A molecular phylogeny of living primates
Open accessAbstract
Comparative genomic analyses of primates offer considerable potential to define and understand the processes that mold, shape, and transform the human genome. However, primate taxonomy is both complex and controversial, with marginal unifying consensus of the evolutionary hierarchy of extant primate species. Here we provide new genomic sequence (~8 Mb) from 186 primates representing 61 (~90%) of the described genera, and we include outgroup species from Dermoptera, Scandentia, and Lagomorpha. The resultant phylogeny is exceptionally robust and illuminates events in primate evolution from ancient to recent, clarifying numerous taxonomic controversies and providing new data on human evolution. Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered. Our resolution of the primate phylogeny provides an essential evolutionary framework with far-reaching applications including: human selection and adaptation, global emergence of zoonotic diseases, mammalian comparative genomics, primate taxonomy, and conservation of endangered species.
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TL;DR
This study presents a highly resolved molecular phylogeny of living primates based on new genomic sequence from 186 primates representing 61 genera, using 34,927 bp from 54 nuclear genes. It clarifies primate taxonomic relationships, divergence dates, and patterns of genome evolution including rate heterogeneity and insertion/deletion variation.
Key findings
- The phylogeny includes 191 taxa (186 primates representing 61 genera, about 90% of described genera) plus outgroups from Dermoptera, Scandentia, and Lagomorpha; 166 of 189 nodes (88%) have bootstrap values of 90–100% and Bayesian posterior probabilities of 0.9–1.0, with only 3 of 189 nodes collapsed into polytomies in bootstrap analyses.
- Strepsirrhini split from Haplorrhini approximately 87 MYA (node 185); tarsiers are supported as sister to Simiiformes (BS = 85 MP; 98 ML; 0.99 PP) to form Haplorrhini, and Dermoptera is affirmed as the closest mammalian order to Primates, followed by Scandentia.
- Platyrrhini diverged from Catarrhini roughly 43.5 MYA; within Cebidae, Cebus and Saimiri emerged about 20 MYA, followed by a lineage splitting to Callitrichinae and Aotus, with Aotus showing 15 synapomorphic indels, the most observed in Simiiformes, and Callitrichinae branching mirroring decreasing body size.
- Cercopithecoidea shows low divergence, especially Papionini; Cercopithecini divergence is nearly twice that of Papionini (mean branch length = 13.1 vs. 7.43, p<0.005), Homo-Pan genetic distance ranges from 6.92 to 7.90×10−3 substitutions/site, and the global nucleotide substitution rate is 6.163×10−4 substitutions/site/MY.
Methods
- New genomic sequence (~8 Mb) was generated from 186 primates representing 61 genera, with outgroups from Dermoptera, Scandentia, and Lagomorpha; 54 nuclear genes yielded a final 34,927 bp after correction for ambiguous sites from an original 43,493 bp per OTU.
- DNA was extracted from blood, buffy coat, hair, buccal swabs, tissues, or cell cultures, PCR-amplified, Sanger-sequenced, aligned with MAFFT, and edited with GBLOCK; partitions included X, Y, autosome, intron, exon, and UTR segments.
- Phylogenetic reconstruction used maximum likelihood and maximum parsimony in PAUP* and GARLI with bootstrap support (1000 MP, 100 ML), plus Bayesian BEAST analyses with an uncorrelated lognormal relaxed clock and nine fossil calibration points; indels were identified with FASTGAP and analyzed by regression and ANOVA.
Limitations
- The paper states that only 3 of 189 nodes are polytomies in bootstrap analyses (nodes 28, 38, 158), that Lemuriformes node 158 collapses into an unresolved trichotomy, that the origin of primates remains unresolved, and that computational constraints limited BEAST analyses to five different species sets.
- The text notes that approximately half of the 261–377 described primate species and 90% of genera are included, that the Y-chromosome tree is based on 127 males as a subset of 191 total taxa, and that some indels were in regions not amplified across all species.
- Evident from the text: despite overall high resolution, some nodes have low support (e.g., node 158; node 187 posterior probability 0.54), and several taxonomic controversies remain, including within Galago, Cercopithecus, and Asian Colobinae.
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Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 55 cited sources checked · 0 supported · 0 flagged
- Findingown data
Strepsirrhines split with Haplorrhini approximately 87 MYA (node 185).
“Here we provide strong evidence that strepsirrhines split with suborder Haplorrhini approximately 87 MYA (node 185).”
Quote in the paperSubstantial claim - Findingown data
Separate phylogenetic analyses of the data partitions are generally concordant.
“Separate phylogenetic analyses of these data partitions are generally concordant.”
Quote in the paperSubstantial claim - Findingown data
Greater frequency of phylogenetic inconsistencies or unresolved nodes occur in subset trees compared with the entire concatenated data set.
“However, greater frequency of phylogenetic inconsistencies or unresolved nodes occur in these subset trees (Figures S2, S3, S4, S5, S6, S7, S8, S9, S10, S11, S12, S13), compared with the entire concatenated data set (Figure 2, Figure S1).”
Quote in the paperSubstantial claim - Findingown data
Only 3 of 189 nodes (nodes 28, 38, 158) are polytomies in the bootstrap analyses.
“Further, only 3 of 189 nodes (nodes 28, 38, 158) are polytomies in the bootstrap analyses (Table 1 and Table 3; Figure 2, Figure S1).”
Quote in the paperSubstantial claim - Findingown data
The greatest proportion of phylogenetically informative sites occurred in Y-linked genes (56%) compared with regions sequenced from the X-chromosome (40%) and autosomes (42%).
“The greatest proportion of phylogenetically informative sites occurred in Y-linked genes (56%) compared with regions sequenced from the X-chromosome (40%) and autosomes (42%) (Table 4, Table S4), a finding also observed in carnivores [6], [7].”
Quote in the paperNot a substantial claim
- Findingown data
The reconstructed primate phylogeny uncovers unequal rates of evolution.
“Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered.”
Quote in the paperSubstantial claim - Findingown data
The reconstructed primate phylogeny uncovers reticulate evolution.
“Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered.”
Quote in the paperSubstantial claim - Findingown data
The reconstructed primate phylogeny uncovers ongoing speciation.
“Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered.”
Quote in the paperSubstantial claim - Findingown data
The reconstructed primate phylogeny uncovers disparate distributions of insertions/deletions among primate lineages.
“Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered.”
Quote in the paperNot a substantial claim - Findingown data
The reconstructed primate phylogeny uncovers ancient relic lineages.
“Ongoing speciation, reticulate evolution, ancient relic lineages, unequal rates of evolution, and disparate distributions of insertions/deletions among the reconstructed primate lineages are uncovered.”
Quote in the paperSubstantial claim - Findingown data
The presented molecular phylogeny is based on 34,927 bp (after correction for ambiguous sites from the original dataset of 43,493 bp per OTU) amplified from 54 nuclear genes in 191 taxa including 186 primates representing 61 genera.
“A comprehensive molecular phylogeny based on 34,927 bp (after correction for ambiguous sites from the original dataset of 43,493 bp per operational taxonomic unit, OTU) amplified from 54 nuclear genes in 191 taxa including 186 primates representing 61 genera is presented (Figure 1, Figure 2, Figure S1, Table S1, and Table S2).”
Quote in the paperSubstantial claim - Findingown data
The sequence phylogeny supports tarsiers as a sister lineage to Simiiformes to form Haplorrhini (BS = 85 MP; 98 ML; 0.99 PP).
“The sequence phylogeny unambiguously supports tarsiers as a sister lineage (albeit distant) to Simiiformes (BS = 85 MP; 98 ML; 0.99 PP) to form Haplorrhini (node 143).”
Quote in the paperSubstantial claim - Findingown data
A long continuous Tarsiiformes branch (node 142) is marked by 25 synapomorphic indels.
“A long continuous Tarsiiformes branch (node 142), marked by 25 synapomorphic indels, is consistent with a relict lineage of ancient origin.”
Quote in the paperSubstantial claim - Findingown data
Mean nucleotide divergence between Lorisidae species is 4-5 times that observed in family Hominidae.
“For example, mean nucleotide divergence between Lorisidae species is 4–5 times that observed in family Hominidae (Figure 3)”
Quote in the paperNot a substantial claim - Findingown data
The Otolemur lineage (node 180) is placed as part of a paraphyletic grouping (node 182) along with two other extant Galago lineages (nodes 181, 183).
“However, the Otolemur lineage (node 180) is placed as part of a paraphyletic grouping (node 182) along with two other extant Galago lineages (nodes 181, 183), suggesting that further taxonomic investigation of Galago is warranted.”
Quote in the paperSubstantial claim - Findingnone given
Platyrrhini diverged from a common ancestor with Catarrhini (node 141) roughly 43.5 MYA during the Eocene.
“Here, Platyrrhini clearly diverged from a common ancestor with Catarrhini (node 141) roughly 43.5 MYA during the Eocene.”
Quote in the paperSubstantial claim - Findingown data
Relatively weak nodal support here collapses Lemuriformes into an unresolved trichotomy of Lemuridae, Indriidae, and the Lepilemuridae + Cheirogaleidae lineage (node 158).
“Further, relatively weak nodal support here collapses Lemuriformes into an unresolved trichotomy of Lemuridae, Indriidae, and the Lepilemuridae + Cheirogaleidae lineage (node 158).”
Quote in the paperNot a substantial claim - Findingown data
The common ancestor to Pitheciidae originated 20.2 MYA (node 140).
“The common ancestor to Pitheciidae (uakaris, titis and sakis) originated 20.2 MYA (node 140)”
Quote in the paperNot a substantial claim - Findingown data
The phylogeny unambiguously resolves the relative divergence pattern among Platyrrhini families from a common ancestor 24.8 MYA (node 78).
“the phylogeny unambiguously resolves the relative divergence pattern among families from a common ancestor 24.8 MYA (node 78).”
Quote in the paperSubstantial claim - Findingown data
During a relatively brief interval (~700,000 years) a lineage arose (node 112) that split to form the Callitrichinae and Aotus.
“Subsequently, during a relatively brief interval (∼700,000 years) a lineage arose (node 112) that split to form the Callitrichinae (marmosets and tamarins) and Aotus (night monkeys).”
Quote in the paperSubstantial claim - Findingown data
Lorisidae divergence significantly (p<0.05) exceeds the average genetic divergence across all Strepsirrhini.
“and significantly (p<0.05) exceed the average genetic divergence across all of Strepsirrhini (nodes 176–178, Table S7, Figure 3).”
Quote in the paperNot a substantial claim - Findingnone given
Aotus, Cebus and Saimiri species are larger than the more derived and smaller squirrel-sized Callitrichinae of Saguinus, Leontopithecus, Callimico, Mico, Cebuella and Callithrix.
“Aotus, Cebus and Saimiri species are larger than the more derived and smaller squirrel-sized Callitrichinae of Saguinus, Leontopithecus, Callimico, Mico, Cebuella and Callithrix.”
Quote in the paperSubstantial claim - Findingcitation
The remainder of Old World monkeys (tribes Papionini and Cercopithecini) arose from a common ancestor approximately 11.5 MYA (node 41).
“The remainder of Old World monkeys (tribes Papionini and Cercopithecini) [2] arose from a common ancestor approximately 11.5 MYA (node 41).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [2] CP Groves, 2001, Primate taxonomy.
Not checked in the free run.
- Findingown data
All genetic studies, including the present, place Trachypithecus vetulus (monticola) nested within the Semnopithecus clade (node 50).
“Nonetheless, all genetic studies, including the present, place Trachypithecus vetulus (monticola) nested within the Semnopithecus clade (node 50), suggesting the need for taxonomic revision.”
Quote in the paperSubstantial claim - Findingown data
Previously ambiguous associations between Trachypithecus and Semnopithecus (nodes 43-51) are clarified.
“Further, previously ambiguous associations between Trachypithecus and Semnopithecus (nodes 43–51) are clarified.”
Quote in the paperSubstantial claim - Findingcitation
Aotus is the sister lineage to Callitrichinae.
“Here, Aotus is the sister lineage to Callitrichinae (marmosets, tamarins) as originally hypothesized by Goodman (1998) [1], [28].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [1] M Goodman, 1998, Toward a phylogenetic classification of Primates based on DNA evidence complemented by fossil evidence., Molecular Phylogenetics and Evolution source
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- cites [28] JC Opazo, 2006, Phylogenetic relationships and divergence times among New World monkeys (Platyrrhini, Primates)., Molecular Phylogenetics and Evolution source
Not checked in the free run.
- Findingown data
The "hominoid slow-down" hypothesized to have occurred in human evolution is confounded by the reduced rates observed in all Catarrhini (not just Homininae) compared with Platyrrhini and Strepsirrhini.
