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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Africa
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East African Lakes
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Lake Tanganyika (1)
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Arctic region
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Brazil
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Utah
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elements, isotopes
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carbon
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hydrogen
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stable isotopes
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metals
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beryllium
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magnesium (1)
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radium
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strontium
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lead
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oxygen
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fossils
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minerals
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Primary terms
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absolute age (16)
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Africa
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Arctic region
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Greenland
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Asia
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Middle East
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Israel (2)
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Atlantic Ocean
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Australasia
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Australia
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biogeography (1)
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Canada
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carbon
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C-14 (15)
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organic carbon (2)
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Cenozoic
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upper Pleistocene
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upper Quaternary (7)
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Tertiary
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Neogene
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Central America
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Vertebrata
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Invertebrata
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lead
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North America
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Basin and Range Province
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oxygen
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Bioturbation increases time averaging despite promoting shell disintegration: a test using anthropogenic gradients in sediment accumulation and burrowing on the southern California shelf
Young death assemblages with limited time-averaging in rocky and Posidonia oceanica habitats in the Mediterranean Sea
Abstract Death assemblages (DAs) are increasingly recognized as a valuable source to reconstruct past ecological baselines, due to the accumulation of skeletal material of non-contemporaneous cohorts. We here quantify the age and time-averaging of DAs on shallow subtidal (5–25 m) rocky substrates and in meadows of Posidonia oceanica in the eastern Mediterranean. We show that such DAs are very young – median ages 9–56 years – with limited time-averaging, one to two orders of magnitude less than on even nearby soft substrates. On rocky substrates, out-of-habitat transport is likely the main cause of loss of older shells. In Posidonia oceanica meadows, the root and rhizome system creates a dense structure – the matte – that quickly entangles and buries shells and limits the potential for bioturbation. The matte is, however, a peculiar feature of Posidonia oceanica , and age and time-averaging in meadows of other seagrass species may be different. The young age of DAs in these habitats requires a careful consideration of their appropriateness as baselines. The large difference in DA age between soft substrates, subject to numerous studies, and hard and seagrass substrates, rarely inspected with geochronological techniques, implies that DA dating is important for studies aiming at using DAs as baselines.
ONSHORE-OFFSHORE TRENDS IN THE TEMPORAL RESOLUTION OF MOLLUSCAN DEATH ASSEMBLAGES: HOW AGE-FREQUENCY DISTRIBUTIONS REVEAL QUATERNARY SEA-LEVEL HISTORY
The taphonomic clock in fish otoliths
Radiocarbon dating supports bivalve-fish age coupling along a bathymetric gradient in high-resolution paleoenvironmental studies
PALEOENVIRONMENTAL IMPLICATIONS OF TIME-AVERAGING AND TAPHONOMIC VARIATION OF SHELL BEDS IN LAKE TANGANYIKA, AFRICA
Tracing the effects of eutrophication on molluscan communities in sediment cores: outbreaks of an opportunistic species coincide with reduced bioturbation and high frequency of hypoxia in the Adriatic Sea
One fossil record, multiple time resolutions: Disparate time-averaging of echinoids and mollusks on a Holocene carbonate platform
SPATIAL VARIATION IN THE TEMPORAL RESOLUTION OF SUBTROPICAL SHALLOW-WATER MOLLUSCAN DEATH ASSEMBLAGES
Stratigraphic unmixing reveals repeated hypoxia events over the past 500 yr in the northern Adriatic Sea
TIME-AVERAGING AND STRATIGRAPHIC RESOLUTION IN DEATH ASSEMBLAGES AND HOLOCENE DEPOSITS: SYDNEY HARBOUR'S MOLLUSCAN RECORD
Rapid and early deglaciation in the central Brooks Range, Arctic Alaska
TRACING BURIAL HISTORY AND SEDIMENT RECYCLING IN A SHALLOW ESTUARINE SETTING (COPANO BAY, TEXAS) USING POSTMORTEM AGES OF THE BIVALVE MULINIA LATERALIS
