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Neutral theory, in ecology, treats all species as if they had the same per capita rates of birth and
death, dispersal, and even speciation. Although this assumption is only a first approximation, neutral
theories in ecology are useful in formulating and testing null hypotheses about how communities and
ecosystems are assembled in landscapes. Recently, neutral theory has been given attention following
the publication of The Unified Neutral theory of biodiversity and Biogeography by Stephen P. Hubbell
(2001). Hubbell went beyond the null hypothesis view to Suggest that neutral theory might actually
give a better explanation for many landscape-level ecological patterns than does current ecological
theory.
Explanation
The neutral theory of biodiversity and biogeography Hubbell (2001) is a
generalization and extension of theory of island biogeography
(MacArthur and Wilson 1967). It is termed neutral theory because all
species are treated as having identical vital rates on a per capita basis
(the same birth and death rates, the same rate of dispersal, and the
same rate of speciation).
Neural theory applies to communities of organism that are the same trophic level and
that compete for the same or similar limiting resources. The theory is derived by
assuming that the dynamics of communities are a zero-sum game for limiting resources
– that is, no species can increase in abundance or biomass without a matching decrease
in the collection abundance or biomass of all other competing species. Neutral theory
assumes that species are largely substitutable in their use of limiting resources, so that
if one species happens to be absents from a community, other species will fully use the
resources freed up by its absence.
https://youtu.be/nPXfLkvnPpo
6. TEMPORAL AND SPATIAL SCALE
Just as the size and quality of landscape patches and corridors (amount of
vegetative cover and food quality, (for example) affect ecological processes and
plant and animal abundances, the geometry and configuration of landscape
elements affect ecological processes at the population and community levels. It
is now widely recognized that the size and shape of landscape patches influence
biotic diversity, home range size and Shape, animal dispersal behavior, and
species abundance.
Recent investigations have a addressed the role that landscape geometry
plays in plant and animal survivorship, Source-sink dynamics, rates of
species invasion, and edge-habitat dynamics. Future investigations need to
address the role of landscape geometry (the study of the shapes, patterns,
and configurations of landscape elements) and landscape architecture
(patch stratification, "soft versus hard" edges, and three-dimensional use of
habitat space) t ecologists are to more fully understand such phenomena
as dispersal behavior. Patterns of animal movement, bioenergetics at the
landscape scale, and ecosystem-landscape sustainability.
Explanation
Civilization seems to reach its most intense development in what was originally
forest and grassland, especially in temperate regions Consequently, most
temperate forests and grasslands have been greatly modified from their
primeval condition, but the basic nature of these ecosystems has by no means
changed Humans, in tact, tend to combine features of both grasslands and
forests into habitats that might be term forest edge.
A forest edge may be defined as at ecotone between forest and grass shrub
communities When humans settle in grassland regions, we plant trees around
our homes, villages, and farms, so that small patches of forest become dispersed
what may have been treeless country Likewise, when human is settle in a forest,
we replace most of it with grasslands and croplands (as lesser amounts of
human force can be obtained from a forest), but leave patches of the original
forest on farms are around residential areas.
AGROECOSYSTEM AND AGROLANDSCAPE