The DOI matches its Crossref record; 74 of the 74 references it cites were found in a registry or an index; none of the 98 sources its claims cite is checked for support yet.
The modern molecular clock
Abstract
The discovery of the molecular clock--a relatively constant rate of molecular evolution--provided an insight into the mechanisms of molecular evolution, and created one of the most useful new tools in biology. The unexpected constancy of rate was explained by assuming that most changes to genes are effectively neutral. Theory predicts several sources of variation in the rate of molecular evolution. However, even an approximate clock allows time estimates of events in evolutionary history, which provides a method for testing a wide range of biological hypotheses ranging from the origins of the animal kingdom to the emergence of new viral epidemics.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
The molecular clock—a relatively constant rate of molecular evolution—was unexpected but is broadly explained by neutral and nearly neutral theory, and it provides a universal tool for dating evolutionary events. However, the clock is “sloppy” and rates vary among lineages, so molecular dates must be treated with appropriate confidence intervals and caution.
Key findings
- Zuckerkandl and Pauling found a strikingly linear accumulation of amino-acid differences over evolutionary time, with each protein having a characteristic rate: histones were exceptionally slow, cytochrome c was faster but slower than haemoglobins, and fibrinopeptides were faster still; Kimura and Ohta explained this by suggesting most amino-acid changes are effectively neutral.
- Rate variation arises through mutation rate, population size, and selective coefficients; examples include murid rodents evolving two to three times faster than hominid primates, and HIV evolving around a million times faster than mammalian genomes.
- Molecular dates can conflict with fossil dates: molecular dates for the origins of animal phyla and orders of mammals and birds are generally twice as old as fossil dates, and published molecular dates for the rodent–primate split vary by as much as 100%.
- A practical application: molecular clock dates place the last common ancestor of the main pandemic HIV strain in the 1930s, countering claims that the virus spread through contaminated polio vaccine in the 1950s.
Methods
- Review article synthesizing the history, theory, and methods of molecular dating; no new primary data or analyses are presented.
- Discusses calibration approaches (fossil record, biogeography, sample dates for viruses), substitution models, and clock tests (relative rates test, Tajima test, likelihood ratio test), plus maximum likelihood and Bayesian methods.
- Uses examples from proteins, Hawaiian island birds and fruitflies, vertebrates, and viruses to illustrate rate constancy and variation.
Limitations
- The paper states that the molecular clock is probabilistic and “sloppy,” with overdispersed substitution intervals adding large confidence intervals; lineage effects can systematically bias date estimates.
- It notes operational errors: uncertain phylogenies, calibration-point errors, and biased genetic-distance estimates; clock tests lack power for shorter or slowly evolving sequences.
- It states that few studies present confidence intervals that accurately portray clock variance, and that molecular dates are often point estimates; as a review, it does not resolve these issues with new data (evident from text).
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
0 of 98 cited sources checked · 0 supported · 0 flagged
None of the sources cited for this claim have been checked yet.
In the paper
“The variation in rate of molecular evolution between lineages warns against using a calibration rate calculated for one lineage to date another, often distantly related, lineage 1,28,48 .”
What the sources say
- Not checked yetcites [1] Smith, A. B. & Peterson, K. J. Dating the time of origin of major clades: molecular clocks and the fossil record. Annu. Rev. Earth Planet. Sci. 30, 65–88 (2002). A review of the controversy surrounding dates for the Cambrian explosion of animal phyla and the early Tertiary radiation of modern mammals and birds. Written by a palaeontologist and a molecular geneticist, this review takes a critical look at the reliability of both fossil and molecular dates. source
- Not checked yetcites [28] Bromham, L. D., Rambaut, A., Hendy, M. D. & Penny, D. he power of relative rates tests depends on the data. J. Mol. Evol. 50, 296–301 (2000). source
- Not checked yetcites [48] Bromham, L. D., Phillips, M. J. & Penny, D. Growing up with dinosaurs: molecular dates and the mammalian radiation. Trends Ecol. Evol. 14, 113–118 (1999). source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The molecular clock arises from the observation that the amount of difference between the DNA of two species is a function of the time since their evolutionary separation.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIn the paper
“The choice of calibration date is crucial to the accuracy of molecular dates, as shown by the difference in date estimates from studies using the same data and methods but different calibration dates 48 .”
What the sources say
- Not checked yetcites [48] Bromham, L. D., Phillips, M. J. & Penny, D. Growing up with dinosaurs: molecular dates and the mammalian radiation. Trends Ecol. Evol. 14, 113–118 (1999). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“However, there is, as yet, no evidence that environmental temperature influences the rate of molecular evolution 40,41 .”
What the sources say
- Not checked yetcites [40] Bromham, L. & Cardillo, M. Testing the link between the latitudinal gradient in species richness and rates of molecular evolution. J. Evol. Biol. 16, 200–207 (2003). source
- Not checked yetcites [41] Held, C. No evidence for slow-down of molecular substitution rates at subzero temperatures in Antarctic serolid isopods (Crustacea, Isopoda, Serolidae). Polar Biol. 24, 497–501 (2001). source
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The rate of accumulation of these neutral mutations would be influenced only by the mutation rate, and so would be relatively constant, as long as the base mutation rate remained unchanged (BOX 3).”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In addition, the strength of selection on particular sites can change, producing bursts of substitutions as a molecule is adapted to a new role or responds to changes in another part of the genome.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“But molecular dates for the origins of animal phyla 27 and orders of mammals and birds 68 are generally twice as old as the dates of origin indicated by the fossil record.”
What the sources say
- Not checked yetcites [27] Bromham, L., Rambaut, A., Fortey, R., Cooper, A. & Penny, D. Testing the Cambrian explosion hypothesis by using a molecular dating technique. Proc. Natl Acad. Sci. USA 95, 12386–12389 (1998). source
- Not checked yetcites [68] Madsen, O. et al.Parallel adaptive radiations in two major clades of placental mammals. Nature 409, 610–614 (2001). Used the quartet method which uses several calibration dates to allow for differences in substitution rate between lineages to support the hypothesis that modern mammals arose long before the final extinction of the dinosaurs. source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“Therefore, the fixation of nearly-neutral alleles of small selective effect is expected to be greatest in small populations 23,24 .”