Long-term accumulation of carbonate shells reflects a 100-fold drop in loss rate
Amino acid ratios in reworked marine bivalve shells constrain Greenland Ice Sheet history during the Holocene
Quantitative comparisons and models of time-averaging in bivalve and brachiopod shell accumulations
Taphonomic bias and time-averaging in tropical molluscan death assemblages: differential shell half-lives in Great Barrier Reef sediment
Bear Lake is a large alkaline lake on a high plateau on the Utah-Idaho border. The Bear River was partly diverted into the lake in the early twentieth century so that Bear Lake could serve as a reservoir to supply water for hydropower and irrigation downstream, which continues today. The northern Rocky Mountain region is within the belt of the strongest of the westerly winds that transport moisture during the winter and spring over coastal mountain ranges and into the Great Basin and Rocky Mountains. As a result of this dominant winter precipitation pattern, most of the water entering the lake is from snowmelt, but with net evaporation. The dominant solutes in the lake water are Ca 2+ , Mg 2+ , and HCO 3 2‒ , derived from Paleozoic carbonate rocks in the Bear River Range west of the lake. The lake is saturated with calcite, aragonite, and dolomite at all depths, and produces vast amounts of carbonate minerals. The chemistry of the lake has changed considerably over the past 100 years as a result of the diversion of Bear River. The net effect of the diversion was to dilute the lake water, especially the Mg 2+ concentration. Bear Lake is oligotrophic and coprecipitation of phosphate with CaCO 3 helps to keep productivity low. However, algal growth is colimited by nitrogen availability. Phytoplankton densities are low, with a mean summer chlorophyll a concentration of 0.4 mg L ‒1 . Phytoplankton are dominated by diatoms, but they have not been studied extensively (but see Moser and Kimball, this volume). Zooplankton densities usually are low (<10 L ‒1 ) and highly seasonal, dominated by calanoid copepods and cladocera. Benthic invertebrate densities are extremely low; chironomid larvae are dominant at depths <30 m, and are partially replaced with ostracodes and oligochaetes in deeper water. The ostracode species in water depths >10 m are all endemic. Bear Lake has 13 species of fish, four of which are endemic.
Bear Lake, on the Idaho-Utah border, lies in a fault-bounded valley through which the Bear River flows en route to the Great Salt Lake. Surficial deposits in the Bear Lake drainage basin provide a geologic context for interpretation of cores from Bear Lake deposits. In addition to groundwater discharge, Bear Lake received water and sediment from its own small drainage basin and sometimes from the Bear River and its glaciated headwaters. The lake basin interacts with the river in complex ways that are modulated by climatically induced lake-level changes, by the distribution of active Quaternary faults, and by the migration of the river across its fluvial fan north of the present lake. The upper Bear River flows northward for ~150 km from its headwaters in the northwestern Uinta Mountains, generally following the strike of regional Laramide and late Cenozoic structures. These structures likely also control the flow paths of groundwater that feeds Bear Lake, and groundwater-fed streams are the largest source of water when the lake is isolated from the Bear River. The present configuration of the Bear River with respect to Bear Lake Valley may not have been established until the late Pliocene. The absence of Uinta Range–derived quartzites in fluvial gravel on the crest of the Bear Lake Plateau east of Bear Lake suggests that the present headwaters were not part of the drainage basin in the late Tertiary. Newly mapped glacial deposits in the Bear River Range west of Bear Lake indicate several advances of valley glaciers that were probably coeval with glaciations in the Uinta Mountains. Much of the meltwater from these glaciers may have reached Bear Lake via ground-water pathways through infiltration in the karst terrain of the Bear River Range. At times during the Pleistocene, the Bear River flowed into Bear Lake and water level rose to the valley threshold at Nounan narrows. This threshold has been modified by aggradation, downcutting, and tectonics. Maximum lake levels have decreased from as high as 1830 m to 1806 m above sea level since the early Pleistocene due to episodic downcutting by the Bear River. The oldest exposed lacustrine sediments in Bear Lake Valley are probably of Pliocene age. Several high-lake phases during the early and middle Pleistocene were separated by episodes of fluvial incision. Threshold incision was not constant, however, because lake highstands of as much as 8 m above bedrock threshold level resulted from aggradation and possibly landsliding at least twice during the late-middle and late Pleistocene. Abandoned stream channels within the low-lying, fault-bounded region between Bear Lake and the modern Bear River show that Bear River progressively shifted northward during the Holocene. Several factors including faulting, location of the fluvial fan, and channel migration across the fluvial fan probably interacted to produce these changes in channel position. Late Quaternary slip rates on the east Bear Lake fault zone are estimated by using the water-level history of Bear Lake, assuming little or no displacement on dated deposits on the west side of the valley. Uplifted lacustrine deposits representing Pliocene to middle Pleistocene highstands of Bear Lake on the footwall block of the east Bear Lake fault zone provide dramatic evidence of long-term slip. Slip rates during the late Pleistocene increased from north to south along the east Bear Lake fault zone, consistent with the tectonic geomorphology. In addition, slip rates on the southern section of the fault zone have apparently decreased over the past 50 k.y.