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Biological dispersal refers to both the movement of individuals (animals, plants, fungi, bacteria, etc.) from their birth site to their breeding site ('natal dispersal') and the movement from one breeding site to another ('breeding dispersal'). Dispersal is also used to describe the movement of propagules such as seeds and spores. Technically, dispersal is defined as any movement that has the potential to lead to gene flow. [1] The act of dispersal involves three phases: departure, transfer, and settlement. There are different fitness costs and benefits associated with each of these phases. [2] Through simply moving from one habitat patch to another, the dispersal of an individual has consequences not only for individual fitness, but also for population dynamics, population genetics, and species distribution. [3] [4] [5] Understanding dispersal and the consequences, both for evolutionary strategies at a species level and for processes at an ecosystem level, requires understanding on the type of dispersal, the dispersal range of a given species, and the dispersal mechanisms involved. Biological dispersal can be correlated to population density. The range of variations of a species' location determines the expansion range. [6]
Biological dispersal may be contrasted with geodispersal, which is the mixing of previously isolated populations (or whole biotas) following the erosion of geographic barriers to dispersal or gene flow. [7] [8] [9]
Dispersal can be distinguished from animal migration (typically round-trip seasonal movement), although within population genetics, the terms 'migration' and 'dispersal' are often used interchangeably.
Furthermore, biological dispersal is impacted and limited by different environmental and individual conditions. [10] This leads to a wide range of consequences on the organisms present in the environment and their ability to adapt their dispersal methods to that environment.
Some organisms are motile throughout their lives, but others are adapted to move or be moved at precise, limited phases of their life cycles. This is commonly called the dispersive phase of the life cycle. The strategies of organisms' entire life cycles often are predicated on the nature and circumstances of their dispersive phases.
In general, there are two basic types:
Due to population density, dispersal may relieve pressure for resources in an ecosystem, and competition for these resources may be a selection factor for dispersal mechanisms. Dispersal of organisms is a critical process for understanding both geographic isolation in evolution through gene flow and the broad patterns of current geographic distributions (biogeography).
A distinction is often made between natal dispersal where an individual (often a juvenile) moves away from the place it was born, and breeding dispersal where an individual (often an adult) moves away from one breeding location to breed elsewhere.
In the broadest sense, dispersal occurs when the fitness benefits of moving outweigh the costs.
There are a number of benefits to dispersal such as locating new resources, escaping unfavorable conditions, avoiding competing with siblings, and avoiding breeding with closely related individuals which could lead to inbreeding depression. [12]
There are also a number of costs associated with dispersal, which can be thought of in terms of four main currencies: energy, risk, time, and opportunity. [2] Energetic costs include the extra energy required to move as well as energetic investment in movement machinery (e.g. wings). Risks include increased injury and mortality during dispersal and the possibility of settling in an unfavorable environment. Time spent dispersing is time that often cannot be spent on other activities such as growth and reproduction. Finally, dispersal can also lead to outbreeding depression if an individual is better adapted to its natal environment than the one it ends up in. In social animals (such as many birds and mammals) a dispersing individual must find and join a new group, which can lead to loss of social rank. [2]
"Dispersal range" refers to the distance a species can move from an existing population or the parent organism. An ecosystem depends critically on the ability of individuals and populations to disperse from one habitat patch to another. Therefore, biological dispersal is critical to the stability of ecosystems.
