European satellites succeed in creating artificial solar eclipse
June 17 (UPI) -- A European space agency created the first "artificial total solar eclipse" using a pair of satellites on Monday.
The space agency Proba-3 showed the first images of the Sun's outer atmosphere -- the solar corona. In its announcement, the agency said that this will help improve the understanding of the sun and its atmosphere.
A pair of spacecrafts was used, the Coronagraph and the Occulter. They flew 492 feet apart for several hours without any control from the ground to create an artificial total solar eclipse's orbit. The two satellites use an optical instrument to take photos of the sun's corona.
The agency's goal for this mission was to observe the sun's corona, which the agency said is important for studying solar wind and understanding coronal mass ejections.
"Many of the technologies which allowed Proba-3 to perform precise formation flying have been developed through ESA's General Support Technology Program, as has the mission itself. It is exciting to see these stunning images validate our technologies in what is now the world's first precision formation flying mission," Dietmar Pilz, ESA director of Technology, Engineering and Quality said.
"I was absolutely thrilled to see the images, especially since we got them on the first try," Andrei Zhukov, principal investigator for ASPIICS at the Royal Observatory of Belgium said.
"Our 'artificial eclipse' images are comparable with those taken during a natural eclipse. The difference is that we can create our eclipse once every 19.6-hour orbit, while total solar eclipses only occur naturally around once, very rarely twice a year. On top of that, natural total eclipses only last a few minutes, while Proba-3 can hold its artificial eclipse for up to 6 hours," said Zhukov.
The Proba-3 mission is led by ESA, managed by Spain's Sener, with more than 29 companies from 14 countries involved.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Medscape
an hour ago
- Medscape
Exceptional Use Recommendation for Nuclear Emergency Drug
The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended an exceptional circumstances marketing authorization for Imreplys. The drug — active ingredient sargramostim and manufactured by Partner Therapeutics Ltd — is intended to treat people with hematopoietic acute radiation syndrome (H-ARS) following acute exposure to myelosuppressive doses of radiation. H-ARS occurs when radiation suppresses bone marrow hematopoiesis, leading to an increased risk for infection and bleeding. It occurs after whole-body radiation doses of about 1-6 Gy, most often associated with acute exposure following radiologic or nuclear emergencies. Sargramostim, a granulocyte-macrophage colony-stimulating factor, counteracts H-ARS by inducing the bone marrow to produce immune-protective leukocytes, including granulocytes, macrophages, and monocytes, as well as red blood cells and platelets. The positive opinion means that Imreplys is now indicated for treatment of patients of all ages with H-ARS following acute exposure to myelosuppressive doses of radiation. It has also been used in the US in patients aged 2 years or older to prevent serious infection in conditions such as leukemia, bone marrow transplant, and prechemotherapy blood cell collection. As well as the infection risk, symptoms of H-ARS may include those of anemia, petechiae, and prolonged bleeding, starting 1-6 hours after exposure and lasting up to 2 days. Exceptional Circumstances Authorization Recommended Medicines can be authorized under exceptional circumstances, subject to certain specific obligations where the applicant was unable to provide comprehensive data on the efficacy and safety of the medicine under normal conditions of use. This may be because the condition that the drug is to be used for is too rare for extensive data gathering; because of limited scientific knowledge in the area concerned; or because collection of full information is not possible or is unethical. Exceptional circumstances authorization must be reviewed annually. The CHMP said that three randomized, blinded, placebo-controlled studies in rhesus monkeys who received H-ARS-inducing total body irradiation showed that Imreplys increased 60-day survival rates compared with placebo. Studies had also shown faster recovery of absolute neutrophil counts and platelets, reduced infection rates, and fewer signs of sepsis. The most common side effects with Imreplys include fever, diarrhea, vomiting, skin reactions, rash, asthenia, metabolic laboratory abnormalities, malaise, high glucose, abdominal pain, weight loss, low albumin, pruritus, gastrointestinal hemorrhage, chills, pharyngitis, bone pain, chest pain, hypomagnesemia, hematemesis, arthralgia, anxiety, and eye hemorrhage. Use Governed by Radiologic/Nuclear Emergency Recommendations The EMA said that Imreplys will be available as a 250 μg powder for solution for injection and should be used in accordance with official radiologic/nuclear emergency recommendations. Detailed recommendations for the use of the product will be described in the summary of product characteristics (SmPC), which will be published on the EMA website in all official European Union languages after the marketing authorization has been granted by the European Commission.
