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The age of Jupiter, the largest planet in our Solar System, is still unknown. Gas-giant planet formation likely involved the growth of large solid cores, followed by the accumulation of gas onto these cores. Thus, the gas-giant cores must have formed before dissipation of the solar nebula, which likely occurred within less than 10 My after Solar System formation. Although such rapid accretion of the gas-giant cores has successfully been modeled, until now it has not been possible to date their formation. Here, using molybdenum and tungsten isotope measurements on iron meteorites, we demonstrate that meteorites derive from two genetically distinct nebular reservoirs that coexisted and remained spatially separated between ∼1 My and ∼3-4 My after Solar System formation. The most plausible mechanism for this efficient separation is the formation of Jupiter, opening a gap in the disk and preventing the exchange of material between the two reservoirs. As such, our results indicate that Jupiter's core grew to ∼20 Earth masses within <1 My, followed by a more protracted growth to ∼50 Earth masses until at least ∼3-4 My after Solar System formation. Thus, Jupiter is the oldest planet of the Solar System, and its solid core formed well before the solar nebula gas dissipated, consistent with the core accretion model for giant planet formation.
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http://dx.doi.org/10.1073/pnas.1704461114 | DOI Listing |
Mon Not R Astron Soc Lett
October 2025
Center for Astrophysics and Space Science (CASS), New York University Abu Dhabi, PO Box 129188, Abu Dhabi, UAE.
The origins of the colours of trans-Neptunian objects (TNOs) represent a crucial unresolved question, central to understanding the history of our Solar system. Recent observational surveys revealed correlations between the eccentricity and inclination of TNOs, and their colours. This rekindled the long-standing debate on whether these colours reflect the conditions of TNO formation or their subsequent evolution.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, PR China; Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt. Electronic address:
Post-synthetic modification (PSM) offers a promising approach for tailoring the compositional, structural, and electronic properties of covalent organic frameworks (COFs), thereby enhancing their exciton dissociation ability and facilitating charge transfer. The effectiveness of these approaches is largely compromised by the harsh conditions, complexity, and alteration of the original structure. Therefore, developing a facile yet effective PSM for modulating COFs' properties without altering the original geometry and/or structure is a challenge.
View Article and Find Full Text PDFSmall
September 2025
School of Nanoscience and Materials Engineering, Henan University, Zhengzhou, 450046, China.
Ru/RuOx/CNTs heterostructured materials are synthesized using an in situ method. The Ru─RuOx heterostructure facilitates active hydrogen dissociation, leading to excellent catalytic performance in nitrate reduction, with ammonia as the primary product at low overpotentials. The process achieves Faradaic efficiencies of ammonia exceeding 90% and a production rate of 1.
View Article and Find Full Text PDFPLoS One
September 2025
Electrical Engineering Determent, Faculty of Engineering, Minia University, Minia, Egypt.
Renewable energy systems are at the core of global efforts to reduce greenhouse gas (GHG) emissions and to combat climate change. Focusing on the role of energy storage in enhancing dependability and efficiency, this paper investigates the design and optimization of a completely sustainable hybrid energy system. Furthermore, hybrid storage systems have been used to evaluate their viability and cost-benefits.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
College of Environmental Sciences and Engineering, Peking University, Beijing 100871, P. R. China.
Current antibiotic-resistant bacteria (ARB) disinfection techniques commonly rely on large dosages of oxidants, resulting in the presence of considerable amounts of residuals and toxic disinfection byproducts (DBPs) in water. Herein, we propose a highly effective ARB disinfection approach via activating an ultralow concentration (10 μM) of chlorite (ClO) by naturally abundant sunlight to generate various reactive species (i.e.
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