raised one of the author’s recurring themes — the blurring of moral lines that is part and parcel of espionage, and the difficulty of distinguishing good guys from bad. Le Carre said it was written at one of the darkest points of the Cold War, just after the building of the Berlin Wall, at a time when he and his colleagues feared nuclear war might be imminent.  “So I wrote a book in great heat which said, ‘a plague on both your houses,'” le Carre told the BBC in 2000.It was immediately hailed as a classic and allowed him to quit the intelligence service to become a full-time writer.  His depictions of life in the clubby, grubby, ethically tarnished world of “The Circus” — the books’ code-name for MI6 — were the antithesis of Ian Fleming’s suave action-hero James Bond and won le Carre a critical respect that eluded Fleming.  Smiley appeared in le Carre’s first two novels and in the trilogy of “Tinker, Tailor, Soldier Spy,” “The Honorable Schoolboy,” and “Smiley’s People.”  Le Carre said the character was based on John Bingham — an MI5 agent who wrote spy thrillers and encouraged le Carre’s literary career — and the ecclesiastical historian Vivian Green, the chaplain of his school and later his Oxford college, “who became effectively my confessor and godfather.” The more than 20 novels touched on the sordid realities of spycraft but le Carre always maintained there was a kind of nobility in the profession. He said in his day spies had seen themselves “almost as people with a priestly calling to tell the truth.””We didn’t shape it or mold it. We were there, we thought, to speak truth to power.”  
“The Perfect Spy,” his most autobiographical book, looks at the formation of a spy in the character of Magnus Pym, a boy whose criminal father and unsettled upbringing bear a strong resemblance to le Carre’s own. His writing continued unabated after the Cold War ended and the front lines of the espionage wars shifted. Le Carre said in 1990 that the fall of the Berlin Wall had come as a relief.  “For me, it was absolutely wonderful,” he said. “I was sick of writing about the Cold War. The cheap joke was to say, ‘Poor old le Carre, he’s run out of material; they’ve taken his wall away.’ The spy story has only to pack up its bags and go where the action is.”  That turned out to be everywhere. “The Tailor of Panama” was set in Central America. “The Constant Gardener,” which was turned into a film starring Ralph Fiennes and Rachel Weisz, was about the pharmaceutical industry’s machinations in Africa.  “A Most Wanted Man,” published in 2008, looked at extraordinary rendition and the war on terror. “Our Kind of Traitor,” released in 2010, took in Russian crime syndicates and the murky machinations of the financial sector.  In 1954, le Carre married Alison Sharp, with whom he had three sons before they divorced in 1971. In 1972 he married Valerie Eustace, with whom he had a son, the novelist Nick Harkaway.  Although he had a home in London, le Carre spent much of his time near Land’s End, England’s southwestern most tip, in a clifftop house overlooking the sea. He was, he said, a humanist but not an optimist.  “Humanity — that’s what we rely on. If only we could see it expressed in our institutional forms, we would have hope then,” he told the AP. “I think the humanity will always be there. I think it will always be defeated.”
 

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Nations Breaking Daily COVID-19 Records for Cases and Deaths 

As more countries approve a coronavirus vaccine, the urgent need for inoculation continues to grow with COVID-19 cases and deaths spiking to record highs in several countries. The Korea Disease Control and Prevention Agency said Sunday that South Korea recorded a record daily increase in coronavirus cases for a second straight day with 1,030 new infections. In the U.S. last week, California recorded more than 25,000 new infections in one day.  “Lives will be lost unless we do more than we’ve ever done,” Governor Gavin Newsom said. 
 
Overall, more than 16 million people in the U.S. have contracted the disease, while nearly 300,000 have died. 
 
A New York Times investigation found that coronavirus deaths have risen faster than the rest of the country in U.S. college town communities where students make up at least 10% of the population. Sorry, but your browser cannot support embedded video of this type, you can
download this video to view it offline.Download File360p | 10 MB480p | 14 MB540p | 17 MB720p | 33 MB1080p | 71 MBOriginal | 545 MB Embed” />Copy Download AudioItaly is poised to overtake Britian as the European country with the most COVID-19 deaths, according to data from Johns Hopkins Coronavirus Resource Center. 
 
Early Sunday, Italy was just 87 deaths behind Britain, but Italy has 6 million fewer people than Britain. 
 
Italy has suffered 25,418 deaths in the weeks since November 1, which is more than it did from April 2 to October 31, when it reported 25,463. 
  
According to Johns Hopkins University, there have been more than 71 million global COVID infections and 1.6 million deaths.  Public health officials say actual numbers are likely higher since not everyone is tested for the disease and some people who are infected do not display any symptoms. Pharmacy supervisor Kevin Weissman wears a thick glove as he opens the door of a special freezer that will hold the Pfizer vaccine at LAC USC Medical Center, during the outbreak of the coronavirus disease, in Los Angeles, California, Dec. 10. 2020.In U.S. states, the first coronavirus vaccine will begin arriving early Monday after the U.S. Food and Drug Administration approved the vaccine made by U.S. drug maker Pfizer and Germany’s BioNTech for emergency use. 
 