What the sources say
- Not checked yetcites [23] Ohta, T. Very slightly deleterious mutations and the molecular clock. J. Mol. Evol. 26, 1–6 (1987). source
- Not checked yetcites [24] Ohta, T. Near-neutrality in evolution of genes and gene regulation. Proc. Natl Acad. Sci. USA 99, 16134–16137 (2002). The most recent exposition of the nearly-neutral model, in which the effects of weak selection depend both on the selection coefficient of the mutation and the size of the population in which the mutant occurs. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This is a fundamental result; it predicts that the long-term rate of neutral molecular evolution in species is the same as the neutral mutation rate in individuals.”
Load-bearingStrength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIn the paper
“They reported a strikingly linear rate of accumulation of amino-acid differences over evolutionary time.”
What the sources say
- Not checked yetcites [3] Zuckerkandl, E. & Pauling, L. in Horizons in Biochemistry (eds Kasha, M. & Pullman, B.) 189–225 (Academic Press, New York, 1962).
Strength:boosted· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes
- Probably not a substantial claim. 19
- It may state two separate claims as one. 27
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The unexpected constancy of rate was explained by assuming that most changes to genes are effectively neutral.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
In the paper
“For example, molecular clock dates that place the last common ancestor of the main pandemic strain of human immunodeficiency virus (HIV) in the 1930s have been used to counter claims that the virus was spread through the distribution of contaminated polio vaccine in the 1950s (allegedly manufactured using tissue from chimpanzees infected with simian immunodeficiency virus) 2 .”
What the sources say
- Not checked yetcites [2] Korber, B. et al.Timing the ancestor of the HIV-1 pandemic strains. Science 288, 1789–1796 (2000). source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The discovery of the molecular clock - a relatively constant rate of molecular evolution provided an insight into the mechanisms of molecular evolution, and created one of the most useful new tools in biology.”
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Theory predicts several sources of variation in the rate of molecular evolution.”
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, extrapolation has few constraints on the variances and biases, so uncertainty increases with the distance between the calibration point and the estimated node.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Selection of the substitution model governs the accuracy of genetic distance estimates and is therefore crucial to the accuracy of molecular dating.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“However, this approach will fail to count 'multiple hits' (repeated changes), so a model of sequence evolution is needed to estimate the true number of substitutions that have occurred, using the observed number 67 .”
What the sources say
- Not checked yetcites [67] Page, R. D. M. & Holmes, E. C. Molecular Evolution: a Phylogenetic Approach (Blackwell Science, Oxford, UK, 1998).
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The reliability of all molecular clock methods depends on the accuracy with which genetic distance is estimated, and on the appropriateness of the calibration rate.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, even an approximate clock allows time estimates of events in evolutionary history, which provides a method for testing a wide range of biological hypotheses ranging from the origins of the animal kingdom to the emergence of new viral epidemics.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Even within mammalian cells, different replication and repair enzymes vary in mutation rate: mitochondrial DNA is copied by DNA polymeraseγ , which has a higher error rate than other mammalian DNA polymerases,and this contributes to the higher mutation rate of mitochondrial genes over nuclear genes.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Small populations are more severely affected by stochastic fluctuations in allele frequencies, so genetic drift (random sampling error on allele frequencies) can overpower selection for alleles with small selection coefficients.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“This constancy of rates is broadly supported by observation: the amount of divergence between genes tends to increase with the time since evolutionary separation, and in many cases the increase seems linear, as in the classic example of globin genes 3 .”
What the sources say
- Not checked yetcites [3] Zuckerkandl, E. & Pauling, L. in Horizons in Biochemistry (eds Kasha, M. & Pullman, B.) 189–225 (Academic Press, New York, 1962).
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“According to the neutral theory of Kimura 4,72 (FIG. 1b) , the overall mutation rate ( µ ) is the sum of deleterious ( µ -), neutral ( µ º), and positive ( µ + ) mutations, µ = µ - +µ º +µ + .”
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“This is consistent with the observations that ECTOTHERMS have lower substitution rates than ENDOTHERMS 36 , that smaller-bodied species of vertebrates with faster metabolic rates have higher substitution rates than larger-bodied species 35,37-39 and that animal mitochondria, which are at the site of oxidative phosporylation, have a higher rate of molecular evolution than nuclear rates 34 (it would”
What the sources say
- Not checked yetcites [36] Martin, A. P. Metabolic rate and directional nucleotide substitution in animal mitochondrial DNA. Mol. Biol. Evol. 12, 1124–1131 (1995).
- Not checked yetcites [35] Martin, A. P. & Palumbi, S. R. Body size, metabolic rate, generation time and the molecular clock. Proc. Natl Acad. Sci. USA 90, 4087–4091 (1993). Showed a relationship between body size and the rate of molecular evolution for vertebrates using estimates of absolute substitution rates. This paper showed that the life history of a species must influence the rate of molecular evolution. source
- Not checked yetcites [37] Bromham, L., Rambaut, A. & Harvey, P. H. Determinants of rate variation in mammalian DNA sequence evolution. J. Mol. Evol. 43, 610–621 (1996). source
- Not checked yetcites [38] Bromham, L. Molecular clocks in reptiles: life history influences rate of molecular evolution. Mol. Biol. Evol. 19, 302–309. (2002). source
- Not checked yetcites [39] Mooers, A. Ø. & Harvey, P. H. Metabolic rate, generation time and the rate of molecular evolution in birds. Mol. Phylogenet. Evol. 3, 344–350 (1994). source
- Not checked yetcites [34] Rand, D. M. Thermal habit, metabolic rate and the evolution of mitochondrial DNA. Trends Ecol. Evol. 9, 125–131 (1994). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“An early and unexpected finding from the molecular revolution was the discovery that a given protein has a characteristic rate of evolution, but that genes differ in their characteristic rates.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Because of the universality of DNA (or RNA), molecular clocks can reach all timescales of evolution, from population divergences to the last common ancestor of the five kingdoms of life.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
None of the sources cited for this claim have been checked yet.
