In ecology, local abundance is the relative representation of a species in a particular ecosystem. [1] It is usually measured as the number of individuals found per sample. The ratio of abundance of one species to one or multiple other species living in an ecosystem is referred to as relative species abundances. [1] Both indicators are relevant for computing biodiversity.
A variety of sampling methods are used to measure abundance. For larger animals, these may include spotlight counts, track counts and roadkill counts, as well as presence at monitoring stations. [2] In many plant communities the abundances of plant species are measured by plant cover, i.e. the relative area covered by different plant species in a small plot. [3] Abundance is in simplest terms usually measured by identifying and counting every individual of every species in a given sector. It is common for the distribution of species to be skewed so that a few species take up the bulk of individuals collected. [4]
Relative species abundance is calculated by dividing the number of species from one group by the total number of species from all groups.
These measures are all a part of community ecology. Understanding patterns within a community is easy when the community has a relatively low number of species. However most communities do not have a low number of species. [4] Measuring species abundance allows for understanding of how species are distributed within an ecosystem. [4] For example, salt water marshes have an influx of sea water, causing only a few species which are adapted to be able to survive in both salt and fresh water to be abundant. Inversely in land locked wetlands, the species abundance is more evenly distributed among the species who live within the wetland. [4]
In most ecosystems in which abundance has been calculated, most often only a small number of species are abundant, while a large number are pretty rare. [4] These abundant species are often generalists, with many rare species being specialists. [4] High density of a species in multiple localities will usually lead to it being relatively abundant over all in an ecosystem. [4] Therefore, high local abundance can be directly linked to high regional distribution. Species with high abundance are likely to have more offspring, and these offspring in turn are more likely to colonize a new sector of the ecosystem than a species which is less abundant. Thus begins a positive feedback loop leading to a species distribution in which a few "core species" are wide spread, and the other species are restricted and scarce known as satellite species. [1]
Species abundance distribution (SAD) is one of the main uses of this measurement. SAD is a measurement of how common, or rare species are within an ecosystem. [5] This allows researchers to assess how different species are distributed throughout an ecosystem. SAD is one of the most basic measurements in ecology and is used very often, therefore many different methods of measurement and analysis have developed. [5]
There are several methods for measuring abundance. An example of this is Semi-Quantitive Abundance ratings. [6] These are measurement methods which involve estimation based on viewing a specific area of a designated size. [6] The two Semi-Quantitive Abundance ratings used are known as the D.A.F.O.R, and the A.C.F.O.R. [6]
The A.C.F.O.R. scale is as follows:
D.A.F.O.R scale:
These methods are useful for getting a rough estimate of the species abundance in a designated area (quadrant), but they are not exact or objective measurements. Therefore, if another method of measuring abundance is available, it should be used, as this will lead to more useful and quantifiable data. [6]
Species diversity is the number of different species that are represented in a given community. The effective number of species refers to the number of equally abundant species needed to obtain the same mean proportional species abundance as that observed in the dataset of interest. Meanings of species diversity may include species richness, taxonomic or phylogenetic diversity, and/or species evenness. Species richness is a simple count of species. Taxonomic or phylogenetic diversity is the genetic relationship between different groups of species. Species evenness quantifies how equal the abundances of the species are.
The unified neutral theory of biodiversity and biogeography is a theory and the title of a monograph by ecologist Stephen P. Hubbell. It aims to explain the diversity and relative abundance of species in ecological communities. Like other neutral theories of ecology, Hubbell assumes that the differences between members of an ecological community of trophically similar species are "neutral", or irrelevant to their success. This implies that niche differences do not influence abundance and the abundance of each species follows a random walk. The theory has sparked controversy, and some authors consider it a more complex version of other null models that fit the data better.
Species richness is the number of different species represented in an ecological community, landscape or region. Species richness is simply a count of species, and it does not take into account the abundances of the species or their relative abundance distributions. Species richness is sometimes considered synonymous with species diversity, but the formal metric species diversity takes into account both species richness and species evenness.
Spatial ecology studies the ultimate distributional or spatial unit occupied by a species. In a particular habitat shared by several species, each of the species is usually confined to its own microhabitat or spatial niche because two species in the same general territory cannot usually occupy the same ecological niche for any significant length of time.
Leaf area index (LAI) is a dimensionless quantity that characterizes plant canopies. It is defined as the one-sided green leaf area per unit ground surface area in broadleaf canopies. In conifers, three definitions for LAI have been used:
The species–area relationship or species–area curve describes the relationship between the area of a habitat, or of part of a habitat, and the number of species found within that area. Larger areas tend to contain larger numbers of species, and empirically, the relative numbers seem to follow systematic mathematical relationships. The species–area relationship is usually constructed for a single type of organism, such as all vascular plants or all species of a specific trophic level within a particular site. It is rarely if ever, constructed for all types of organisms if simply because of the prodigious data requirements. It is related but not identical to the species discovery curve.
