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841.
842.
Tissues of bowhead, beluga, and gray whales were analyzed for Ag, Cd, Cu, Se, Zn, THg and MeHg (belugas only). Delta15N and delta13C in muscle were used to estimate trophic position and feeding habitat, respectively. Trace element concentrations in tissues were significantly different among whale species. Hepatic Ag was higher in belugas than bowheads and gray whales. Gray whales had lower Cd concentrations in liver and kidney than bowhead and belugas and a sigmoid correlation of Cd with length was noted for all whales. Renal and hepatic Se and THg were higher in belugas than in baleen whales. The hepatic molar ratio of Se:THg exceeded 1:1 in all species and was negatively correlated to body length. Hepatic and renal Zn in subsistence-harvested gray whales was lower than concentrations for stranded whales. Se:THg molar ratios and tissue concentrations of Zn may show promise as potential indicators of immune status and animal health.  相似文献   
843.
For sixteen years following the 1989 Exxon Valdez oil spill adult returns of pink salmon in Prince William Sound, Alaska were monitored to assess spill effects on survival. No evidence of spill effects was detected for either intertidal or whole-stream spawning fish. From 1989 through 2004 mean densities for oiled and reference streams tracked each other, illustrating similar responses of oiled and reference stream adult populations to naturally changing oceanographic and climactic conditions. Hatchery fish strayed into the study streams, but similar incursions occurred in oiled and reference streams, and their presence was compensated for to eliminate their influence on determining the success of the returning natural populations. These results, showing no detectable effects of oiling on pink salmon spawning populations, are supported by published field studies on pink salmon incubation success in oiled streams.  相似文献   
844.
The Met Office Hadley Centre Unified Model (HadAM3) with the tiled version of the Met Office Surface Exchange Scheme (MOSES2) land surface scheme is used to assess the impact of a comprehensive imposed vegetation annual cycle on global climate and hydrology. Two 25-year numerical experiments are completed: the first with structural vegetation characteristics (Leaf Area Index, LAI, canopy height, canopy water capacity, canopy heat capacity, albedo) held at annual mean values, the second with realistic seasonally varying vegetation characteristics. It is found that the seasonalities of latent heat flux and surface temperature are widely affected. The difference in latent heat flux between experiments is proportional to the difference in LAI. Summer growing season surface temperatures are between 1 and 4 K lower in the phenology experiment over a majority of grid points with a significant vegetation annual cycle. During winter, midlatitude surface temperatures are also cooler due to brighter surface albedo over low LAI surfaces whereas during the dry season in the tropics, characterized by dormant vegetation, surface temperatures are slightly warmer due to reduced transpiration. Precipitation is not as systematically affected as surface temperature by a vegetation annual cycle, but enhanced growing season precipitation rates are seen in regions where the latent heat flux (evaporation) difference is large. Differences between experiments in evapotranspiration, soil moisture storage, the timing of soil thaw, and canopy interception generate regional perturbations to surface and sub-surface runoff annual cycles in the model.  相似文献   
845.
846.
The biodiversity record of graptolites from the Cheeseman's Creek Formation, considered herein as late Gisbornian (Caradoc) in age, has been substantially increased to fifteen taxa, including the new species Dicellograptus praemorrisi sp. nov. and Climacograptus vandenbergi sp. nov. Some of the records have global correlative significance enabling us to identify the wilsoni Biozone ( = calcaratus Biozone of eastern Australia). Several evolutionary lineages have been recognized:
  • 1 Dicellograptus moffatensis (Carruthers, 1858) → D. praemorrisi sp. nov → D. morrisi Hopkinson, 1871
  • 2 Glossograptus hincksi Hopkinson, 1872 → Glossograptus? sp.
  • 3 Climacograptus bicornis (J. Hall, 1847) → C. vandenbergi sp. nov. → C. lanceolatus VandenBerg, 1990.
Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   
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