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The following summary outlines a combined computer and laboratory exercise conducted in "Quantitative Ecology of Marine Systems," a class I developed at the Shannon Point Marine Center, Western Washin...
We measured the nutrient stoichiometry of inputs, outputs, retention, storage, and recycling in three seasonally nitrogen (N)-deficient reservoirs by incorporating watershed mass balances with measur...
We studied the feeding behavior of the nauplii and adult females of the marine cyclopoid copepod Oithona davisae in the laboratory. Functional response experiments showed that O. davisae can feed on ...
We created a model physical system to investigate the role of blade rigidity in setting forces and rates of mass exchange for a blade exposed to unsteady flow in a vortex street. Using a combination ...
In ~ 50% of the ocean, iron (Fe) limits phytoplankton growth, including that of the diatom Pseudo-nitzschia. Fe-limited Pseudo-nitzschia spp. may produce the potent neurotoxin domoic acid (DA) to acce...
We hypothesized that mats of a nonnative macroalga, Gracilaria vermiculophylla, which is often found incorporated several centimeters into intertidal mudflat sediments, would increase net denitrifica...
Using 31-yr data from measurements in a lake that has experienced change in eutrophication status, I showed that the effects of global warming on chlorophyll a (Chl a)–normalized maximum rates of phot...
Results from a study of benthic nitrogen cycling in two Arctic fjords are presented. Intact sediment core incubations were used to quantify net fluxes of dissolved inorganic nitrogen, organic nitroge...
The ability of propagules (fertilized eggs) of five species of fucoid algae(Hormosira banksii, Durvillaea antarctica, Cystophora torulosafrom New Zealand, and Fucus gardneriandPelvetiopsis limitatafro...
A mesocosm experiment was conducted to determine the effects of nutrient enrichment on competitive interactions between a hard coral, a green alga, and a sea anemone. In the low-nutrient controls, ab...
The distributions of water-surface slopes and wave heights were measured under suddenly started and stopped winds. The root-mean-square slopes and average wave heights are found to grow and decay expo...
Growth Rates of a Topographic Instability     Topographic Instability  Growth Rates       font style='font-size:12px;'> 2009/2/6
We consider a linear model of a topographically induced shear instability, described by Pedlosky (1980). The perturbation technique used by Pedlosky, to establish the existence of unstable normal mode...
Isopycnal maps of 3H–3He age (τ) with about 100 km resolution have been obtained for a 1000-km scale area in the eastern subtropical North Atlantic. The midscale texture of the maps is consistent with...
Why Oceanic Dissipation Rates Are Not Lognormal     Oceanic Dissipation Rates  Not Lognormal  turbulent flow       font style='font-size:12px;'> 2008/12/30
In their derivation of the lognormal probability density function for volume-averaged dissipation rates, Gurvich and Yaglom assumed explicitly that these dissipation rates are statistically homogeneou...
The transport of mass between a mixed layer, exposed to mechanical and thermodynamic forcing, and an adiabatic thermocline is studied for gyre-scale motions. It is shown that if the mixed layer can be...

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