搜索结果: 1-15 共查到“理学 growth rates”相关记录23条 . 查询时间(0.125 秒)
Growth rates of lava domes with respect to viscosity of magmas
lava domes squeeze of magma growth rates of domes Hagen-Poiseuille Law macroscopic viscosity
2015/9/10
In the discussion of lava dome formation, viscosity of magma plays an important role. Measurements of viscosity
of magmas in field and laboratory are briefly summarized. The types of lava dome emplac...
We study the abelian sandpile growth model, where n particles are added at the origin on a stable background configuration in Zd. Any site with at least 2d particles then topples by sending one partic...
Iron and copper limitations differently affect growth rates and photosynthetic and physiological parameters of the marine diatom Pseudo-nitzschia delicatissima
Iron and copper limitations differently affect growth rates photosynthetic and physiological parameters marine diatom Pseudo-nitzschia delicatissima
2014/4/2
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...
Growth rates, Hausdorff measure and stability for the p-obstacle problem(3/2≤p≤2)
growth rate Hausdorff measure obstacle problem stability
2011/10/17
In this paper, we consider the free boundary for the inho-mogeneous obstacle problem with zero obstacle. We firstly establish the growth rates for the solution u(x) and the gradient of u(x), awa...
Numerical values of the growth rates of power-free languages
Numerical values growth rates power-free languages
2010/12/16
We present upper and two-sided bounds of the exponential growth rate for a wide range of power-free languages. All bounds are obtained with the use of algorithms previously developed by the author.
Charged and total particle formation and growth rates during EUCAARI 2007 campaign in Hyytiälä
growth rates EUCAARI 2007 campaign Hyytiä lä
2009/6/23
Despite the fact that frequent aerosol formation has been observed in various locations in the atmosphere, the overall magnitude of the new particle formation as a particle source is still unclear. In...
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...
Airborne measurements of nucleation mode particles I: coastal nucleation and growth rates
Airborne measurements nucleation mode particles I coastal nucleation growth rates
2008/12/4
A light aircraft was equipped with a bank of Condensation Particle Counters (CPCs) (50% cut from 3–5.4–9.6 nm) and a nano-Scanning Mobility Particle Sizer (nSMPS) and deployed along the west coast of ...
The Michelson Interferometer for Passive Atmospheric Sounding onboard ENVISAT (MIPAS-E) offers the opportunity to detect and spectrally resolve many atmospheric minor constituents affecting atmospheri...
Fatigue crack growth rates of rotor steel at elevated temperatures
rotor steels (30CrlMolV) fatigue crack propagation rate temperature
2011/9/14
Low fatigue samples were obtained from the outer edges of rotor steel (30CrlMolV) which had operated under different temperatures conditions.Based on this data,the effects of temperature on fatigue cr...
Predicting marine phytoplankton maximum growth rates from temperature:Improving on the Eppley curve using quantile regression
marine phytoplankton maximum growth rates temperature:Improving the Eppley curve quantile regression
2014/4/21
The Eppley curve describes an exponential function that defines the maximum attainable daily growth rate of marine phytoplankton as a function of temperature. The curve was originally fitted by eye as...
CO2 control of Trichodesmium N2 fixation, photosynthesis, growth rates, and elemental ratios: Implications for past, present, and future ocean biogeochemistry
CO2 control Trichodesmium N2 fixation photosynthesis growth rates elemental ratios past present future ocean biogeochemistry
2014/4/22
Diazotrophic marine cyanobacteria in the genus Trichodesmium contribute a large fraction of the new nitrogen entering the oligotrophic oceans, but little is known about how they respond to shifts in g...
Does low temperature constrain the growth rates of heterotrophic protists? Evidence and implications for algal blooms in cold waters
low temperature growth rates of heterotrophic protists Evidence and implications algal blooms cold waters
2014/4/23
Literature review and synthesis of growth rates of aquatic protists focused on the role of temperature in the formation of massive annual algal blooms in high-latitude ecosystems. Maximal growth rates...
atural growth rates in Antarctic krill (Euphausia superba): II. Predictive models based on food, temperature, body length, sex, and maturity stage
sex maturity stage
2014/5/4
We used the instantaneous growth rate method to determine the effects of food, temperature, krill length, sex, and maturity stage on in situ summer growth of krill across the southwest Atlantic sector...
Diatom fatty acid biomarkers indicate recent growth rates in Antarctic krill
Diatom fatty acid biomarkers indicate growth rates Antarctic krill
2014/5/9
We investigated the relationship between nutritional condition (levels of specific fatty acids) and growth increment (percentage growth per intermoult period, percentage IMP-1) for Antarctic krill (Eu...