“For example, the “hominoid slow-down” hypothesized to have occurred in human evolution, is confounded by the reduced rates observed in all Catarrhini (not just Homininae) compared with Platyrrhini and Strepsirrhini (Figure 3, Table S10).”
Quote in the paperNot a substantial claim - Findingown data
Sequence divergence between tribes is unequal with Cercopithecini nearly twice that of Papionini (mean branch length = 13.1, 7.43, respectively, p<0.005).
“Lastly, sequence divergence between tribes is unequal with Cercopithecini nearly twice that of Papionini (mean branch length = 13.1, 7.43, respectively, p<0.005)”
Quote in the paperNot a substantial claim - Findingnone given
The relative branching patterns among infraorders, parvorders, superfamilies, families, subfamilies, genera and species are resolved with high measures of support for all but three nodes.
“Additional insights are possible because the relative branching patterns among infraorders, parvorders, superfamilies, families, subfamilies, genera and species are resolved with high measures of support for all but three nodes.”
Quote in the paperSubstantial claim - Findingnone given
The Lorisidae are marked by extraordinary divergence relative to other primate lineages.
“By contrast, the Lorisidae are marked by extraordinary divergence relative to other primate lineages.”
Quote in the paperNot a substantial claim - Findingown data
The major correlate of indel frequency is not substitution rate, but overall genome divergence represented by branch length (R-square = 0.659 Lorisiformes; 0.610 Lemuriformes; 0.3286 Simiiformes; P<0.05).
“The major correlate of indel frequency is not substitution rate, but overall genome divergence represented by branch length (R-square = 0.659 Lorisiformes; 0.610 Lemuriformes; 0.3286 Simiiformes; P<0.05).”
Quote in the paperSubstantial claim - Findingown data
Old World monkeys (Cercopithecoidea) display remarkably low levels of divergence, particularly within Papionini.
“For example, Old World monkeys (Cercopithecoidea) display remarkably low levels of divergence, particularly within Papionini”
Quote in the paperNot a substantial claim - Findingown data
The "phyletic dwarfism" of the Callitrichinae (nodes 97, 85) and the evolution of nocturnalism in Aotinae are correlated with increased rates along specific branches (see nodes 99, 100) rather than being a function of an average rate among all branches within the lineage.
“By contrast, the “phyletic dwarfism” of the Callitrichinae (nodes 97, 85) and the evolution of nocturnalism in Aotinae are correlated with increased rates along specific branches (see nodes 99, 100) rather than an being a function of an average rate among all branches within the lineage (Figure 3)”
Quote in the paperSubstantial claim - Interpretationown data
Resolving differences among previous studies that used only single genes, mtDNA, and smaller numbers of primate taxa requires both genome-wide datasets and maximum representation of species.
“Thus, these findings illustrate the need for both genome-wide datasets and maximum representation of species to resolve differences among previous studies that used only single genes, the uniparentally inherited mtDNA molecular marker and smaller numbers of primate taxa.”
Quote in the paperSubstantial claim - Premisecitation
Efforts to overcome the deficiency using a supermatrix approach with published sequences culled from prior studies are inherently flawed by a prohibitively large proportion of missing data for each taxon (e.g. 59-85%).
“Efforts to overcome this deficiency using a supermatrix approach [4], [5] with published sequences culled from these prior studies are inherently flawed by a prohibitively large proportion of missing data for each taxon (e.g. 59–85% see [5]).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [4], [5]
Not checked in the free run.
- cites [5] PH Fabre, 2009, Patterns of macroevolution among Primates inferred from a supermatrix of mitochondrial and nuclear DNA., Molecular Phylogenetics and Evolution source
Not checked in the free run.
- Interpretationown data
The long continuous Tarsiiformes branch is consistent with a relict lineage of ancient origin.
“A long continuous Tarsiiformes branch (node 142), marked by 25 synapomorphic indels, is consistent with a relict lineage of ancient origin.”
Quote in the paperNot a substantial claim - Interpretationown data
Common ancestors of Chiromyiformes and Lemuriformes likely colonized the island of Madagascar prior to 58.6 MYA (node 174).
“Common ancestors of Chiromyiformes and Lemuriformes likely colonized the island of Madagascar prior to 58.6 MYA (node 174).”
Quote in the paperSubstantial claim - Interpretationcitation
Chiromyiformes diverged from a common ancestor with Lemuriformes shortly after colonisation of Madagascar.
“Chiromyiformes diverged from a common ancestor with Lemuriformes shortly after colonisation of Madagascar [14], [19]”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [14] A Matsui, 2009, Molecular phylogeny and evolution of prosimians based on complete sequences of mitochondrial DNAs., Gene source
Not checked in the free run.
- cites [19] C Roos, 2004, Primate jumping genes elucidate strepsirrhine phylogeny., Proceedings of the National Academy of Sciences of the United States of America source
Not checked in the free run.
- Interpretationcitation
"Phyletic dwarfism" is supported in Cebidae.
“Another case of adaptation termed “phyletic dwarfism,” defined as a gradient in morphological size partially correlated with evolutionary time [32], is supported in Cebidae.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [32] SM Ford, 1992, Systematics and body size: implications for feeding adaptations in New World monkeys., American Journal of Physical Anthropology source
Not checked in the free run.
- Interpretationown data
Rapid speciation into the 3 genera occurred early in Homininae evolution.
“and suggests rapid speciation into the 3 genera occurred early in Homininae evolution.”
Quote in the paperSubstantial claim - Premisecitation
Hylobatidae are noted for exceptional rates of chromosome re-arrangement, 10-20 times faster than in most mammals.
“Hylobatidae (siamang, gibbons, hoolock) are noted for exceptional rates of chromosome re-arrangement [52], [53], 10–20 times faster than in most mammals [54].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [52] S Muller, 2003, Chromosomal phylogeny and evolution of gibbons (Hylobatidae)., Human Genetics source
Not checked in the free run.
- cites [53] A Jauch, 1992, Reconstruction of genomic rearrangements in great apes and gibbons by chromosome painting., Proceedings of the National Academy of Sciences of the United States of America source
Not checked in the free run.
- cites [54] D Misceo, 2008, Tracking the complex flow of chromosome rearrangements from the Hominoidea Ancestor to extant Hylobates and Nomascus Gibbons by high-resolution synteny mapping., Genome Research source
Not checked in the free run.
- Interpretationreasoning
Hylobatidae exhibits episodes of rapid divergence perhaps related to excessive genome re-organization.
“Thus, Hylobatidae exhibits episodes of rapid divergence perhaps related to excessive genome re-organization and warrants additional investigation.”
Quote in the paperSubstantial claim - Interpretationreasoning
Resolution of Allenopithecus (node 40) and Miopithecus (node 35) speciation herein suggests a single evolutionary transition from an arboreal to a terrestrial lifestyle in E. patas, C. l'hoesti, and Chlorocebus species.
“Further, resolution of Allenopithecus (node 40) and Miopithecus (node 35) speciation herein suggests a single evoluiontary transition from an arboreal to a terrestrial lifestyle in E. patas, C. l'hoesti, and Chlorocebus species.”
Quote in the paperSubstantial claim - Interpretationown data
The molecular genetic resolution of the primate phylogeny provides a robust comparative genomic resource to affirm, alter, and extend previous taxonomic inferences.
“The molecular genetic resolution of the primate phylogeny provides a robust comparative genomic resource to affirm, alter, and extend previous taxonomic inferences.”
Quote in the paperSubstantial claim - Premisecitation
The TMRCA of Catarrhini is 29.0 MYA (stdev 6.0).
“C) mean = 29.0 MYA, stdev = 6.0 for TMRCA of Catarrhini [80]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [80] C Poux, 2004, Primate phylogeny, evolutionary rate variations, and divergence times: a contribution from the nuclear gene IRBP., American Journal of Physical Anthropology source
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
- Study design and conductown data
The Y-chromosome tree is not directly comparable to the topologies of the other data partitions because the number of males (N = 127) was a subset of the total (N = 191).
“It should be noted that the Y-chromosome tree is not directly comparable to the topologies of the other data partitions because the number of males (N = 127) was a subset of the total (N = 191).”
Quote in the paperNot a substantial claim - Interpretationown data
The large amount of sequence available here for each well-recognized species in Hominidae provides a baseline estimate of average genetic divergence per taxonomic level in primates.
“In the context of human evolution, the large amount of sequence available here for each well-recognized species in Hominidae provides a baseline estimate of average genetic divergence per taxonomic level in primates.”
Quote in the paperSubstantial claim - Interpretationreasoning
An adaptive "speed-up" occurred in the common ancestors of these extant species.
“suggesting that an adaptive “speed-up” occurred in the common ancestors of these extant species.”
Quote in the paperSubstantial claim - Premisecitation
The TMRCA of Platyrrhini is 23.5 MYA (stdev 3.0).
“D) mean = 23.5 MYA, stdev = 3.0 for TMRCA of Platyrrhini [26], [81]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [26], [81]
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
- Premisecitation
The TMRCA of Homo-Pan is 6.5 MYA (stdev 0.8).
“H) mean = 6.5 MYA, stdev = 0.8 for TMRCA of Homo-Pan [84]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [84] P Vignaud, 2002, Geology and palaeontology of the Upper Miocene Toros-Menalla hominid locality, Chad., Nature source
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
- Premisecitation
The TMRCA of Theropithecus clade is 4.0 MYA (stdev 0.4).
“F) mean = 4.0 MYA, stdev = 0.4 for TMRCA of Theropithecus clade [40], [83]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [40], [83]
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
- Premisecitation
The TMRCA of Papionini is 7 MYA (stdev 1.0).
“E) mean = 7 MYA, stdev = 1.0 for TMRCA of Papionini [82]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [82] ME Steiper, 2004, Genomic data support the hominoid slowdown and an Early Oligocene estimate for the hominoid-cercopithecoid divergence., Proceedings of the National Academy of Sciences of the United States of America source
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
- May combine two claims. 60
- Classified as probably not a substantial claim. 21
May combine two claims.
FindingcitationDermoptera is the closest mammalian order relative to Primates, followed by Scandentia.
“Rooted by Lagomorpha, the phylogeny affirms Dermoptera as the closest mammalian order relative to Primates, followed by Scandentia [16], [17].”
- Also stated in: § Conclusions · plain
“Dermoptera is the closest mammalian order to Primates;”
Quote in the paperSubstantial claim0 of 2 sources checked- Also stated in: § Conclusions · plain
May combine two claims.
Findingown dataThe study provides new genomic sequence (~8 Mb) from 186 primates representing 61 (~90%) of the described genera, and includes outgroup species from Dermoptera, Scandentia, and Lagomorpha.
“Here we provide new genomic sequence (∼8 Mb) from 186 primates representing 61 (∼90%) of the described genera, and we include outgroup species from Dermoptera, Scandentia, and Lagomorpha.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe ancient lineage is monophyletic and defined by a long branch and eight shared insertions/deletions (indels) (node 144).
“The ancient lineage is monophyletic and defined by a long branch and eight shared insertions/deletions (indels) (node 144).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe phylogeny is highly resolved, with bootstrap values of 90-100% and Bayesian posterior probabilities of 0.9-1.0 at 166 of the 189 nodes (88%).
“The phylogeny is highly resolved, with bootstrap values of 90–100% and Bayesian posterior probabilities of 0.9–1.0 at 166 of the 189 nodes (88%)(Table 1, Table 2, Table 3).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataDaubentonia is a single relict genus defined by a long branch with high indel frequency (N = 14).
“and today consists of a single relict genus Daubentonia defined by a long branch with high indel frequency (N = 14) (Figure 2, Figure S1, Table S7).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe Cebidae radiation initiated with the emergence of sister taxa Cebus (Cebinae) and Saimiri (Saimirinae) approximately 20 MYA (node 113), in agreement with other molecular studies.
“The Cebidae radiation initiated with the emergence of sister taxa Cebus (Cebinae) and Saimiri (Saimirinae) approximately 20 MYA (node 113), in agreement with other molecular studies [27]-[30].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [27]-[30]
Not checked in the free run.
May combine two claims.
Findingown dataWithin Lorisidae, the four extant genera split into the African subfamily Perodicticinae (Arctocebus, Perodictus) and the Asian subfamily Lorisinae (Nycticebus, Loris) and are the most divergent within all of primates.
“Within Lorisidae, the four extant genera split into the African subfamily Perodicticinae (Arctocebus, Perodictus) and the Asian subfamily Lorisinae (Nycticebus, Loris) and are the most divergent within all of primates.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataNext to radiate are the Atelidae (node 126), with the most basal lineage leading to Alouatta, followed by the divergence of Ateles from a South American lineage comprised of sister genera Lagothrix and Brachyteles.