A diversity index is a quantitative measure that reflects how many different types there are in a dataset, and that can simultaneously take into account the phylogenetic relations among the individuals distributed among those types, such as richness, divergence or evenness. These indices are statistical representations of biodiversity in different aspects.
In ecology, alpha diversity (α-diversity) is the mean species diversity in a site at a local scale. The term was introduced by R. H. Whittaker together with the terms beta diversity (β-diversity) and gamma diversity (γ-diversity). Whittaker's idea was that the total species diversity in a landscape is determined by two different things, the mean species diversity in sites at a more local scale and the differentiation among those sites.
Species distribution, or speciesdispersion, is the manner in which a biological taxon is spatially arranged. The geographic limits of a particular taxon's distribution is its range, often represented as shaded areas on a map. Patterns of distribution change depending on the scale at which they are viewed, from the arrangement of individuals within a small family unit, to patterns within a population, or the distribution of the entire species as a whole (range). Species distribution is not to be confused with dispersal, which is the movement of individuals away from their region of origin or from a population center of high density.
A rank abundance curve or Whittaker plot is a chart used by ecologists to display relative species abundance, a component of biodiversity. It can also be used to visualize species richness and species evenness. It overcomes the shortcomings of biodiversity indices that cannot display the relative role different variables played in their calculation.
In ecology, gamma diversity (γ-diversity) is the total species diversity in a landscape. The term was introduced by R. H. Whittaker together with the terms alpha diversity (α-diversity) and beta diversity (β-diversity). Whittaker's idea was that the total species diversity in a landscape (γ) is determined by two different things, the mean species diversity in sites at a more local scale (α) and the differentiation among those sites (β). According to this reasoning, alpha diversity and beta diversity constitute independent components of gamma diversity:
In ecology, the occupancy–abundance (O–A) relationship is the relationship between the abundance of species and the size of their ranges within a region. This relationship is perhaps one of the most well-documented relationships in macroecology, and applies both intra- and interspecifically. In most cases, the O–A relationship is a positive relationship. Although an O–A relationship would be expected, given that a species colonizing a region must pass through the origin and could reach some theoretical maximum abundance and distribution, the relationship described here is somewhat more substantial, in that observed changes in range are associated with greater-than-proportional changes in abundance. Although this relationship appears to be pervasive, and has important implications for the conservation of endangered species, the mechanism(s) underlying it remain poorly understood
In ecology, rarefaction is a technique to assess species richness from the results of sampling. Rarefaction allows the calculation of species richness for a given number of individual samples, based on the construction of so-called rarefaction curves. This curve is a plot of the number of species as a function of the number of samples. Rarefaction curves generally grow rapidly at first, as the most common species are found, but the curves plateau as only the rarest species remain to be sampled.
Ecological dominance is the degree to which one or several species have a major influence controlling the other species in their ecological community or make up more of the biomass. Both the composition and abundance of species within an ecosystem can be affected by the dominant species present.
Mechanistic models for niche apportionment are biological models used to explain relative species abundance distributions. These niche apportionment models describe how species break up resource pool in multi-dimensional space, determining the distribution of abundances of individuals among species. The relative abundances of species are usually expressed as a Whittaker plot, or rank abundance plot, where species are ranked by number of individuals on the x-axis, plotted against the log relative abundance of each species on the y-axis. The relative abundance can be measured as the relative number of individuals within species or the relative biomass of individuals within species.
Relative species abundance is a component of biodiversity and is a measure of how common or rare a species is relative to other species in a defined location or community. Relative abundance is the percent composition of an organism of a particular kind relative to the total number of organisms in the area. Relative species abundances tend to conform to specific patterns that are among the best-known and most-studied patterns in macroecology. Different populations in a community exist in relative proportions; this idea is known as relative abundance.
Plant ecology is a subdiscipline of ecology that studies the distribution and abundance of plants, the effects of environmental factors upon the abundance of plants, and the interactions among plants and between plants and other organisms. Examples of these are the distribution of temperate deciduous forests in North America, the effects of drought or flooding upon plant survival, and competition among desert plants for water, or effects of herds of grazing animals upon the composition of grasslands.
Conservation biologists have designed a variety of objective means to empirically measure biodiversity. Each measure of biodiversity relates to a particular use of the data. For practical conservationists, measurements should include a quantification of values that are commonly shared among locally affected organisms, including humans. For others, a more economically defensible definition should allow the ensuring of continued possibilities for both adaptation and future use by humans, assuring environmental sustainability.
The abundances of plant species are often measured by plant cover, which is the relative area covered by different plant species in a small plot. Plant cover is not biased by the size and distributions of individuals, and is an important and often measured characteristic of the composition of plant communities.
Rare biosphere refers to a large number of rare species of microbial life, i.e. bacteria, archaea and fungi, that can be found in very low concentrations in an environment.