Ghost lineage

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Phylogeny of ichthyosaurs. Thick horizontal lines signify the existence of a fossil record for the respective time and taxa. Thin lines represent ghost lineages. Ichthyosauria phylogeny.jpg
Phylogeny of ichthyosaurs. Thick horizontal lines signify the existence of a fossil record for the respective time and taxa. Thin lines represent ghost lineages.

A ghost lineage is a hypothesized ancestor in a species lineage that has left no fossil evidence, but can still be inferred to exist or have existed because of gaps in the fossil record or genomic evidence. [1] [2] The process of determining a ghost lineage relies on fossilized evidence before and after the hypothetical existence of the lineage and extrapolating relationships between organisms based on phylogenetic analysis. [3] Ghost lineages assume unseen diversity in the fossil record and serve as predictions for what the fossil record could eventually yield; these hypotheses can be tested by unearthing new fossils or running phylogenetic analyses. [4]

Contents

Ghost lineages and Lazarus taxa are related concepts, as both stem from gaps in the fossil record. [2] A ghost lineage is any gap in a taxon's fossil record, with or without reappearance, while a Lazarus taxon is a type of ghost lineage wherein a species is believed to have gone extinct due to an absence of it in the fossil record, but then reappears after a period of time. [2] Examples of Lazarus taxa include the famous coelacanths, as well as the Philippine naked-backed fruit bat. [5]

Name

In 1992, an article stated: "These additional entities are taxa [groups] that are predicted to occur by the internal branching structure of phylogenetic trees.... I refer to these as ghost lineages because they are invisible to the fossil record." [6] Phylogenetic trees constructed based on fossil records and Darwin's theory of evolution often give an indication that species with similar phenotypes existed, although its fossil has not been discovered. [7]

It is important to note that ghost lineages and ghost taxa are not the same. A ghost lineage is a one direct connection between the descendant and the ancestor, whereas a ghost taxon has many split descendants. [3]

Examples

A selection of gaps within the fossil record of animals having hard body parts. Other notable examples are Chronoperates and Protanguilla. Fossil record gaps - animals with hard body parts.svg
A selection of gaps within the fossil record of animals having hard body parts. Other notable examples are Chronoperates and Protanguilla .

When looking back at extinct organisms, there are some groups of organisms (or lineages) that have gaps in their fossil records. These organisms or species may be closely related to one another, but there are no traces in the fossil records or sediment beds that might shed some light on their origins. Biologists may infer the existence of ghost lineages by examining sequential stratigraphic units in the fossil record. [8] Fossils can then be mapped onto cladograms and range charts to assess which lineages are missing in the fossil record. [8] A classic example is the coelacanth, a type of fish related to the lungfishes and to primitive tetrapods. Coelacanths have been around for the past 80 million years but have failed to leave any fossils. The reason for this is their environment, which is deep water near volcanic islands; therefore, these sediments are hard to get to, giving these coelacanths an 80 million year gap or ghost lineage. [2] Another ghost lineage was that of the averostran theropods, a ghost lineage now reduced considerably due to the discovery of Tachiraptor . [9]

Duration and diversification

The duration between distinct fossils can be measured and used to derive information about the evolutionary history of a species. A study conducted in 1998 showed that a correlation exists between the diversification of a species and the duration of its ghost lineage; namely that a shorter ghost lineage implies that there will be greater species diversification. [10]

Genetic evidence

Genetic evidence has revealed ghost populations in many species, including modern bonobos and chimpanzees, allopolyploid frogs, polyploid parthenogenetic crayfish, a variety of plants, and humans. [11] [12] [13] A study comparing the genomes of 69 modern bonobos and chimpanzees found between 0.94.2% of gene flow from ancient bonobos and an archaic great ape lineage to modern bonobos, allowing researchers to reconstruct 4.8% of this ghost population's genome. [11] Furthermore, previous models for European ancestry suggested that European populations descended from two ancient populations, but genetic evidence now suggests that a third ghost population, the Ancient North Eurasians, has also contributed to European ancestry. [13]

See also

Related Research Articles

In biology, phylogenetics is the study of the evolutionary history of life using genetics, which is known as phylogenetic inference. It establishes the relationship between organisms with the empirical data and observed heritable traits of DNA sequences, protein amino acid sequences, and morphology. The results are a phylogenetic tree—a diagram setting the hypothetical relationships between organisms and their evolutionary history.