Mexico also approved the emergency use of Pfizer’s coronavirus vaccine late Friday, bringing to six the number of countries that are using or plan to use it. Britain, Bahrain, Canada and Saudi Arabia have also approved the vaccine. Mexico City said Saturday that shops in the capital’s center and other busy areas would temporarily close at 5 p.m. to reduce the risk spreading the virus as authorities battle a surge in cases. Brazil is steadily approaching 7 million COVID-19 cases and has recorded more than 181,000 deaths.  Brazilian President Jair Bolsonaro has been skeptical about the seriousness of the disease, even though he is a coronavirus survivor.  The South American country’s Supreme Court gave Brazil’s government a deadline to come up with a plan to fight the spread of the disease. A Health Ministry document sent to Brazil’s Supreme Court said 108 million doses of the vaccine would be set aside for priority groups, such as health care workers, the elderly and members of indigenous communities, Reuters reports.  The plan, however, did not provide a date for starting inoculations for priority groups or the rest of the population.  Last week, Brazil’s health minister vowed to vaccinate the entire country during the course of next year. 

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COVID-19 Vaccine Approved as Cases Surge

As more countries approve a coronavirus vaccine, the urgent need for inoculation continues to grow with COVID-19 cases and deaths spiking to record highs in several countries.The Korea Disease Control and Prevention Agency said Sunday that South Korea recorded a record daily increase in coronavirus cases for a second straight day with 1,030 new infections.In the U.S. last week, California recorded more than 25,000 new infections in one day.  “Lives will be lost unless we do more than we’ve ever done,” Gov. Gavin Newsom said.Overall, more than 16 million people in the U.S. have contracted the disease, while nearly 300,000 have died.A New York Times investigation found that coronavirus deaths have risen faster than the rest of the country in U.S. college town communities where students make up at least 10% of the population.Italy is poised to overtake Britian as the European country with the most COVID-19 deaths, according to data from Johns Hopkins Coronavirus Resource Center.Early Sunday, Italy was just 87 deaths behind Britain, but Italy has 6 million fewer people than Britain.Italy has suffered 25,418 deaths in the weeks since Nov. 1, which is more than it did from April 2 to Oct. 31, when it reported 25,463.According to Johns Hopkins University, there have been more than 71 million global COVID infections and 1.6 million deaths.Public health officials say actual numbers are likely higher since not everyone is tested for the disease and some people who are infected do not display any symptoms.Sorry, but your browser cannot support embedded video of this type, you can
download this video to view it offline.Download File360p | 10 MB480p | 14 MB540p | 17 MB720p | 33 MB1080p | 71 MBOriginal | 545 MB Embed” />Copy Download AudioIn U.S. states, the first coronavirus vaccine will begin arriving early Monday after the U.S. Food and Drug Administration approved the vaccine made by U.S. drugmaker Pfizer and Germany’s BioNTech for emergency use.Mexico also approved the emergency use of Pfizer’s coronavirus vaccine late Friday, bringing to six the number of countries that are using or plan to use it.Britain, Bahrain, Canada and Saudi Arabia have also approved the vaccine.Mexico City said Saturday that shops in the capital’s center and other busy areas would temporarily close at 5 p.m. to reduce the risk spreading the virus as authorities battle a surge in cases.Brazil is steadily approaching 7 million COVID-19 cases and has recorded more than 181,000 deaths.Brazilian President Jair Bolsonaro has been skeptical about the seriousness of the disease, even though he is a coronavirus survivor.The South American country’s Supreme Court gave Brazil’s government a deadline to come up with a plan to fight the spread of the disease.A health ministry document sent to Brazil’s Supreme Court said 108 million doses of the vaccine would be set aside for priority groups, such as health care workers, the elderly and members of indigenous communities, Reuters reports. The plan, however, did not provide a date for starting inoculations for priority groups or the rest of the population.Last week, Brazil’s health minister vowed to vaccinate the entire country during the course of next year.

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Chinese Capsule with Moon Rocks Begins Return to Earth

A Chinese space capsule bringing back the first moon rocks in more than four decades started its three-day return to Earth on Sunday.The Chang’e 5 lunar probe, which had been orbiting the moon for about a week, fired up four engines for about 22 minutes to move out of the moon’s orbit, the China National Space Administration said in a social media post.The craft’s lander touched down on the moon earlier this month close to a formation called the Mons Rumker, an area believed to have been the site of ancient volcanic activity. It collected about 2 kilograms of samples.The return capsule is expected to land in northern China in the Inner Mongolia region after separating from the rest of the spacecraft and floating down on parachutes. The material would be the first brought back since the Soviet Union’s Luna 24 probe in 1976.The rocks and other debris were obtained both by drilling into the moon’s crust and scooping directly off the surface. They may be billions of years younger than those brought back by earlier U.S. and Soviet missions, possibly offering insights into the moon’s history and that of other bodies in the solar system.China has set up labs to analyze the samples for age and composition and is also expected to share some of them with other countries, as was done with the hundreds of kilograms brought back by the U.S. and former Soviet Union.China’s space program has a series of ambitious missions underway, including a probe en route to Mars. The Chang’e lunar program, named after the ancient Chinese moon goddess, has been operating the Chang’e 4 probe on the moon’s less explored far side for the past two years.Future plans call for returning a human to the moon and perhaps a permanent moon base. China is also building a space station to begin operating as early as 2022.