“Next to radiate are the Atelidae (node 126), with the most basal lineage leading to Alouatta (howler monkeys), currently widely distributed from Mexico to northern Argentina, followed by the divergence of Ateles (spider monkeys) from South American lineage comprised of sister genera (node 121) of Lagothrix (woolly monkeys) and Brachyteles (muriquis).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataA few indels define alternate evolutionary topologies, such as tarsiers aligned with Strepsirrhini (1 indel, ZFX) or Scandentia (1 indel, DCTN2), compared with those that support an ancestral grouping of Tarsiiformes + Strepsirrhini + Dermoptera + Scandentia (2 indels, PLCB4, POLA1).
“A few indels (Table S5) define alternate evolutionary topologies, such as tarsiers aligned with Strepsirrhini (1 indel, ZFX) or Scandentia (1 indel, DCTN2), compared with those that support an ancestral grouping of Tarsiiformes +Strepsirrhini +Dermoptera +Scandentia (2 indels, PLCB4, POLA1).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataOur data affirm the ancient split of Strepsirrhini, approximately 68.7 MYA (node 144), into the progenitors of Lemuriformes/Chiromyiformes (origin 58.6 MYA, node 174) and Lorisiformes (origin 40.3 MYA, node 184).
“Our data affirm the ancient split of Strepsirrhini, approximately 68.7 MYA (node 144), into the progenitors of Lemuriformes/Chiromyiformes (origin 58.6 MYA, node 174) and Lorisiformes (origin 40.3 MYA, node 184).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationThis branching pattern among Lemuriformes families agrees with earlier nuclear gene segment findings and differs from studies using mtDNA sequence and Alu insertion variation.
“This branching pattern among families agrees with earlier nuclear gene segment findings [20] that differ from studies using mtDNA sequence and Alu insertion variation which were unable to resolve these hierarchical associations [19].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [20] JE Horvath, 2007, Primate comparative genomics: lemur biology and evolution., Trends in Genetics source
Not checked in the free run.
- cites [19] C Roos, 2004, Primate jumping genes elucidate strepsirrhine phylogeny., Proceedings of the National Academy of Sciences of the United States of America source
Not checked in the free run.
May combine two claims.
Findingown dataLorisiformes evolution includes the radiation of Lorisidae (37 MYA, node 179) and Galagidae (19.9 MYA, node 183) species.
“Lorisiformes evolution includes the radiation of Lorisidae (pottos and lorises, 37 MYA, node 179) and Galagidae (19.9 MYA, node 183) species.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe evolution of the four Lemuriformes families began 38.6 MYA (node 173) with the emergence of Lemuridae, followed by Indriidae and a monophyletic lineage that split 32.9 MYA (node 152) to form the sister lineages of Lepilemuridae and Cheirogaleidae.
“The evolution of the four Lemuriformes families began 38.6 MYA (node 173) with the emergence of Lemuridae, followed by Indriidae and a monophyletic lineage that split 32.9 MYA (node 152) to form the sister lineages of Lepilemuridae and Cheirogaleidae.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenThe hierarchical branching order among the remaining Callitrichinae of Leontopithecus, Callimico, Callithrix and Mico mirrors decreasing body size and culminates with the smallest platyrrhine species, Cebuella pygmaea, as most derived.
“The hierarchical branching order among the remaining Callitrichinae of Leontopithecus, Callimico, Callithrix and Mico mirrors decreasing body size and culminates with the smallest platyrrhine species, Cebuella pygmaea, as most derived.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataAsian (tribe Presbytini) and African (tribe Colobini) genera are monophyletic (nodes 53 and 61, respectively), supporting earlier genetic findings over morphology-based taxonomy.
“Asian (tribe Presbytini) and African (tribe Colobini) genera are monophyletic (nodes 53 and 61, respectively), supporting earlier genetic findings [4], [40] over morphology-based taxonomy [2], [45].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [4] HJ Chatterjee, 2009, Estimating the phylogeny and divergence times of primates using a supermatrix approach., BMC Evolutionary Biology source
Not checked in the free run.
- cites [40] N Ting, 2008, Phylogenetic incongruence between nuclear and mitochondrial markers in the Asian colobines and the evolution of the langurs and leaf monkeys., Molecular Phylogenetics and Evolution source
Not checked in the free run.
- cites [2] CP Groves, 2001, Primate taxonomy.
Not checked in the free run.
May combine two claims.
Findingown dataThe Presbytis lineage, distinguished by 3 indel events (node 56), diverged first within Asian Colobinae, followed by the odd-nosed group (Rhinopithecus, Nasalis, Pygathrix), Trachypithecus and Semnopithecus.
“Here, the Presbytis lineage, distinguished by 3 indel events (node 56), diverged first within Asian Colobinae, followed by the odd-nosed group (Rhinopithecus, Nasalis, Pygathrix), Trachypithecus and Semnopithecus.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenColobinae radiation started approximately 12 MYA (node 42) with species adapted to an arboreal, leaf-eating existence.
“Colobinae radiation started approximately 12 MYA (node 42) with species adapted to an arboreal, leaf-eating existence.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenIn Callitrichinae, Saguinus is the first to diverge with S. fuscicollis currently distributed south of the Amazon River.
“In Callitrichinae, Saguinus is the first to diverge with S. fuscicollis currently distributed south of the Amazon River.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataAotus species divide into sister lineages, with the "grey-necked" species (A. trivirgatus + A. lemurinus griseimembra) distributed north of the Amazon River, and "red-necked" species A. nancymaae, A. azarae species and associated subspecies located most to the south (nodes 98, 101, 102).
“Aotus species divide into sister lineages, with the “grey-necked” species (A. trivirgatus + A. lemurinus griseimembra) distributed north of the Amazon River, and “red-necked” species A. nancymaae, A. azarae species and associated subspecies located most to the south (nodes 98, 101, 102).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingnone givenCercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62).
“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62)”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe Aotus lineage (node 98) radiated with unusually high numbers of synapomorphic indels (N = 15), the most observed in Simiiformes.
“The Aotus lineage (node 98) radiated with unusually high numbers of synapomorphic indels (N = 15), the most observed in Simiiformes (Table 2 and Table 3)”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe genus diversified into northern (S. bicolor, S. midas, S. martinsi, S. geoffroyi, S. oedipus) and south Amazonian species (S. imperator, S. mystax, S. labiatus); a trend generally similar to findings based on mtDNA and single nuclear genes.
“Subsequently, the genus diversified into northern (S. bicolor, S. midas, S. martinsi, S. geoffroyi, S. oedipus) and south Amazonian species (S. imperator, S. mystax, S. labiatus); a trend generally similar to findings based on mtDNA [33] and single nuclear genes [34].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [33] SJ Cropp, 1999, Historical biogeography of tamarins, genus Saguinus: The molecular phylogenetic evidence., American Journal of Physical Anthropology source
Not checked in the free run.
- cites [34] FC Canavez, 1999, Phylogenetic relationships of the callitrichinae (Platyrrhini, Primates) based on beta(2)-microglobulin DNA sequences., American Journal of Primatology source
Not checked in the free run.
May combine two claims.
FindingcitationDifferences in behavior, morphology, karyology, and genetic data between the two island populations support the taxonomic designation as two separate species of Bornean (P. pygmaeus) and Sumatran orangutans (P. abelii), and these designations are upheld by the data presented here.
“Differences in behavior, morphology, karyology, and genetic data between the two island populations [2] support the taxonomic designation as two separate species of Bornean (P. pygmaeus) and Sumatran orangutans (P. abelii), and these designations are upheld by the data presented here.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [2] CP Groves, 2001, Primate taxonomy.
Not checked in the free run.
May combine two claims.
Findingnone givenGenerally arboreal, Miopithecus and Allenopithecus are early offshoots with respect to the two Cercopithecini subclades formed approximately 7 MYA.
“Generally arboreal, Miopithecus and Allenopithecus are early offshoots with respect to the two Cercopithecini subclades formed approximately 7 MYA.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataCercopithecini include lineages rooted by divergent monotypic genera followed by more recent speciation, characterized by transition from an arboreal to a terrestrial lifestyle.
“Cercopithecini (guenons, patas monkey, talapoin, green monkeys) include lineages rooted by divergent monotypic genera followed by more recent speciation, characterized by transition from an arboreal to a terrestrial lifestyle.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataBased on 54 gene regions, Homo-Pan genetic distance range from 6.92 to 7.90×10−3 substitutions/site (P. paniscus and P. troglodytes, respectively), which is less than previous estimates based on large scale sequencing of specific regions such as chromosome 7.
“Based on 54 gene regions, Homo-Pan genetic distance range from 6.92 to 7.90×10−3 substitutions/site (P. paniscus and P. troglodytes, respectively), which is less than previous estimates based on large scale sequencing of specific regions such as chromosome 7 [50].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [50] N Elango, 2006, Variable molecular clocks in hominoids., Proceedings of the National Academy of Sciences of the United States of America source
Not checked in the free run.
May combine two claims.
Findingown dataThe branch forming the Homo and Pan lineage apart from Gorilla is relatively short (node 73, 27 steps MP, 0 indels) compared with that of the Pan genus (node 72, 91 steps MP, 2 indels).
“The branch forming the Homo and Pan lineage apart from Gorilla is relatively short (node 73, 27 steps MP, 0 indels) compared with that of the Pan genus (node 72, 91 steps MP, 2 indels)”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe global rate of nucleotide substitution across the entire primate phylogeny is 6.163×10−4 substitutions/site/MY, but exhibits significant heterogeneity across lineages and among branches.
“The global rate of nucleotide substitution across the entire primate phylogeny is 6.163×10−4 substitutions/ site/ MY, but exhibits significant heterogeneity across lineages (Figure 3) and among branches (Table 1, Table 2, Table 3; Tables S6, S7, S8).”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenThe Cercopithecus lineage (node 34) radiated after Miopithecus and retained an arboreal lifestyle.
“The Cercopithecus lineage (node 34) radiated after Miopithecus and retained an arboreal lifestyle.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataNomascus species appear more recent than Symphalangus and Hylobates, with node divergence dates estimated at less than 1 MY.
“Moreover, Nomascus species appear more recent than Symphalangus and Hylobates, with node divergence dates estimated at less than 1 MY (Table 3, Table S9, Figure 2).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe phylogeny affirms Groves proposal that Lophocebus and Theropithecus are distinct clades apart from Papio (nodes 18, 19), although the average nucleotide divergence among these three genera are generally less than between other recognized Papionin genera (Macaca, Mandrillus, Cercocebus).
“Moreover, the phylogeny affirms Groves [2] proposal that Lophocebus and Theropithecus are distinct clades apart from Papio (nodes 18, 19), although the average nucleotide divergence among these three genera are generally less than between other recognized Papionin genera (Macaca, Mandrillus, Cercocebus) (Figure 2, Figure S1, Table 3, Table S9).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [2] CP Groves, 2001, Primate taxonomy.
Not checked in the free run.
May combine two claims.
FindingcitationMacaca diverged 5.1 MYA and today is represented by an African lineage comprised of a single species M. sylvanus, and an Asian lineage consisting of well-defined species groups (fascicularis, sinica, mulatta, nemestrina, Sulawesi) inhabiting India and Asia, SE Asia and Sundaland.
“One of the more familiar genera within Cercopithecoidea, Macaca (macaques) diverged 5.1 MYA and today is represented by an African lineage comprised of a single species M. sylvanus, and an Asian lineage consisting of well-defined species groups (fascicularis, sinica, mulatta, nemestrina, Sulawesi) inhabiting India and Asia, SE Asia and Sundaland [49].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [49] T Ziegler, 2007, Molecular phylogeny and evolutionary history of Southeast Asian macaques forming the M. silenus group., Molecular Phylogenetics and Evolution source
Not checked in the free run.
May combine two claims.
Findingown dataThe eight species included in this study form three clades that coincide with genus designation (absent is Hoolock; nodes 64-69) that diverged rapidly 8.9 MYA.
“The eight species included in this study form three clades that coincide with genus designation (absent is Hoolock; nodes 64–69) that diverged rapidly 8.9 MYA.”
Quote in the paperSubstantial claimMay combine two claims.
FindingreasoningGenome divergence varies across primate lineages, with the least inter-specific differences observed in Cercopithecidae lineages and the most in Lorisidae.
“Genome divergence varies across primate lineages, with the least inter-specific differences observed in Cercopithecidae lineages and the most in Lorisidae”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe second Cercopithecini subclade, rooted by Allenopithecus, forms a terrestrial clade of Erythrocebus patas and Chlorocebus species, with Cercopithecus l'hoesti separated from the other Cercopithecus.
“The second, rooted by Allenopithecus, forms a terrestrial clade of Erythrocebus patas and Chlorocebus species, with Cercopithecus l'hoesti separated the other Cercopithecus.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe highly endangered orangutan forms the single genus Pongo in subfamily Ponginae (nodes 75-76), the sister lineage to Homininae.
