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Ring species
Ring species
from Wikipedia
In a ring species, gene flow occurs between neighbouring populations of a species, but at the ends of the ring the populations don't interbreed.
The coloured bars show natural populations (colours), varying along a cline. Such variation may occur in a line (e.g. up a mountain slope) as in A, or may wrap around as in B.
Where the cline bends around, populations next to each other on the cline can interbreed, but at the point at which the beginning meets the end again, as at C, the differences along the cline prevent interbreeding (gap between pink and green). The interbreeding populations are then called a ring species.

In biology, a ring species is a connected series of neighbouring populations, each of which interbreeds with closely sited related populations, but for which there exist at least two end populations in the series which are too distantly related to interbreed, though there is a potential gene flow between linked neighbouring populations.[1] Such non-breeding, though genetically connected, end populations may co-exist in the same region (sympatry) thus closing a ring. The German term Rassenkreis, meaning "circle of races", is also used.

Ring species represent speciation and have been cited as evidence of evolution. They illustrate what happens over time as populations genetically diverge, specifically because they represent, in living populations, what normally happens over time between long-deceased ancestor populations and living populations, in which the intermediates have become extinct. The evolutionary biologist Richard Dawkins remarks that ring species "are only showing us in the spatial dimension something that must always happen in the time dimension".[2]

Formally, the issue is that interfertility (ability to interbreed) is not a transitive relation; if A breeds with B, and B breeds with C, it does not mean that A breeds with C, and therefore does not define an equivalence relation. A ring species is a species with a counterexample to the transitivity of interbreeding.[3] However, it is unclear whether any of the examples of ring species cited by scientists actually permit gene flow from end to end, with many being debated and contested.[4]

History

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The classic ring species is the Larus gull. In 1925 Jonathan Dwight found the genus to form a chain of varieties around the Arctic Circle. However, doubts have arisen as to whether this represents an actual ring species.[5] In 1938, Claud Buchanan Ticehurst argued that the greenish warbler had spread from Nepal around the Tibetan Plateau, while adapting to each new environment, meeting again in Siberia where the ends no longer interbreed.[6] These and other discoveries led Mayr to first formulate a theory on ring species in his 1942 study Systematics and the Origin of Species. Also in the 1940s, Robert C. Stebbins described the Ensatina salamanders around the Californian Central Valley as a ring species;[7][8] but again, some authors such as Jerry Coyne consider this classification incorrect.[4] Finally in 2012, the first example of a ring species in plants was found in a spurge, forming a ring around the Caribbean Sea.[9]

Speciation

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The evolutionary biologist Ernst Mayr championed the concept of ring species, stating that it unequivocally demonstrated the process of speciation.[10] A ring species is an alternative model to allopatric speciation, "illustrating how new species can arise through 'circular overlap', without interruption of gene flow through intervening populations…"[11] However, Jerry Coyne and H. Allen Orr point out that rings species more closely model parapatric speciation.[4]

Ring species often attract the interests of evolutionary biologists, systematists, and researchers of speciation leading to both thought provoking ideas and confusion concerning their definition.[1] Contemporary scholars recognize that examples in nature have proved rare due to various factors such as limitations in taxonomic delineation[12] or, "taxonomic zeal"[10]—explained by the fact that taxonomists classify organisms into "species", while ring species often cannot fit this definition.[1] Other reasons such as gene flow interruption from "vicariate divergence" and fragmented populations due to climate instability have also been cited.[10]

Ring species also present an interesting case of the species problem for those seeking to divide the living world into discrete species. All that distinguishes a ring species from two separate species is the existence of the connecting populations; if enough of the connecting populations within the ring perish to sever the breeding connection then the ring species' distal populations will be recognized as two distinct species. The problem is whether to quantify the whole ring as a single species (despite the fact that not all individuals interbreed) or to classify each population as a distinct species (despite the fact that it interbreeds with its near neighbours). Ring species illustrate that species boundaries arise gradually and often exist on a continuum.[10]

Examples

[edit]
Ensatina salamanders, an example of a ring species
Speculated evolution and spread of the greenish warbler, Phylloscopus trochiloides:
  P. t. trochiloides
  P. t. obscuratus
  P. t. plumbeitarsus
  P. t. ludlowi
  P. t. viridanus
Note: The P. t. nitidus in Caucasus Mountains not shown.

