Abstract We report the Earth's rate of radiogenic heat production and (anti)neutrino luminosity from geologically relevant short‐lived radionuclides (SLR) and long‐lived radionuclides (LLR) using decay constants from the geological community, updated nuclear physics parameters, and calculations of theβspectra. We track the time evolution of the radiogenic power and luminosity of the Earth over the last 4.57 billion years, assuming an absolute abundance for the refractory elements in the silicate Earth and key volatile/refractory element ratios (e.g., Fe/Al, K/U, and Rb/Sr) to set the abundance levels for the moderately volatile elements. The relevant decays for the present‐day heat production in the Earth (19.9 ± 3.0 TW) are from40K,87Rb,147Sm,232Th,235U, and238U. Given element concentrations in kg‐element/kg‐rock and densityρin kg/m3, a simplified equation to calculate the present‐day heat production in a rock isurn:x-wiley:ggge:media:ggge22244:ggge22244-math-0001 The radiogenic heating rate of Earth‐like material at solar system formation was some 103to 104times greater than present‐day values, largely due to decay of26Al in the silicate fraction, which was the dominant radiogenic heat source for the first∼10 Ma. Assuming instantaneous Earth formation, the upper bound on radiogenic energy supplied by the most powerful short‐lived radionuclide26Al (t1/2= 0.7 Ma) is 5.5×1031 J, which is comparable (within a factor of a few) to the planet's gravitational binding energy. 
                        more » 
                        « less   
                    
                            
                            A C α finite difference method for the Caputo time‐fractional diffusion equation
                        
                    
    
            Abstract We begin with a treatment of the Caputo time‐fractional diffusion equation, by using the Laplace transform, to obtain a Volterra integro‐differential equation. We derive and utilize a numerical scheme that is derived in parallel to the L1‐method for the time variable and a standard fourth‐order approximation in the spatial variable. The main method derived in this article has a rate of convergence ofO(kα + h4)foru(x,t) ∈ Cα([0,T];C6(Ω)),0 < α < 1, which improves previous regularity assumptions that requireC2[0,T]regularity in the time variable. We also present a novel alternative method for a first‐order approximation in time, under a regularity assumption ofu(x,t) ∈ C1([0,T];C6(Ω)), while exhibiting order of convergence slightly more thanO(k)in time. This allows for a much wider class of functions to be analyzed which was previously not possible under the L1‐method. We present numerical examples demonstrating these results and discuss future improvements and implications by using these techniques. 
        more » 
        « less   
        
    
                            - Award ID(s):
- 2012235
- PAR ID:
- 10452591
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Numerical Methods for Partial Differential Equations
- Volume:
- 37
- Issue:
- 3
- ISSN:
- 0749-159X
- Format(s):
- Medium: X Size: p. 2261-2277
- Size(s):
- p. 2261-2277
- Sponsoring Org:
- National Science Foundation
More Like this
- 
            
- 
            Abstract Jeffbenite (Mg3Al2Si3O12) is a tetragonal phase found in so far only in superdeep diamonds, and its thermoelastic parameters are a prerequisite for determining entrapment pressures as it is regarded as a potential indicator for superdeep diamonds. In this study, the thermoelastic properties of synthetic Fe3+‐jeffbenite were measured up to 33.7 GPa and 750 K. High‐temperature static compression data were fitted, giving (∂KT0/∂T)P = −0.0107 (4) GPa/K andαT = 3.50 (3) × 10−5 K−1. The thermoelastic properties and phase stability are applied to modeling isomekes, orP‐Tpaths intersecting possible conditions of entrapment in diamond. We calculate that under ideal exhumation, jeffbenite entrapped at mantle transition zone conditions will exhibit a high remnant pressure at 300 K (Pinc) of ∼5.0 GPa. Elastic geobarometry on future finds of jeffbenite inclusions can use the new equation of state to estimate entrapment pressures for this phase with still highly uncertain stability field in the mantle.more » « less
- 
            Abstract Reactions of (O=)PH(OCH2CH3)2and BrMg(CH2)mCH=CH2(4.9–3.2 equiv;m=4 (a), 5 (b), 6 (c)) give the dialkylphosphine oxides (O=)PH[(CH2)mCH=CH2]2(2 a–c; 77–81 % after workup), which are treated with NaH and then α,ω‐dibromides Br(CH2)nBr (0.49–0.32 equiv;n=8 (a′), 10 (b′), 12 (c′), 14 (d′)) to yield the bis(trialkylphosphine oxides) [H2C=CH(CH2)m]2P(=O)(CH2)n(O=)P[(CH2)mCH=CH2]2(3 ab′,3 bc′,3 cd′,3 ca′; 79–84 %). Reactions of3 bc′and3 ca′with Grubbs’ first‐generation catalyst and then H2/PtO2afford the dibridgehead diphosphine dioxides(4 bc′,4 ca′; 14–19 %,n′=2m+2);31P NMR spectra show two stereoisomeric species (ca. 70:30). Crystal structures of two isomers of the latter are obtained,out,out‐4 ca′and a conformer ofin,out‐4 ca′that features crossed chains, such that the (O=)P vectors appearout,out. Whereas4 bc′resists crystallization, a byproduct derived from an alternative metathesis mode, (CH2)12P(=O)(CH2)12(O=)P(CH2)12, as well as3 ab′and3 bc′, are structurally characterized. The efficiencies of other routes to dibridgehead diphosphorus compounds are compared.more » « less
- 
            Motivated by gradient methods in optimization theory, we give methods based onψ‐fractional derivatives of orderαin order to solve unconstrained optimization problems. The convergence of these methods is analyzed in detail. This paper also presents an Adams–Bashforth–Moulton (ABM) method for the estimation of solutions to equations involvingψ‐fractional derivatives. Numerical examples using the ABM method show that the fractional orderαand weightψare tunable parameters, which can be helpful for improving the performance of gradient descent methods.more » « less
- 
            Abstract Potassium (K) informs on the radiogenic heat production, atmospheric composition, and volatile element depletion of the Earth and other planetary systems. Constraints on the abundance of K in the Earth, Moon, and other rocky bodies have historically hinged on K/U values measured in planetary materials, particularly comparisons of the continental crust and mid‐ocean ridge basalts (MORBs), for developing compositional models of the bulk silicate Earth (BSE). However, a consensus on the most representative K/U value for global MORB remains elusive despite numerous studies. Here, we statistically analyze a critical compilation of MORB data to determine the K/U value of the MORB source. Covariations in the log‐normal abundances of K and U establish that K is 3–7 times less incompatible than U during melting and/or crystallization processes, enabling inverse modeling to infer the K/U of the MORB source region. These comprehensive data have a mean K/U for global MORB = 13,900 ± 200 (2σm;n = 4,646), and define a MORB source region with a K/U between 14,000 and 15,500, depending on the modeled melting regime. However, this range represents strictly a lower limit due to the undefined role of fractional crystallization in these samples and challenges preserving the signatures of depleted components in the MORB mantle source. This MORB source model, when combined with recent metadata analyses of ocean island basalt (OIB) and continental crust, suggests that the BSE has a K/U value >12,100 and contains >260 × 10−6 kg/kg K, resulting in a global production of∼3.5 TW of radiogenic heat today and 1.5 × 1017 kg of40Ar over the lifetime of the planet.more » « less
 An official website of the United States government
An official website of the United States government 
				
			 
					 
					