“The highly endangered orangutan forms the single genus Pongo in subfamily Ponginae (nodes 75–76), the sister lineage to Homininae.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataWith the exception of the fascicularis group, which is split in this study whereby M. arctoides [fascicularis] is more closely aligned with M. thibetana [sinica] rather than M. fascicularis as expected, our data otherwise strongly support these macaque species groups (nodes 6, 11).
“With the exception of the fascicularis group, which is split in this study whereby M. arctoides [fascicularis] is more closely aligned with M. thibetana [sinica] rather than M. fascicularis as expected, our data otherwise strongly support these macaque species groups (nodes 6, 11).”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenIn the New World, the phylogenetic placement of the unique, nocturnal Aotinae is unambiguously resolved, diverging rapidly after the sister lineage of Cebinae+Saimirinae and prior to the Callitrichinae within the family Cebidae.
“In the New World, the phylogenetic placement of the unique, nocturnal Aotinae is unambiguously resolved, diverging rapidly after the sister lineage of Cebinae+Saimirinae and prior to the Callitrichinae within the family Cebidae.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataExcluding the infraorders Tarsiiformes (25 indels) and Chiromyiformes (14 indels) due to statistically inadequate sampling, the indel frequency per branch varies by a factor of 20 with the greatest accumulation within Lorisidae (particularly Arctocebus calabarensis) and the least in Cercopithecidae.
“Excluding the infraorders Tarsiiformes (25 indels) and Chiromyiformes (14 indels) due to statistically inadequate sampling, the indel frequency per branch varies by a factor of 20 (Table 1, Table 2, Table 3; Tables S7, S8, S9) with the greatest accumulation within Lorisidae (particularly Arctocebus calabarensis) and the least in Cercopithecidae (Figure 3).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationThe pattern of divergence of Callitrichinae is correlated with a gradation in species size, supporting "phyletic dwarfism".
“Further, the pattern of divergence of Callitrichinae is correlated with a gradation in species size, supporting “phyletic dwarfism” [32], [35].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [32] SM Ford, 1992, Systematics and body size: implications for feeding adaptations in New World monkeys., American Journal of Physical Anthropology source
Not checked in the free run.
- cites [35] SM Ford, 1980, Callitrichids as phyletic dwarfs, and the place of Callitrichidae in Platyrrhini., Primates source
Not checked in the free run.
May combine two claims.
Findingown dataThe distribution of indels is ubiquitous in both coding and noncoding segments, but is markedly disjunct among primate lineages.
“Here, the distribution of indels is ubiquitous in both coding and noncoding segments (Tables S4, S5, S6), but is markedly disjunct among primate lineages (Figure 3).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingnone givenApproximately half of the 261-377 species and 90% of the genera are included, facilitating resolution of long-standing phylogenetic ambiguities.
“Approximately half of the 261–377 species and 90% of the genera are included facilitating resolution of long-standing phylogenetic ambiguities.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationCurrent views concur that 67-69 primate genera originated from a common ancestor during the Cretaceous/Paleocene boundary roughly 80-90 MYA.
“Primate taxonomy has undergone considerable revision but current views [1]-[3] concur that 67–69 primate genera originated from a common ancestor during the Cretaceous/Paleocene boundary roughly 80–90 MYA.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1]-[3]
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe exact number of primate genera is controversial and species counts range from 261-377.
“The exact number of primate genera is controversial and species counts range from 261–377 [1]-[3].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1]-[3]
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAn Eocene expansion formed the major extant primate lineages: Strepsirrhini (Lorisiformes, Chiromyiformes, Lemuriformes), Tarsiiformes, and Simiiformes (Platyrrhini and Catarrhini).
“An Eocene expansion formed the major extant lineages of 1) Strepsirrhini, which is composed of Lorisiformes (galagos, pottos, lorises), Chiromyiformes (Malagasy aye-aye) and Lemuriformes (Malagasy lemurs); 2) Tarsiiformes (tarsiers) and 3) Simiiformes composed of Platyrrhini (New World monkeys) and Catarrhini”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1]-[3]
Not checked in the free run.
May combine two claims.
Interpretationown dataOptimal resolution of node 158 is observed with exon sequences, indicating that intron sites may be saturated, while more conserved coding regions remain informative and reflect the ancient rapid radiation of Lemuriformes families.
“Optimal resolution of this node is observed with exon sequences (Figures S8 and S9), indicating that intron sites may be saturated, while more conserved coding regions remain informative and reflect the ancient rapid radiation of Lemuriformes families.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataInter-specific genetic differences are roughly half those observed among other colobine genera and may indicate that recent speciation, taxonomic over-splitting, reticulate evolution, or a combination thereof are common within the Asian Colobinae radiation.
“Inter-specific genetic differences are roughly half those observed among other colobine genera (Figure 2, Figure S1, Table 3, Table S9) and may indicate that recent speciation, taxonomic over-splitting, reticulate evolution, or a combination thereof, (e. g. see [40], [44], [46]) are common within the Asian Colobinae radiation.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [40] N Ting, 2008, Phylogenetic incongruence between nuclear and mitochondrial markers in the Asian colobines and the evolution of the langurs and leaf monkeys., Molecular Phylogenetics and Evolution source
Not checked in the free run.
- cites [44] KP Karanth, 2008, Molecular phylogeny and biogeography of langurs and leaf monkeys of South Asia (Primates : Colobinae)., Molecular Phylogenetics and Evolution source
Not checked in the free run.
- cites [46] KP Karanth, 2008, Primate numts and reticulate evolution of capped and golden leaf monkeys (Primates: Colobinae)., Journal of biosciences source
Not checked in the free run.
May combine two claims.
InterpretationcitationThis phylogenetic depiction of Callitrichinae is concordant with several other morphological and reproductive traits related to dwarfism and perhaps reflects adaptive evolution selected by fluctuating resource availability within the Amazon and Atlantic coast rainforests.
“This phylogenetic depiction of Callitrichinae is concordant with several other morphological and reproductive traits [32], [35] related to dwarfism and perhaps reflects adaptive evolution selected by fluctuating resource availability within the Amazon and Atlantic coast rainforests [36].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [32] SM Ford, 1992, Systematics and body size: implications for feeding adaptations in New World monkeys., American Journal of Physical Anthropology source
Not checked in the free run.
- cites [35] SM Ford, 1980, Callitrichids as phyletic dwarfs, and the place of Callitrichidae in Platyrrhini., Primates source
Not checked in the free run.
- cites [36] M Moynihan, 1976, The New World primates : adaptive radiation and the evolution of social behavior, languages, and intelligence.
Not checked in the free run.
May combine two claims.
InterpretationcitationThe unusual depth of divergence in Aotus may exemplify adaptive speciation as Aotus are the only nocturnal Simiiformes, and thereby may have reduced competition with diurnal small-bodied platyrrhines inhabiting the same neotropical environments.
“The unusual depth of divergence (i.e. sizeable nucleotide substitutions/site; high indel frequency) may exemplify adaptive speciation as Aotus are the only nocturnal Simiiformes [31], and thereby may have reduced competition with diurnal small-bodied platyrrhines inhabiting the same neotropical environments.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [31] F Ankel-Simons, 2008, Diurnality, Nocturnality, and the Evolution of Primate Visual Systems., American Journal of Physical Anthropology source
Not checked in the free run.
May combine two claims.
InterpretationreasoningAs odd-nosed species are not exclusively arboreal and folivorous, the results indicate either morphological convergence between Presbytis with Trachypithecus and Semnopithecus, adaptation for an expanded diet in the odd-nosed group, or that a folivorous diet is a symplesiomorphic trait within Asian colobines.
“As odd-nosed species are not exclusively arboreal and folivorous, the results indicate either 1) morphological convergence between Presbytis with Trachypithecus and Semnopithecus, 2) adaptation for an expanded diet in the odd-nosed group, or 3) that a folivorous diet is a symplesiomorphic trait within Asian colobines.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataThe least inter-specific differences in Cercopithecidae reflect recent speciation, and the most in Lorisidae reflect the more ancient origins of the latter.
“reflecting recent speciation in the former and the more ancient origins of the latter (Figure 3, Table 1, Table 3, Tables S7 and S9).”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThis paraphyly, also reported in earlier genetic studies and counter to initial morphological classifications, suggests taxonomic revision of Cercopithecus.
“This paraphyly, also reported in earlier genetic studies [39], [47], [48] and counter to initial morphological classifications [2], suggests taxonomic revision of Cercopithecus.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [39] J Xing, 2007, A mobile element-based evolutionary history of guenons (tribe Cercopithecini)., BMC Biology source
Not checked in the free run.
- cites [47] AJ Tosi, 2004, Sex chromosome phylogenetics indicate a single transition to terrestriality in the guenons (tribe Cercopithecini)., Journal of Human Evolution source
Not checked in the free run.
- cites [48] AJ Tosi, 2003, Cercopithecine Y-chromosome data provide a test of competing morphological evolutionary hypotheses., Molecular Phylogenetics and Evolution source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationLarge-scale genome sequence analysis demonstrate that indel formation is an indicator of genome plasticity, positively correlated with adjacent nucleotide substitution rate, gene segmental duplication, chromosomal position, hybridization between species and speciation, and is enhanced by molecular mechanisms of recombination among repetitive elements.
“Further, large-scale genome sequence analysis demonstrate that indel formation is an indicator of genome plasticity, positively correlated with adjacent nucleotide substitution rate [56], [57], gene segmental duplication, chromosomal position, hybridization between species and speciation, and is enhanced by molecular mechanisms of recombination among repetitive elements [58]-[60].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [56] LC Zhu, 2009, Genomewide Association between Insertions/Deletions and the Nucleotide Diversity in Bacteria., Molecular Biology and Evolution source
Not checked in the free run.
- cites [57] DC Tian, 2008, Single-nucleotide mutation rate increases close to insertions/deletions in eukaryotes., Nature
Not checked in the free run.
- cites [58]-[60]
Not checked in the free run.
Classified as probably not a substantial claim.
PremisecitationThe TMRCA of Simiiformes is 43.0 MYA (stdev 4.5).
“B) mean = 43.0 MYA, stdev = 4.5 for TMRCA of Simiiformes [79], [80]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [79], [80]
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningResolution of the primate species phylogeny here provides a validated framework essential in the development, interpretation and discovery of the genetic underpinnings of human adaptation and disease.
“Resolution of the primate species phylogeny here provides a validated framework essential in the development, interpretation and discovery of the genetic underpinnings of human adaptation and disease.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenA negative control (no template) was included in every whole-genome amplification and was verified by downstream PCR and sequencing.
“A negative control (no template) was included in every WGA and was verified by downstream PCR and sequencing.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductnone givenOnly PCR products that produced single bands were sequenced.
“Only PCR products that produced single bands were sequenced.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductcitationRegions of sequence ambiguity within the alignment were identified by GBLOCK and removed from subsequent phylogenetic analyses.
“Regions of sequence ambiguity within the alignment were identified by GBLOCK version 0.91b [72], and removed from subsequent phylogenetic analyses.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [72] G Talavera, 2007, Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments., Systematic Biology source
Not checked in the free run.
May combine two claims.
Interpretationown dataThe low divergence in Cercopithecoidea is consistent with reticulate evolution, recent speciation and possibly augmented by taxonomic over-splitting.
“consistent with reticulate evolution, recent speciation and possibly augmented by taxonomic over-splitting.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenSupport for nodes within the phylogeny used bootstrap analysis with identical settings established for each method of phylogenetic reconstruction and values greater than 50% were retained.
“Support for nodes within the phylogeny used bootstrap analysis with identical settings established for each method of phylogenetic reconstruction and values greater than 50% were retained.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
PremisecitationThe TMRCA of galagids and lorisids is 40.0 MYA (stdev 3.0).
“A) mean = 40.0 MYA, standard deviation (stdev) = 3.0 for time to most recent common ancestor (TMRCA) of galagids and lorisids [78]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [78] ER Seiffert, 2003, Fossil evidence for an ancient divergence of lorises and galagos., Nature source
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
May combine two claims.
InterpretationreasoningA parsimonious interpretation of the present data suggests an Asian origin for primates because the ancient Asian Tarsiiformes and the strepsirrhine Lorisinae are most basal and the closest relatives of primates, Dermoptera and Scandentia, are also exclusive to Asia.
“A parsimonious interpretation of the present data would suggest an Asian origin as the ancient Asian Tarsiiformes and the strepsirrhine Lorisinae are most basal and the closest relatives of primates, Dermoptera and Scandentia, are also exclusive to Asia.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductcitationMultiple sequence files for each gene segment were aligned by MAFFT, imported into Se-Al, and verified by eye.