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US Approves Emergency Use of Vaccine

The U.S. has approved emergency use of the Pfizer–BioNTech coronavirus vaccine, paving the way for Americans to start getting vaccinated within days. But public skepticism about the safety of the vaccine remains, with polls showing many adults say they won’t get the shot or are unsure about getting it. White House Correspondent Patsy Widakuswara has the latest.

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Pakistan Decides Against New Coal-fired Power

Pakistan Prime Minister Imran Khan announced Saturday that his country would have no new coal-fired power generation as part of its contribution in global efforts against climate change.Khan gave details of the substantial undertaking while addressing the international Climate Ambition Summit 2020, held virtually because of the coronavirus pandemic.The United Nations, United Kingdom, France, Chile and Italy hosted the event, bringing world leaders together to press for greater efforts in curbing global warming.“We have decided we will not have any more power based on coal,” Khan told the summit. “We have already scrapped two coal power projects, which were supposed to produce 2,600 megawatts of energy, and replaced it by hydroelectricity.”By 2030, Khan said, 60% of all energy produced in Pakistan will be clean and obtained through renewable resources, while 30% of all vehicles will run on electricity.The prime minister said that while Pakistan accounts for less than 1% of global carbon emissions, it is the “fifth most vulnerable” to effects of climate change, citing data from the 2019 Global Climate Risk Index report.“I assure you that Pakistan will be doing its best to make its contribution to mitigate the effects of climate change,” Khan said.FILE – Cargo trains carrying shipping containers and coal dust cross under a bridge with the backdrop of City Station, built in the British Raj era, in Karachi, Pakistan, Sept. 24, 2018.Pakistan had just one coal-fired power plant until 2016. China has since invested billions of dollars in the South Asian nation, installing at least nine coal-based power plants with more under construction.Official data show Pakistan’s coal-based power generation surged to 57% through fiscal 2020, which ended in June, thanks to Beijing’s investments under its Belt and Road Initiative. The collaboration helped Islamabad overcome years of power shortages in the country.Khan’s government, which took power more than two years ago, has also undertaken a countrywide reforestation campaign to plant more than 3 billion trees by mid-2023 to mitigate the effects of climate change. The massive program, dubbed the Ten Billion Tree Tsunami, went into effect last year, and officials say it has planted more than 500 million saplings across Pakistan.Addressing the summit, U.N. chief Antonio Guterres urged world leaders to declare a “state of climate emergency” in their respective countries. “If we don’t change course, we may be headed for a catastrophic temperature rise of more than 3.0 degrees this century,” he warned.The summit marked five years since the landmark Paris Agreement on climate change, which seeks to limit global warming to 1.5 degrees Celsius, compared with pre-industrial levels.

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Charley Pride, Country Music’s First Black Star, Dies at 86

Charley Pride, country music’s first Black star whose rich baritone on such hits as “Kiss an Angel Good Morning” helped sell millions of records and made him the first Black member of the Country Music Hall of Fame, has died. He was 86.Pride died Saturday in Dallas of complications from COVID-19, according to Jeremy Westby of the public relations firm 2911 Media.”I’m so heartbroken that one of my dearest and oldest friends, Charley Pride, has passed away. It’s even worse to know that he passed away from COVID-19. What a horrible, horrible virus. Charley, we will always love you,” Dolly Parton tweeted.Pride released dozens of albums and sold more than 25 million records during a career that began in the mid-1960s. Hits besides “Kiss an Angel Good Morning” in 1971 included “Is Anybody Goin’ to San Antone,” “Burgers and Fries,” “Mountain of Love” and “Someone Loves You Honey.”FILE – Charley Pride poses with the Pioneer Award he received at the 29th Academy of Country Music Awards show in Universal City, Calif., May 3, 1994. In 2000, Pride was inducted into the Country Music Hall of Fame.He received three Grammy Awards, had more than 30 No. 1 hits between 1969 and 1984, won the Country Music Association’s Top Male Vocalist and Entertainer of the Year awards in 1972 and was inducted into the Country Music Hall of Fame in 2000.The Smithsonian in Washington acquired memorabilia from Pride, including a pair of boots and one of his guitars, for the National Museum of African American History and Culture.Singer Ronnie Milsap called him a pioneer and said that without his encouragement, Milsap might never gone to Nashville.”To hear this news tears out a piece of my heart,” he said in a statement.Until the early 1990s, when Cleve Francis came along, Pride was the only Black country singer signed to a major label.In 1993, he joined the Grand Ole Opry cast in Nashville.’Skin hang-ups'”They used to ask me how it feels to be the ‘first colored country singer,’ ” he told The Dallas Morning News in 1992. “Then it was ‘first Negro country singer,’ then ‘first Black country singer.’ Now I’m the ‘first African-American country singer.’ That’s about the only thing that’s changed. This country is so race-conscious, so ate up with colors and pigments. I call it ‘skin hang-ups’ — it’s a disease.”Pride was raised in Sledge, Mississippi, the son of a sharecropper. He had seven brothers and three sisters.In 2008 while accepting a Lifetime Achievement Award as part of the Mississippi Governor’s Awards for Excellence in the Arts, Pride said he never focused on race.”My older sister one time said, ‘Why are you singing THEIR music?’ ” Pride said. “But we all understand what the y’all-and-us-syndrome has been. See, I never as an individual accepted that, and I truly believe that’s why I am where I am today.”As a young man before launching his singing career, he was a pitcher and outfielder in the Negro American League with the Memphis Red Sox and in the Pioneer League in Montana.FILE – Brad Paisley and Charley Pride perform “Kiss an Angel Good Morning” at the 50th annual CMA Awards at the Bridgestone Arena, Nov. 2, 2016, in Nashville, Tenn.After playing minor league baseball a couple of years, he ended up in Helena, Montana, where he worked in a zinc smelting plant by day and played country music in clubs at night.After a tryout with the New York Mets, he visited Nashville and broke into country music when Chet Atkins, head of RCA Records, heard two of his demo tapes and signed him.To ensure that Pride was judged on his music and not his race, his first few singles were sent to radio stations without a publicity photo. After his identity became known, a few country radio stations refused to play his music.WelcomedFor the most part, though, Pride said he was well-received. Early in his career, he would put white audiences at ease when he joked about his “permanent tan.””Music is the greatest communicator on the planet Earth,” he said in 1992. “Once people heard the sincerity in my voice and heard me project and watched my delivery, it just dissipated any apprehension or bad feeling they might have had.”Throughout his career, he sang positive songs instead of sad ones often associated with country music.”Music is a beautiful way of expressing oneself and I truly believe music should not be taken as a protest,” he told The Associated Press in 1985. “You can go too far in anything — singing, acting, whatever — and become politicized to the point you cease to be an entertainer.”In 1994, he wrote his autobiography, “Pride: The Charley Pride Story,” in which he disclosed he was mildly manic depressive.He had surgery in 1997 to remove a tumor from his right vocal cord.He received the Living Legend award from The Nashville Network/Music City News, recognizing 30 years of achievement, in 1997.”I’d like to be remembered as a good person who tried to be a good entertainer and made people happy, was a good American who paid his taxes and made a good living,” he said in 1985. “I tried to do my best and contribute my part.”