Urban areas can be seen to have their own unique effects on the dispersal range and dispersal abilities of different organisms. For plant species, urban environments largely provide novel dispersal vectors. While animals and physical factors (i.e. wind, water, etc) have played a role in dispersal for centuries, motor vehicles have recently been considered as major dispersal vectors. Tunnels that connect rural and urban environments have been shown to expedite a large amount of and diverse set of seeds from urban to rural environments. This could lead to possible sources of invasive species on the urban-rural gradient. [13] Another example of the effects of urbanization could be seen next to rivers. Urbanization has led to the introduction of different invasive species through direct planting or wind dispersal. In turn, rivers next to these invasive plant species have become vital dispersal vectors. Rivers could be seen to connect urban centers to rural and natural environments. Seeds from the invasive species were shown to be transported by the rivers to natural areas located downstream, thus building upon the already established dispersal distance of the plant. [14]
In contrast, urban environments can also provide limitations for certain dispersal strategies. Human influence through urbanization greatly affects the layout of landscapes, which leads to the limitation of dispersal strategies for many organisms. These changes have largely been exhibited through pollinator-flowering plant relationships. As the pollinator's optimal range of survival is limited, it leads to a limited supply of pollination sites. Subsequently, this leads to less gene flow between distantly separated populations, in turn decreasing the genetic diversity of each of the areas. [15] Likewise, urbanization has been shown to impact the gene flow of distinctly different species (ex. mice and bats) in similar ways. While these two species may have different ecological niches and living strategies, urbanization limits the dispersal strategies of both species. This leads to genetic isolation of both populations, resulting in limited gene flow. While the urbanization did have a greater effect on mice dispersal, it also led to a slight increase in inbreeding among bat populations. [16]
Few species are ever evenly or randomly distributed within or across landscapes. In general, species significantly vary across the landscape in association with environmental features that influence their reproductive success and population persistence. [17] [18] Spatial patterns in environmental features (e.g. resources) permit individuals to escape unfavorable conditions and seek out new locations. [19] This allows the organism to "test" new environments for their suitability, provided they are within animal's geographic range. In addition, the ability of a species to disperse over a gradually changing environment could enable a population to survive extreme conditions. (i.e. climate change).
As the climate changes, prey and predators have to adapt to survive. This poses a problem for many animals, for example, the Southern Rockhopper Penguins. [20] These penguins are able to live and thrive in a variety of climates due to the penguins' phenotypic plasticity. [21] However, they are predicted to respond by dispersal, not adaptation this time. [21] This is explained due to their long life spans and slow microevolution. Penguins in the subantarctic have very different foraging behavior from those of subtropical waters; it would be very hard to survive by keeping up with the fast-changing climate because these behaviors took years to shape. [20]
A dispersal barrier may result in a dispersal range of a species much smaller than the species distribution. An artificial example is habitat fragmentation due to human land use. By contrast, natural barriers to dispersal that limit species distribution include mountain ranges and rivers. An example is the separation of the ranges of the two species of chimpanzee by the Congo River.
On the other hand, human activities may also expand the dispersal range of a species by providing new dispersal methods (e.g., ballast water from ships). Many such dispersed species become invasive, like rats or stinkbugs, but some species also have a slightly positive effect to human settlers like honeybees and earthworms. [22]
Most animals are capable of locomotion and the basic mechanism of dispersal is movement from one place to another. Locomotion allows the organism to "test" new environments for their suitability, provided they are within the animal's range. Movements are usually guided by inherited behaviors.
The formation of barriers to dispersal or gene flow between adjacent areas can isolate populations on either side of the emerging divide. The geographic separation and subsequent genetic isolation of portions of an ancestral population can result in allopatric speciation.
Seed dispersal is the movement or transport of seeds away from the parent plant. Plants are limited by vegetative reproduction and consequently rely upon a variety of dispersal vectors to transport their propagules, including both abiotic and biotic vectors. Seeds can be dispersed away from the parent plant individually or collectively, as well as dispersed in both space and time. The patterns of seed dispersal are determined in large part by the specific dispersal mechanism, and this has important implications for the demographic and genetic structure of plant populations, as well as migration patterns and species interactions. There are five main modes of seed dispersal: gravity, wind, ballistic, water, and by animals.
