Hybrid swarm

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A red-bellied paradise flycatcher (Terpsiphone rufiventer) found in the gallery forests of Abuko, The Gambia (where many of the T. rufiventer are part of a hybrid swarm with T. viridis). Flickr - Rainbirder - Red-bellied Paradise Flycatcher (Terpsiphone rufiventer) male.jpg
A red-bellied paradise flycatcher (Terpsiphone rufiventer) found in the gallery forests of Abuko, The Gambia (where many of the T. rufiventer are part of a hybrid swarm with T. viridis).

A hybrid swarm is a population of hybrids that has survived beyond the initial hybrid generation, with interbreeding between hybrid individuals and backcrossing with its parent types. Such population are highly variable, with the genetic and phenotypic characteristics of individuals ranging widely between the two parent types. [1] Hybrid swarms thus blur the boundary between the parent taxa. Precise definitions of which populations can be classified as hybrid swarms vary, with some specifying simply that all members of a population should be hybrids, while others differ in whether all members should have the same or different levels of hybridization. [2]

Contents

Hybrid swarms occur when the hybrid is viable and at least as vigorous as its parent types; and there are no barriers to crossbreeding between the hybrid and parent types. Swarms cannot occur if one of these conditions is not met: if the hybrid type has low viability, the hybrid population cannot maintain itself except by further hybridisation of the parent types, resulting in a hybrid population of low variability. On the other hand, if hybrids are vigorous but cannot backcross with parent populations, the result is hybrid speciation, which, aside from the contribution of new hybrids, evolves independently of its parent types. In either situation, it is possible for the hybrid population to overtake the parent populations. [3] In some cases, this can even occur within the span of just a few generations. [3] If the hybrid species has the greater viability, they can simply outcompete the parent species for resources, resulting in competitive exclusion, whereas if the parent species has the greater viability, gene flow between the two populations can result in decreased genetic variation. [3]

Hybrid swarms form within hybrid zones, an area where two similar species come into contact and hybridize. [4] [5] These develop as a result of secondary contact between the parent species. [4] After a long period of geographic isolation, the cause of which may be either natural or man-made, the reoccurrence of the parent species in the same environment can lead to interbreeding, hybridization, and potentially, a hybrid swarm. [4] [6] Hybrid swarms can lead to introgressive hybridization, or introgression, in which there is gene flow from the hybrid gene pool to the parental gene pool, or vice versa, occurring due to backcrossing between the populations. [6] When introgression has occurred, there will be a high level of diversity in alleles near the vicinity of the hybrid swarm. [7]

Examples

In plants, it is possible for a hybrid swarm to form between self-pollinating and outcrossing species. [8] One such example is hybridization between the self-pollinating wood aven and the mostly outcrossing water aven in the UK. [8] In one study of a young hybrid swarm of these two species, the population was found to be composed of the parent species, F1 generation offspring, and backcrosses with the water aven, but no backcrosses with the wood aven and no F2 generation, which would result from self-pollinating F1s. [8]

Hybrid swarms can also form between domestic and wild species, with one study proposing that wild rice is a hybrid swarm that has genetically mixed with domesticated rice. [9]

Invasive species

Hybrid swarms can pose a significant threat to an ecosystem when they involve invasive species, as invasive hybrids are frequently able to easily outcompete native species. [10] As with other hybrid swarms, the hybrid genotypes may be more or less fit than the parent genotypes. In the event of a particular hybrid genotype having the greatest fitness, not only the native parent species, but also the exotic parent species may be outcompeted. [10] On the other hand, if there is not one dominant genotype but rather trade-offs between different hybrid genotypes, a high degree of variability will occur between the hybrids, native species, and exotic species. [10]

One example of an invasive hybrid swarm occurs among shiners in the upper Coosa River. [11] A hybrid swarm was formed between the blacktail shiner, a species native to the river, and the red shiner, an invasive species. [11] The population has expanded its range over time, moving both downstream and upstream while the proportion of hybrid individuals in the system is increasing. [11] In addition, the size of the hybrid swarm has experienced a great degree of flux, experiencing alternating growth and decline over time. [11]

See also

Related Research Articles

<span class="mw-page-title-main">Hybrid (biology)</span> Offspring of cross-species reproduction

In biology, a hybrid is the offspring resulting from combining the qualities of two organisms of different varieties, species or genera through sexual reproduction. Generally, it means that each cell has genetic material from two different organisms, whereas an individual where some cells are derived from a different organism is called a chimera. Hybrids are not always intermediates between their parents, but can show hybrid vigor, sometimes growing larger or taller than either parent. The concept of a hybrid is interpreted differently in animal and plant breeding, where there is interest in the individual parentage. In genetics, attention is focused on the numbers of chromosomes. In taxonomy, a key question is how closely related the parent species are.