In the paper
“Conversely, many palaeontologists suggest that the discrepancy between molecular and palaeontological dates shows that molecular clocks can be systematically inaccurate, because some process associated with explosive radiations could speed the molecular clock 69,70 (although no supporting evidence has yet been found for this hypothesis 49 ).”
What the sources say
- Not checked yetcites [69] Conway Morris, S. Early metazoan evolution: reconciling paleontology and molecular biology. Am. Zool. 38, 867–877 (1998). source
- Not checked yetcites [70] Valentine, J., Jablonski, D. & Erwin, D. Fossils, molecules and embryos: new perspectives on the Cambrian explosion. Development 126, 851–859 (1999). source
- Not checked yetcites [49] Bromham, L. Molecular clocks and explosive radiations. J. Mol. Evol. (in the press). source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✗ Asserted: fails✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The authors may not put it forward as true. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“For example, murid rodents (rats, mice and hamsters) have less efficient excisionrepair mechanisms than humans 31 and this is consistent with the higher rate of molecular evolution in murid rodents than in hominids 32 .”
What the sources say
- Not checked yetcites [31] Hart, R. W. & Setlow, R. B. Correlation between deoxyribonucleic acid excision-repair and life-span in a number of mammal species. Proc. Natl Acad. Sci. USA 71, 2169–2173 (1974). source
- Not checked yetcites [32] Li, W. -H., Ellesworth, D. L., Krushkal, J., Chang, B. H. -J. & Hewett-Emmett, D. Rates of nucleotide substitution in primates and rodents and the generation-time effect hypothesis. Mol. Phylogenet. Evol. 5, 182–187 (1996). source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Some researchers suggest that the pace and degree of change in explosive radiations is too great to be explained by Darwinian MICROEVOLUTIONARY processes, and that special mechanisms must be invoked,such as rapid change by developmental macromutations involving the HOX GENE COMPLEX 70,71 .”
What the sources say
- Not checked yetcites [70] Valentine, J., Jablonski, D. & Erwin, D. Fossils, molecules and embryos: new perspectives on the Cambrian explosion. Development 126, 851–859 (1999). source
- Not checked yetcites [71] Carroll, R. C. Towards a new evolutionary synthesis. Trends Ecol. Evol. 15, 27–32 (2000). source
Strength:hedged· not yet calibratedTests✗ Asserted: fails✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The authors may not put it forward as true. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“However, it could be related to population size effects if rapidly speciating lineages undergo frequent population subdivision 40 .”
What the sources say
- Not checked yetcites [40] Bromham, L. & Cardillo, M. Testing the link between the latitudinal gradient in species richness and rates of molecular evolution. J. Evol. Biol. 16, 200–207 (2003). source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“if the rate of molecular evolution is relatively constant, then the amount of genetic difference between two species gives a measure of the time since their evolutionary separation”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds. It may state two separate claims as one.
In the paper
“Mutation rate clearly varies between taxa 29 and much of this variation is due to differences in repair equipment (biochemical factors).”
What the sources say
- Not checked yetcites [29] Drake, J., Charlesworth, B., Charlesworth, D. & Crow, J. Rates of spontaneous mutation. Genetics 148, 1667–1686 (1998). Observable mutation rates, when measured per genome per generation, are remarkably similar across widely divergent organisms, indicating that natural selection might shape optimum mutation rates. source
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“It is possible that the population size effect could also account for the intriguing association between the diversification rate of flowering plant lineages (speciation minus extinction) and rates of molecular evolution 46 .”
What the sources say
- Not checked yetcites [46] Barraclough, T. G. & Savolainen, V. Evolutionary rates and species diversity in flowering plants. Evolution 55, 677–683 (2001). source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“So, the nearly neutral theory describes how the rate of molecular evolution can vary not only with changes in the mutation rate, but also through the changing balance between selection and drift.”
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“There are three approaches to allowing for the variation in the rate of molecular evolution.”
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
In the paper
“However, these clock tests lack power for shorter sequences (or genes with low rates of change) and will detect only a relatively low proportion of cases of rate variation for the types of sequence that are typically used in molecular clock studies 28 .”
What the sources say
- Not checked yetcites [28] Bromham, L. D., Rambaut, A., Hendy, M. D. & Penny, D. he power of relative rates tests depends on the data. J. Mol. Evol. 50, 296–301 (2000). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“A likelihood ratio test is used to compare the fit of a single substitution rate with a multiple-rate model.”
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Mutations are divided into three categories: mutations for which selection is the predominant force (4N e σ s > 3); nearly neutral mutations, which are governed by both selection and drift (3 ≥ 4N e σ s ≤ 0.2); and effectively neutral mutations, the fate of which is determined only by drift (4N e σ s < 0.2).”
What the sources say
- Not checked yetcites [22] Ohta, T. & Kimura, M. On the constancy of the evolutionary rate of cistrons. J. Mol. Evol. 1, 18–25 (1971). source
- Not checked yetcites [23] Ohta, T. Very slightly deleterious mutations and the molecular clock. J. Mol. Evol. 26, 1–6 (1987). source
- Not checked yetcites [24] Ohta, T. Near-neutrality in evolution of genes and gene regulation. Proc. Natl Acad. Sci. USA 99, 16134–16137 (2002). The most recent exposition of the nearly-neutral model, in which the effects of weak selection depend both on the selection coefficient of the mutation and the size of the population in which the mutant occurs. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
In the paper
“Second, the nearly neutral theory predicts that the rate of molecular evolution is influenced by mutation rate, population size and the relative proportions of sites with different selective coefficients; these factors might differ between genes, between species and over time, potentially resulting in consistent bias in date estimates 28 .”
