Muto, A. | Engineering Papers

NASA NTRS2019

Possible Role for Tectonics in the Evolving Stability of the Greenland Ice Sheet

The history of the Greenland Ice Sheet has been influenced by the geodynamic response to ice sheet fluctuations, and this interaction may help explain past deglaciations under modest climate forcing. We hypothesize that when the Iceland hot spot passed beneath north‐central Greenland, it thinned the lithosphere and left anomalous heat likely with partially melted rock; however, it did not break through the crust to supply voluminous flood basalts. Subsequent Plio‐Pleistocene glacial‐interglacial cycles caused large and rapidly migrating stresses, driving dike formation and other processes that shifted melted rock toward the surface. The resulting increase in surface geothermal flux favored a thinner, faster‐responding ice sheet that was more prone to deglaciation. If this hypothesis of control through changes in geothermal flux is correct, then the long‐term (10 (sup 5) to 10 (sup 6) years) trend now is toward lower geothermal flux, but with higher‐frequency (less than or equal to 10( sup 4) to 10 (sup 5) years) oscillations linked to glacial‐interglacial cycles. Whether the geothermal flux is increasing or decreasing now is not known but is of societal relevance due to its possible impact on ice flow. We infer that projections of the future of the ice sheet and its effect on sea level must integrate geologic and geophysical data as well as glaciological, atmospheric, oceanic, and paleoclimatic information.

Greenland Ice Sheet↗

NASA NTRS1992

Recent evidence for evolution of the genetic code

The genetic code, formerly thought to be frozen, is now known to be in a state of evolution. This was first shown in 1979 by Barrell et al. (G. Barrell, A. T. Bankier, and J. Drouin, Nature [London] 282:189-194, 1979), who found that the universal codons AUA (isoleucine) and UGA (stop) coded for methionine and tryptophan, respectively, in human mitochondria. Subsequent studies have shown that UGA codes for tryptophan in Mycoplasma spp. and in all nonplant mitochondria that have been examined. Universal stop codons UAA and UAG code for glutamine in ciliated protozoa (except Euplotes octacarinatus) and in a green alga, Acetabularia. E. octacarinatus uses UAA for stop and UGA for cysteine. Candida species, which are yeasts, use CUG (leucine) for serine. Other departures from the universal code, all in nonplant mitochondria, are CUN (leucine) for threonine (in yeasts), AAA (lysine) for asparagine (in platyhelminths and echinoderms), UAA (stop) for tyrosine (in planaria), and AGR (arginine) for serine (in several animal orders) and for stop (in vertebrates). We propose that the changes are typically preceded by loss of a codon from all coding sequences in an organism or organelle, often as a result of directional mutation pressure, accompanied by loss of the tRNA that translates the codon. The codon reappears later by conversion of another codon and emergence of a tRNA that translates the reappeared codon with a different assignment. Changes in release factors also contribute to these revised assignments. We also discuss the use of UGA (stop) as a selenocysteine codon and the early history of the code.

Review↗