<span class="mw-page-title-main">Coelacanth</span> Order of lobe-finned fishes

Coelacanths are an ancient group of lobe-finned fish (Sarcopterygii) in the class Actinistia. As sarcopterygians, they are more closely related to lungfish and tetrapods than to ray-finned fish.

The molecular clock is a figurative term for a technique that uses the mutation rate of biomolecules to deduce the time in prehistory when two or more life forms diverged. The biomolecular data used for such calculations are usually nucleotide sequences for DNA, RNA, or amino acid sequences for proteins.

<span class="mw-page-title-main">Living fossil</span> Organism resembling a form long shown in the fossil records

A living fossil is an extant taxon that phenotypically resembles related species known only from the fossil record. To be considered a living fossil, the fossil species must be old relative to the time of origin of the extant clade. Living fossils commonly are of species-poor lineages, but they need not be. While the body plan of a living fossil remains superficially similar, it is never the same species as the remote relatives it resembles, because genetic drift would inevitably change its chromosomal structure.

<i>Homo</i> Genus of hominins that includes humans and their closest extinct relatives

Homo is a genus of great ape that emerged from the genus Australopithecus and encompasses only a single extant species, Homo sapiens, along with a number of extinct species classified as either ancestral or closely related to modern humans; these include Homo erectus and Homo neanderthalensis. The oldest member of the genus is Homo habilis, with records of just over 2 million years ago. Homo, together with the genus Paranthropus, is probably most closely related to the species Australopithecus africanus within Australopithecus. The closest living relatives of Homo are of the genus Pan, with the ancestors of Pan and Homo estimated to have diverged around 5.7-11 million years ago during the Late Miocene.

<span class="mw-page-title-main">Lazarus taxon</span> Taxon that disappears from the fossil record, only to reappear later

In paleontology, a Lazarus taxon is a taxon that disappears for one or more periods from the fossil record, only to appear again later. Likewise in conservation biology and ecology, it can refer to species or populations that were thought to be extinct, and are rediscovered. The term Lazarus taxon was coined by Karl W. Flessa and David Jablonski in 1983 and was then expanded by Jablonski in 1986. Paul Wignall and Michael Benton defined Lazarus taxa as, "At times of biotic crisis many taxa go extinct, but others only temporarily disappeared from the fossil record, often for intervals measured in millions of years, before reappearing unchanged". Earlier work also supports the concept though without using the name Lazarus taxon, like work by Christopher R. C. Paul.

Anagenesis is the gradual evolution of a species that continues to exist as an interbreeding population. This contrasts with cladogenesis, which occurs when there is branching or splitting, leading to two or more lineages and resulting in separate species. Anagenesis does not always lead to the formation of a new species from an ancestral species. When speciation does occur as different lineages branch off and cease to interbreed, a core group may continue to be defined as the original species. The evolution of this group, without extinction or species selection, is anagenesis.

Evidence of common descent of living organisms has been discovered by scientists researching in a variety of disciplines over many decades, demonstrating that all life on Earth comes from a single ancestor. This forms an important part of the evidence on which evolutionary theory rests, demonstrates that evolution does occur, and illustrates the processes that created Earth's biodiversity. It supports the modern evolutionary synthesis—the current scientific theory that explains how and why life changes over time. Evolutionary biologists document evidence of common descent, all the way back to the last universal common ancestor, by developing testable predictions, testing hypotheses, and constructing theories that illustrate and describe its causes.

Neontology is a part of biology that, in contrast to paleontology, deals with living organisms. It is the study of extant taxa : taxa with members still alive, as opposed to (all) being extinct. For example:

Computational phylogenetics, phylogeny inference, or phylogenetic inference focuses on computational and optimization algorithms, heuristics, and approaches involved in phylogenetic analyses. The goal is to find a phylogenetic tree representing optimal evolutionary ancestry between a set of genes, species, or taxa. Maximum likelihood, parsimony, Bayesian, and minimum evolution are typical optimality criteria used to assess how well a phylogenetic tree topology describes the sequence data. Nearest Neighbour Interchange (NNI), Subtree Prune and Regraft (SPR), and Tree Bisection and Reconnection (TBR), known as tree rearrangements, are deterministic algorithms to search for optimal or the best phylogenetic tree. The space and the landscape of searching for the optimal phylogenetic tree is known as phylogeny search space.