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Mexico Approves Coronavirus Vaccine

Mexico approved the emergency use of a coronavirus vaccine late Friday, bringing to six the number of countries that are inoculating or plan to inoculate with shots produced by U.S. drugmaker Pfizer and Germany’s BioNTech.Britain, Bahrain, Canada, Saudi Arabia and the United States have also approved the vaccine.Mexican Assistant Health Secretary and epidemiologist Hugo Lopez-Gatell called the vaccine approval “a reason for hope.” Reuters reports Mexico signed an agreement with Pfizer to acquire 34 million doses of the vaccine, with the first batch expected later this month.Mexico has recorded 1.2 million COVID-19 cases and 113,000 deaths, according to Johns Hopkins University.The vaccine’s approval by the U.S. Food and Drug Administration Friday came as the United States topped 295,000 fatalities from COVID-19, the world’s highest death toll, according to Johns Hopkins University, which calculates the United States has had 15.8 million of the world’s more than 71 million COVID infections.Hospitalizations are at record levels in America’s most populous state, California. Los Angeles County reported its highest-ever daily number for new COVID-19 cases at more than 12,000 earlier this week. A public health official said the county is “on a very dangerous track to seeing unprecedented and catastrophic suffering and death … if we can’t stop the surge.”Meanwhile, the World Health Organization and the International Federation of Red Cross and Red Crescent Societies signed an agreement, the Emergency Medical Team (EMT) Initiative, on Friday to strengthen the delivery of emergency medical and health services during humanitarian crises.“We are very committed to working together with WHO to provide quality emergency health services that communities desperately need in times of crisis.” said IFRC Secretary-General Jagan Chapagain.India said early Saturday that it recorded 30,000 new cases in the past 24 hours. The South Asian nation follows the U.S. in the number of COVID cases with 9.8 million infections. Brazil comes in third with more than 6 million COVID infections.

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Trump Hails Approved Coronavirus Vaccine as ‘Medical Miracle’

U.S. President Donald Trump late Friday hailed what he termed “a medical miracle” – the immediate but extremely limited availability of a coronavirus vaccine less than a year after the first cases of COVID-19 were reported in the United States.In a video message posted on Twitter, Trump said the first doses of the Pfizer-BioNTech vaccine the U.S. Food and Drug Administration approved for emergency use will be administered “within 24 hours” and will be “free [of charge] for all Americans.”The president said the vaccine “will save millions of lives and soon end the pandemic once and for all.” The assertion contradicted health officials who note that it will be months before many Americans can be inoculated and that eradication of COVID-19 is far from assured.There was no immediate reaction from President-elect Joe Biden, who earlier this week promised that 100 million vaccine doses would be administered in the first 100 days of his administration. Biden will be sworn in Jan. 20.The top Democrat in Congress, House Speaker Nancy Pelosi, said “Americans should have full confidence in this vaccine knowing that it has been reviewed and recommended by the independent experts of the FDA’s advisory panel.”In a statement, Pelosi urged federal action to accelerate vaccine manufacturing, adding, “We must ensure that the vaccine will be free and distributed in a fair and equitable manner to as many Americans as possible as soon as possible.”Health and Human Services Secretary Alex Azar, meanwhile, said millions of vaccine doses are being shipped but that, despite the good news, Americans must “double down” on public health measures.“As Americans get vaccinated, we need to continue taking steps like washing our hands, social distancing, and wearing face coverings to protect ourselves, our loved ones, and our communities,” Azar said in a statement.The chairman of the Senate Health Committee, Tennessee Republican Lamar Alexander, tweeted that the American public should be “grateful to the scientists in pharmaceutical companies and the federal government who produced this result, both the Trump Administration for leading it and Congress for funding it.”