Many examples have been documented in nature. Debate exists concerning much of the research, with some authors citing evidence against their existence entirely.[4][13][self-published source?] The following examples provide evidence that—despite the limited number of concrete, idealized examples in nature—continuums of species do exist and can be found in biological systems.[10] This is often characterized by sub-species level classifications such as clines, ecotypes, complexes, and varieties. Many examples have been disputed by researchers, and equally "many of the [proposed] cases have received very little attention from researchers, making it difficult to assess whether they display the characteristics of ideal ring species."[1]

The following list gives examples of ring species found in nature. Some of the examples such as the Larus gull complex, the greenish warbler of Asia, and the Ensatina salamanders of America, have been disputed.[13][14][15][16]

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
A ring species is a phenomenon in where a series of geographically adjacent populations of a single forms a continuous chain around a central geographic barrier, such that neighboring populations can interbreed and produce viable offspring, but the populations at the opposite ends of the chain, despite being connected through the intermediate forms, are reproductively isolated and behave as distinct . This pattern demonstrates how gradual genetic and phenotypic divergence can lead to over geographic space without complete physical separation. Classic examples include the salamander complex (Ensatina eschscholtzii) in , where populations form a ring around the arid Central Valley, with intergrading along the chain but between the coastal E. e. eschscholtzii and inland E. e. klauberi forms in . Similarly, the (Phylloscopus trochiloides) complex encircles the , with six showing clinal variation in , song, and genetics; the western P. t. viridanus and eastern P. t. plumbeitarsus coexist in central without interbreeding, despite through southern populations. These cases illustrate the role of isolation by distance in promoting divergence, often driven by adaptation to local environments or , and highlight challenges in defining species boundaries under . Although true ring species are rare due to factors like secondary contact and hybridization, they serve as natural experiments for studying the process.

Definition and Fundamentals

Definition

A ring species is defined as a chain of intergrading populations that form a geographic loop around an impassable barrier, where neighboring populations can interbreed freely, but the populations at the opposite ends of the chain are reproductively isolated from one another despite occupying overlapping ranges. This configuration arises from a single ancestral population expanding outward in two directions around the barrier, leading to gradual genetic and morphological divergence over time. Ring species illustrate a key challenge to the biological species concept, which defines species as groups of actually or potentially interbreeding natural populations that are reproductively isolated from other such groups. In this setup, the continuous chain of interbreeding populations suggests a single species, yet the reproductive isolation between the terminal forms implies multiple species, highlighting how gradual evolutionary change blurs discrete boundaries. This paradox underscores speciation as a gradual process rather than an abrupt event. Conceptually, the structure of a ring species can be visualized as a linear sequence of populations arranged in a circular encircling a central geographic barrier, such as a or , with occurring along the chain but ceasing at the points of secondary contact between the ends.

Key Characteristics

Ring species exhibit a spatial arrangement where populations form a continuous chain encircling a geographic barrier, such as a or , with adjacent populations capable of interbreeding and exchanging . This configuration results in gradual genetic and morphological divergence that increases linearly with geographic distance along the chain, reflecting ongoing between neighboring groups while allowing cumulative differentiation over the ring's extent. At the points of secondary contact where the chain's terminal populations overlap, however, typically occurs, manifesting as reduced hybrid viability, fertility, or behavioral incompatibilities between these non-adjacent forms. Identification of ring species relies on several diagnostic criteria, including the presence of an unbroken or nearly continuous ring-like distribution around an impassable central barrier that prevents direct across the loop. Evidence of interbreeding zones—regions of hybridization and —must be demonstrable between successive populations along the ring, confirming connectivity, while the terminal forms coexist sympatrically without significant interbreeding. Genetic analyses often reveal a single species boundary at the overlap zone, with no internal boundaries disrupting the chain's integrity, underscoring the structure's role in demonstrating speciation gradients. Unlike linear clines, where populations vary gradually along a straight or open-ended without closing the loop, ring species close the spatial circuit, leading to of the most divergent ends and highlighting without intermediate bridging them. This closed-loop distinguishes ring species by enabling the observation of secondary contact dynamics that linear arrangements cannot produce.

Historical Development

Early Observations

The ring species concept was first hypothesized in 1905 by herpetologist Leonhard Stejneger, as reported by , to explain how closely related forms might coexist without interbreeding due to a circular geographic distribution around a barrier. A key early detailed example came from ornithologist Jonathan Dwight's extensive study of gulls in the genus . In his 1925 monograph, Dwight described a series of intergrading gull forms distributed in a circumpolar chain around the , extending from the herring gull (Larus argentatus) in through various intermediate populations to the Vega gull (Larus vegae or L. argentatus ponticus) in , with notable variation in plumage, size, and bill morphology along the chain. This pattern suggested gradual clinal variation encircling a geographic barrier, though Dwight did not explicitly term it a "ring species." Subsequent field observations in provided another foundational example among amphibians. In 1949, herpetologist Robert C. Stebbins conducted detailed surveys of the Ensatina eschscholtzii across , documenting a ring-shaped distribution of radiating from the central Sierra Nevada and curving around the southern end of the Central Valley. Stebbins noted distinct color patterns and morphological differences—such as blotched orange forms in the north transitioning to uniform yellow or black in the south—among seven , with adjacent populations showing intergradation while the terminal forms in the exhibited reduced hybridization. Prior to 2012, reports of potential ring species in remained anecdotal and lacked systematic validation, often limited to observations of clinal variation in isolated floral groups without confirmed circular distributions or interbreeding patterns. These scattered accounts, drawn from regional floras and taxonomic surveys, hinted at possible ring-like structures in species like certain spurges or oaks but did not achieve formal recognition as ring species due to insufficient geographic or morphological data.