What the sources say
- Not checked yetcites [28] Bromham, L. D., Rambaut, A., Hendy, M. D. & Penny, D. he power of relative rates tests depends on the data. J. Mol. Evol. 50, 296–301 (2000). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Slightly deleterious mutations will tend to be removed by selection in very large populations; however, they can be fixed by chance in smaller populations in which selection can be overpowered by random sampling events (GENETIC DRIFT) .”
What the sources say
- Not checked yetcites [22] Ohta, T. & Kimura, M. On the constancy of the evolutionary rate of cistrons. J. Mol. Evol. 1, 18–25 (1971). source
- Not checked yetcites [23] Ohta, T. Very slightly deleterious mutations and the molecular clock. J. Mol. Evol. 26, 1–6 (1987). source
- Not checked yetcites [24] Ohta, T. Near-neutrality in evolution of genes and gene regulation. Proc. Natl Acad. Sci. USA 99, 16134–16137 (2002). The most recent exposition of the nearly-neutral model, in which the effects of weak selection depend both on the selection coefficient of the mutation and the size of the population in which the mutant occurs. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Molecular dates for Hemignathus (panel b ) and Drosophila (panel c ) confirm this order of colonization, and produce a remarkably linear relationship between genetic divergence and time when DNA distance is plotted against island age.”
What the sources say
- Not checked yetcites [10] Fleischer, R. C., McIntosh, C. E. & Tarr, C. L. Evolution on a volcanic conveyor belt: using phylogeographic reconstructions and K-Ar based ages of the Hawaiian islands to estimate molecular evolutionary rates. Mol. Ecol. 7, 533–545 (1998). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Molecular evolutionary theory has led to the prediction that species can differ in their rate of molecular evolution through changes to traits that influence mutation rate, population size or selective coefficients, but the measurable effect of these predicted influences has only recently begun to be investigated for a wide range of taxa.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Several dates can be used to fit a linear relationship between genetic distance and time, which might subsequently be used to estimate the rate of molecular evolution 62 or the time of origin of the last common ancestor of all included samples 2 .”
What the sources say
- Not checked yetcites [62] Shankarappa, R. et al. Consistent viral evolutionary changes associated with the progression of human immunodeficiency virus type 1 infection. J. Virol. 73, 10489–10502 (1999). source
- Not checked yetcites [2] Korber, B. et al.Timing the ancestor of the HIV-1 pandemic strains. Science 288, 1789–1796 (2000). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Estimating maximum and minimum possible rates for a given data set requires several calibration dates, which are not always available, and gives conservative assessments of molecular dates that are suitable only for rejecting particular hypotheses as being inconsistent with the data 55 .”
What the sources say
- Not checked yetcites [55] Bromham, L. D. & Hendy, M. D. Can fast early rates reconcile molecular dates to the Cambrian explosion? Proc. R. Soc. Lond. B 267, 1041–1047 (2000). source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The high variance that arises from residual effects makes date estimates imprecise, but lineage effects, in which different species have different characteristic rates, might bias date estimates - that is, estimates based on the assumption of a constant rate might produce consistently over- or under-estimated dates.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Failure to detect rate variation can cause systematic error in date estimates, because undetected rate variation can lead to consistently overestimated dates of divergence 28 .”
What the sources say
- Not checked yetcites [28] Bromham, L. D., Rambaut, A., Hendy, M. D. & Penny, D. he power of relative rates tests depends on the data. J. Mol. Evol. 50, 296–301 (2000). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Similar methods have been developed that use Bayesian statistics to select the most likely parameters of molecular evolution for a set of viral sequences, including the substitution rates and timing of ancestral nodes 64 .”
What the sources say
- Not checked yetcites [64] Drummond, A., Pybus, O. G. & Rambaut, A. Inference of viral evolutionary rates from molecular sequences. Adv. Parasitol. (in the press). A review of the methods used to estimate substitution rates in viruses, including estimating molecular dates when rates vary.
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, the method relies on the validity of many assumptions, some of which might be inappropriate for the data being tested (such as the assumption that a constant rate of lineage origination and extinction, counter to the proposed 'explosion') (BOX 2).”
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Compounding these residual and lineage errors in the clock are operational errors in measuring the rate of molecular evolution, which include uncertainty in the relationships between taxa (the evolutionary tree), errors in calibration points and uncertainties in the mechanism of evolution 1,49 .”
What the sources say
- Not checked yetcites [1] Smith, A. B. & Peterson, K. J. Dating the time of origin of major clades: molecular clocks and the fossil record. Annu. Rev. Earth Planet. Sci. 30, 65–88 (2002). A review of the controversy surrounding dates for the Cambrian explosion of animal phyla and the early Tertiary radiation of modern mammals and birds. Written by a palaeontologist and a molecular geneticist, this review takes a critical look at the reliability of both fossil and molecular dates. source
- Not checked yetcites [49] Bromham, L. Molecular clocks and explosive radiations. J. Mol. Evol. (in the press). source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“All molecular clock methods rely on accurate estimates of the genetic distance between sequences, and, in some cases, this measurement might be biased.”
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds. It may state two separate claims as one.
The paper relies on this without support.
Molecular dates are frequently presented as point estimates, or with sample errors that represent the difference between estimates in the same study.
“Part of the difficulty of assessing the reliability of molecular clocks is that molecular dates are frequently presented as point estimates, or with sample errors that represent the difference between estimates in the same study.”
The paper relies on this without support.
Few studies present molecular date estimates with confidence intervals that accurately portray the variance in the clock due to the sloppiness of the tick rate, or the lineage variation in rates.
“Few studies present molecular date estimates with confidence intervals that accurately portray the variance in the clock due to the sloppiness of the tick rate, or the lineage variation in rates.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Actually, single fossils may also bear their load of uncertainty in taxonomy identification and geological ages (11).”
From The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils? (2004) · cites this paper as [11]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Nearly neutral and effectively neutral categories overlap
MinorThe stated inequality for nearly neutral mutations includes values below 0.2, which the next category also classifies as effectively neutral. The categories therefore overlap rather than defining separate ranges.