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Brazil Nears 180,000 Deaths in Second Coronavirus Wave

Brazil, which is second to the U.S. in deaths from COVID-19 and third in the world in positive cases, is approaching 180,000 deaths as it suffers through its second wave of the disease caused by the coronavirus.In the past day, more than 53,000 cases and 770 deaths have been reported, according to the Johns Hopkins Coronavirus Resource Center. Since the start of the pandemic, Brazil has recorded more than 6.7 million cases.Brazil, with a population of 212 million, is entering its summer, when beaches fill with weekend crowds.”The situation is likely to worsen with the summer, because people will move around more, without any control, most of the restriction measures having already been lifted,” Christovam Barcellos, a researcher at the Fiocruz institute, told AFP.The coronavirus crisis in the U.S. continued to intensify Friday, as more than 2,700 people died of COVID-19, according to Johns Hopkins data, down from the record toll of 3,124 set Wednesday. The country’s deaths now stand at more than 292,000, the most in the world.The U.S. Food and Drug Administration authorized Friday the emergency use of a vaccine produced by U.S. drugmaker Pfizer and Germany’s BioNTech.An FDA advisory panel voted to recommend approval of the vaccine late Thursday.And the U.S. purchased 100 million more doses of another vaccine, one by Moderna. Friday’s agreement brings the number of Moderna doses to 200 million, enough shots for 100 million people. Both the Pfizer and Moderna vaccines require two shots.”Securing another 100 million doses from Moderna by June 2021 further expands our supply of doses across the Operation Warp Speed portfolio of vaccines,” said Health and Human Services Secretary Alex Azar.With the U.S. on the verge of its inoculation program, human rights group Amnesty International’s director of economic and social justice issued a warning. Steve Cockburn told The New York Times, “Rich countries have clear human rights obligations not only to refrain from actions that could harm access to vaccines elsewhere, but also to cooperate and provide assistance to countries that need it.”The Johns Hopkins University Coronavirus Resource Center said Friday night there are 70 million coronavirus infections worldwide, with nearly 1.6 million deaths.The U.S. continues to lead the world in the number of cases with more than 15.8 million infections, followed by India with almost 9.8 million and Brazil with nearly 6.8 million.

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EU Vaccine Agency Victim of Cyberattack

The head of the European Union’s medical agency confirmed Friday it had been the subject of a cyberattack for the past two weeks but said it will not impact its ongoing evaluation of COVID-19 vaccines.The cyberattack was originally announced Wednesday, with the agency providing few details. During an online meeting with the European Parliament, European Medicines Agency (EMA) executive director, Emer Cooke, said the agency had “launched a full investigation in close cooperation with the law enforcement officials and other relevant entities.”In a brief statement on its website, Pfizer partner BioNTech said it had been informed that some of the documents related to regulatory submission for its COVID-19 vaccine candidate, which has been stored on an EMA server, had been “unlawfully accessed.” The company said it did not believe any personal data of trial participants had been compromised.Cooke said Friday, “We can assure you that the timelines for the evaluation of the COVID-19 vaccines and treatments are not impacted. And the agency as you see today continues to be fully functional.”The Amsterdam–based agency is evaluating the Pfizer-BioNTech’s COVID-19 vaccine already approved by Britain and Canada, as well as the vaccine candidate from Moderna. The agency said it will make a decision on conditional approval at a meeting to be held by December 29, while a decision on Moderna’s version should follow by January 12.Cooke said based on the data for the two vaccines so far, “the safety and efficacy look very promising, and we have not seen the adverse events coming up that would be a concern.”Earlier this week, Cooke said the vaccine developed by Oxford University and AstraZeneca is also being considered but complete data for that vaccine has not yet been submitted. 

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US Allows Emergency COVID-19 Vaccine in Bid to End Pandemic 

