scholarly journals On the complex dynamics of savanna landscapes

2018 ◽  
Vol 115 (7) ◽  
pp. E1336-E1345 ◽  
Author(s):  
Jonathan David Touboul ◽  
Ann Carla Staver ◽  
Simon Asher Levin

Simple mathematical models can exhibit rich and complex behaviors. Prototypical examples of these drawn from biology and other disciplines have provided insights that extend well beyond the situations that inspired them. Here, we explore a set of simple, yet realistic, models for savanna–forest vegetation dynamics based on minimal ecological assumptions. These models are aimed at understanding how vegetation interacts with both climate (a primary global determinant of vegetation structure) and feedbacks with chronic disturbances from fire. The model includes three plant functional types—grasses, savanna trees, and forest trees. Grass and (when they allow grass to persist in their subcanopy) savanna trees promote the spread of fires, which in turn, demographically limit trees. The model exhibits a spectacular range of behaviors. In addition to bistability, analysis reveals (i) that diverse cyclic behaviors (including limit and homo- and heteroclinic cycles) occur for broad ranges of parameter space, (ii) that large shifts in landscape structure can result from endogenous dynamics and not just from external drivers or from noise, and (iii) that introducing noise into this system induces resonant and inverse resonant phenomena, some of which have never been previously observed in ecological models. Ecologically, these results raise questions about how to evaluate complicated dynamics with data. Mathematically, they lead to classes of behaviors that are likely to occur in other models with similar structure.

2021 ◽  
Vol 748 (1) ◽  
pp. 012009
Author(s):  
Agusyadi Ismail ◽  
Yayan Hendrayana ◽  
Dadan Ramadani ◽  
Sri Umiyati

Abstract Mount Ciremai National Park forest that area had been encroached. Because of that condition, stand structure especially the species composition and vegetation structure need to be researched. The aim of this research was to identify plant species and analyze forest vegetation structure. This research was conducted between March–April 2018 in the 15.500 ha area with 0.02% sampling intensity. Data was collected using grid line method that consisted of 34 sample plots with the 10 m distance between the plots and 20 m between the lines. The numbers of identified plant species at the research location were 43 species, classified by 10 families and 24 genera. Cinnamomum sintoc has a high level of dominance species. The forest vegetation was consisting by the different growth phases. The tree phase has the highest density of 3672 species/ha, while the seedling phase was lowest density of 1060 species/ha. The forest crown stratification were consisting of A, B, C, D and E stratum. The highest number of plants were from C strata for 4651 trees and the least from A strata with 25 trees with the highest tree was 42 m. Could be concluded that the composition of Mount Ciremai National Park forest have so many number of species and complex structure vegetation forest.


2013 ◽  
Vol 23 (12) ◽  
pp. 1330041 ◽  
Author(s):  
HONGJUN CAO ◽  
YANGUO WU

Based on the detailed bifurcation analysis and the master stability function, bursting types and stable domains of the parameter space of the Rulkov map-based neuron network coupled by the mean field are taken into account. One of our main findings is that besides the square-wave bursting, there at least exist two kinds of triangle burstings after the mean field coupling, which can be determined by the crisis bifurcation, the flip bifurcation, and the saddle-node bifurcation. Under certain coupling conditions, there exists two kinds of striking transitions from the square-wave bursting (the spiking) to the triangle bursting (the square-wave bursting). Stable domains of fixed points, periodic solutions, quasiperiodic solutions and their corresponding firing regimes in the parameter space are presented in a rigorous mathematical way. In particular, as a function of the intrinsic control parameters of each single neuron and the external coupling strength, a stable coefficient of the Neimark–Sacker bifurcation is derived in a parameter plane. These results show that there exist complex dynamics and rich firing regimes in such a simple but thought-provoking neuron network.


2016 ◽  
Author(s):  
Maria A. Zoran ◽  
Liviu Florin V. Zoran ◽  
Adrian I. Dida

1998 ◽  
Vol 122 (1) ◽  
pp. 240-245 ◽  
Author(s):  
M. Basso ◽  
L. Giarre´ ◽  
M. Dahleh ◽  
I. Mezic´

In this paper we model the microcantilever-sample interaction in an atomic force microscope (AFM) via a Lennard-Jones potential and consider the dynamical behavior of a harmonically forced system. Using nonlinear analysis techniques on attracting limit sets, we numerically verify the presence of chaotic invariant sets. The chaotic behavior appears to be generated via a cascade of period doubling, whose occurrence has been studied as a function of the system parameters. As expected, the chaotic attractors are obtained for values of parameters predicted by Melnikov theory. Moreover, the numerical analysis can be fruitfully employed to analyze the region of the parameter space where no theoretical information on the presence of a chaotic invariant set is available. In addition to explaining the experimentally observed chaotic behavior, this analysis can be useful in finding a controller that stabilizes the system on a nonchaotic trajectory. The analysis can also be used to change the AFM operating conditions to a region of the parameter space where regular motion is ensured. [S0022-0434(00)01401-5]


2021 ◽  
Vol 31 (14) ◽  
Author(s):  
Haijun Wang ◽  
Hongdan Fan ◽  
Jun Pan

Combining qualitative analysis and numerical technique, the present work revisits a four-dimensional circuit system in [Ma et al., 2016] and mainly reveals some of its rich dynamics not yet investigated: pitchfork bifurcation, Hopf bifurcation, singularly degenerate heteroclinic cycle, globally exponentially attractive set, invariant algebraic surface and heteroclinic orbit. The main contributions of the work are summarized as follows: Firstly, it is proved that there exists a globally exponentially attractive set with three different exponential rates by constructing a suitable Lyapunov function. Secondly, the existence of a pair of heteroclinic orbits is also proved by utilizing two different Lyapunov functions. Finally, numerical simulations not only are consistent with theoretical results, but also illustrate potential existence of hidden attractors in its Lorenz-type subsystem, singularly degenerate heteroclinic cycles with distinct geometrical structures and nearby hyperchaotic attractors in the case of small [Formula: see text], i.e. hyperchaotic attractors and nearby pseudo singularly degenerate heteroclinic cycles, i.e. a short-duration transient of singularly degenerate heteroclinic cycles approaching infinity, or the true ones consisting of normally hyperbolic saddle-foci (or saddle-nodes) and stable node-foci, giving some kind of forming mechanism of hyperchaos.


2019 ◽  
pp. 82-95
Author(s):  
William J. Bond

Boundaries between open and closed ecosystems often coincide with soil differences of greater or lesser degree. It has long been argued that these soil differences explain the striking differences in vegetation structure. But the nature of the vegetation itself feeds back on soil properties so that it is far from trivial to determine whether soil differences are a cause or consequence of the vegetation growing at a site. This chapter reviews soil physical and chemical characteristics and their potential to determine open and closed vegetation mosaics. The chapter also explores competitive exclusion of forest trees by grasses, herbs, and shrubs.


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