<span class="mw-page-title-main">Signor–Lipps effect</span> Sampling bias in the fossil record raising difficulties to characterize extinctions

The Signor–Lipps effect is a paleontological principle proposed in 1982 by Philip W. Signor and Jere H. Lipps which states that, since the fossil record of organisms is never complete, neither the first nor the last organism in a given taxon will be recorded as a fossil. The Signor–Lipps effect is often applied specifically to cases of the youngest-known fossils of a taxon failing to represent the last appearance of an organism. The inverse, regarding the oldest-known fossils failing to represent the first appearance of a taxon, is alternatively called the Jaanusson effect after researcher Valdar Jaanusson, or the Sppil–Rongis effect.

<span class="mw-page-title-main">Autapomorphy</span> Distinctive feature, known as a derived trait, that is unique to a given taxon

In phylogenetics, an autapomorphy is a distinctive feature, known as a derived trait, that is unique to a given taxon. That is, it is found only in one taxon, but not found in any others or outgroup taxa, not even those most closely related to the focal taxon. It can therefore be considered an apomorphy in relation to a single taxon. The word autapomorphy, introduced in 1950 by German entomologist Willi Hennig, is derived from the Greek words αὐτός, autos "self"; ἀπό, apo "away from"; and μορφή, morphḗ = "shape".

In phylogenetics, basal is the direction of the base of a rooted phylogenetic tree or cladogram. The term may be more strictly applied only to nodes adjacent to the root, or more loosely applied to nodes regarded as being close to the root. Note that extant taxa that lie on branches connecting directly to the root are not more closely related to the root than any other extant taxa.

<span class="mw-page-title-main">Species</span> Basic unit of taxonomic classification, below genus

A species is a population of organisms in which any two individuals of the appropriate sexes or mating types can produce fertile offspring, typically by sexual reproduction. It is the basic unit of classification and a taxonomic rank of an organism, as well as a unit of biodiversity. Other ways of defining species include their karyotype, DNA sequence, morphology, behaviour, or ecological niche. In addition, paleontologists use the concept of the chronospecies since fossil reproduction cannot be examined. The most recent rigorous estimate for the total number of species of eukaryotes is between 8 and 8.7 million. About 14% of these had been described by 2011. All species are given a two-part name, called a "binomial". The first part of a binomial is the genus to which the species belongs. The second part is called the specific name or the specific epithet. For example, Boa constrictor is one of the species of the genus Boa, with constrictor being the species' epithet.

<i>Xiongguanlong</i> Extinct genus of dinosaurs

Xiongguanlong is an extinct genus of tyrannosauroid theropod from the Early Cretaceous period of what is now China. The type and only species is X. baimoensis. The generic name comes from Jiayuguan City and the Mandarin word "long" which means dragon. The specific epithet, "baimoensis" is a latinization of the Mandarin word for "white ghost" in reference to one of the geological features of the type locality.

<span class="mw-page-title-main">Gavialoidea</span> Superfamily of large reptiles

Gavialoidea is one of three superfamilies of crocodylians, the other two being Alligatoroidea and Crocodyloidea. Although many extinct species are known, only the gharial Gavialis gangeticus and the false gharial Tomistoma schlegelii are alive today, with Hanyusuchus having become extinct in the last few centuries.

Incomplete lineage sorting (ILS) (also referred to as hemiplasy, deep coalescence, retention of ancestral polymorphism, or trans-species polymorphism) is a phenomenon in evolutionary biology and population genetics that results in discordance between species and gene trees. By contrast, complete lineage sorting results in concordant species and gene trees. ILS occurs in the context of a gene in an ancestral species which exists in multiple alleles. If a speciation event occurs in this situation, either complete lineage sorting will occur, and both daughter species will inherit all alleles of the gene in question, or incomplete lineage sorting will occur, when one or both daughter species inherits a subset of alleles present in the parental species. For example, if two alleles of a gene are present and a speciation event occurs, one of the two daughter species might inherit both alleles, but the second daughter species only inherits one of the two alleles. In this case, incomplete lineage sorting has occurred.

<span class="mw-page-title-main">Molecular paleontology</span>

Molecular paleontology refers to the recovery and analysis of DNA, proteins, carbohydrates, or lipids, and their diagenetic products from ancient human, animal, and plant remains. The field of molecular paleontology has yielded important insights into evolutionary events, species' diasporas, the discovery and characterization of extinct species.

<span class="mw-page-title-main">Outline of evolution</span> Overview of and topical guide to change in the heritable characteristics of organisms

The following outline is provided as an overview of and topical guide to evolution:

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.

References

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