“Multiple sequence files for each gene segment amplified were aligned by MAFFT version 6 [69], [70], imported into Se-Al ver 2.0a11 [71] and verified by eye.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [69], [70]
Not checked in the free run.
- cites [71] A Rambaut, 2007, Se-Al. Sequence Alignment Editor.
Not checked in the free run.
Classified as probably not a substantial claim.
Study design and conductnone givenOnly indels that correctly conformed to the species associations of the primate phylogeny were used and identified as a subset of synapomorphic events.
“Second, only indels that correctly conformed to the species associations of the primate phylogeny (Figure 2) were used and identified as a subset of synapomorphic events (Table 1, Table 2, Table 3; Tables S5, S6).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenIndels in regions that did not amplify across all species were identified as synapomorphic for a lineage providing ∼70% of the relevant species were successfully PCR amplified, and that species with missing sequence for the indel did not all occur on the same node within the lineage.
“Infrequently, some indels included in the analysis were positioned in regions that did not amplify across all species. In these cases, indels were identified as synapomorphic for a lineage providing ∼70% of the relevant species were successfully PCR amplified, and that species with missing sequence for the indel did not all occur on the same node within the lineage.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductnone givenTrees sampled from the first 1 million generations were discarded.
“Log files from each run were imported into Tracer ver 1.4.1, and trees sampled from the first 1 million generations were discarded.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductown dataMixing of trees was assessed in Tracer by examination of ESS values.
“Mixing of trees was assessed in Tracer by examination of ESS values.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenAll indels were identified using FASTGAP on GBLOCKED alignments and verified by eye.
“First, all indels were identified using FASTGAP on GBLOCKED alignments and verified by eye.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductnone givenFour to seven independent MCMC runs for each analysis were run for 20-100 million generations to ensure sampling of ESS values.
“Four to seven independent Markov chain Monte Carlo (MCMC) runs for each analysis were run for 20–100 million generations to ensure sampling of estimated sample size (ESS) values.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
PremisecitationThe mean root height of all Primates is 90.0 MYA (stdev 6.0) based on molecular estimates.
“A normal prior for the mean root height of 90.0 MYA with stdev = 6.0 was used based on molecular estimates of MRCA of all Primates [14], [82], [85].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [14], [82], [85]
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
Classified as probably not a substantial claim. May combine two claims.
Premisenone givenThe calibration points selected are based on fossil dates that have undergone extensive review in previous publications and are supported by a consensus of paleoanthropologists.
“The calibration points selected are based on fossil dates that have undergone extensive review in previous publications and are supported by a consensus of paleoanthropologists.”
Quote in the paperSubstantial claimMay combine two claims.
Study design and conductown dataThe number of MCMC steps was more than adequate, with ESS of all parameters often exceeding 200, and Tracer plots showing strong equilibrium after discarding burn-in.
“Analysis of these parameters in Tracer suggested that the number of MCMC steps was more than adequate, with ESS of all parameters often exceeding 200, and Tracer plots showing strong equilibrium after discarding burn-in.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe TMRCA of Hominidae is 15.5 MYA (stdev 2.5).
“G) mean = 15.5 MYA, stdev = 2.5 for TMRCA of Hominidae [14]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [14] A Matsui, 2009, Molecular phylogeny and evolution of prosimians based on complete sequences of mitochondrial DNAs., Gene source
Not checked in the free run.
- The authors state this as an assumption: The ingroup is monophyletic with respect to the outgroup.
The paper relies on this without support.
Primate taxonomy is complex and controversial, with marginal unifying consensus on the evolutionary hierarchy of extant primate species.
“However, primate taxonomy is both complex and controversial, with marginal unifying consensus of the evolutionary hierarchy of extant primate species.”
The paper relies on this without support.
The phylogenetic hierarchy of primate species has only modest local (family and genus level) molecular resolution with little consensus on overall primate radiations.
“Markedly absent from these many advances however, is a formal evolutionary context to interpret these findings, as the phylogenetic hierarchy of primate species has only modest local (family and genus level) molecular resolution with little consensus on overall primate radiations.”
The paper relies on this without support.
Recent application of molecular genetic data to resolve primate systematics has been informative but limited in scope and constrained to specific subsets of taxa.
“Recent application of molecular genetic data to resolve primate systematics has been informative, but limited in scope and constrained to just specific subsets of taxa.”
The paper relies on this without support.
Whole genome sequencing of 12 primate species is now completed or nearly so.
“Although whole genome sequencing of 12 primate species are now completed, or nearly so, broader genome representation of man's closest relatives is necessary to interpret human evolution, adaptation and genome structure to assist in biomedical advances.”
The authors state this as an assumption.
The ingroup is monophyletic with respect to the outgroup.
“with the ingroup assumed to be monophyletic with respect to the outgroup.”
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?
New World monkeys comprise the parvorder Platyrrhini, and divergence of this taxon from Old World primates and hominoids occurred approximately 43 million years ago.
“NWM comprise the parvorder Platyrrhini, and estimates based on molecular clocks suggest a divergence of this taxon from Old World primates and hominoids ~43 Mya”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Perelman et al., 2011
Primates as an Order diverged from other mammalian forms approximately 80-90 million years ago.
“Primates as an Order diverged from other mammalian forms approximately 80-90 million years ago (Mya; (Perelman et al., 2011)”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Perelman et al., 2011
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.
A fourth node is marked as collapsed in bootstrap analyses
MinorThe text names only nodes 28, 38, and 158 as bootstrap polytomies, but Table 2 marks node 81 with Note A for both bootstrap analyses. Note A is defined as a node collapsed into a polytomy by bootstrap analyses.
“only 3 of 189 nodes (nodes 28, 38, 158) are polytomies in the bootstrap analyses”
“| 81 | 1.53 | 0.59 | 2.28 | 6.00 | 1.42 | 13.06 | 11.34 | 21 | 0 | Note A | Note A | 1.00 |”
Node 144 has eight indels in the text but nine in Table 1
MinorThe text assigns eight shared indels to node 144, whereas Table 1 lists nine indels for that node.
“eight shared insertions/deletions (indels) (node 144)”
“| 144 | 68.74 | 58.77 | 76.61 | 9.91 | 5.98 | 14.30 | 188.50 | 591 | 9 | 100 | 100 | 1.00 |”
Y-linked informative-site proportion is overstated
MinorTable 4 gives 1,312 informative Y-linked sites out of 2,630 Y-linked sites, or 49.89%, rather than the stated 56%. Its tabulated value of 55.59% is also inconsistent with those counts.
Reported 56 · recomputed 49.885932
“The greatest proportion of phylogenetically informative sites occurred in Y-linked genes (56%)”
Coding and non-coding lengths do not total the analyzed sequence
MinorThe stated coding and non-coding lengths sum to 31,927 bp, not the reported 34,927 bp analyzed.
Reported 34927 · recomputed 31927
“Roughly equal amounts of coding (14742 bp) and non-coding (17185 bp) genomic regions were sampled”
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BackgroundComparative anchor tagged sequences (CATS) for integrative mapping of mammalian genomes
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“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62), but classification schemes [2] are marked by inconsistencies between morphological [37,38] and genetic data, as well as differences among genetic data studies [4,27,39-44].”
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MethodFossil evidence for an ancient divergence of lorises and galagos
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BackgroundSingle origin of Malagasy Carnivora from an African ancestor
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Single-nucleotide mutation rate increases close to insertions/deletions in eukaryotes
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BackgroundArrival and Diversification of Caviomorph Rodents and Platyrrhine Primates in South America
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Primate adaptation and evolution
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“, E) mean = 7 MYA, stdev = 1.0 for TMRCA of Papionini”
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Callitrichids as Phyletic Dwarfs, and the Place of the Callitrichidae in Platyrrhini
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“Further, large-scale genome sequence analysis demonstrate that indel formation is an indicator of genome plasticity, positively correlated with adjacent nucleotide substitution rate [56,57], gene segmental duplication, chromosomal position, hybridization between species and speciation, and is enhanced by molecular mec…”
BackgroundX-chromosomal window into the evolutionary history of the guenons (Primates: Cercopithecini)
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“4 for TMRCA of Theropithecus clade [40,83], G) mean = 15.”
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“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62), but classification schemes [2] are marked by inconsistencies between morphological [37,38] and genetic data, as well as differences among genetic data studies [4,27,39-44].”
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The anatomy of Dolichocebus gaimanensis, a stem platyrrhine monkey from Argentina
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“0 for TMRCA of Platyrrhini [26,81], E) mean = 7 MYA, stdev = 1.”
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“Hylobatidae (siamang, gibbons, hoolock) are noted for exceptional rates of chromosome re-arrangement [52,53], 10–20 times faster than in most mammals [54].”
BackgroundMolecular Phylogeny of the Major Hylobatid Divisions
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“Classification schemes of the 12 species range from two genera (Hylobates and Symphalangus) to four subgenera and/or genera (Hylobates, Nomascus, Symphalangus, Hoolock), defined by unique numbers of chromosomes [54,55].”
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Molecular phylogeny and evolution of prosimians based on complete sequences of mitochondrial DNAs.
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Successive radiations, not stasis, in the South American primate fauna
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“However, the debate continues over the geographic locale most consistent with the existing fossil record [9,10,12,16,23,26,61-63].”
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“Trachypithecus and Semnopithecus genera consist of closely related, often sympatric species (node 51), distributed in the Indian subcontinent and SE Asia, with inconsistent phylogenetic resolution among species [4,27,40,44,46].”
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“Further, large-scale genome sequence analysis demonstrate that indel formation is an indicator of genome plasticity, positively correlated with adjacent nucleotide substitution rate [56,57], gene segmental duplication, chromosomal position, hybridization between species and speciation, and is enhanced by molecular mec…”
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“However, the debate continues over the geographic locale most consistent with the existing fossil record [9,10,12,16,23,26,61-63].”
BackgroundTosi, A. J., Melnick, D. J., & Disotell, T. R. (2004) · Journal of Human Evolution · doi:10.1016/j.jhevol.2003.11.006 · Cited by 106 · cited 1× · see citing works
“This paraphyly, also reported in earlier genetic studies [39,47,48] and counter to initial morphological classifications [2], suggests taxonomic revision of Cercopithecus.”
ResultVariable molecular clocks in hominoids
Elango, N., Thomas, J. W., Program§, N. C. S., & Yi, S. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510716103 · Cited by 105 · cited 1× · see citing works
“, respectively), which is less than previous estimates based on large scale sequencing of specific regions such as chromosome 7”
ResultPoux, C., & Douzery, E. J. P. (2004) · American Journal of Physical Anthropology · doi:10.1002/ajpa.10322 · Cited by 103 · cited 14× · see citing works
“5 for TMRCA of Simiiformes [79,80], C) mean = 29.”
BackgroundInfluentialGene-specific universal mammalian sequence-tagged sites: Application to the canine genome
Venta, P. J., Brouillette, J. A., Yuzbasiyan‐Gurkan, V., & Brewer, G. J. (1996) · Biochemical Genetics · doi:10.1007/bf02399951 · Cited by 102 · cited 1× · see citing works
“This list includes primers from earlier studies [12,16,21,64-68], as well as those designed specifically for this study using a unique bioinformatics approach (Pontius, unpublished data).”
MethodZiegler, T., Abegg, C., Meijaard, E., Perwitasari‐Farajallah, D., Walter, L., Hodges, J. K., & Roos, C. (2006) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2006.11.015 · Cited by 97 · cited 2× · see citing works
“sylvanus, and an Asian lineage consisting of well-defined species groups (fascicularis, sinica, mulatta, nemestrina, Sulawesi) inhabiting India and Asia, SE Asia and Sundaland [49].”
BackgroundInfluentialSelf-citationSteiper, M. E. (2006) · Journal of Human Evolution · doi:10.1016/j.jhevol.2005.12.005 · Cited by 96 · cited 1× · see citing works
“in subfamily Ponginae (nodes 75–76), the sister lineage to Homininae. Currently restricted to the islands of Borneo and Sumatra, orangutans once inhabited all of Southeast Asia during the Pleistocene”
BackgroundMolecular Phylogeny of Old World Monkeys (Cercopithecidae) as Inferred from γ-Globin DNA Sequences
Page, S. L., Chiu, C.-H., & Goodman, M. (1999) · Molecular Phylogenetics and Evolution · doi:10.1006/mpev.1999.0653 · Cited by 92 · cited 1× · see citing works
“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62), but classification schemes [2] are marked by inconsistencies between morphological [37,38] and genetic data, as well as differences among genetic data studies [4,27,39-44].”