The U.S. gave the final go-ahead Friday to the nation’s first COVID-19 vaccine, marking what could be the beginning of the end of an outbreak that has killed nearly 300,000 Americans, according to a person familiar with the decision but not authorized to discuss it publicly.Shots for health workers and nursing home residents are expected to begin in the coming days after the Food and Drug Administration authorized an emergency rollout of what promises to be a strongly protective vaccine from Pfizer Inc. and its German partner BioNTech.Initial doses are scarce and will be rationed as the U.S. joins Britain and several other countries in scrambling to vaccinate as many people as possible ahead of winter. It will take months of work to tamp down the coronavirus that has surged to catastrophic levels in recent weeks and already claimed 1.5 million lives globally.While the FDA decision came only after public review of data from a huge, ongoing study, it has also been dogged by intense political pressure from the Trump administration, which has accused the agency of being too slow and even threatened to remove FDA chief Stephen Hahn if a ruling did not come Friday.The move sets off what will be the largest vaccination campaign in U.S. history — but it also has global ramifications because it’s a role model to many other countries facing the same decision.The world desperately needs multiple vaccines for enough to go around, and the Pfizer-BioNTech shot is the first based on rigorous scientific testing to emerge from that worldwide race — a record-setting scientific achievement that shaved years off the usual process.”I don’t think you would have found a scientist on this planet that would have predicted this 11 months ago,” said Dr. Paul Offit, a vaccine expert at Children’s Hospital of Philadelphia who advises the FDA.Second vaccineThe U.S. is considering a second vaccine, made by Moderna Inc., that could roll out in another week. In early January, Johnson & Johnson expects to learn if its vaccine is working in final testing.Europe is set to make its own decision on the Pfizer-BioNTech and Moderna shots later this month, an important step as some other candidates that multiple countries were anxiously awaiting have hit roadblocks. Friday, Sanofi and GSK announced a monthslong delay after early tests showed their vaccine didn’t work well enough in older adults.FILE – A medic at a regional hospital receives Russia’s “Sputnik-V” vaccine shot against the COVID-19 disease in Tver, Russia, Oct. 12, 2020.And China and Russia didn’t wait for final-stage tests before beginning vaccinations with some homegrown shots.About 3 million doses of the Pfizer-BioNTech vaccine are expected in the first shipments around the country, according to officials with Operation Warp Speed, the Trump administration’s vaccine development program. A similar amount is to be held in reserve for those recipients’ second dose.A Centers for Disease Control and Prevention advisory committee is poised to recommend who’s first in line. Expected to follow health workers and those in nursing homes are other essential workers, older adults and people at high risk because of other health problems. U.S. authorities don’t expect enough for the general population before spring, and that’s assuming there are no manufacturing glitches.In a still unfinished study of nearly 44,000 people, the FDA found the vaccine was safe and more than 90% effective across recipients of different ages, including older adults, races and those with health problems that put them at high risk from the coronavirus.FILE – A health care worker at LAC USC Medical Center swabs a person at a drive-through testing center during the coronavirus outbreak, in Los Angeles, Dec. 10, 2020.Emergency use means the vaccine still is experimental. Most important for would-be recipients to know: — Some protection begins after the first dose, but it takes a second dose three weeks later for full protection. It’s unclear how long protection lasts.— The vaccine protects against COVID-19 illness, but no one yet knows if it can stop the silent, symptomless spread that accounts for roughly half of all cases. The ongoing study will attempt to answer that, but for now, the vaccinated still will need to wear masks and keep their distance.— Expect a sore arm and some flu-like symptoms such as fever, fatigue, headache and chills after the second dose. While uncomfortable, those reactions last only about a day. “That’s just your immune system working. It’s a good thing,” Offit said.— Authorities are investigating several allergic reactions reported in Britain by people with a history of severe allergies. Offit said it is routine in the U.S. for the vaccinated to stick around for a half-hour so they could get prompt treatment if such reactions appear.If emergency use of Moderna’s vaccine also is authorized, the U.S. expects to vaccinate 20 million people by the end of December. They hope to have enough for another 30 million people in January and 50 million in February.ReluctanceGetting shots into arms is the big challenge, especially as a new poll from The Associated Press-NORC Center for Public Affairs Research found only half of Americans want the vaccine when it’s their turn. About a quarter say they won’t get it and the rest aren’t sure.Political interference has complicated health authorities’ message that the testing was rigorous and cut no corners.President Donald Trump bashed the FDA, again, Friday for taking too long, complaining that the agency “is still a big, old, slow turtle.” One of his deputies even pressed Hahn to clear the shots by the end of the day or face possible firing, two administration officials said.The FDA is unique in analyzing drugmakers’ raw data, a process that takes longer than many other countries’ regulatory reviews. In addition, the FDA insisted that large COVID-19 vaccine studies track at least half the participants for two months to look for side effects, a time period when historically any vaccine problems appear.

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Can China Become Self-reliant in Semiconductors?