There are numerous animal forms that are non-motile, such as sponges, bryozoans, tunicates, sea anemones, corals, and oysters. In common, they are all either marine or aquatic. It may seem curious that plants have been so successful at stationary life on land, while animals have not, but the answer lies in the food supply. Plants produce their own food from sunlight and carbon dioxide—both generally more abundant on land than in water. Animals fixed in place must rely on the surrounding medium to bring food at least close enough to grab, and this occurs in the three-dimensional water environment, but with much less abundance in the atmosphere.
All of the marine and aquatic invertebrates whose lives are spent fixed to the bottom (more or less; anemones are capable of getting up and moving to a new location if conditions warrant) produce dispersal units. These may be specialized "buds", or motile sexual reproduction products, or even a sort of alteration of generations as in certain cnidaria.
Corals provide a good example of how sedentary species achieve dispersion. Broadcast spawning corals reproduce by releasing sperm and eggs directly into the water. These release events are coordinated by the lunar phase in certain warm months, such that all corals of one or many species on a given reef will be released on the same single or several consecutive nights. The released eggs are fertilized, and the resulting zygote develops quickly into a multicellular planula . This motile stage then attempts to find a suitable substratum for settlement. Most are unsuccessful and die or are fed upon by zooplankton and bottom-dwelling predators such as anemones and other corals. However, untold millions are produced, and a few do succeed in locating spots of bare limestone, where they settle and transform by growth into a polyp. All things being favorable, the single polyp grows into a coral head by budding off new polyps to form a colony.
The majority of animals are motile. Motile animals can disperse themselves by their spontaneous and independent locomotive powers. For example, dispersal distances across bird species depend on their flight capabilities. [23] On the other hand, small animals utilize the existing kinetic energies in the environment, resulting in passive movement. Dispersal by water currents is especially associated with the physically small inhabitants of marine waters known as zooplankton. The term plankton comes from the Greek, πλαγκτον, meaning "wanderer" or "drifter".
Many animal species, especially freshwater invertebrates, are able to disperse by wind or by transfer with an aid of larger animals (birds, mammals or fishes) as dormant eggs, dormant embryos or, in some cases, dormant adult stages. Tardigrades, some rotifers and some copepods are able to withstand desiccation as adult dormant stages. Many other taxa (Cladocera, Bryozoa, Hydra, Copepoda and so on) can disperse as dormant eggs or embryos. Freshwater sponges usually have special dormant propagules called gemmulae for such a dispersal. Many kinds of dispersal dormant stages are able to withstand not only desiccation and low and high temperature, but also action of digestive enzymes during their transfer through digestive tracts of birds and other animals, high concentration of salts, and many kinds of toxicants. Such dormant-resistant stages made possible the long-distance dispersal from one water body to another and broad distribution ranges of many freshwater animals.
Dispersal is most commonly quantified either in terms of rate or distance.
Dispersal rate (also called migration rate in the population genetics literature) or probability describes the probability that any individual leaves an area or, equivalently, the expected proportion of individual to leave an area.
The dispersal distance is usually described by a dispersal kernel which gives the probability distribution of the distance traveled by any individual. A number of different functions are used for dispersal kernels in theoretical models of dispersal including the negative exponential distribution, [24] extended negative exponential distribution, [24] normal distribution, [24] exponential power distribution, [25] inverse power distribution, [24] and the two-sided power distribution. [26] The inverse power distribution and distributions with 'fat tails' representing long-distance dispersal events (called leptokurtic distributions) are thought to best match empirical dispersal data. [24] [27]
Dispersal not only has costs and benefits to the dispersing individual (as mentioned above), it also has consequences at the level of the population and species on both ecological and evolutionary timescales. Organisms can be dispersed through multiple methods. Carrying through animals is especially effective as it allows traveling of far distances. Many plants depend on this to be able to go to new locations, preferably with conditions ideal for precreation and germination. With this, dispersal has major influence in the determination of population and spread of plant species. [28]
Many populations have patchy spatial distributions where separate yet interacting sub-populations occupy discrete habitat patches (see metapopulations). Dispersing individuals move between different sub-populations which increases the overall connectivity of the metapopulation and can lower the risk of stochastic extinction. If a sub-population goes extinct by chance, it is more likely to be recolonized if the dispersal rate is high. Increased connectivity can also decrease the degree of local adaptation.