BackgroundDiurnality, nocturnality, and the evolution of primate visual systems
Ankel‐Simons, F., & Rasmussen, D. T. (2008) · American Journal of Physical Anthropology · doi:10.1002/ajpa.20957 · Cited by 90 · cited 10× · see citing works
“The Aotus lineage (node 98) radiated with unusually high numbers of synapomorphic indels (N = 15), the most observed in Simiiformes (Table 2 and Table 3), to form a complex species group of controversial taxonomic designation as subfamily or family and uncertainty over its exact placement relative to other Cebidae lin…”
BackgroundInfluentialMosaic retroposon insertion patterns in placental mammalsPreprint
Churakov, G., Kriegs, J. O., Baertsch, R., Zemann, A., Brosius, J., & Schmitz, J. (2009) · Genome Research · doi:10.1101/gr.090647.108 · Cited by 83 · cited 1× · see citing works
“These incongruent alternatives suggest further investigation of more complex rare genomic changes as cladistic markers of ancient speciation is needed [17,18].”
BackgroundA mobile element-based evolutionary history of guenons (tribe Cercopithecini)
Xing, J., Wang, H., Zhang, Y., Ray, D. A., Tosi, A. J., Disotell, T. R., & Batzer, M. A. (2007) · BMC Biology · doi:10.1186/1741-7007-5-5 · Cited by 78 · see citing works
Molecular phylogeny and biogeography of langurs and leaf monkeys of South Asia (Primates: Colobinae)
Karanth, K. P., Singh, L., Collura, R. V., & Stewart, C. (2008) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2007.11.026 · Cited by 75 · cited 3× · see citing works
“see [40,44,46]) are common within the Asian Colobinae radiation.”
BackgroundPrimate phylogeny: molecular evidence from retroposons
Schmitz, J., Roos, C., & Zischler, H. (2004) · Cytogenetic and Genome Research · doi:10.1159/000080799 · Cited by 72 · see citing works
Self-citationTing, N., Tosi, A. J., Li, Y., Zhang, Y.-P., & Disotell, T. R. (2007) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2007.11.008 · Cited by 70 · cited 5× · see citing works
“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62), but classification schemes [2] are marked by inconsistencies between morphological [37,38] and genetic data, as well as differences among genetic data studies [4,27,39-44].”
BackgroundResultInfluentialRetropositional events consolidate the branching order among New World monkey genera.
Osterholz, M., Walter, L., & Roos, C. (2009) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2008.12.014 · Cited by 68 · see citing works
Self-citationPecon‐Slattery, J., Wilkerson, A. J. P., Murphy, W. J., & O’Brien, S. J. (2004) · Molecular Biology and Evolution · doi:10.1093/molbev/msh241 · Cited by 67 · see citing works
Self-citationPhylogenomics of African guenons
Moulin, S., Gerbault‐Seureau, M., Dutrillaux, B., & Richard, F. A. (2008) · Chromosome Research · doi:10.1007/s10577-008-1226-6 · Cited by 64 · cited 1× · see citing works
“Cercopithecidae includes two subfamilies, Colobinae and Cercopithecinae, which diverged 18 MYA (node 62), but classification schemes [2] are marked by inconsistencies between morphological [37,38] and genetic data, as well as differences among genetic data studies [4,27,39-44].”
BackgroundNew World monkey phylogeny based on X-linked G6PD DNA sequences
Steiper, M. E., & Ruvolo, M. (2003) · Molecular Phylogenetics and Evolution · doi:10.1016/s1055-7903(02)00375-5 · Cited by 59 · see citing works
Molecular Phylogeny and Dating of Early Primate Divergences
Eduardo Eizirik, C., Murphy, W. J., Springer, M. S., & O’Brien, S. J. (2004) · Springer eBooks · doi:10.1007/978-1-4419-8873-7_2 · Cited by 53 · see citing works
Self-citationGenomewide Association between Insertions/Deletions and the Nucleotide Diversity in Bacteria
Zhu, L., Wang, Q., Tang, P., Araki, H., & Tian, D. (2009) · Molecular Biology and Evolution · doi:10.1093/molbev/msp144 · Cited by 49 · see citing works
Misceo, D., Capozzi, O., Roberto, R., Dell’Oglio, M. P., Rocchi, M., Stanyon, R., & Archidiacono, N. (2008) · Genome Research · doi:10.1101/gr.078295.108 · Cited by 46 · see citing works
Lilly, A. A., Mehlman, P. T., & Higley, J. D. (1999) · American Journal of Primatology · doi:10.1002/(sici)1098-2345(1999)48:3 · Cited by 43 · see citing works
Self-citationPrimate comparative genomics: lemur biology and evolution
Horvath, J. E., & Willard, H. F. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.02.007 · Cited by 40 · cited 2× · see citing works
“This branching pattern among families agrees with earlier nuclear gene segment findings [20] that differ from studies using mtDNA sequence and Alu insertion variation which were unable to resolve these hierarchical associations [19].”
BackgroundResultSelf-citationSRY Evolution in Cebidae (Platyrrhini: Primates)
Angelo, M. (2002) · Journal of Molecular Evolution · doi:10.1007/s00239-001-2308-7 · Cited by 37 · see citing works
Primate numts and reticulate evolution of capped and golden leaf monkeys (Primates: Colobinae)
Karanth, K. P. (2008) · Journal of Biosciences · doi:10.1007/s12038-008-0096-6 · Cited by 27 · cited 2× · see citing works
“see [40,44,46]) are common within the Asian Colobinae radiation.”
BackgroundVolfovsky, N., Oleksyk, T. K., Cruz, K. C., Truelove, A. L., Stephens, R. M., & Smith, M. W. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-51 · Cited by 17 · see citing works
Groves, C. P. (1989) · Science · doi:10.1126/science.244.4906.860 · Cited by 3 · cited 1× · see citing works
“Asian (tribe Presbytini) and African (tribe Colobini) genera are monophyletic (nodes 53 and 61, respectively), supporting earlier genetic findings [4,40] over morphology-based taxonomy [2,45].”
ResultBeall (1999) · doi:10.1002/(sici)1096-8644(199901)108:1
Flagged first, then by citations
3 of the 89 references couldn’t be matched to a known paper.
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Mash: fast genome and metagenome distance estimation using MinHash
(2016) · Genome biology · doi:10.1186/s13059-016-0997-x · Cited by 3,373 · see citing works
“which the Mash topology is more similar to past phylogenetic studies [27] and mitochondrial trees [13].”
BackgroundThe brain’s default network: updated anatomy, physiology and evolving insights
Buckner, R. L., & DiNicola, L. M. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0212-7 · Cited by 1,058 · see citing works
Genetic Management of Fragmented Animal and Plant Populations
Frankham, R., Ballou, J. D., Ralls, K., Eldridge, M. D. B., Dudash, M. R., Fenster, C. B., Lacy, R. C., & Sunnucks, P. (2017) · doi:10.1093/oso/9780198783398.001.0001 · Cited by 525 · see citing works
A developmental coordinate of pluripotency among mice, monkeys and humans
Nakamura, T., Okamoto, I., Sasaki, K., Yabuta, Y., Iwatani, C., Tsuchiya, H., Seita, Y., Nakamura, S., Yamamoto, T., & Saitou, M. (2016) · Nature · doi:10.1038/nature19096 · Cited by 516 · see citing works
Springer, M. S., Meredith, R. W., Gatesy, J., Emerling, C. A., Park, J. S., Rabosky, D. L., Stadler, T., Steiner, C., Ryder, O. A., Janečka, J. E., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049521 · Cited by 518 · see citing works
“[12], who included 219, 271, and 186 primate species, respectively.”
BackgroundResultInfluentialCaptivity humanizes the primate microbiome
Clayton, J. B., Vangay, P., Huang, H., Ward, T., Hillmann, B., Al‐Ghalith, G. A., Travis, D. A., Long, H. T., Tuan, B. V., Minh, V. V., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521835113 · Cited by 510 · see citing works
“(22) for the 10 unique primate species sampled in this study.”
BackgroundA glimpse on the pattern of rodent diversification: a phylogenetic approach
Fabre, P., Hautier, L., Dimitrov, D., & Douzery, E. (2012) · BMC Evolutionary Biology · doi:10.1186/1471-2148-12-88 · Cited by 506 · see citing works
“Fabre PH, Rodrigues A, Douzery EJP: Patterns of macroevolution among Primates inferred from a supermatrix of mitochondrial and nuclear DNA.”
BackgroundParham, P., & Moffett, A. (2013) · Nature reviews. Immunology · doi:10.1038/nri3370 · Cited by 481 · see citing works
Primate brain size is predicted by diet but not sociality
DeCasien, A. R., Williams, S. A., & Higham, J. P. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0112 · Cited by 479 · see citing works
Reveley, C., Seth, A. K., Pierpaoli, C., Silva, A. C., Yu, D., Saunders, R. C., Leopold, D. A., & Ye, F. Q. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418198112 · Cited by 417 · see citing works
“Moreover, although in many respects the macaque brain is a good approximation of the human brain, both species have undergone profound evolutionary changes since the time of their most recent common ancestor living more than 20 million years ago (10), particularly in regard to the massive expansion of the cerebral cor…”
BackgroundSelf-citationLactobacilli Dominance and Vaginal pH: Why Is the Human Vaginal Microbiome Unique?
Miller, E. A., Beasley, D. E., Dunn, R. R., & Archie, E. A. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01936 · Cited by 411 · see citing works
“…University, Raleigh, NC, USA, 4Center for Macroecology, Evolution and Climate, Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark, 5 Institute of Primate Research, National Museums of Kenya, Nairobi, Kenya The human vaginal microbiome is dominated by bacteria from…”
BackgroundEvolutionary trends in host physiology outweigh dietary niche in structuring primate gut microbiomes
Amato, K. R., Sanders, J. G., Song, S. J., Nute, M., Metcalf, J. L., Thompson, L., Morton, J. T., Amir, A., McKenzie, V. J., Humphrey, G., et al. (2018) · The ISME Journal · doi:10.1038/s41396-018-0175-0 · Cited by 368 · see citing works
Primate phylogenetic relationships and divergence dates inferred from complete mitochondrial genomes
Pozzi, L., Hodgson, J. A., Burrell, A. S., Sterner, K. N., Raaum, R. L., & Disotell, T. R. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.02.023 · Cited by 313 · see citing works
“, 2013), but in contrast with nuclear data (Perelman et al., 2011; but see Guschanski et al., 2013).”
InfluentialTransposable elements are the primary source of novelty in primate gene regulationPreprint
Trizzino, M., Park, Y., Beltrame, M. H., Aracena, K. A., Mika, K. M., Çalışkan, M., Perry, G. H., Lynch, V. J., & Brown, C. D. (2017) · Genome Research · doi:10.1101/gr.218149.116 · Cited by 273 · see citing works
“We performed ChIP-seq for histone H3 lysine 27 acetylation (H3K27ac)andhistoneH3lysine4monomethylation(H3K4me1), whichmarkfunctionalandpoisedregulatoryelements,intheliver of six primate species, including at least one species from each major primate clade (Perelman et al. 2011).”
Springer, M. S., & Gatesy, J. (2015) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2015.07.018 · Cited by 281 · see citing works
Onabajo, O. O., Banday, A. R., Stanifer, M. L., Yan, W., Obajemu, A., Santer, D. M., Florez-Vargas, O., Piontkivska, H., Vargas, J. M., Ring, T. J., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-00731-9 · Cited by 261 · see citing works
Rossier, B. C., Baker, M. E., & Studer, R. A. (2015) · Physiological Reviews · doi:10.1152/physrev.00011.2014 · Cited by 269 · see citing works
“(255), based on a wealth of new genomic data, comparative genomic analyses of primates allow resolving the primate phylogeny with a much greater accuracy.”
BackgroundThe common marmoset genome provides insight into primate biology and evolution
Worley, K. C., Rogers, J., Muzny, D. M., Weinstock, G. M., Chandrabose, M. N., Cree, A., Dao, M., Dinh, H. H., Fowler, R. G., Gabisi, R. A., et al. (2014) · Nature Genetics · doi:10.1038/ng.3042 · Cited by 261 · see citing works
A Mitogenomic Phylogeny of Living Primates
Finstermeier, K., Zinner, D. P., Brameier, M., Meyer, M., Kreuz, E., Hofreiter, M., & Roos, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069504 · Cited by 266 · see citing works
“In our mt genome data, Erythrocebus clusters with Cercopithecus and not with Chlorocebus as suggested by all available nuclear sequence and retroposon data [18,42,58,59], but monophyly of Erythrocebus and Chlorocebus is not rejected by alternative tree topology tests (P > 0.”
BackgroundMethodResultInfluentialSelf-citationLim, E. S., Fregoso, O. I., McCoy, C. O., Matsen, F. A., IV, Malik, H. S., & Emerman, M. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.01.004 · Cited by 261 · see citing works
“The phylogeny constructed from the primate SAMHD1 sequences was congruent with the generally accepted primate species phylogeny (Perelman et al., 2011), confirming that the sequences are orthologous.”