The U.S. added China’s biggest computer chipmaker SMIC to a blacklist of alleged Chinese military companies last week, a move that will further widen the gap between China’s chip technology and the rest of the world.Despite its status as the world’s factory, China has never figured out how to make advanced chips. In recent years, Beijing has been planning a series of sweeping government policies and pouring billions of dollars into the industry to fulfill its chip self-sufficiency goal.So far, under ever-tightening international export controls, however, the country has only found itself mired in some of the most embarrassing industrial failures in its recent history. Most notably, one of the nation’s most high-profile chipmakers was taken over by municipal authorities in its home city of Wuhan, and a Beijing-based chipmaker, the Tsinghua Unigroup, defaulted on a corporate bond.FILE – A Chinese microchip is seen through a microscope set up at the booth for the state-controlled Tsinghua Unigroup project which is driving China’s semiconductor ambitions during the 21st China Beijing International High-tech Expo in Beijing.In this highly internationally integrated industry, experts say, no country can manufacture chips on its own, and China’s efforts to develop its semiconductor sector remains out of reach.Highly globalized chainSemiconductor production is considered one of the most sophisticated manufacturing processes in the world, involving more than 50 disciplines. Billions of transistor structures must be built within a few millimeters.The core equipment used to manufacture computer chips includes lithography machines. A Dutch company called ASML is the only company in the world currently capable of producing high-end extreme ultraviolet lithography machines. Of its 17 core suppliers, though, more than half are from the United States, and the rest are companies located throughout Europe.The company is jointly owned by shareholders from dozens of countries. According to its official website, among the top three major shareholders, two are from the United States and one is from the United Kingdom. Capital Research and Management Co. is the largest shareholder, and the second largest is the BlackRock Group; both are in the U.S. Additionally, Taiwan’s TSMC and South Korea’s Samsung also hold shares in ASML, allowing these two manufacturers to enjoy the priority right to purchase the machine.   In Bid to Rely Less on US, China Firms Stockpile Taiwan Tech HardwareChina wants to become technologically self-reliant in 10 years but needs help for nowWhile ASML may dominate the chipmaking machine market, it is only one part of the long chain in the industry. The lens of its lithography machine is manufactured by Zeiss of Germany, the laser technology is owned by Cymer of the United States, and a French company provides key valves.Jan-Peter Kleinhans, a senior researcher at the Berlin think tank New Responsibility Foundation and director of the Technology and Geopolitics Project, said no country can make chips without foreign companies’ technology. He told VOA in a telephone interview that it took ASML more than two decades to develop their machines, and “they rely themselves on a network of around 5,000 suppliers to build this machine.”Kleinhans said that without the participation of any one of these companies, the entire global semiconductor chain would break.Kobe Goldberg, a researcher at the New American Security Research Center, told VOA that what China is trying to do is to build a totally nationalized supply chain in a highly internationalized industry. “That is much more difficult in an industry like semiconductors since it is so internationally integrated.”John Lee, a senior researcher at the Mercator Institute for China Studies, a think tank in Germany, said several Chinese firms already have the capacity to manufacture or fabricate some semiconductors. But they can easily face a crackdown by the U.S. government since American companies have a very strong dominance in the upstream segment of the supply chain, such as chip design.
 Huawei’s Survival at Stake as US Sanctions LoomStarting Sept. 15, China’s telecom giant Huawei will be cut off from essential supplies of semiconductors and without those chips, Huawei cannot make smartphones or 5G equipment on which its business depends, business analysts say”The dominance of U.S.-origin technology in upstream sectors of the global semiconductor supply chain means that Chinese ICT [information and communications technology] firms across the board are exposed to U.S. export controls, regardless of what happens to SMIC or Huawei as individual companies,” Lee added.Multilateral export controlThe multilateral export control implemented by democratic countries can be traced back to the informal multilateral regime called the Coordinating Committee for Multilateral Export Controls (CoCom).  Established in 1949, the 17-member organization, including the United States, the United Kingdom, Japan, France and Australia, attempted to coordinate controls over the export of strategic materials and technology to communist countries. In 1952, a separate group was established to scrutinize exports to China.US Imposes Curbs on Exports by China’s Top Chipmaker SMICNew Commerce Department requirements mean American suppliers of certain technology products to SMIC must apply for individual licenses before they can exportAlthough CoCom ceased to function on March 31, 1994, the list of prohibited items it formulated was later inherited by another multilateral export agreement, the Wassenaar Arrangement, which was signed in 1996. As many as 42 European, American and Asian countries joined the program, which allows member states to exercise control over their own technology exports, and China is again included in the list of targeted countries.Last December, the group reached an agreement to add chip manufacturing technology to the list of items subject to export controls.  While this revision does not explicitly target China, it points out that export restrictions are targeted at nonmember states, while China, along with Iran and North Korea, are not member states. Some Chinese observers called the jointly implemented move a “collective action” against China by countries that dominate the chip manufacturing supply chain.The Bureau of Industrial Security of the U.S. Commerce Department also announced in October of this year that six emerging technologies would be included in a new export control under the Wassenaar Agreement. All these technologies are directly related to chip manufacturing, including extreme ultraviolet lithography necessary for advanced chip manufacturing.Martijn Rasser, a senior researcher at the Center for New American Security’s Technology and National Security Project, told VOA the world’s liberal democracies have a huge advantage in their network of alliances and partnerships, adding: “It’s something that China just completely lacks, and that’s a big, a big headwind for them.”

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White House Threatens FDA Chief’s Job Over Vaccine Approval

White House chief of staff Mark Meadows on Friday pressed Food and Drug Administration chief Stephen Hahn to grant an emergency use authorization for Pfizer’s coronavirus vaccine by the end of the day or face possible firing, two administration officials said.The vaccine produced by Pfizer Inc. and its German partner BioNTech won a critical endorsement Thursday from an FDA panel of outside advisers, and signoff from the agency — which is expected within days — is the next step needed to get the shots to the public.US On Verge of Launching COVID VaccinationsFood and Drug Administration has approved vaccine by Pfizer and Germany’s BioNTech The FDA is not required to follow the guidance of its advisory committees, but often does.Meadows spoke to Hahn by telephone on Friday, according to a senior administration official who was familiar with the conversation but was not authorized to discuss private conversations.Hahn disputed characterizations of his conversation with Meadows.The chief of staff also told Hahn his job was in jeopardy if the emergency use authorization was not issued before Saturday, said a second administration official familiar with the conversation.

