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To clarify geomagnetic field behavior in the Late Cretaceous, paleointensity and rock-magnetic studies were carried out on basalts with K-Ar ages of 78.6 ± 2.5 and 73.1 ± 1.6 Ma in northwest South Korea. A total of 314 samples (262 from six lava flows and 52 from massive basalts) were subjected to Thellier-type IZZI paleointensity experiments. Through the application of seven paleointensity selection criteria that mainly verify the thermal alteration of magnetic minerals and the stability of remanence direction, fifteen paleointensity data were obtained from five of the lava flows. Based on rock-magnetic experiments and microscopic observations, it is revealed that the measured paleointensity is carried by single-domain (titano)magnetite. The site-mean paleointensities ranged 13.1-21.3 μT, which corresponds to a virtual axial dipole moment of 2.3-3.8 × 10 22 Am 2 . The combination of this result with selected data from the IAGA paleointensity database establishes the existence of different dipole moments according to rock type. In particular, the geomagnetic field strength recorded in Late Cretaceous crystalline volcanic rock was relatively low and stable, with a mean dipole moment of 4.0 ± 1.9 × 10 22 Am 2 regardless of geomagnetic field reversals.

The preferential incorporation of carboxylic acids into aragonite and its effects on the crystal growth and physicochemical properties of aragonite were systematically investigated using a seeded co-precipitation system with different carboxylic acids (citric, malic, acetic, glutamic, and phthalic). Aragonite synthesized in the presence of citric and malic acids showed a remarkable decrease in the crystallinity and size of crystallite, and the retardation of crystal growth distinctively changed the crystal morphology. The contents of citric acid and malic acid in the aragonite samples were 0.65 wt % and 0.19 wt %, respectively, revealing that the changes in the physicochemical properties of aragonite were due to the preferential incorporation of such carboxylic acids. Speciation modeling further confirmed that citric acid with three carboxyl groups dominantly existed as a metal–ligand, (Ca–citrate)−, which could have a strong affinity toward the partially positively charged surface of aragonite. This indicates why citric acid was most favorably incorporated among other carboxylic acids. Our results demonstrate that the number of carboxyl functional groups strongly affects the preferential incorporation of carboxylic acids into aragonite; however, it could be suppressed by the presence of other functional groups or the structural complexity of organic molecules.

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