Human interference with the environment has been seen to have an effect on dispersal. Some of these occurrences have been accidents, like in the case of zebra mussels, which are indigenous to Southeast Russia. A ship had accidentally released them into the North American Great Lakes and they became a major nuisance in the area, as they began to clog water treatment and power plants. Another case of this was seen in Chinese bighead and silver carp, which were brought in with the purpose of algae control in many catfish ponds across the U.S. Unfortunately, some had managed to escape into the neighboring rivers of Mississippi, Missouri, Illinois, and Ohio, eventually causing a negative impact for the surrounding ecosystems. [11] However, human-created habitats such as urban environments have allowed certain migrated species to become urbanophiles or synanthropes. [29]
Dispersal has caused changes to many species on a genetic level. A positive correlation has been seen for differentiation and diversification of certain species of spiders in the Canary Islands. These spiders were residing in archipelagos and islands. Dispersion was identified as a key factor in the rate of both occurrences. [30]
Human impact has had a major influence on the movement of animals through time. An environmental response occurs in due to this, as dispersal patterns are important for species to survive major changes. There are two forms of human-mediated dispersal:
Long-distance dispersals are observed when seeds are carried through human vectors. A study was conducted to test the effects of human-mediated dispersal of seeds over long distances in two species of Brassica in England. The main methods of dispersal compared with movement by wind versus movement by attachment to outerwear. It was concluded that shoes were able to transport seeds to further distances than what would be achievable through wind alone. It was noted that some seeds were able to stay on the shoes for long periods of time, about 8 hours of walking, but evenly came off. Due to this, the seeds were able to travel far distances and settle into new areas, where they were previously not inhabiting. However, it is also important that the seeds land in places where they are able to stick and grow. Specific shoe size did not seem to have an effect on prevalence. [32]
Biological dispersal can be observed using different methods. To study the effects of dispersal, observers use the methods of landscape genetics. [33] This allows scientists to observe the difference between population variation, climate and well as the size and shape of the landscape. An example of the use of landscape genetics as a means to study seed dispersal, for example, involves studying the effects of traffic using motorway tunnels between inner cities and suburban area. [34]
Genome wide SNP dataset and species distribution modelling are examples of computational methods used to examine different dispersal modes. [33] A genome-wide SNP dataset can be used to determine the genomic and demographic history within the range of collection or observation [Reference needed]. Species distribution models are used when scientists wish to determine which region is best suited for the species under observation [Reference needed]. Methods such as these are used to understand the criteria the environment provides when migration and settlement occurs such as the cases in biological invasion.
Human-aided dispersal, an example of an anthropogenic effect, can contribute to biological dispersal ranges and variations. [35]
Informed dispersal is a way to observe the cues of biological dispersal suggesting the reasoning behind the placement. [36] This concept implies that the movement between species also involve information transfer. Methods such as GPS location are used to monitor the social cues and mobility of species regarding habitat selection. [37] GPS radio-collars can be used when collecting data on social animals such a meerkats. [38] Consensus data such as detailed trip records and point of interest (POI) data can be used to predict the movement of humans from rural to urban areas are examples of informed dispersal [Reference needed].
Direct tracking or visual tracking allows scientists to monitor the movement of seed dispersal by color coding. [14] Scientists and observers can track the migration of individuals through the landscape. The pattern of transportation can then be visualized to reflect the range in which the organism expands.
Urban ecology is the scientific study of the relation of living organisms with each other and their surroundings in an urban environment. An urban environment refers to environments dominated by high-density residential and commercial buildings, paved surfaces, and other urban-related factors that create a unique landscape. The goal of urban ecology is to achieve a balance between human culture and the natural environment.