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Pollstar: Pandemic Cost Live Events Industry $30B

Concert trade publication Pollstar says the live events industry’s revenue is off more than $30 billion in 2020 because of the coronavirus pandemic.Pollstar released its year-end report Friday, explaining that the live events industry should have hit a record-setting $12.2 billion this year but instead incurred $9.7 billion in losses. The company added that the projected $30 billion figure in losses includes “unreported events, ancillary revenues, including sponsorships, ticketing, concessions, merch, transportation, restaurants, hotels and other economic activity tied to the live events.” Those losses accounted for more than $8 billion.In March, hundreds of artists announced their current or upcoming tours would need to be postponed or canceled because of the pandemic. While a small number of performers have played drive-in concerts and others have held digital concerts, the majority of artists have not played live in 2020.With just a few months on the road, Elton John’s “Farewell Yellow Brick Road Tour” tops the year’s Top 100 Worldwide Tours list with $87.1 million grossed from November 30 through March 7. John’s tour ranked No. 2 last year with $212 million grossed.Celine Dion came in second this year with $71.2 million, followed by Trans-Siberian Orchestra ($58.2 million), U2 ($52.1 million) and Queen + Adam Lambert ($44.6 million). Post Malone, Eagles, Jonas Brothers, Dead & Company and Andrea Bocelli rounded out the Top 10.”It’s been an extraordinarily difficult year for the events industry, which has been disproportionately impacted by the coronavirus. As painful as it is to chronicle the adversity and loss our industry and many of our colleagues faced, we understand it is a critical undertaking toward facilitating our recovery, which is thankfully on the horizon,” Ray Waddell, president of Oak View Group’s Media & Conferences Division, which oversees Pollstar and VenuesNow, said in a statement Friday.”With vaccines, better testing, new safety and sanitization protocols, smart ticketing and other innovations, the live industry will be ramping up in the coming months, and we’re sure that at this time next year we’ll have a very different story to tell.”

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EU Vaccine Agency Victim of Cyber-attack

The head of the European Union’s medical agency confirmed Friday it had been the subject of a cyberattack for the past two weeks but said it will not impact its ongoing evaluation of COVID-19 vaccines.The cyberattack was originally announced Wednesday, with the agency providing few details. During an online meeting with the European Parliament, European Medicines Agency (EMA) executive director, Emer Cooke, said the agency had “launched a full investigation in close cooperation with the law enforcement officials and other relevant entities.”In a brief statement on its website, Pfizer partner BioNTech said it had been informed that some of the documents related to regulatory submission for its COVID-19 vaccine candidate, which has been stored on an EMA server, had been “unlawfully accessed.” The company said it did not believe any personal data of trial participants had been compromised.Cooke said Friday, “We can assure you that the timelines for the evaluation of the COVID-19 vaccines and treatments are not impacted. And the agency as you see today continues to be fully functional.”The Amsterdam–based agency is evaluating the Pfizer-BioNTech’s COVID-19 vaccine already approved by Britain and Canada, as well as the vaccine candidate from Moderna. The agency said it will make a decision on conditional approval at a meeting to be held by December 29, while a decision on Moderna’s version should follow by January 12.Cooke said based on the data for the two vaccines so far, “the safety and efficacy look very promising, and we have not seen the adverse events coming up that would be a concern.”Earlier this week, Cooke said the vaccine developed by Oxford University and AstraZeneca is also being considered but complete data for that vaccine has not yet been submitted. 

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WHO Seeks Global Access to Approved Coronavirus Vaccines

The World Health Organization (WHO) says action and money are needed to ensure coronavirus vaccines are available around the world as Western nations approve them.
During Friday’s COVID-19 briefing at WHO headquarters in Geneva, Director-General Tedros Adhanom Ghebreyesus applauded the fact Britain was already vaccinating its citizens and that Canada, the United states and others would not be far behind. He said to have safe and effective vaccines for a virus that was completely unknown a year ago is an “astounding scientific achievement.”
The WHO chief noted it would be an even greater achievement to ensure all countries have equal access to those vaccines. Tedros said the U.N. agency has worked hard over the past year to secure political commitments from world leaders for equal access to vaccines and he said he wants to see those commitments translated into action.  
He said the WHO needs $4.3 billion to procure vaccines for the world’s neediest countries and urged donors to help fill a funding gap.  
The director-general said the organization is working with its partners to ensure developing countries have infrastructure in place to deliver vaccines to their populations. Through its COVAX vaccine cooperative and the 189 countries participating, Tedros said the WHO has secured nearly a billion doses of three potential vaccines.  Americans Await Final Approval of First COVID-19 Vaccine as Deaths Reach Record HighUS Food and Drug Administration widely expected to authorize emergency use after special panel votes to recommend approval   But Tedros said closing the funding gap is crucial to ensuring the entire world is protected.
“We have all seen images of people being vaccinated against COVID-19. We want to see these same images all over the world, and that will be a true sign of solidarity,” he said Friday.

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At-Home Kits Aim to Close COVID-19 Testing Gap

Getting a COVID test can mean long lines and delayed results. Matt Dibble looks into recent breakthroughs that may have more of us performing a test at home.
Camera: Matt Dibble       Producer: Matt Dibble

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