Biological exponential growth is the unrestricted growth of a population of organisms, occurring when resources in its habitat are unlimited. Most commonly apparent in species that reproduce quickly and asexually, like bacteria, exponential growth is intuitive from the fact that each organism can divide and produce two copies of itself. Each descendent bacterium can itself divide, again doubling the population size (as displayed in the above graph). [1] The bacterium Escherichia coli, under optimal conditions, may divide as often as twice per hour. Left unrestricted, the growth could continue, and a colony would cover the Earth's surface in less than a day. [2] [3] Resources are the determining factor in establishing biological exponential growth, and there are different mathematical equations used to analyze and quantify it.
Resource availability is essential for the unimpeded growth of a population. Examples of resources organisms use are food, water, shelter, sunlight, and nutrients.[1][2] Ideally, when resources in the habitat are unlimited, each species can fully realize its innate potential to grow in number, as Charles Darwin observed while developing his theory of natural selection. Any species growing exponentially under unlimited resource conditions can reach enormous population densities in a short time. Darwin showed how even a slow-growing animal like the elephant could theoretically reach an enormous population if there were unlimited resources for its growth in its habitat.[3] This is unrealistic in almost all situations (with exceptions, such as a laboratory). There is simply a finite quantity of everything necessary for life, and individuals in a population will compete with their own or other species for these finite resources.[4]
One equation used to analyze biological exponential growth uses the birth and death rates in a population. If, in a hypothetical population of size N, the birth rates (per capita) are represented as b and death rates (per capita) as d, then the increase or decrease in N during a time period t will be
(b-d) is called the 'intrinsic rate of natural increase' and is a parameter chosen for assessing the impacts of any biotic or abiotic factor on population growth. [4]
As the population approaches its carrying capacity, the rate of growth decreases, and the population trend will become logistic. [5] Once the carrying capacity, or K, is incorporated to account for the finite resources that a population will be competing for within an environment, the aforementioned equation becomes the following:
The variable is the population's maximum growth rate, which is also known as biotic potential. [5] A graph of this equation creates an S-shaped curve, which demonstrates how initial population growth is exponential due to the abundance of resources and lack of competition. When factors that limit an organisms growth are not available in constant supply to meet the growing demand, such as RNA and protein amounts in bacteria, the growth of the organism cannot continue at this exponential rate. [6] As resources become more limited, the growth rate tapers off, and eventually, once growth rates are at the carrying capacity of the environment, the population size will taper off. [5] This S-shaped curve observed in logistic growth is a more accurate model than exponential growth for observing real-life population growth of organisms. [7]
Biological exponential growth has ties to other scientific fields such as chemical ecology and microbiology. In relation to chemical ecology, the reactions that occur between the chemicals termed secondary metabolites of organisms impacts how they reproduce, feed, and defend themselves. [8] Therefore, secondary metabolites are a type of resource that influences the growth of organisms as well.
The exponential function is a mathematical function denoted by or . Unless otherwise specified, the term generally refers to the positive-valued function of a real variable, although it can be extended to the complex numbers or generalized to other mathematical objects like matrices or Lie algebras. The exponential function originated from the operation of taking powers of a number, but various modern definitions allow it to be rigorously extended to all real arguments , including irrational numbers. Its ubiquity in pure and applied mathematics led mathematician Walter Rudin to consider the exponential function to be "the most important function in mathematics".
Half-life is the time required for a quantity to reduce to half of its initial value. The term is commonly used in nuclear physics to describe how quickly unstable atoms undergo radioactive decay or how long stable atoms survive. The term is also used more generally to characterize any type of exponential decay. For example, the medical sciences refer to the biological half-life of drugs and other chemicals in the human body. The converse of half-life is doubling time.
Theoretical ecology is the scientific discipline devoted to the study of ecological systems using theoretical methods such as simple conceptual models, mathematical models, computational simulations, and advanced data analysis. Effective models improve understanding of the natural world by revealing how the dynamics of species populations are often based on fundamental biological conditions and processes. Further, the field aims to unify a diverse range of empirical observations by assuming that common, mechanistic processes generate observable phenomena across species and ecological environments. Based on biologically realistic assumptions, theoretical ecologists are able to uncover novel, non-intuitive insights about natural processes. Theoretical results are often verified by empirical and observational studies, revealing the power of theoretical methods in both predicting and understanding the noisy, diverse biological world.
A logistic function or logistic curve is a common S-shaped curve with the equation
Exponential growth occurs when a quantity grows at a rate directly proportional to its present size. For example, when it is 3 times as big as it is now, it will be growing 3 times as fast as it is now.