“nearly neutral mutations, which are governed by both selection and drift (3 ≥ 4N e σ s ≤ 0.2)”
“effectively neutral mutations, the fate of which is determined only by drift (4N e σ s < 0.2)”
Citations
Cites
Evolutionary trees from DNA sequences: A maximum likelihood approach.
Felsenstein, J. (1981) · Journal of Molecular Evolution · doi:10.1007/bf01734359 · Cited by 14,571
The Neutral Theory of Molecular Evolution
Kimura, M. (1979) · Scientific American · doi:10.1038/scientificamerican1179-98 · Cited by 7,687
The Neutral Theory of Molecular Evolution
Kimura, M. (1983) · Cambridge University Press eBooks · doi:10.1017/cbo9780511623486 · Cited by 6,300
On the Origin of Species by Means of Natural Selection
Livezey, R. L., & Darwin, C. R. (1953) · The American Midland Naturalist · doi:10.2307/2485224 · Cited by 5,431
A molecular timescale for vertebrate evolution
Kumar, S., & Hedges, S. B. (1998) · Nature · doi:10.1038/31927 · Cited by 1,936
Drake, J. W., Charlesworth, B., Charlesworth, D., & Crow, J. F. (1998) · Genetics · doi:10.1093/genetics/148.4.1667 · Cited by 1,932
King, J. L., & Jukes, T. H. (1969) · Science · doi:10.1126/science.164.3881.788 · Cited by 1,772
Body size, metabolic rate, generation time, and the molecular clock.
Martin, A. P., & Palumbi, S. R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.9.4087 · Cited by 1,239 · cited 1×
“, then species with higher metabolic rates might generate higher concentrations of mutagens and incur more DNA damag”
BackgroundThe causes of molecular evolution
Gillespie, J. H. (1992) · Choice Reviews Online · doi:10.5860/choice.30-2064 · Cited by 1,214
A nonparametric approach to estimating divergence times in the absence of rate constancy.
Sanderson, M. J. (1997) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a025731 · Cited by 1,156 · cited 1×
“A more promising approach is to explicitly model rate variation over the phylogen”
Background
Flagged first, then by citations
Research works printed but not linked: 1
- Zuckerkandl, E. & Pauling, L. in Horizons in Biochemistry (eds Kasha, M. & Pullman, B.) 189–225 (Academic Press, New York, 1962).
Cited by
Sorted by citations
Items 301–400 of 615
The Molecular Clock in the Evolution of Protein Structures
Pascual‐García, A., Arenas, M., & Bastolla, U. (2019) · Systematic Biology · doi:10.1093/sysbio/syz022 · Cited by 20
Elayadeth‐Meethal, M., Aravindakshan, T. V., Muhasin Asaf, V. N., Pramod, S., Maloney, S. K., Martin, G. B., Rivero, M. J., Sejian, V., Naseef, P. P., Kuruniyan, M. S., et al. (2021) · Animals · doi:10.3390/ani11082368 · Cited by 21
Edwards, D. L., Roberts, J. D., & Keogh, J. S. (2008) · Journal of Biogeography · doi:10.1111/j.1365-2699.2008.01927.x · Cited by 21
Congruence test of molecular clock calibration hypotheses based on B ayes factor comparisons
Andújar, C., Soria‐Carrasco, V., Serrano, J., & Gómez‐Zurita, J. (2013) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.12151 · Cited by 21
Diversity of bat astroviruses in Lao PDR and Cambodia
Lacroix, A., Duong, V., Hul, V., Sorn, S., Holl, D., Keo, O., Chea, S., Hassanin, A., Theppangna, W., Silithammavong, S., et al. (2016) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2016.11.013 · Cited by 21
Genetic Isolation Discovered among Previously Described Sympatric Morphs of a Meiobenthic Copepod
Staton, J. L., Garlitska, L. A., Wickliffe, L. C., Coull, B. C., & Villanueva, S. M. (2005) · Journal of Crustacean Biology · doi:10.1651/c-2600.1 · Cited by 21
Spontaneous mutations of a model heterotrophic marine bacterium
Sun, Y., Powell, K. E., Sung, W., Lynch, M., Moran, M. A., & Luo, H. (2017) · The ISME Journal · doi:10.1038/ismej.2017.20 · Cited by 21
Evolutionary dynamics of predicted G-quadruplexes in human and other great apes
Mohanty, S. K., Chiaromonte, F., & Makova, K. D. (2025) · Genome biology · doi:10.1186/s13059-025-03635-1 · Cited by 21
Martínez‐Cruz, B., & Godoy, J. A. (2007) · BMC Evolutionary Biology · doi:10.1186/1471-2148-7-170 · Cited by 20
Stem cells as common ancestors in a colorectal cancer ancestral tree
Shibata, D. K. (2008) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3282f2a2e9 · Cited by 20
Silliman, K., Indorf, J. L., Knowlton, N., Browne, W. E., & Hurt, C. R. (2021) · BMC Ecology and Evolution · doi:10.1186/s12862-021-01836-3 · Cited by 19
Allegrucci, G., Massa, B., Trasatti, A., & Sbordoni, V. (2013) · Systematic Entomology · doi:10.1111/syen.12031 · Cited by 19
Price, B. W., Villet, M. H., WALTON, S. M., & Barker, N. P. (2010) · Systematic Entomology · doi:10.1111/j.1365-3113.2010.00560.x · Cited by 19
Biogeography and the molecular dating game: a futile revival of phenetics?
