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141.
142.
Stephen G. Warren 《Climatic change》1982,4(4):329-340
The growth and decay of ice sheets are driven by forces affecting the seasonal cycles of snowfall and snowmelt. The external forces are likely to be variations in the earth's orbit which cause differences in the solar radiation received. Radiational control of snowmelt is modulated by the seasonal cycles of snow albedo and cloud cover. The effects of orbital changes can be magnified by feedbacks involving atmospheric CO2 content, ocean temperatures and desert areas. Climate modeling of the causes of the Pleistocene ice ages involves modeling the interactions of all components of the climate system; snow, sea ice, glacier ice, the ocean, the atmosphere, and the solid earth. Such modeling is also necessary for interpreting oxygen isotope records from ice and ocean as paleoclimatic evidence. 相似文献
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Stephen A. Hall 《Quaternary Research》1982,17(3):391-407
Analyses of pollen and land snails from rocksheter sites in the Osage Hills of northeastern Oklahoma indicate that the period 2000-1000 yr B.P. was moister than today. During that time, colonies of the prairie vole Microtus ochrogaster were present in the Texas Panhandle. About 1000 yr B.P. the climate changed to dry conditions that have persisted to the present. Disjunct colonies of small mammals in Texas became extinct at the beginning of the dry episode, thereby establishing the composition of the modern fauna. The climatic model for the origin of the Panhandle Aspect (A.D. 1200–1500) is questioned on the grounds that the Southern Plains experienced a long period of dry climate commencing A.D. 950. 相似文献
145.
S.Stephen Streeter Paul E. Belanger Thomas B. Kellogg Jean Claude Duplessy 《Quaternary Research》1982,18(1):72-90
Fluctuations in benthic foraminiferal faunas over the last 130,000 yr in four piston cores from the Norwegian Sea are correlated with the standard worldwide oxygen-isotope stratigraphy. One species, Cibicides wuellerstorfi, dominates in the Holocene section of each core, but alternates downcore with Oridorsalis tener, a species dominant today only in the deepest part of the basin. O. tener is the most abundant species throughout the entire basin during periods of particularly cold climate when the Norwegian Sea presumably was ice covered year round and surface productivity lowered. Portions of isotope Stages 6, 3, and 2 are barren of benthic foraminifera; this is probably due to lowered benthic productivity, perhaps combined with dilution by ice-rafted sediment; there is no evidence that the Norwegian Sea became azoic. The Holocene and Substage 5e (the last interglacial) are similar faunally. This similarity, combined with other evidence, supports the presumption that the Norwegian Sea was a source of dense overflows into the North Atlantic during Substage 5e as it is today. Oxygen-isotope analyses of benthic foraminifera indicate that Norwegian Sea bottom waters warmer than they are today from Substage 5d to Stage 2, with the possible exception of Substage 5a. These data show that the glacial Norwegian Sea was not a sink for dense surface water, as it is now, and thus it was not a source of deep-water overflows. The benthic foraminiferal populations of the deep Norwegian Sea seem at least as responsive to near-surface conditions, such as sea-ice cover, as they are to fluctuations in the hydrography of the deep water. Benthic foraminiferal evidence from the Norwegian Sea is insufficient in itself to establish whether or not the basin was a source of overflows into the North Atlantic at any time between the Substage 5e/5d boundary at 115,000 yr B.P. and the Holocene. 相似文献
146.
J. Stewart Turner Herbert E. Huppert R.Stephen J. Sparks 《Journal of Volcanology and Geothermal Research》1983,16(3-4)
Previous laboratory experiments investigating the fluid dynamics of replenished magma chambers have been extended to model effects resulting from the release of gas. Turbulent transfer of heat between a layer of dense, hot and volatile-rich mafic magma overlying cooler more evolved magma can lead to crystallization and exsolution of volatiles in the lower layer. Small gas bubbles can cause the bulk density to decrease to that of the upper layer and thus produce sudden overturning and initiate mixing, followed by further exsolution of gas and explosive eruption. These processes have been modelled in the laboratory using a chemical reaction between sodium or potassium carbonate and nitric acid to release small bubbles of CO2. We have investigated both the initial overturning produced by gas release in the lower layer, and the subsequent evolution of gas due to intimate mixing of the two layers. The latter experiments, in which the reactants remained isolated in the two layers until overturning occurred, demonstrated unambiguously that the fluxes of chemical components across the interfaces between convecting layers are very slow compared to the flux of heat. This shows that the evolution of layers of magma of different origins and composition can take place nearly independently of each other. The magmas can coexist in the same stratified chamber, until their bulk densities become equal and they mix together. The processes illustrated in these experiments could occur in H2O-bearing magmas such as in the calcalkaline association and in CO2-bearing mafic magmas such as in silica undersaturated suites. 相似文献
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150.
Primary productivity and phytoplankton size fraction dominance in a temperate North Atlantic estuary
Stephen F. Bruno Robert D. Staker Gurdial M. Sharma Jefferson T. Turner 《Estuaries and Coasts》1983,6(3):200-211
The composition, productivity, and standing crop of net (>20 μm) and nano-(<20 μm) phytoplankton of Peconic Bay, Long Island, New York was examined from June 1978 through May 1979. Nanoplankton, primarily small solitary flagellates, chlorophytes, and diatoms, dominated from May through September accounting for 88.5% of the productivity and 88.1% of the standing crop (measured as chlorophyll a). An apparent net plankton bloom began in December and continued through March. The dominant organism through most of the winter bloom was the chain-forming diatom Skeletonema costatum (Grev.) Cl. Net plankton at this time represented 66.4% of the standing crop. For both size fractions, productivity/chlorophyll a (g C per g chl a per d, integrated through the euphotic zone) was a function of light energy over the year with the exception of a few sampling dates during the post-winter bloom period. Assimilation numbers (g C per g chl a per h at saturating light intensities) were a function of temperature between 0 and 20°C. Nitrogen deficiency did not appear to be a factor in regulating phytoplankton growth rate through the euphotic zone, as ratios of 14C assimilation for dark bottles enriched with NH3 and with no enrichment exhibited no relationship to environmental dissolved inorganic nitrogen concentrations. Zooplankton grazing pressure appeared to have been an important factor in regulating the upper limit of phytoplankton biomass and in influencing size fraction dominance. Dominance of one phytoplankton size fraction over the other on any given date was not based on physiological differences between the two groups since both fractions were composed of the same species. Apparent net phytoplankton blooms (in terms of productivity and chlorophyll a) were artifacts of increased chain lengths of nanoplankton diatoms such as Skeletonema costatum, and to a lesser extent, Thalassiosira nordenskioldii Cl. and Detonula confervacea (Cl.) Gran, rather than to the dominance of large, solitary cells. 相似文献