In population genetics, gene flow is the transfer of genetic material from one population to another. If the rate of gene flow is high enough, then two populations will have equivalent allele frequencies and therefore can be considered a single effective population. It has been shown that it takes only "one migrant per generation" to prevent populations from diverging due to drift. Populations can diverge due to selection even when they are exchanging alleles, if the selection pressure is strong enough. Gene flow is an important mechanism for transferring genetic diversity among populations. Migrants change the distribution of genetic diversity among populations, by modifying allele frequencies. High rates of gene flow can reduce the genetic differentiation between the two groups, increasing homogeneity. For this reason, gene flow has been thought to constrain speciation and prevent range expansion by combining the gene pools of the groups, thus preventing the development of differences in genetic variation that would have led to differentiation and adaptation. In some cases dispersal resulting in gene flow may also result in the addition of novel genetic variants under positive selection to the gene pool of a species or population
In spermatophyte plants, seed dispersal is the movement, spread or transport of seeds away from the parent plant. Plants have limited mobility and rely upon a variety of dispersal vectors to transport their seeds, including both abiotic vectors, such as the wind, and living (biotic) vectors such as birds. Seeds can be dispersed away from the parent plant individually or collectively, as well as dispersed in both space and time. The patterns of seed dispersal are determined in large part by the dispersal mechanism and this has important implications for the demographic and genetic structure of plant populations, as well as migration patterns and species interactions. There are five main modes of seed dispersal: gravity, wind, ballistic, water, and by animals. Some plants are serotinous and only disperse their seeds in response to an environmental stimulus. These modes are typically inferred based on adaptations, such as wings or fleshy fruit. However, this simplified view may ignore complexity in dispersal. Plants can disperse via modes without possessing the typical associated adaptations and plant traits may be multifunctional.
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.
Colonisation or colonization is the spread and development of an organism in a new area or habitat. Colonization comprises the physical arrival of a species in a new area, but also its successful establishment within the local community. In ecology, it is represented by the symbol λ to denote the long-term intrinsic growth rate of a population.
Myrmecochory ( ; from Ancient Greek: μύρμηξ, romanized: mýrmēks and χορεία khoreíā is seed dispersal by ants, an ecologically significant ant–plant interaction with worldwide distribution. Most myrmecochorous plants produce seeds with elaiosomes, a term encompassing various external appendages or "food bodies" rich in lipids, amino acids, or other nutrients that are attractive to ants. The seed with its attached elaiosome is collectively known as a diaspore. Seed dispersal by ants is typically accomplished when foraging workers carry diaspores back to the ant colony, after which the elaiosome is removed or fed directly to ant larvae. Once the elaiosome is consumed, the seed is usually discarded in underground middens or ejected from the nest. Although diaspores are seldom distributed far from the parent plant, myrmecochores also benefit from this predominantly mutualistic interaction through dispersal to favourable locations for germination, as well as escape from seed predation.
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.
In landscape ecology, landscape connectivity is, broadly, "the degree to which the landscape facilitates or impedes movement among resource patches". Alternatively, connectivity may be a continuous property of the landscape and independent of patches and paths. Connectivity includes both structural connectivity and functional connectivity. Functional connectivity includes actual connectivity and potential connectivity in which movement paths are estimated using the life-history data.
Revegetation is the process of replanting and rebuilding the soil of disturbed land. This may be a natural process produced by plant colonization and succession, manmade rewilding projects, accelerated process designed to repair damage to a landscape due to wildfire, mining, flood, or other cause. Originally the process was simply one of applying seed and fertilizer to disturbed lands, usually grasses or clover. The fibrous root network of grasses is useful for short-term erosion control, particularly on sloping ground. Establishing long-term plant communities requires forethought as to appropriate species for the climate, size of stock required, and impact of replanted vegetation on local fauna. The motivations behind revegetation are diverse, answering needs that are both technical and aesthetic, but it is usually erosion prevention that is the primary reason. Revegetation helps prevent soil erosion, enhances the ability of the soil to absorb more water in significant rain events, and in conjunction reduces turbidity dramatically in adjoining bodies of water. Revegetation also aids protection of engineered grades and other earthworks.
