A vast shadow will sweep over Saturn's cloud tops early on July 18: Here's how to see it
Early risers will get a rare opportunity to see something extraordinary in the early hours of July 18 — the dark shadow of Saturn's largest moon, Titan, sweeping across the planet's cloud tops.
Once every 15 years, Saturn's tilted orbit brings its iconic rings — and Titan's orbital path — into an edge-on alignment with Earth. This event, known as a ring-plane crossing, heralds the onset of a season of dramatic 'shadow transits', as Titan's vast umbral silhouette periodically sweeps across the gas giant's surface.
"Sighting a shadow transit of Titan for an amateur astronomer is somewhat the equivalent of a fisherman hooking and reeling in a particularly large or elusive fish," Hayden Planetarium instructor and lecturer Joe Rao told Space.com in an email. "It is so unusual a sight that doesn't happen very often, which is why even veteran skywatchers are excited at the possibility of making such a sighting."
When is Titan's shadow transit?
Titan's next shadow transit will get underway at 3 a.m. EDT (0700 GMT) on July 18, at which time the moon's dark outline will be visible slowly progressing across Saturn's cloudy disk, according to Sky and Telescope.
Look for Saturn in the southeastern sky, just below the stars of the constellation Pisces shining like a bright star to the naked eye, with the moon in the east.
Observers in the U.S. will have a good view of the first two hours of the shadow transit, but by the time Titan's shadow leaves Saturn's disk at 8:05 a.m. EDT (12:05 GMT), the brightening dawn will overpower the view.
How powerful does a telescope need to be to spot Titan's shadow?
At the time of the shadow transit, Titan and Saturn will be separated by approximately 846 million miles (1.36 billion kilometers) from Earth — far beyond the capabilities of the naked eye or binoculars, but well within reach of many amateur telescopes.
We asked Rao for guidance on the kind of scope needed to view Titan's shadow transit. "An 8-inch telescope at 200-power or a 10-inch telescope at 250-power should provide a good view of Titan's shadow, especially on a night of good seeing," Rao explained.
To calculate the magnifcation of your telescope, you need only divide its focal length by the focal length of your chosen eyepiece. For example, a 1000 mm telescope with a 10 mm eyepiece yields 100-power magnification.
Rao also emphasised that stable atmospheric conditions are crucial to obtaining a clear view. This becomes more important when using higher power with a smaller aperture scope. It's best to use one-half magnification/power when viewing distant objects to avoid them appearing to "boil", or "scintilate" when viewed through the eyepiece.
"At least 200-power is necessary for getting a reasonably good view of the dark 'shadow dot' projected on Saturn's disk," continued Rao. "The general rule of thumb is to utilize 50-power for every inch of aperture of the telescope objective, or mirror. So, for a 4-inch telescope, the maximum magnification to be used is 200-power, which is considered the limit for a telescope of that size."
When are the next Titan shadow transits?
After the July 18 event, five more Titan shadow transits will be visible from Earth. Each occurs roughly16 days after the last — a result of Titan's 16-day orbital period — and starting progressively earlier in the night for viewers in the U.S.
Date
Start
End
Aug 3
2:25 a.m.
7:04 a.m.
Aug 19
1:52 a.m.
6:00 a.m.
Sept 4
1:25 a.m.
4:50 a.m.
Sept 20
1:09 a.m.
3:34 a.m.
Oct 6
1:32 a.m.
The next transit after this week will begin at 2:25 a.m. (0625 GMT) on August 3, while the last chance to catch the moon's shadow fall on Saturn will take place on October 6.
After the October event, stargazers will have to wait another 15 years before the next ring crossing brings Titan — and its shadow — into alignment once more!
Titan's shadow through the eyes of the Cassini spacecraft
Without question, the most spectacular views of a Titan shadow transit came courtesy of NASA's Cassini spacecraft, which witnessed the moon's dark outline fall over Saturn's cloud surface in November 2009, while it travelled a mere 1.3 million miles (2.1 million km) from the colossal gas giant. Cassini has long since found its resting place beneath the cloud surface of Saturn, but amateur astronomers will have an opportunity to follow in Cassini's steps later this week and witness the next Titan shadow transit for themselves when it takes place on July 18.
