Local ice caps in Finderup Land,North Greenland,survived the Holocene Thermal Maximum     

Nicolaj K. Larsen  Laura B. Levy  Astrid Strunk  Anne Sofie Sndergaard  Jesper Olsen  Torben L. Lauridsen 《Boreas: An International Journal of Quaternary Research》2019,48(3):551-562

Local glaciers and ice caps (GICs) comprise only ~5.4% of the total ice volume, but account for ~14–20% of the current ice loss in Greenland. The glacial history of GICs is not well constrained, however, and little is known about how they reacted to Holocene climate changes. Specifically, in North Greenland, there is limited knowledge about past GIC fluctuations and whether they survived the Holocene Thermal Maximum (HTM, ~8 to 5 ka). In this study, we use proglacial lake records to constrain the ice‐marginal fluctuations of three local ice caps in North Greenland including Flade Isblink, the largest ice cap in Greenland. Additionally, we have radiocarbon dated reworked marine molluscs in Little Ice Age (LIA) moraines adjacent to the Flade Isblink, which reveal when the ice cap was smaller than present. We found that outlet glaciers from Flade Isblink retreated inland of their present extent from ~9.4 to 0.2 cal. ka BP. The proglacial lake records, however, demonstrate that the lakes continued to receive glacial meltwater throughout the entire Holocene. This implies that GICs in Finderup Land survived the HTM. Our results are consistent with other observations from North Greenland but differ from locations in southern Greenland where all records show that the local ice caps at low and intermediate elevations disappeared completely during the HTM. We explain the north–south gradient in glacier response as a result of sensitivity to increased temperature and precipitation. While the increased temperatures during the HTM led to a complete melting of GICs in southern Greenland, GICs remained in North Greenland probably because the melting was counterbalanced by increased precipitation due to a reduction in Arctic sea‐ice extent and/or increased poleward moisture transport.  相似文献   

THE BLOOMINGTON (LL6) CHONDRITE AND ITS SHOCK MELT GLASSES     

Robert T. Dodd  Edward J. Olsen  Roy S. Clarke 《Meteoritics & planetary science》1985,20(3):575-581

The Bloomington meteorite, a 67.8 gram veined, brecciated chondrite, fell during the summer of 1938 in Bloomington, Illinois. Its olivine, orthopyroxene and metal compositions (fo₆₉, en₇₄ and Fe₅₂ Ni₄₈ respectively) and its texture identify it as a brecciated LL6 chondrite of shock facies d. Shock melt glasses occur in Bloomington as sparse melt pockets and veins in clasts and as isolated masses in the black, clast-rich matrix. The vein glasses chemically resemble bulk LL-group chondrites and thus appear to reflect total melting of the host meteorite. The melt pocket and matrix glasses, like those described previously in L-group chondrites, have more varied compositions and are typically enriched in normative plagioclase. All glasses that we analyzed in Bloomington have FeO/MgO and Na/Al ratios similar to those of LL-group chondrites, indicating that melting of this meteorite involved neither a significant change in the oxidation state of iron nor loss of sodium to a vapor phase. Bloomington is a monomict breccia whose components formed in place as a result of a single episode of shock and attendant melting.  相似文献   

Authors' Reply     

Kaare L. Rasmussen  Hans J. F. Olsen  Raymond Gwozdz  Evgeniy M. Kolesnikov 《Meteoritics & planetary science》2001,36(7):1001-1006

Abstract— Jull et al. propose an alternative interpretation of our depth vs. ¹⁴C data measured on a peat core from the central Tunguska impact site (Rasmussen et al., 1999). We find that the proposed alternative is untenable.  相似文献   

Oxalate-promoted forsterite dissolution at low pH     

Amanda Albright Olsen 《Geochimica et cosmochimica acta》2008,72(7):1758-1766

We ran a series of 124 semi-batch reactor experiments to measure the dissolution rate of forsterite in solutions of nitric and oxalic acid solutions over a pH range of 0-7 and total oxalate concentrations between 0 and 0.35 m at 25 °C. We found that the empirical rate law for the dissolution of forsterite in these solutions is