Nelson, G. J., & Ladiges, P. Y. (2009) · Bulletin de la Société Géologique de France · doi:10.2113/gssgfbull.180.1.39 · Cited by 19
Lakatos, F., Grodzki, W., Zhang, Q., & Stauffer, C. (2007) · Journal of Forest Research · doi:10.1007/s10310-007-0025-9 · Cited by 19
The molecular clock and evolutionary timescales
Luo, A., & Ho, S. Y. W. (2018) · Biochemical Society Transactions · doi:10.1042/bst20180186 · Cited by 19
Ribera, I., & Balke, M. (2007) · Journal of Biogeography · doi:10.1111/j.1365-2699.2007.01694.x · Cited by 18
Razeto‐Barry, P., Díaz, J., & Vásquez, R. A. (2012) · Genetics · doi:10.1534/genetics.112.138628 · Cited by 19
Postgenomic taxonomy of human ureaplasmas – a case study based on multiple gene sequences
Kong, F., & Gilbert, G. L. (2004) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63073-0 · Cited by 18
A somatic genetic clock for clonal species
Yu, L., Renton, J., Burian, A., Khachaturyan, M., Bayer, T., Kotta, J., Stachowicz, J. J., DuBois, K., Baums, I. B., Werner, B., et al. (2024) · Nature Ecology & Evolution · doi:10.1038/s41559-024-02439-z · Cited by 21
Inferring relative numbers of human leucocyte genome replications
Chu, M. W., Siegmund, K. D., Hao, Q., Crooks, G. M., Tavaré, S., & Shibata, D. K. (2008) · British Journal of Haematology · doi:10.1111/j.1365-2141.2008.07142.x · Cited by 17
Log Transformation Improves Dating of Phylogenies
Mai, U., & Mirarab, S. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msaa222 · Cited by 19
Liu, J., Lindström, A. J., Marler, T. E., & Gong, X. (2021) · Annals of Botany · doi:10.1093/aob/mcab118 · Cited by 17
Molecular Clock of Neutral Mutations in a Fitness-Increasing Evolutionary Process
Kishimoto, T., Ying, B., Tsuru, S., Iijima, L., Suzuki, S., Hashimoto, T., Oyake, A., Kobayashi, H., Someya, Y., Narisawa, D., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005392 · Cited by 17
Lattuada, E., Cavallaro, R., Benedetti, F., Cocchi, F., Lorenzi, C., & Smeraldi, E. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.05.084 · Cited by 16
Liao, J., Orsi, R. H., Carroll, L. M., & Wiedmann, M. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15014 · Cited by 16
Cliff, H. B., Wapstra, E., & Burridge, C. P. (2015) · BMC Evolutionary Biology · doi:10.1186/s12862-015-0397-y · Cited by 16
Grouzdev, D. S., Kuznetsov, B. B., Keppen, O. I., Krasilnikova, E. N., Lebedeva, N. V., & Ivanovsky, R. N. (2014) · Microbiology · doi:10.1099/mic.0.082313-0 · Cited by 16
Hershler, R., Liu, H., & Sada, D. W. (2007) · Journal of Molluscan Studies · doi:10.1093/mollus/eym014 · Cited by 16
Cooper, W. G. (2012) · International Journal of Quantum Chemistry · doi:10.1002/qua.22834 · Cited by 16
Stanton, D. W. G., Hart, J. A., Galbusera, P., Helsen, P., Shephard, J. M., Kümpel, N. F., Wang, J., Ewen, J. G., & Bruford, M. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101081 · Cited by 17
A common root for coevolution and substitution rate variability in protein sequence evolution
Rizzato, F., Zamuner, S., Pagnani, A., & Laio, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-53958-w · Cited by 15
REGγ regulates circadian clock by modulating BMAL1 protein stability
Kubra, S., Zhang, H., Si, Y., Gao, X. C., Wang, T., Pan, L., Li, L., Zhong, N., Fu, J., Zhang, B., et al. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00704-9 · Cited by 15
Holmes, R. S., Glenn, J. P., VandeBerg, J. L., & Cox, L. A. (2009) · Journal of Medical Primatology · doi:10.1111/j.1600-0684.2008.00315.x · Cited by 15
Mello, B., & Schrago, C. G. (2012) · Ecology and Evolution · doi:10.1002/ece3.94 · Cited by 14
The Molecular Clock and Evolutionary Rates Across the Tree of Life
Ho, S. Y. W. (2020) · Springer eBooks · doi:10.1007/978-3-030-60181-2_1 · Cited by 16
Phylogeny and evolutionary history of queen polymorphic Myrmecina ants (Hymenoptera: Formicidae)
Steiner, F. M., Schlick-Steiner, B. C., Konrad, H., Linksvayer, T. A., Quek, S., Christian, E., Stauffer, C., & Buschinger, A. (2006) · European Journal of Entomology · doi:10.14411/eje.2006.083 · Cited by 14
Broughton, J. M., & Smith, G. R. (2016) · Developments in earth surface processes · doi:10.1016/b978-0-444-63590-7.00012-3 · Cited by 14
Briones, C., Manrubia, S. C., Lázaro, E., Lazcano, A., & Amils, R. (2004) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2004.10.020 · Cited by 14
Matute, D. R., Torres, I. P., Salgado‐Salazar, C., Restrepo, Á., & McEwen, J. G. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2007.01.006 · Cited by 14
Hedderson, T. A. J., & Zander, R. H. (2007) · Journal of Bryology · doi:10.1179/174328207x205171 · Cited by 14
Correlated evolutionary rates across genomic compartments in Annonaceae
Hoekstra, P. H., Wieringa, J. J., SMETS, E. F., Brandão, R. D., Lopes, J. D. C., Erkens, R. H. J., & Chatrou, L. W. (2017) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2017.05.026 · Cited by 13
