Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Equations model ecosystem

The notion of persistence attempts to capture the idea that if the equations (D.l) represent a model ecosystem then all components of the ecosystem survive. The system (D.l) is said to be persistent if... [Pg.277]

PEST. This code ( 3) was developed within the framework of Rensselaer Polytechnic Institute s CLEAN (Comprehensive Lake Ecosystem Analyzer) model. It includes highly elaborated algorithms for biological phenomena, as described in this volume (44). For example, biotransformation is represented via second-order equations in bacterial population density (Equation 5) in the other codes described in this section PEST adds to this effects of pH and dissolved oxygen on bacterial activity, plus equations for metabolism in higher organisms. PEST allows for up to 16 compartments (plants, animals, etc.), but does not include any spatially resolved computations or transport processes other than volatilization. [Pg.36]

The high degree of packing of the organisms within a volume can lead to the formation of floes (suspended aggregates), where millions of cells cluster to form particles with dimensions in the order of millimetres [29]. Models for uptake by such ecosystems also assume sphericity, and start from a continuity equation accounting for the consumption of the species throughout the floe ... [Pg.192]

Competition modeling is one of the more challenging aspects of mathematical biology. Competition is clearly important in nature, yet there are so many ways for populations to compete that the modeling is difficult to carry out in any generality. On the other hand, the mathematical idea seems quite simple when one population increases, the growth rate of the others should diminish (or at least not increase), a concept that is quite easily expressed by partial derivatives of the specific growth rates. If an ecosystem is modeled by a system of ordinary differential equations - for example, by... [Pg.1]

To estimate isotopic discrimination at the ecosystem, local or regional scales, an estimate of the exchange flux, or the 6 C value of NEE, at the relevant scale is required. Such estimates are obtained by sampling air in and above plant canopies, or in the and above the atmospheric boundary layer (ABL). A simple and powerful approach employs a two-member mixing model as first proposed by Keeling (1958, 1961). The equation used in the Keeling approach is derived from the basic assumption that the atmospheric concentration of a substance in an ecosystem reflects the combination of some background amount of the substance that is already present in the atmosphere and some amount of substance that is added or removed by a source or sink in the ecosystem ... [Pg.2103]

A great future challenge for modeling the Baltic Sea ecosystem is related to the task of conceptual and numerical ecosystem model formulation. Before a numerical ecosystem model can be implemented and simulations are carried out, a conceptual view on the ecosystem must be developed and formulated. This includes the determination of the major links in the biogeochemical cycles, identification of the leading players in these cycles, and to find estimates for their activity in the transport and transformation of matter. This requires accomplishing the difficult task of a far-reaching simplification of a complex conceptual ecosystem model, the formulation as mathematical equations and the numerical implementation of suitable solution methods. Little is known about many model parameters. [Pg.617]

Application ofGIS techniques for calculation and mapping of critical loads Critical loads ofpollutants at an ecosystem can be calculated on the basis of the Steady-State Mass Balance (SSMB) biogeochemical model (see Chapter 10). All equations of this model include a quantitative estimation of the greatest possible number of... [Pg.234]

For process optimization with respect to several economic criteria such as net present worth, payback period and operating cost, the classical Williams and Otto (WO) process and an industrial low-density polyethylene (LDPE) plant are considered. Results show that either single optimal solution or Pareto-optimal solutions are possible for process design problems depending on the objectives and model equations. Subsequently, industrial ecosystems are studied for optimization with respect to both economic and environmental objectives. Economic objective is important as companies are inherently profit-driven, and there is often a tradeoff between profit and environmental impact. Pareto-optimal fronts were successfully obtained for the 6-plant industrial ecosystem optimized for multiple objectives by NSGA-ll-aJG. The study and results reported in this chapter show the need and potential for optimization of processes for multiple economic and environmental objectives. [Pg.302]

While several researchers have attempted mass balances for mercury in rivers and lakes [74,75,93,94], none have attempted to collect quantitative mercury measurements with a whole-ecosystem approach. The purpose of the study was to examine a complete set of mercury fluxes in the BDW Lake basin. A detailed explanation of the mass balance model, mass flux equations and the calculation of error is available in other publications [86,92]. [Pg.231]

It is likely that natural ecosystems (forest, grassland) emit no or only small amounts of ammonia because normally there is a deficit of fixed nitrogen in landscapes. Reported emissions factors over forests span three orders of magnitude and are likely be influenced by re-emission of wet deposited ammonium. Older publications considerably overestimated emission by using simple models considering soil ammonium concentrations obtained from relative decomposition and nitrification rates, where Henry s law gives the equilibrium concentration of ammonia gas in the soil, and a simplified diffusion equation yields the flux to the atmosphere, for example, Dawson (1977) calculated it to be about 47 Tg N yr b... [Pg.221]

Deterministic models (most commonly systems of nonlinear differential equations) have been used to model the dynamics of lake ecosystems (Park et ai, 1974 Chen Orlob, 1975 Joergensen, 1976 Di Toro et ai, 1979). These models have been satisfactory to describe the main trends of ecological phenomena however, deterministic models are not capable of reflecting the inherently random behaviour of ecosystems. This source of uncertainty is/ especially important in large multiparameter models. /... [Pg.203]

Various kinds of models are also proposed for an ecosystem modeF "" ° it also solves conservation equations for relevant components with appropriate source and sink terms. If C is the concentration of some component in a model, the time rate of variation of C is given by ... [Pg.918]

Monarch populations share their habitat with com ecosystems to a degree previously undocumented (4). Despite this, die portion of the monarch population diat is potentially exposed to toxic levels of Bt com pollen is negligible and declining as planting of event 176 is phased out. Because the effects portion of the risk probability equations described above (Pt) is such a small value for the dominant com hytirids currendy planted, the sensitivity of die model to factors describing ecological exposure ( ) and for risk (R) will remain low. [Pg.60]


See other pages where Equations model ecosystem is mentioned: [Pg.131]    [Pg.418]    [Pg.34]    [Pg.40]    [Pg.604]    [Pg.274]    [Pg.279]    [Pg.179]    [Pg.138]    [Pg.269]    [Pg.4062]    [Pg.341]    [Pg.588]    [Pg.618]    [Pg.235]    [Pg.22]    [Pg.152]    [Pg.105]    [Pg.255]    [Pg.146]    [Pg.668]    [Pg.3]    [Pg.277]    [Pg.182]    [Pg.212]    [Pg.554]    [Pg.309]    [Pg.358]    [Pg.198]   
See also in sourсe #XX -- [ Pg.112 ]




SEARCH



Model ecosystem

Model equations

Modeling equations

Modelling equations

© 2024 chempedia.info