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Grew, ES, Bada JL, Hazen RM.  2011.  Borate Minerals and Origin of the RNA World. Origins of Life and Evolution of Biospheres. 41:307-316.   10.1007/s11084-010-9233-y   AbstractWebsite

The RNA World is generally thought to have been an important link between purely prebiotic (>3.7 Ga) chemistry and modern DNA/protein biochemistry. One concern about the RNA World hypothesis is the geochemical stability of ribose, the sugar moiety of RNA. Prebiotic stabilization of ribose by solutions associated with borate minerals, notably colemanite, ulexite, and kernite, has been proposed as one resolution to this difficulty. However, a critical unresolved issue is whether borate minerals existed in sufficient quantities on the primitive Earth, especially in the period when prebiotic synthesis processes leading to RNA took place. Although the oldest reported colemanite and ulexite are 330 Ma, and the oldest reported kernite, 19 Ma, boron isotope data and geologic context are consistent with an evaporitic borate precursor to 2400-2100 Ma borate deposits in the Liaoning and Jilin Provinces, China, as well as to tourmaline-group minerals at 33003450 Ma in the Barberton belt, South Africa. The oldest boron minerals for which the age of crystallization could be determined are the metamorphic tourmaline species schorl and dravite in the Isua complex (metamorphism between ca. 3650 and ca. 3600 Ma). Whether borates such as colemanite, ulexite and kernite were present in the Hadean (>4000 Ma) at the critical juncture when prebiotic molecules such as ribose required stabilization depends on whether a granitic continental crust had yet differentiated, because in its absence we see no means for boron to be sufficiently concentrated for borates to be precipitated.

Bada, JL, Vrolijk CD, Brown S, Druffel ERM, Hedges REM.  1987.  Bomb Radiocarbon in Metabolically Inert Tissues from Terrestrial and Marine Mammals. Geophysical Research Letters. 14:1065-1067.   10.1029/GL014i010p01065   Website
Fang, LS, Bada JL.  1990.  The Blue-Green Blood-Plasma of Marine Fish. Comparative Biochemistry and Physiology B-Biochemistry & Molecular Biology. 97:37-45.   10.1016/0305-0491(90)90174-r   Website
Bada, JL.  1995.  Biomolecules - Origins of Homochirality. Nature. 374:594-595.   10.1038/374594a0   Website
Bada, JL.  1998.  Biogeochemistry of organic nitrogen compounds. Nitrogen-Containing Macromolecules in the Bio- and Geosphere. 707( Stankiewicz BA, VanBergen PF, Eds.).:64-73., Washington: Amer Chemical Soc Abstract

Nitrogen containing organic compounds represent the second most abundant reservoir of nitrogen on the surface of the Earth. However, the organic compounds that make up this global nitrogen pool are not well characterized. Although amino acids and the nitrogenous bases of nucleic acids make up only a few percent of the total organic nitrogen reservoir, the geochemical reactions of these compounds have been extensively studied. Because hydrolysis reactions are rapid on the geologic time scale, both proteins and nucleic acids (DNA and RNA) are not preserved for more than 10(3) to 10(5) years in most environments. The racemization reaction of amino acids converts the L-amino acids present in the biosphere into a racemic mixture (D/L amino acid ratio = 1.0) in the geosphere in less than 10(6) years. Anhydrous conditions, such as those that may be associated with amber entombed insects, may retard both biopolymer hydrolysis and racemization. Condensation reactions between amino acids and sugars, including sugars at apurinic sites in nucleic acid fragments, likely result in the incorporation of these compounds into geopolymers such as humic acids. Although rearrangement reactions in geopolymers may scramble the original molecular structures, part of the global organic nitrogen inventory was originally derived from amino acids and nucleic acid bases.

Fang, LS, Bada JL.  1982.  Biliverdin Reductase-Activity in Marine Fishes. Marine Biology Letters. 3:121-130.Website
Low, PS, Bada JL.  1974.  Bile-Pigments in Blood Serum of Fish from Family Cottidae. Comparative Biochemistry and Physiology. 47:411-418.   10.1016/0300-9629(74)90003-6   Website