A quantity is subject to exponential decay if it decreases at a rate proportional to its current value. Symbolically, this process can be expressed by the following differential equation, where N is the quantity and λ (lambda) is a positive rate called the exponential decay constant, disintegration constant, rate constant, or transformation constant:
In population ecology and economics, maximum sustainable yield (MSY) is theoretically, the largest yield that can be taken from a species' stock over an indefinite period. Fundamental to the notion of sustainable harvest, the concept of MSY aims to maintain the population size at the point of maximum growth rate by harvesting the individuals that would normally be added to the population, allowing the population to continue to be productive indefinitely. Under the assumption of logistic growth, resource limitation does not constrain individuals' reproductive rates when populations are small, but because there are few individuals, the overall yield is small. At intermediate population densities, also represented by half the carrying capacity, individuals are able to breed to their maximum rate. At this point, called the maximum sustainable yield, there is a surplus of individuals that can be harvested because growth of the population is at its maximum point due to the large number of reproducing individuals. Above this point, density dependent factors increasingly limit breeding until the population reaches carrying capacity. At this point, there are no surplus individuals to be harvested and yield drops to zero. The maximum sustainable yield is usually higher than the optimum sustainable yield and maximum economic yield.
The Lotka–Volterra equations, also known as the Lotka–Volterra predator–prey model, are a pair of first-order nonlinear differential equations, frequently used to describe the dynamics of biological systems in which two species interact, one as a predator and the other as prey. The populations change through time according to the pair of equations:
Pierre François Verhulst was a Belgian mathematician and a doctor in number theory from the University of Ghent in 1825. He is best known for the logistic growth model.
Population dynamics is the type of mathematics used to model and study the size and age composition of populations as dynamical systems.
Compartmental models are a very general modelling technique. They are often applied to the mathematical modelling of infectious diseases. The population is assigned to compartments with labels – for example, S, I, or R,. People may progress between compartments. The order of the labels usually shows the flow patterns between the compartments; for example SEIS means susceptible, exposed, infectious, then susceptible again.
The Allee effect is a phenomenon in biology characterized by a correlation between population size or density and the mean individual fitness of a population or species.
In chemistry, the rate equation is an empirical differential mathematical expression for the reaction rate of a given reaction in terms of concentrations of chemical species and constant parameters only. For many reactions, the initial rate is given by a power law such as
When a quantity grows towards a singularity under a finite variation it is said to undergo hyperbolic growth. More precisely, the reciprocal function has a hyperbola as a graph, and has a singularity at 0, meaning that the limit as is infinite: any similar graph is said to exhibit hyperbolic growth.
Intraspecific competition is an interaction in population ecology, whereby members of the same species compete for limited resources. This leads to a reduction in fitness for both individuals, but the more fit individual survives and is able to reproduce. By contrast, interspecific competition occurs when members of different species compete for a shared resource. Members of the same species have rather similar requirements for resources, whereas different species have a smaller contested resource overlap, resulting in intraspecific competition generally being a stronger force than interspecific competition.
In science, e-folding is the time interval in which an exponentially growing quantity increases by a factor of e; it is the base-e analog of doubling time. This term is often used in many areas of science, such as in atmospheric chemistry, medicine and theoretical physics, especially when cosmic inflation is investigated. Physicists and chemists often talk about the e-folding time scale that is determined by the proper time in which the length of a patch of space or spacetime increases by the factor e mentioned above.
The Gompertz curve or Gompertz function is a type of mathematical model for a time series, named after Benjamin Gompertz (1779–1865). It is a sigmoid function which describes growth as being slowest at the start and end of a given time period. The right-side or future value asymptote of the function is approached much more gradually by the curve than the left-side or lower valued asymptote. This is in contrast to the simple logistic function in which both asymptotes are approached by the curve symmetrically. It is a special case of the generalised logistic function. The function was originally designed to describe human mortality, but since has been modified to be applied in biology, with regard to detailing populations.
A Malthusian growth model, sometimes called a simple exponential growth model, is essentially exponential growth based on the idea of the function being proportional to the speed to which the function grows. The model is named after Thomas Robert Malthus, who wrote An Essay on the Principle of Population (1798), one of the earliest and most influential books on population.
A population model is a type of mathematical model that is applied to the study of population dynamics.
In aquatic toxicology, bioconcentration is the accumulation of a water-borne chemical substance in an organism exposed to the water.
John A. Miller and Stephen B. Harley zoology 4th edition