Yahoo
2 hours ago
- Yahoo
Actor Alan Cumming to receive honorary degree from University of St Andrews
ACTOR Alan Cumming is to receive an honorary degree from the University of St Andrews during a week of graduations for students from almost 90 countries. More than 2200 students will gather at the University of St Andrews from June 30 for summer graduation ceremonies. Graduates from 88 different countries, including Canada, Australia and Nepal will receive their awards in the Younger Hall from June 30 to July 4. READ MORE: Scottish Government removes WhatsApp from all official devices The graduation ceremony season will include nine 'distinguished individuals' honoured for their contributions to sport, politics, science, medicine and the arts. Marvel actor and The Traitors US presenter Alan Cumming will receive an honorary degree on Thursday July 3, while BBC security correspondent Frank Gardner will be presented with one on Friday July 4. Sustainability campaigner Sara Parkin and US golfer Judy Rankin will also receive the accolade during the week. Also recognised will be Russian-American scientist Eugene Koonin and political theorist and feminist writer Professor Cynthia Enloe. There is one ceremony on June 30 at 2pm, while the other ceremonies will occur twice in one day.


Medscape
3 hours ago
- Medscape
Preemptive TIPS Promising for Fundal Variceal Bleeding
TOPLINE: In patients with cirrhosis and acute fundal variceal bleeding, the use of preemptive transjugular intrahepatic portosystemic shunt (p-TIPS) with a covered stent within 72 hours of initial bleeding resulted in superior outcomes, with a higher probability of patients being free of death or rebleeding at 1 year than those using standard treatment. METHODOLOGY: Researchers conducted a randomised trial across 17 tertiary centres in France to compare two strategies for preventing rebleeding of non-type 1 gastro-oesophageal varices. They included 101 patients with cirrhosis and acute fundal variceal bleeding (mean age, 58.2 years; 80% men) from January 3, 2019, to February 25, 2023, who achieved initial haemostasis with endoscopic glue injection for at least 12 hours. Patients were randomly assigned to either receive p-TIPS within 72 hours of the initial endoscopic glue injection (n = 47) or continue with on-demand glue obliteration combined with non-selective beta blockers (n = 54). The primary composite endpoint was all-cause mortality or clinically significant rebleeding, defined as recurrent melena or haematemesis requiring hospitalisation or blood transfusion or causing a 3 g/dL drop in haemoglobin, within 1 year from the initial haemostasis. Analyses were conducted in the modified intention-to-treat population. TAKEAWAY: The 1-year probability of being free from death or rebleeding was higher in the p-TIPS group than in the glue obliteration and non-selective beta-blocker group (77% vs 37%; hazard ratio, 0.25; P < .0001). The overall survival did not differ significantly between the two groups; however, 37% of patients in the glue obliteration and non-selective beta-blocker group required TIPS after a median of 25 days. The cumulative incidence of hepatic encephalopathy at 1 year was 35% in the p-TIPS group and 32% in the glue obliteration and non-selective beta-blocker group. Complications related to glue injection occurred in 22 procedures, including 13 bleeding episodes, eight glue migrations (three in the p-TIPS group and five in the glue obliteration group), and one case of cardiac decompensation in the p-TIPS group. The number of patients who experienced any adverse or serious adverse event did not differ significantly between the groups, and no deaths were considered related to the treatment. IN PRACTICE: "The results of the present study strongly support the use of p-TIPS in the management of acute gastric variceal bleeding and add an additional argument in favour of TIPS, which improves prognosis by effectively treating the haemodynamic disorders associated with cirrhosis," the authors of the study wrote. "In patients with cirrhosis and bleeding from fundal varices, p-TIPS with a covered stent is associated with markedly decreased death or rebleeding and should therefore be considered as a first-line therapy," they added. SOURCE: This study was led by Jean-Paul Cervoni, MD, Service d'Hépatologie et de Soins Intensifs, CHU Besançon, Besançon, France. It was published online on June 12, 2025, in The Lancet Gastroenterology & Hepatology. LIMITATIONS: A small sample size precluded definitive subgroup analyses (eg, variceal type). An overrepresentation of alcohol-related cirrhosis may have limited the applicability of the findings to other aetiologies. Eight patients in the p-TIPS group were treated beyond the 72-hour window. DISCLOSURES: This study was funded by the French Ministry of Health. Two authors reported receiving payment for lectures and one author reported receiving consulting fees from Gore. This article was created using several editorial tools, including AI, as part of the process. Human editors reviewed this content before publication.