Geology topics

J. Rosenbaum

Publications and source records attributed to J. Rosenbaum.

3 recordsLinked to original sources

USGS2008

A 2650-year-long record of environmental change from northern Yellowstone National Park based on a comparison of multiple proxy data

Geochemical, stable-isotope, pollen, charcoal, and diatom records were analyzed at high-resolution in cores obtained from Crevice Lake, a varved-sediment lake in northern Yellowstone National Park. The objective was to reconstruct the ecohydrologic, vegetation, and fire history of the watershed for the last 2650 years to better understand past climate variations at the forest-steppe transition. The data suggest a period of limited bottom-water anoxia, relatively wet winters, and cool springs and summers from 2650 to 2100 cal yr BP (700-150 BC). Dry warm conditions occurred between 2100 and 850-800 cal yr BP (150 BC and AD 1100-1150), when the lake was anoxic, winter precipitation was low, and summer stratification was protracted. The data are consistent with overall warmer/drier conditions during the Medieval Climate Anomaly, although they suggest a shift towards wetter winters within that period. The period from 850 to 800 cal yr BP (AD 1100-1150) to 250 cal yr BP (AD 1700) was characterized by greater water-column mixing and cooler spring/summer conditions than before. In addition, fire activity shifted towards infrequent large events and pollen production was low. From 250 to 150 cal yr BP (AD 1700-1800), winter precipitation was moderate compared to previous conditions, and the lake was again stratified, suggesting warm summers. Between 150 and 42 cal yr BP (AD 1800-1908), winter precipitation increased and spring and summer conditions became moderate. Metal pollution, probably from regional mining operations, is evident in the 1870s. Large fires occurred between ca. 1800-1880, but in general the forests were more closed than before. The Crevice Lake record suggests that the last 150 years of Yellowstone's environmental history were characterized by intermediate conditions when compared with the previous 2500 years. ?? 2007 Elsevier Ltd and INQUA.

Quaternary International↗

USGS2006

Unusual Holocene and late Pleistocene carbonate sedimentation in Bear Lake, Utah and Idaho, USA

Bear Lake (Utah-Idaho, USA) has been producing large quantities of carbonate minerals of varying mineralogy for the past 17,000 years. The history of sedimentation in Bear Lake is documented through the study of isotopic ratios of oxygen, carbon, and strontium, percent organic carbon, percent CaCO3, X-ray diffraction mineralogy, HCl-leach inorganic geochemistry, and magnetic properties on samples from three piston cores. Historically, the Bear River, the main source of water for Great Salt Lake, did not enter Bear Lake until it was artificially diverted into the lake at the beginning of the 20th century. However, during the last glacial interval, the Bear River did enter Bear Lake depositing red, calcareous, silty clay. About 18,000 years ago, the Bear River became disconnected from Bear Lake. A combination of warmer water, increased evaporation, and increased organic productivity triggered the precipitation of calcium carbonate, first as calcite. As the salinity of the lake increased due to evaporation, aragonite began to precipitate about 11,000 years ago. Aragonite is the dominant mineral that accumulated in bottom sediments of the lake during the Holocene, comprising an average of about 70 wt.% of the sediments. Aragonite formation in a large, cold, oligotrophic, high latitude lake is highly unusual. Lacustrine aragonite usually is found in small, saline lakes in which the salinity varies considerably over time. However, Bear Lake contains endemic ostracodes and fish, which indicate that the chemistry of the lake has remained fairly constant for a long time. Stable isotope data from Holocene aragonite show that the salinity of Bear Lake increased throughout the Holocene, but never reached highly evolved values of ??18O in spite of an evaporation-dominated water balance. Bear Lake hydrology combined with evaporation created an unusual situation that produced large amounts of aragonite, but no evaporite minerals.

Sedimentary Geology↗

USGS1998

Field-dependence of AC susceptibility in titanomagnetites

AC susceptibility measurements as a function of field amplitude Hac and of frequency show a strong field dependence for a set of synthetic titanomagnetites (Fe3-xTixO4) and for certain basalts from the SOH-1 Hawaiian drill hole and from Iceland. In-phase susceptibility is constant below fields of about 10-100 A/m, and then increases by as much as a factor of two as Hsc is increased to 2000 A/m. Both the initial field-independent susceptibilities and field-dependence of susceptibility are systematically related to composition: initial susceptibility is 3 SI for a single-crystal sphere of TMO (x = 0) and decreases with increasing titanium content; field-dependence is nearly zero for TM0 and increases systematically to a maximum near TM60 (x = 0.6). This field dependence can in some cases be mistaken for frequency dependence, and leaf to incorrect interpretations of magnetic grain size and composition when titanomagnetite is present.

Earth and Planetary Science Letters↗