Key Theoretical Contributions

The ring species concept received significant theoretical grounding through the works of , who in his influential book Genetics and the Origin of Species (first published in 1937 and revised in 1941) linked such formations to processes. Dobzhansky described ring species as chains of locally adapted populations where occurs between neighboring groups but diminishes over distance, ultimately leading to between the terminal populations in the ring. This framework integrated genetic principles with geographic divergence, illustrating how partial isolation could drive evolutionary splitting without complete geographic barriers. Ernst Mayr further advanced the in his 1942 book Systematics and the Origin of Species, where he explicitly integrated ring species into the biological , defining as groups reproductively isolated from others. Mayr highlighted ring species as exemplars of in statu nascendi—speciation caught in the process—demonstrating how continuous intergradation along a chain could culminate in discrete at the points of secondary contact. He argued that these structures provided for the gradual origin of isolating mechanisms, challenging earlier views of abrupt species formation. The term "ring species" was formally coined by A.J. Cain in 1954 in his book Animal Species and Their Evolution, providing a precise for these geographic and evolutionary patterns. Post-1942 developments built on these foundations by emphasizing clinal variation and behavioral dynamics. , in his 1942 synthesis Evolution: The Modern Synthesis, stressed the importance of clinal variation in ring species, portraying them as gradients of phenotypic change shaped by environmental gradients across the geographic loop, which underscored the continuity between intraspecific variation and . In the 1970s, Guy L. Bush refined the theory in his review "Modes of Animal " (1975), incorporating the role of in contact zones, where favors stronger premating barriers to minimize costly hybridization between terminal populations, thus stabilizing the ring as a model of ongoing divergence.

Formation and Speciation Mechanisms

Geographic and Evolutionary Processes

Ring species arise through the geographic expansion of an ancestral population from a peripheral location around an impermeable barrier, such as mountain ranges or large bodies of water, which prevents direct crossing and promotes in the encircling populations. This expansion forms a continuous ring-shaped distribution, where populations at the ends of the ring eventually come into secondary contact, often exhibiting despite interbreeding among adjacent segments. Such barriers are relatively common in global for certain taxa, with cohesive barriers under 50,000 km² facilitating the process in low-dispersal species, though composite barriers spanning millions of km² are rarer and suit higher-dispersal organisms. The evolutionary timeline of ring species formation involves gradual over thousands of generations, driven by , , and as populations adapt to varying environmental conditions along the ring. persists between neighboring populations, maintaining connectivity and a of interbreeding links around the barrier, but this flow weakens over longer distances, allowing cumulative genetic differences to accumulate linearly with geographic separation. Ring closure occurs when the expanding fronts meet, typically after approximately 2,000 generations in modeled scenarios, at which point the degree of isolation at the depends on the extent of prior and landscape features like habitable area size. This process exemplifies , an intermediate mode between allopatric (complete geographic separation) and sympatric (no geographic separation) , where partial isolation from the barrier enables divergence while adjacency supports limited gene exchange. In parapatric scenarios, the continuous yet obstructed distribution fosters isolation by distance, with reproductive barriers emerging primarily at the secondary contact points despite ongoing connectivity elsewhere in the ring.

Genetic Mechanisms

In ring species, occurs predominantly between adjacent populations along the ring, facilitating genetic exchange over short distances while accumulating divergence over longer spans, a process known as isolation by distance. This pattern arises because dispersal is typically limited, allowing local genetic cohesion but enabling stepwise differentiation as populations adapt to varying selective pressures around the geographic loop. Models of spatial demonstrate that such restricted migration maintains connectivity without homogenizing the entire ring, as evidenced in the complex where markers revealed high locally but sharp genetic breaks at distant terminals. Divergence in ring species is driven by multiple genetic factors, including local to heterogeneous environments, on mating traits, and in peripheral populations. Local promotes shifts in response to environmental gradients, such as variations encircling a barrier, leading to phenotypic and genotypic differences that accumulate cumulatively. contributes through divergence in signals like s or colors, reducing mating success between distant forms, as observed in genomic analyses of greenish warblers where traits show elevated differentiation. further amplifies divergence in small or isolated segments of the ring, particularly where population sizes fluctuate. In overlap zones between terminal populations, strengthens prezygotic barriers, such as mate preferences, to minimize costly hybridization, enhancing . At the points where terminal populations meet, hybrid zones form with dynamics shaped by reduced hybrid fitness, which selects for assortative mating and maintains genetic clines. Hybrids often exhibit lower viability or fertility due to genetic incompatibilities, creating tension zones where selection against intermediates balances dispersal, thereby promoting parental assortative mating to avoid unfit offspring. This process is illustrated in the Ensatina salamander ring, where fine-scale genetic analysis of hybrid zones shows strong selection against hybrids, favoring prezygotic isolation. Gene flow models describe cline width in these zones using the basic for allele spread: pt=D2px2\frac{\partial p}{\partial t} = D \frac{\partial^2 p}{\partial x^2} where pp represents allele frequency, tt is time, xx is spatial position, and DD is the diffusion coefficient reflecting dispersal rate; equilibrium cline width scales as D/s\sqrt{D / s}
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