The Genome Landscape of the African Green Monkey Kidney-Derived Vero Cell Line
Osada, N., Kohara, A., Yamaji, T., Hirayama, N., Kasai, F., Sekizuka, T., Kuroda, M., & Hanada, K. (2014) · DNA Research · doi:10.1093/dnares/dsu029 · Cited by 250 · see citing works
“42, 43 The estimated divergence between the rhesus macaque and Vero cell line genomes was 2.2%.”
BackgroundInfluentialPlohl, M., Meštrović, N., & Mravinac, B. (2012) · Genome dynamics · doi:10.1159/000337122 · Cited by 238 · see citing works
Next-Generation Museomics Disentangles One of the Largest Primate Radiations
Guschanski, K., Krause, J., Sawyer, S., Valente, L., Bailey, S., Finstermeier, K., Sabin, R., Gilissen, E., Sonet, G., Nagy, Z. T., et al. (2013) · Systematic Biology · doi:10.1093/sysbio/syt018 · Cited by 232 · see citing works
Evolution of Multilevel Social Systems in Nonhuman Primates and Humans
Grueter, C. C., Chapais, B., & Zinner, D. P. (2012) · International Journal of Primatology · doi:10.1007/s10764-012-9618-z · Cited by 230 · see citing works
“On the other hand, when OMUs congregate on an irregular basis and bands are more fluid and not as consistently assembled or behaviorally integrated as in strict modular systems, this would constitute a flexible system, e.g., Theropithecus gelada (Table II; see also Grueter and Zinner 2004).”
BackgroundHERV Envelope Proteins: Physiological Role and Pathogenic Potential in Cancer and Autoimmunity
Grandi, N., & Tramontano, E. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00462 · Cited by 227 · see citing works
“The estimated period in which the different primate species evolutionary diverged (as derived from Steiper and Young, 2006; Perelman et al., 2011) is indicated in the underlying tree at each node of separation, and is depicted in the graph by colored blocks corresponding to the first primate…”
BackgroundStegelmeier, A. A., Müller, K. M., Weese, J. S., & Neufeld, J. D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801302115 · Cited by 221 · see citing works
Molecular ecology and adaptation of visual photopigments in craniates
Davies, W. I. L., Collin, S. P., & Hunt, D. M. (2012) · Molecular Ecology · doi:10.1111/j.1365-294x.2012.05617.x · Cited by 214 · see citing works
A comprehensive atlas of immunological differences between humans, mice, and non-human primates
Bjornson-Hooper, Z. B., Fragiadakis, G. K., Spitzer, M. H., Chen, H., Madhireddy, D., Hu, K., Lundsten, K., McIlwain, D. R., & Nolan, G. P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.867015 · Cited by 215 · see citing works
Byrne, H., Rylands, A. B., Carneiro, J. C., Alfaro, J. W. L., Bertuol, F., da Silva, M. N. F., Messias, M. R., Groves, C. P., Mittermeier, R. A., Farias, I. P., et al. (2016) · Frontiers in Zoology · doi:10.1186/s12983-016-0142-4 · Cited by 215 · see citing works
“1758. Syst. Nat. 10th ed., 1: 25. In part. Humboldt, A. von. 1811. Rec. Obs. Zool. Anat. Comp. 1: 319. Simia lugens (= Callicebus lugens). Cebus Erxleben, C. P. 1777. Systema Regni Anim. Mammalia, p. 44. In part. Hoffmannsegg, G. von. 1807. Mag. Ges. Naturf. Freunde, Berlin, 9: 97. Cebus moloch (= Callicebus moloch).…”
BackgroundKelava, I., Reillo, I., Murayama, A. Y., Kalinka, A. T., Stenzel, D., Tomančák, P., Matsuzaki, F., Lebrand, C., Sasaki, E., Schwamborn, J. C., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr301 · Cited by 212 · see citing works
“Therefore, we assembled an anthropoid phylogeny using topology and branch lengths estimated previously (Perelman et al. 2011) based on ~8 Mb of genomic sequence (Supplementary Fig.”
A global catalog of whole-genome diversity from 233 primate species
Kuderna, L. F. K., Gao, H. C., Janiak, M. C., Kuhlwilm, M., Orkin, J. D., Bataillon, T. M., Manu, S., Valenzuela, A., Bergman, J., Rousselle, M. M. C., et al. (2023) · Science · doi:10.1126/science.abn7829 · Cited by 206 · see citing works
Self-citationThe Ancient Evolutionary History of Polyomaviruses
Buck, C. B., Doorslaer, K. V., Peretti, A., Geoghegan, E. M., Tisza, M. J., An, P., Katz, J. P., Pipas, J. M., McBride, A. A., Camus, A. C., et al. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005574 · Cited by 211 · see citing works
“Based on the posterior distributions obtained for the host [84, 100], normal priors were imposed on specific nodes used to calibrate the evolutionary rates (S5 File).”
MethodMetabolic rate and body size are linked with perception of temporal information
Healy, K., McNally, L., Ruxton, G. D., Cooper, N., & Jackson, A. L. (2013) · Animal Behaviour · doi:10.1016/j.anbehav.2013.06.018 · Cited by 202 · see citing works
“We used Benton & Donoghue’s (2007) estimation of divergence time between anopsids (Testudines and Aves) and suarapids (Squamata and Rhynchocephalia) while Perelman et al. (2011) was used for the divergence and phylogenetic relationships among Squamata, Rhynchocephalia, Testudines and Aves.”
dos Reis, M., Gunnell, G. F., Barba‐Montoya, J., Wilkins, A., Yang, Z., & Yoder, A. D. (2018) · Systematic Biology · doi:10.1093/sysbio/syy001 · Cited by 188 · see citing works
“…been inordinately and repeatedly the subject of divergence time analysis, with the first studies appearing at the very outset of molecular clock studies (Sarich and Wilson 1967), up to phylogenomic studies encompassing a large set of primate species (Perelman et al. 2011; Springer et al. 2012).”
BackgroundMethodThe ABO blood group is a trans-species polymorphism in primates
Ségurel, L., Thompson, E. E., Flutre, T., Lovstad, J. N., Venkat, A., Margulis, S. W., Moyse, J. A., Ross, S., Gamble, K. C., Sella, G., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210603109 · Cited by 192 · see citing works
“We assumed that B arose ∼8 Mya (the minimum age indicated by Fig.”
InfluentialGlutaredoxin: Discovery, redox defense and much more
Ogata, F. T., Branco, V., Vale, F. F., & Coppo, L. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101975 · Cited by 189 · see citing works
Centromere repositioning in mammals
Rocchi, M., Archidiacono, N., Schempp, W., Capozzi, O., & Stanyon, R. (2011) · Heredity · doi:10.1038/hdy.2011.101 · Cited by 183 · see citing works
“15 MYA (Perelman et al., 2011), therefore the origin of the ENC has to be somewhere between 15 and 1.”
BackgroundInfluentialBraga, R. M., Van Dijk, K. R. A., Polimeni, J. R., Eldaief, M. C., & Buckner, R. L. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00808.2018 · Cited by 162 · see citing works
Alfaro, J. W. L., Boubli, J. P., Paim, F. P., RIBAS, C. C., da Silva, M. N. F., Messias, M. R., Röhe, F., Mercês, M. P., Júnior, J. S. S., Silva, C. R., et al. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.09.004 · Cited by 180 · see citing works
Hecht, E. E., Gutman, D. A., Bradley, B. A., Preuss, T. M., & Stout, D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.039 · Cited by 175 · see citing works
“In this scenario, the macaque–chimpanzee–human last common ancestor (~25–32 million years ago (Goodman et al., 1998; Chatterjee et al., 2009; Perelman et al., 2011)) did not have SLF”
Phylogenomic analyses provide insights into primate evolution
Shao, Y., Zhou, L., Li, F., Zhao, L., Zhang, B.-L., Shao, F., Chen, J., Chen, C., Bi, X., Zhuang, X.-L., et al. (2023) · Science · doi:10.1126/science.abn6919 · Cited by 170 · see citing works
“2B), which contradicts the 218 Hominini slowdown hypothesis on the nucleotide substitution rates (35).”
BackgroundMethodInfluentialSelf-citationLaguette, N., Rahm, N., Sobhian, B., Chable-Bessia, C., Münch, J., Snoeck, J., Sauter, D., Switzer, W. M., Heneine, W., Kirchhoff, F., et al. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.01.007 · Cited by 174 · see citing works
Human mortality improvement in evolutionary context
Bürger, O., Baudisch, A., & Vaupel, J. W. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215627109 · Cited by 172 · see citing works
“6 million years (14), since the split from a common ancestor with chimpanzees.”
BackgroundA quantitative review of MHC ‐based mating preference: the role of diversity and dissimilarity
Kamiya, T., O’Dwyer, K., Westerdahl, H., Senior, A. M., & Nakagawa, S. (2014) · Molecular Ecology · doi:10.1111/mec.12934 · Cited by 170 · see citing works
“taxonomy database, and polytomies were resolved using the following studies (Steppan et al. 2004; Hackett et al. 2008; Perelman et al. 2011; Crête-Lafreni ere et al. 2012).”
MethodThe Ancient Evolutionary History of Polyomaviruses
Buck, C., Van Doorslaer, K., Peretti, A., Geoghegan, E., Tisza, M., An, P., Katz, J., Pipas, J., McBride, A., Camus, A., et al. (2016) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 170 · see citing works
Fan, H., Ives, A. R., Surget‐Groba, Y., & Cannon, C. H. (2015) · BMC Genomics · doi:10.1186/s12864-015-1647-5 · Cited by 165 · see citing works
“1) as those previously published using traditional methods [30, 31], even though AAF did not use any information about assembly or alignment.”
BackgroundMethodResultInfluentialPrimate vaginal microbiomes exhibit species specificity without universal Lactobacillus dominance
Yıldırım, S., Yeoman, C. J., Janga, S. C., Thomas, S. M., Ho, M., Leigh, S. R., Microbiome, P., White, B. A., Wilson, B. A., & Stumpf, R. M. (2014) · The ISME Journal · doi:10.1038/ismej.2014.90 · Cited by 166 · see citing works
“The aligned sequences based on 54 concatenated primate genes were used to build the maximum parsimony tree (Perelman et al., 2011).”
MethodMolecular evolution of hydrogen peroxide degrading enzymes
Zámocký, M., Gasselhuber, B., Furtmüller, P. G., & Obinger, C. (2012) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2012.01.017 · Cited by 168 · see citing works
Pacheco, M. A., Matta, N. E., Valkiūnas, G., Parker, P. G., Mello, B., Stanley, C. E., Lentino, M., García-Amado, M. A., Cranfield, M. R., Pond, S. L. K., et al. (2017) · Molecular Biology and Evolution · doi:10.1093/molbev/msx285 · Cited by 167 · see citing works
“This event is used to inform a calibration prior with a maximum of 65 Ma that allows this parasite clade to be as old as the origin of primates, if the data support that (Perelman et al. 2011).”
Mitchell, P. S., Patzina, C., Emerman, M., Haller, O., Malik, H. S., & Kochs, G. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.09.005 · Cited by 142 · see citing works
“A phylogenetic tree generated from these MxA sequences was congruent with a previously published primate phylogeny (Perelman et al., 2011) confirming that the MxA sequences obtained were orthologous (Figure 1A).”
ResultPhylogeny and Divergence Times of Lemurs Inferred with Recent and Ancient Fossils in the Tree
Herrera, J. P., & Dávalos, L. M. (2016) · Systematic Biology · doi:10.1093/sysbio/syw035 · Cited by 156 · see citing works
Conservation Genomics of Threatened Animal Species
Steiner, C., Putnam, A. S., Hoeck, P. E. A., & Ryder, O. A. (2013) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-031412-103636 · Cited by 159 · see citing works
Crottini, A., Madsen, O., Poux, C., Strauß, A., Vieites, D. R., & Vences, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112487109 · Cited by 153 · see citing works
Roux, C., Tsagkogeorga, G., Bierne, N., & Galtier, N. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst066 · Cited by 154 · see citing works
“This is equivalent to the divergence between humans and marmosets 1581 Downloaded from https://academic.oup.com/mbe/article-abstract/30/7/1574/972546 by guest on 29 July 2018 (Perelman et al. 2011).”
BackgroundEarly primate evolution in Afro‐Arabia
Seiffert, E. R. (2012) · Evolutionary Anthropology Issues News and Reviews · doi:10.1002/evan.21335 · Cited by 152 · see citing works
The systematics and evolution of New World primates – A review
Schneider, H., & Sampaio, I. (2013) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2013.10.017 · Cited by 150 · see citing works
“were based on Perelman et al. (2011) estimates.”