"Though we, living in the 21st century, have grown accustomed to seeing the Saturnian system through the eyes of Cassini, there still remains the thrill of witnessing, with one's own eyes, a major celestial event in the life of another planet a billion miles away," Carolyn Porco, planetary scientists and imaging team leader for NASA's Cassini mission told Space.com in an email.
Editor's Note: If you would like to share your images of the Titan shadow transit with Space.com's readers, then please send your photo(s), comments, and your name and location to spacephotos@space.com.
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The Company's novel nanoviricide™ class of drug candidates and the nanoviricide™ technology are based on intellectual property, technology and proprietary know-how of TheraCour Pharma, Inc. The Company has a Memorandum of Understanding with TheraCour for the development of drugs based on these technologies for all antiviral infections. The MoU does not include cancer and similar diseases that may have viral origin but require different kinds of treatments. The Company has obtained broad, exclusive, sub-licensable, field licenses to drugs developed in several licensed fields from TheraCour Pharma, Inc. The Company's business model is based on licensing technology from TheraCour Pharma Inc. for specific application verticals of specific viruses, as established at its foundation in 2005. Our lead drug candidate is NV-387, a broad-spectrum antiviral drug that we plan to develop as a treatment of RSV, COVID, Long COVID, Influenza, and other respiratory viral infections, as well as MPOX/Smallpox infections. Our other advanced drug candidate is NV-HHV-1 for the treatment of Shingles. The Company cannot project an exact date for filing an IND for any of its drugs because of dependence on a number of external collaborators and consultants. The Company is currently focused on advancing NV-387 into Phase II human clinical trials. The Company is also developing drugs against a number of viral diseases including oral and genital Herpes, viral diseases of the eye including EKC and herpes keratitis, H1N1 swine flu, H5N1 bird flu, seasonal Influenza, HIV, Hepatitis C, Rabies, Dengue fever, and Ebola virus, among others. NanoViricides' platform technology and programs are based on the TheraCour® nanomedicine technology of TheraCour, which TheraCour licenses from AllExcel. NanoViricides holds a worldwide exclusive perpetual license to this technology for several drugs with specific targeting mechanisms in perpetuity for the treatment of the following human viral diseases: Human Immunodeficiency Virus (HIV/AIDS), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Rabies, Herpes Simplex Virus (HSV-1 and HSV-2), Varicella-Zoster Virus (VZV), Influenza and Asian Bird Flu Virus, Dengue viruses, Japanese Encephalitis virus, West Nile Virus, Ebola/Marburg viruses, and certain Coronaviruses. The Company intends to obtain a license for RSV, Poxviruses, and/or Enteroviruses if the initial research is successful. As is customary, the Company must state the risk factor that the path to typical drug development of any pharmaceutical product is extremely lengthy and requires substantial capital. As with any drug development efforts by any company, there can be no assurance at this time that any of the Company's pharmaceutical candidates would show sufficient effectiveness and safety for human clinical development. Further, there can be no assurance at this time that successful results against coronavirus in our lab will lead to successful clinical trials or a successful pharmaceutical product. This press release contains forward-looking statements that reflect the Company's current expectation regarding future events. Actual events could differ materially and substantially from those projected herein and depend on a number of factors. Certain statements in this release, and other written or oral statements made by NanoViricides, Inc. are 'forward-looking statements' within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company's control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. The Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company's expectations include, but are not limited to, those factors that are disclosed under the heading 'Risk Factors' and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Although it is not possible to predict or identify all such factors, they may include the following: demonstration and proof of principle in preclinical trials that a nanoviricide is safe and effective; successful development of our product candidates; our ability to seek and obtain regulatory approvals, including with respect to the indications we are seeking; the successful commercialization of our product candidates; and market acceptance of our products. The phrases 'safety', 'effectiveness' and equivalent phrases as used in this press release refer to research findings including clinical trials as the customary research usage and do not indicate evaluation of safety or effectiveness by the US FDA. FDA refers to US Food and Drug Administration. IND application refers to 'Investigational New Drug' application. cGMP refers to current Good Manufacturing Practices. CMC refers to 'Chemistry, Manufacture, and Controls'. CHMP refers to the Committee for Medicinal Products for Human Use, which is the European Medicines Agency's (EMA) committee responsible for human medicines. API stands for 'Active Pharmaceutical Ingredient'. WHO is the World Health Organization. R&D refers to Research and Development. Contact: NanoViricides, Inc. [email protected] Public Relations Contact: [email protected] press release