<span class="mw-page-title-main">Gene flow</span> Transfer of genetic variation from one population to another

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

Backcrossing is a crossing of a hybrid with one of its parents or an individual genetically similar to its parent, to achieve offspring with a genetic identity closer to that of the parent. It is used in horticulture, animal breeding, and production of gene knockout organisms.

<span class="mw-page-title-main">Sympatry</span> Biological concept

In biology, two related species or populations are considered sympatric when they exist in the same geographic area and thus frequently encounter one another. An initially interbreeding population that splits into two or more distinct species sharing a common range exemplifies sympatric speciation. Such speciation may be a product of reproductive isolation – which prevents hybrid offspring from being viable or able to reproduce, thereby reducing gene flow – that results in genetic divergence. Sympatric speciation may, but need not, arise through secondary contact, which refers to speciation or divergence in allopatry followed by range expansions leading to an area of sympatry. Sympatric species or taxa in secondary contact may or may not interbreed.

Inbreeding depression is the reduced biological fitness which has the potential to result from inbreeding. Biological fitness refers to an organism's ability to survive and perpetuate its genetic material. Inbreeding depression is often the result of a population bottleneck. In general, the higher the genetic variation or gene pool within a breeding population, the less likely it is to suffer from inbreeding depression, though inbreeding and outbreeding depression can simultaneously occur.

In biology, outbreeding depression happens when crosses between two genetically distant groups or populations result in a reduction of fitness. The concept is in contrast to inbreeding depression, although the two effects can occur simultaneously. Outbreeding depression is a risk that sometimes limits the potential for genetic rescue or augmentations. It is considered postzygotic response because outbreeding depression is noted usually in the performance of the progeny.

<i>Crepis</i> Genus of flowering plants in the family Asteraceae

Crepis, commonly known in some parts of the world as hawksbeard or hawk's-beard, is a genus of annual and perennial flowering plants of the family Asteraceae superficially resembling the dandelion, the most conspicuous difference being that Crepis usually has branching scapes with multiple heads. The genus name Crepis derives from the Greek krepis, meaning "slipper" or "sandal", possibly in reference to the shape of the fruit.

<span class="mw-page-title-main">Introgression</span> Transfer of genetic material from one species to another

Introgression, also known as introgressive hybridization, in genetics is the transfer of genetic material from one species into the gene pool of another by the repeated backcrossing of an interspecific hybrid with one of its parent species. Introgression is a long-term process, even when artificial; it may take many hybrid generations before significant backcrossing occurs. This process is distinct from most forms of gene flow in that it occurs between two populations of different species, rather than two populations of the same species.

Allogamy or cross-fertilization is the fertilization of an ovum from one individual with the spermatozoa of another. By contrast, autogamy is the term used for self-fertilization. In humans, the fertilization event is an instance of allogamy. Self-fertilization occurs in hermaphroditic organisms where the two gametes fused in fertilization come from the same individual. This is common in plants and certain protozoans.

<span class="mw-page-title-main">Hybrid zone</span>

A hybrid zone exists where the ranges of two interbreeding species or diverged intraspecific lineages meet and cross-fertilize. Hybrid zones can form in situ due to the evolution of a new lineage but generally they result from secondary contact of the parental forms after a period of geographic isolation, which allowed their differentiation. Hybrid zones are useful in studying the genetics of speciation as they can provide natural examples of differentiation and (sometimes) gene flow between populations that are at some point between representing a single species and representing multiple species in reproductive isolation.

The mechanisms of reproductive isolation are a collection of evolutionary mechanisms, behaviors and physiological processes critical for speciation. They prevent members of different species from producing offspring, or ensure that any offspring are sterile. These barriers maintain the integrity of a species by reducing gene flow between related species.