Connecting within-host dynamics to the rate of viral molecular evolution
Peck, K. M., Chan, C. H. S., & Tanaka, M. M. (2015) · Virus Evolution · doi:10.1093/ve/vev013 · Cited by 12
Bator, J., Marshall, D. C., Hill, K. B. R., Cooley, J. R., Leston, A., & Simon, C. M. (2021) · Zoological Journal of the Linnean Society · doi:10.1093/zoolinnean/zlab065 · Cited by 13
Martn-Bravo, S., & Escudero, M. (2012) · InTech eBooks · doi:10.5772/32313 · Cited by 13
The Influence of Rickettsiologists on Post-Modern Microbiology
Georgiades, K., Merhej, V., & Raoult, D. (2011) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2011.00008 · Cited by 13
Pushing the envelope on molecular dating
Shields, R. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.03.011 · Cited by 13
Human germline mutation and the erratic evolutionary clockPreprint
Moorjani, P., Gao, Z., & Przeworski, M. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/058024 · Cited by 13
The Use of Bioinformatics for Studying HIV Evolutionary and Epidemiological History in South America
Bello, G., Soares, M. A., & Schrago, C. G. (2011) · AIDS Research and Treatment · doi:10.1155/2011/154945 · Cited by 12
Dates and rates in grape’s plastomes: evolution in slow motion
Zecca, G., Grassi, F., Tabidze, V., Pipia, I., Kotorashvili, A., Kotaria, N., & Beridze, T. (2019) · Current Genetics · doi:10.1007/s00294-019-01004-7 · Cited by 16
Babarinde, I. A., & Saitou, N. (2020) · Genome Biology and Evolution · doi:10.1093/gbe/evaa157 · Cited by 11
Cooper, W. G. (2009) · Biochemical Genetics · doi:10.1007/s10528-009-9293-8 · Cited by 12
Soria‐Hernanz, D. F., Braverman, J. M., & Hamilton, M. B. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn074 · Cited by 13
Disorders of Sleep and Circadian Rhythms
Overeem, S., Lammers, G. J., & Tafti, M. (2007) · Elsevier eBooks · doi:10.1016/b978-012369509-3.50028-7 · Cited by 12
Biodiversity of octopuses in the Americas
González-Gómez, R., Avendaño, O., Barriga-Sosa, I. D. L. A., Bastos, P., Caamal‐Monsreal, C., Castillo-Estrada, G., Cedillo-Robles, C. E., Daw, A. L., Díaz‐Santana‐Iturrios, M., Galindo-Cortés, G., et al. (2024) · Marine Biology · doi:10.1007/s00227-024-04489-0 · Cited by 11
Extreme Deviations from Expected Evolutionary Rates in Archaeal Protein Families
Petitjean, C., Makarova, K. S., Wolf, Y. I., & Koonin, E. V. (2017) · Genome Biology and Evolution · doi:10.1093/gbe/evx189 · Cited by 10
Does the Evolution of Complex Life Depend on the Stellar Spectral Energy Distribution?
Haqq-Misra, J. (2019) · Astrobiology · doi:10.1089/ast.2018.1946 · Cited by 11
Arab, D. A., & Lo, N. C. (2021) · Journal of Molecular Evolution · doi:10.1007/s00239-021-10001-9 · Cited by 11
Ernst Mayr, the tree of life, and philosophy of biology
O’Malley, M. A. (2010) · Biology & Philosophy · doi:10.1007/s10539-010-9214-6 · Cited by 12
Strength and Limitations of DNA Barcode under the Multidimensional Species Perspective.
Sbordoni, V. (2010) · OpenstarTs (Univeristy of Trieste https://www.units.it/) · Cited by 11
Admixture of evolutionary rates across a butterfly hybrid zone
Xiong, T., Li, X., Yago, M., & Mallet, J. (2022) · eLife · doi:10.7554/elife.78135 · Cited by 10
The Cambrian explosion triggered by critical turning point in genome size evolution
Li, D. J., & Zhang, S. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.01.032 · Cited by 10
Andonov, A. P., Coulthart, M. B., Pérez‐Losada, M., Crandall, K. A., Posada, D., Padmore, R., Giulivi, A., Oger, J. J.-F., Peters, A. A., & Dekaban, G. A. (2012) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2012.07.015 · Cited by 10
Leber, M. F., Hoyler, B., Prien, S., Neault, S., Engeland, C. E., Förster, J. M., Bossow, S., Springfeld, C., Kalle, C. V., Jäger, D., et al. (2020) · Journal of General Virology · doi:10.1099/jgv.0.001395 · Cited by 10
Stem Cell Chronicles: Autobiographies Within Genomes
Shibata, D. K., & Tavaré, S. (2007) · Stem Cell Reviews and Reports · doi:10.1007/s12015-007-0022-6 · Cited by 10
Cooper, W. G. (2011) · Interdisciplinary Sciences Computational Life Sciences · doi:10.1007/s12539-011-0065-x · Cited by 10
Neutral and adaptive protein evolution
Yang, Z. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198567028.003.0008 · Cited by 10
Ślesak, I., & Ślesak, H. (2024) · New Phytologist · doi:10.1111/nph.19633 · Cited by 9
Fusca, D. D., Dall’Acqua, M. N., Ramirez, S. S., & Cutter, A. D. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011852 · Cited by 11
Adaptive tracking with antagonistic pleiotropy results in seemingly neutral molecular evolution
Song, S., Chen, P., Shen, X., & Zhang, J. (2025) · Nature Ecology & Evolution · doi:10.1038/s41559-025-02887-1 · Cited by 9
Ancestral inference in tumors: How much can we know?