Source–sink dynamics is a theoretical model used by ecologists to describe how variation in habitat quality may affect the population growth or decline of organisms.
A wildlife corridor, also known as a habitat corridor, or green corridor, is an designated area that connects wildlife populations that have been separated by human activities or structures, such as development, roads, or land clearings. These corridors enable movement of individuals between populations, which helps to prevent negative effects of inbreeding and reduced genetic diversity, often caused by genetic drift, that can occur in isolated populations. Additionally, corridors support the re-establishment of populations that may have been reduced or wiped out due to random events like fires or disease. They can also mitigate some of the severe impacts of habitat fragmentation, a result of urbanization that divides habitat areas and restricts animal movement. Habitat fragmentation from human development poses an increasing threat to biodiversity, and habitat corridors help to reduce its harmful effects.
A genetic isolate is a population of organisms that has little to no genetic mixing with other organisms of the same species due to geographic isolation or other factors that prevent reproduction. Genetic isolates form new species through an evolutionary process known as speciation. All modern species diversity is a product of genetic isolates and evolution.
Defaunation is the global, local, or functional extinction of animal populations or species from ecological communities. The growth of the human population, combined with advances in harvesting technologies, has led to more intense and efficient exploitation of the environment. This has resulted in the depletion of large vertebrates from ecological communities, creating what has been termed "empty forest". Defaunation differs from extinction; it includes both the disappearance of species and declines in abundance. Defaunation effects were first implied at the Symposium of Plant-Animal Interactions at the University of Campinas, Brazil in 1988 in the context of Neotropical forests. Since then, the term has gained broader usage in conservation biology as a global phenomenon.
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.
A dispersal vector is an agent of biological dispersal that moves a dispersal unit, or organism, away from its birth population to another location or population in which the individual will reproduce. These dispersal units can range from pollen to seeds to fungi to entire organisms.
Forest migration is the movement of large seed plant dominated communities in geographical space over time.
Microbial biogeography is a subset of biogeography, a field that concerns the distribution of organisms across space and time. Although biogeography traditionally focused on plants and larger animals, recent studies have broadened this field to include distribution patterns of microorganisms. This extension of biogeography to smaller scales—known as "microbial biogeography"—is enabled by ongoing advances in genetic technologies.
Ran Nathan is an Israeli biologist, ornithologist, and academic.
Diplochory, also known as “secondary dispersal”, “indirect dispersal” or "two-phase dispersal", is a seed dispersal mechanism in which a plant's seed is moved sequentially by more than one dispersal mechanism or vector. The significance of the multiple dispersal steps on the plant fitness and population dynamics depends on the type of dispersers involved. In many cases, secondary seed dispersal by invertebrates or rodents moves seeds over a relatively short distance and a large proportion of the seeds may be lost to seed predation within this step. Longer dispersal distances and potentially larger ecological consequences follow from sequential endochory by two different animals, i.e. diploendozoochory: a primary disperser that initially consumes the seed, and a secondary, carnivorous animal that kills and eats the primary consumer along with the seeds in the prey's digestive tract, and then transports the seed further in its own digestive tract.
Migration, in ecology, is the large-scale movement of members of a species to a different environment. Migration is a natural behavior and component of the life cycle of many species of mobile organisms, not limited to animals, though animal migration is the best known type. Migration is often cyclical, frequently occurring on a seasonal basis, and in some cases on a daily basis. Species migrate to take advantage of more favorable conditions with respect to food availability, safety from predation, mating opportunity, or other environmental factors.