<span class="mw-page-title-main">Hybrid speciation</span> Form of speciation involving hybridization between two different species

Hybrid speciation is a form of speciation where hybridization between two different species leads to a new species, reproductively isolated from the parent species. Previously, reproductive isolation between two species and their parents was thought to be particularly difficult to achieve, and thus hybrid species were thought to be very rare. With DNA analysis becoming more accessible in the 1990s, hybrid speciation has been shown to be a somewhat common phenomenon, particularly in plants. In botanical nomenclature, a hybrid species is also called a nothospecies. Hybrid species are by their nature polyphyletic.

<span class="mw-page-title-main">Genetic pollution</span> Problematic gene flow ⇨ wild populations

Genetic pollution is a term for uncontrolled gene flow into wild populations. It is defined as "the dispersal of contaminated altered genes from genetically engineered organisms to natural organisms, esp. by cross-pollination", but has come to be used in some broader ways. It is related to the population genetics concept of gene flow, and genetic rescue, which is genetic material intentionally introduced to increase the fitness of a population. It is called genetic pollution when it negatively impacts the fitness of a population, such as through outbreeding depression and the introduction of unwanted phenotypes which can lead to extinction.

<span class="mw-page-title-main">Bateson–Dobzhansky–Muller model</span> Model of the evolution of genetic incompatibility

The Bateson–Dobzhansky–Muller model, also known as Dobzhansky–Muller model, is a model of the evolution of genetic incompatibility, important in understanding the evolution of reproductive isolation during speciation and the role of natural selection in bringing it about. The theory was first described by William Bateson in 1909, then independently described by Theodosius Dobzhansky in 1934, and later elaborated in different forms by Herman Muller, H. Allen Orr and Sergey Gavrilets.

Hybrizyme is a term coined to indicate novel or normally rare gene variants that are associated with hybrid zones, geographic areas where two related taxa meet, mate, and produce hybrid offspring. The hybrizyme phenomenon is widespread and these alleles occur commonly, if not in all hybrid zones. Initially considered to be caused by elevated rates of mutation in hybrids, the most probable hypothesis infers that they are the result of negative (purifying) selection. Namely, in the center of the hybrid zone, negative selection purges alleles against hybrid disadvantage. Stated differently, any allele that will decrease reproductive isolation is favored and any linked alleles also increase their frequency by genetic hitchhiking. If the linked alleles used to be rare variants in the parental taxa, they will become more common in the area where the hybrids are formed.

<span class="mw-page-title-main">Hybridogenesis in water frogs</span>

The fertile hybrids of European water frogs reproduce by hybridogenesis (hemiclonally). This means that during gametogenesis, they discard the genome of one of the parental species and produce gametes of the other parental species. The first parental genome is restored by fertilization of these gametes with gametes from the first species. In all-hybrid populations of the edible frog Pelophylax kl. esculentus, however, triploid hybrids provide this missing genome.

Eukaryote hybrid genomes result from interspecific hybridization, where closely related species mate and produce offspring with admixed genomes. The advent of large-scale genomic sequencing has shown that hybridization is common, and that it may represent an important source of novel variation. Although most interspecific hybrids are sterile or less fit than their parents, some may survive and reproduce, enabling the transfer of adaptive variants across the species boundary, and even result in the formation of novel evolutionary lineages. There are two main variants of hybrid species genomes: allopolyploid, which have one full chromosome set from each parent species, and homoploid, which are a mosaic of the parent species genomes with no increase in chromosome number.

<span class="mw-page-title-main">Introgressive hybridization in plants</span>

Introgressive hybridization, also known as introgression, is the flow of genetic material between divergent lineages via repeated backcrossing. In plants, this backcrossing occurs when an generation hybrid breeds with one or both of its parental species.

The agricultural weed syndrome is the set of common traits which make a plant a successful agricultural weed. Most of these traits are not, themselves, phenotypes but are instead methods of rapid adaptation. So equipped, plants of various origins - invasives, natives, mildly successful marginal weeds of agriculture, weeds of other settings - accumulate other characteristics which allow them to compete in an environment with a high degree of human management.

Hybridization, when new offspring arise from crosses between individuals of the same or different species, results in the assemblage of diverse genetic material and can act as a stimulus for evolution. Hybrid species are often more vigorous and genetically differed than their ancestors. There are primarily two different forms of hybridization: natural hybridization in an uncontrolled environment, whereas artificial hybridization occurs primarily for the agricultural purposes.

References

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