Zhao, J., Siegmund, K. D., Shibata, D. K., & Marjoram, P. (2014) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2014.05.027 · Cited by 9
Lack, J., & Bussche, R. A. V. D. (2009) · Acta Chiropterologica · doi:10.3161/150811009x465668 · Cited by 8
Mays, H. L., Oehler, D. A., Morrison, K. W., Morales, A. E., Lycans, A., Perdue, J., Battley, P. F., Cherel, Y., Chilvers, B. L., Crofts, S., et al. (2019) · Journal of Heredity · doi:10.1093/jhered/esz051 · Cited by 9
Toward a syntactic phylogeny of modern Indo-European languages
Longobardi, G., Guardiano, C., Silvestri, G., Boattini, A., & Ceolin, A. (2015) · Benjamins current topics · doi:10.1075/bct.75.07lon · Cited by 9
Osugi, A., Tamaru, A., Yoshiyama, T., Iwamoto, T., Mitarai, S., & Murase, Y. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04289-23 · Cited by 8
Terrestrial Fauna and Hominin DNA from Sedimentary Archives
Murchie, T. J., Giguet‐Covex, C., Heintzman, P. D., Slon, V., & Wang, Y. (2023) · Developments in paleoenvironmental research · doi:10.1007/978-3-031-43799-1_11 · Cited by 9
On the number of genomic pacemakers: a geometric approach
Snir, S. (2014) · Algorithms for Molecular Biology · doi:10.1186/s13015-014-0026-0 · Cited by 8
Protein Conformational Dynamics and Signaling in Evolution and Pathophysiology
Schweizer, L., & Mueller, L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-411460-9.00007-0 · Cited by 8
Comparative Microbial Genomics and Forensics
Massey, S. E. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.emf-0001-2013 · Cited by 8
Change! Combining Analytic Approaches with Street Wisdom
Bammer, G. (2015) · ANU Press eBooks · doi:10.22459/ccaasw.07.2015 · Cited by 16
The species problem in biology – another look
Pavlinov, I. Y. (2009) · Proceedings of the Zoological Institute RAS · doi:10.31610/trudyzin/2009.supl.1.250 · Cited by 8
Understanding Neutral Genomic Molecular Clocks
Yi, S. V. (2007) · Evolutionary Biology · doi:10.1007/s11692-007-9010-7 · Cited by 10
Scarpa, F., Sanna, D., Cossu, P., Lai, T., Curini-Galletti, M. C., & Casu, M. (2017) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2017.08.011 · Cited by 8
Biogeografia dos peixes marinhos do Atlântico Sul ocidental: Padrões e Processos
Caires, R. A. (2014) · Arquivos de Zoologia · doi:10.11606/issn.2176-7793.v45iespp5-24 · Cited by 8
Lichen-Forming Fungi, Diversification of
Lumbsch, H. T. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800049-6.00249-3 · Cited by 8
Bai, X., Guo, X., Zhang, X. J., Song, W., Li, Y. H., Luo, W., Cao, X., & Wang, W. M. (2013) · Mitochondrial DNA · doi:10.3109/19401736.2013.823166 · Cited by 7
Mays, H. L., McKay, B. D., Tietze, D. T., Yao, C., Miller, L. N., Moreland, K. N., & Lei, F. (2015) · Avian Research · doi:10.1186/s40657-015-0025-y · Cited by 7
Naydenov, K. D., Naydenov, M. K., Alexandrov, A. K., Gurov, T. V., Gyuleva, V., Hinkov, G., Ivanovska, S., Tsarev, A., Nikolic, B. M., Goudiaby, V., et al. (2023) · European Journal of Forest Research · doi:10.1007/s10342-022-01513-0 · Cited by 8
Covariation of Branch Lengths in Phylogenies of Functionally Related Genes
Li, W. L. S., & Rodrigo, A. G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008487 · Cited by 8
Edwards, D. L., & Roberts, J. D. (2011) · Australian Journal of Zoology · doi:10.1071/zo11005 · Cited by 7
Phylogenetics and Conservation in New Zealand: The Long and the Short of It
Trewick, S. A., & Morgan‐Richards, M. (2016) · Topics in biodiversity and conservation · doi:10.1007/978-3-319-22461-9_5 · Cited by 7
GONZÁLEZ-WEVAR, C. A., Hüne, M., Rosenfeld, S., Saucède, T., Féral, J., Mansilla, A., & Poulin, É. (2016) · Biodiversity · doi:10.1080/14888386.2016.1181573 · Cited by 7
Florio, A. M., & Raxworthy, C. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154144 · Cited by 7
Simulating molecular evolution
Yang, Z. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198567028.003.0009 · Cited by 7
Phylogenetic Analyses: A Toolbox Expanding towards Bayesian Methods
Aris‐Brosou, S., & Xia, X. (2008) · International Journal of Plant Genomics · doi:10.1155/2008/683509 · Cited by 7
Ragupathy, R., Banks, T. W., & Cloutier, S. (2010) · Molecular Genetics and Genomics · doi:10.1007/s00438-009-0509-8 · Cited by 7
Koch, N. M., Thompson, J. R., Mooi, R., & Rouse, G. W. (2025) · Systematic Biology · doi:10.1093/sysbio/syaf055 · Cited by 9
Reconstructing species responses to past climatic changes using niche modeling and genetic data
Ježková, T. (2020) · PubMed · doi:10.34917/2026082 · Cited by 6
Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages
Översti, S., & Palo, J. U. (2022) · Genome Biology and Evolution · doi:10.1093/gbe/evac097 · Cited by 9
Metadata
- Authors
- Bromham, L., & Penny, D.
- Affiliations
- University of Sussex (GB)
- Allan Wilson Centre (NZ)
- Corresponding author
- Bromham, Lindell
- ORCID
- Bromham, Lindell
- Venue
- Nature Reviews Genetics
- Published
- 2003-03
- Volume
- 4
- Issue
- 3
- Pages
- 216-224
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2062220010
- Semantic Scholar
- 07e298aa4bc7299c0bfd8164d900b90ce80102a2
- Cited by
- 615
- References
- 74
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 17 · 2023: 14 · 2022: 11 · 2021: 25 · 2020: 21 · 2019: 21 · 2018: 17 · 2017: 20 · 2016: 27 · 2015: 24 · 2014: 50 · 2013: 40 · 2012: 27
- FWCI
- 3.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Figshare (submittedVersion)
- ANU Open Research (Australian National University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Keywords
- molecular clock, molecular evolution rate, neutral theory of molecular evolution, rate variation, divergence time estimation, evolutionary history, viral epidemics
- MeSH terms
- Animals, Disease Outbreaks, DNA, Genetics, Population, Humans, Models, Genetic, Mutation, Population Density, Proteins, Selection, Genetic, Time Factors, Evolution, Molecular, Communicable Diseases, Emerging, History, Ancient
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-06, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-06 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review