BackgroundMethodInfluentialExonization of transposed elements: A challenge and opportunity for evolution
Schmitz, J., & Brosius, J. (2011) · Biochimie · doi:10.1016/j.biochi.2011.07.014 · Cited by 150 · see citing works
Marine origin of retroviruses in the early Palaeozoic Era
Aiewsakun, P., & Katzourakis, A. (2017) · Nature Communications · doi:10.1038/ncomms13954 · Cited by 148 · see citing works
Ebeling, M., Küng, E., See, A., Broger, C., Steiner, G., Berrera, M., Heckel, T., Iniguez, L. A., Albert, T., Schmucki, R., et al. (2011) · Genome Research · doi:10.1101/gr.123117.111 · Cited by 146 · see citing works
“These primates share a commonancestorwithhumans that is estimated to have lived about 32million years ago (Perelman et al. 2011).”
BackgroundComparative RNA sequencing reveals substantial genetic variation in endangered primatesPreprint
Perry, G. H., Melsted, P., Marioni, J. C., Wang, Y., Bainer, R. O., Pickrell, J. K., Michelini, K., Zehr, S. M., Yoder, A. D., Stephens, M., et al. (2011) · Genome Research · doi:10.1101/gr.130468.111 · Cited by 147 · see citing works
“This conclusion is further supported by our ability to nearly perfectly recapitulate the known primate phylogeny (Perelman et al. 2011) based on either the sequence data or the estimates of gene expression levels (Fig.”
BackgroundMeaning, intention, and inference in primate vocal communication
Fischer, J., & Price, T. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.10.014 · Cited by 144 · see citing works
Steiper, M. E., & Seiffert, E. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119506109 · Cited by 143 · see citing works
“(7); green, theCYP7A1 region (16); blue, Jamesonet al.”
BackgroundBaboon phylogeny as inferred from complete mitochondrial genomes
Zinner, D. P., Wertheimer, J., Liedigk, R., Groeneveld, L. F., & Roos, C. (2012) · American Journal of Physical Anthropology · doi:10.1002/ajpa.22185 · Cited by 142 · see citing works
“Estimated divergence times for all nodes are in a similar range as dates from other molecular studies (Chan et al., 2010; Perelman et al., 2011; Roos et al., 2011; Liedigk et al., 2012; Steiper and Seiffert, 2012).”
ResultSelf-citationTime-Dependent Rate Phenomenon in Viruses
Aiewsakun, P., & Katzourakis, A. (2016) · Journal of Virology · doi:10.1128/jvi.00593-16 · Cited by 132 · see citing works
“On the basis of these observations, their rates have been estimated to be of the order of 10 7 to 10 9 nucleotide substitutions per site per year (s/n/y) (1–5), comparable to those of their hosts (6, 7).”
BackgroundNiimura, Y., Matsui, A., & Touhara, K. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy042 · Cited by 134 · see citing works
Faurby, S., & Svenning, J. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.11.001 · Cited by 133 · see citing works
“Family monophyly and family assignment in the New World monkeys are unsettled, although the monophyly of the NewWorld monkey superfamily is settled beyond doubt (Perelman et al., 2011).”
BackgroundSystems Biology of the Vervet Monkey
Jasinska, A. J., Schmitt, C. A., Service, S. K., Cantor, R. M., Dewar, K., Jentsch, J. D., Kaplan, J. R., Turner, T. R., Warren, W. C., Weinstock, G. M., et al. (2013) · ILAR Journal · doi:10.1093/ilar/ilt049 · Cited by 131 · see citing works
“…differentiation of the vervet from other members of its tribe is estimated to be about 1.5 to 3 million years ago, based on molecular phylogeny analyses from 54 nuclear genes in 191 primate taxa (Perelman et al. 2011) and similar analyses from mitochondrial genome data (Wertheim and Worobey 2007).”
InfluentialAnimal models of human pregnancy and placentation: alternatives to the mouse
Carter, A. M. (2020) · Reproduction · doi:10.1530/rep-20-0354 · Cited by 130 · see citing works
“Figure 5 Classification of primates (Perelman et al. 2011).”
Manipulation complexity in primates coevolved with brain size and terrestriality
Heldstab, S. A., Kosonen, Z. K., Koski, S. E., Burkart, J. M., van Schaik, C. P., & Isler, K. (2016) · Scientific Reports · doi:10.1038/srep24528 · Cited by 128 · see citing works
Münk, C., Willemsen, A., & Bravo, I. G. (2012) · BMC Evolutionary Biology · doi:10.1186/1471-2148-12-71 · Cited by 127 · see citing works
“This timing could be compatible with the Hylobatidae/Hominidae split some 18–24 Mya, although it matches well the Cercopithecidae/Hominoidea split some 26–34 Mya [44].”
ResultVoice pitch: a window into the communication of social power
Aung, T., & Puts, D. A. (2019) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2019.07.028 · Cited by 126 · see citing works
Kay, R. F. (2013) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2013.12.002 · Cited by 125 · see citing works
“phylogeny (Opazo et al., 2006; Osterholz et al., 2009; Wildman et al., 2009; Perelman et al., 2011; Springer et al., 2012).”
ResultInfluentialLinking the Investigations of Character Evolution and Species Diversification
Magnuson-Ford, K., & Otto, S. P. (2012) · The American Naturalist · doi:10.1086/666649 · Cited by 121 · see citing works
“…of primate diversification, we recommend that future analyses include trait information for more species, use the most recent molecular data (e.g., see Perelman et al. 2011), and be conducted over a set of trees that are consistent with the data, to account for phylogenetic uncertainty.”
MethodCortés‐Ortiz, L., Rylands, A. B., & Mittermeier, R. A. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1957-4_3 · Cited by 121 · see citing works
Esselstyn, J. A., Oliveros, C. H., Swanson, M. T., & Faircloth, B. C. (2017) · Genome Biology and Evolution · doi:10.1093/gbe/evx168 · Cited by 123 · see citing works
Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host
Palesch, D., Bosinger, S. E., Tharp, G. K., Vanderford, T. H., Paiardini, M., Chahroudi, A., Johnson, Z. P., Kirchhoff, F., Hahn, B. H., Norgren, R. B., et al. (2018) · Nature · doi:10.1038/nature25140 · Cited by 119 · see citing works
“…more closely related to sooty mangabeys and drills than to rhesus macaques, the phylogeny of Old World monkeys is compatible with the possibility of a single G-to-A mutation creating the truncated form of the protein in the common ancestor of baboons, rhesus macaques and sooty mangabeys 12,14 (Fig.”
BackgroundIdentification of a Genomic Reservoir for New TRIM Genes in Primate Genomes
Han, K., Lou, D. I., & Sawyer, S. L. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002388 · Cited by 120 · see citing works
“(C) The relationships of the species discussed in this study are shown, along with approximate dates of divergence [78,79].”
BackgroundThe evolution and functions of nuclei of the visual pulvinar in primates
Baldwin, M. K. L., Balaram, P., & Kaas, J. H. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24272 · Cited by 119 · see citing works
“Thus, current classification schemes divide living primates into two large clades, the strepsirrhine (prosimians, except for tarsiers), and the haplorhines (tarsiers and anthropoids (Kay, Ross, & Williams, 1997; Jameson et al., 2011; Perelman et al., 2011).”
BackgroundRabenold, D., & Pearson, O. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028379 · Cited by 116 · see citing works
“(DOC) Figure S1 Phylogeny of the species included in the study with ages of splits indicated in millions of years (data from Perelman et al., 2011 [70]).”
BackgroundMethodBiogeography of the marmosets and tamarins (Callitrichidae)
Buckner, J. C., Alfaro, J. W. L., Rylands, A. B., & Alfaro, M. E. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.04.031 · Cited by 116 · see citing works
Compton, A. A., & Emerman, M. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003135 · Cited by 112 · see citing works
“The resulting A3G phylogeny and the currently accepted phylogeny of OWM species [37] are similar but not identical, most likely due to rampant selection.”
BackgroundMethodInfluentialOld World Monkeys Compare to Apes in the Primate Cognition Test Battery
Schmitt, V., Pankau, B., & Fischer, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032024 · Cited by 112 · see citing works
“Within the hominoidea (apes and humans), the last common ancestor of humans and their closest relatives, the chimpanzees and bonobos, is dated at about 6 mya [1], while the split between the Hominoidea and the Cercopithecoidea (Old World monkeys) occurred between 29 and 24 mya [2].”
The population genomics of rhesus macaques ( Macaca mulatta ) based on whole-genome sequencesPreprint
Xue, C., Raveendran, M., Harris, R. A., Fawcett, G. L., Liu, X., White, S. J., Dahdouli, M., Deiros, D. R., Below, J. E., Salerno, W. J., et al. (2016) · Genome Research · doi:10.1101/gr.204255.116 · Cited by 111 · see citing works
“caques are Old World monkeys (Family Cercopithecidae, Superfamily Cercopithecoidea) and thus are phylogenetically closely related to humans, sharing a common ancestor roughly 25million years ago (Perelman et al. 2011).”
BackgroundSelf-citationHuman KIR repertoires: shaped by genetic diversity and evolution
Manser, A. R., Weinhold, S., & Uhrberg, M. (2015) · Immunological Reviews · doi:10.1111/imr.12316 · Cited by 113 · see citing works
“5 million years of evolution from humans (97, 98).”
BackgroundMorphology of the Nasal Capsule of Primates—With Special Reference to D aubentonia and H omo
Maier, W., & Ruf, I. (2014) · The Anatomical Record · doi:10.1002/ar.23023 · Cited by 112 · see citing works
“Phylogenetically, Daubentonia seems to be a basal branch to the Madagascan strepsirhines, which probably arrived on this island somewhat <60 million year ago (Roos et al., 2004; Perelman et al., 2011).”
BackgroundEvidence of Alternative Dietary Syndromes and Nutritional Goals in the Genus Alouatta
Garber, P. A., Righini, N., & Kowalewski, M. M. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1960-4_4 · Cited by 110 · see citing works
Schlenker, P., Chemla, E., Schel, A. M., Fuller, J. L., Gautier, J., Kuhn, J. D., Veselinović, D., Arnold, K., Cäsar, C., Keenan, S., et al. (2016) · Theoretical Linguistics · doi:10.1515/tl-2016-0001 · Cited by 110 · see citing works
“Colobus monkeys and cercopithecines probably have a most recent common ancestor that lived – very approximately – 18 million years ago (Perelman et al. 2011).”
New approaches for genome assembly and scaffolding
Rice, E. S., & Green, R. E. (2019) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-020518-115344 · Cited by 110 · see citing works
Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors
Blanco-Melo, D., Gifford, R. J., & Bieniasz, P. D. (2017) · eLife · doi:10.7554/elife.22519 · Cited by 109 · see citing works
“Expected branch lengths were calculated for the minimum and maximum estimates of the origin of hominids (13.45 and 19.68 MY respectively) (Perelman et al., 2011) using the neutral substitution for humans.”
MethodInfluentialA Severe Lack of Evidence Limits Effective Conservation of the World's Primates
Junker, J., Petrovan, S. O., Arroyo‐Rodríguez, V., Boonratana, R., Byler, D., Chapman, C. A., Chetry, D., Cheyne, S. M., Cornejo, F. M., Cortés‐Ortiz, L., et al. (2020) · BioScience · doi:10.1093/biosci/biaa082 · Cited by 108 · see citing works
Self-citationViral evolution in deep time: lentiviruses and mammals
Gifford, R. J. (2011) · Trends in Genetics · doi:10.1016/j.tig.2011.11.003 · Cited by 105 · see citing works
McCord, A. I., Chapman, C. A., Weny, G., Tumukunde, A., Hyeroba, D., Klotz, K., Koblings, A. S., Mbora, D. N. M., Cregger, M. A., White, B. A., et al. (2013) · American Journal of Primatology · doi:10.1002/ajp.22238 · Cited by 104 · see citing works
“Specifically, although black‐and‐white colobus and red colobus are closely related [Perelman et al., 2011], microbiomes of these two colobine species were as different from each other as either was from the microbiomes of more distantly related red‐tailed guenons.”
S cones: Evolution, retinal distribution, development, and spectral sensitivity
HUNT, D. M., & Peichl, L. (2013) · Visual Neuroscience · doi:10.1017/s0952523813000242 · Cited by 103 · see citing works
“If codon changes at site 86 are placed on to a primate phylogeny (Perelman et al., 2011 ) using the tree shrew as an outgroup (Petry & Harosi, 1990 ; Hunt et al., 2009 a ), then this codon would appear to have passed unchanged into the SWS1 pigment of the aye-aye ( Fig.”
Primate mosaic brain evolution reflects selection on sensory and cognitive specialization
DeCasien, A. R., & Higham, J. P. (2019) · Nature Ecology & Evolution · doi:10.1038/s41559-019-0969-0 · Cited by 103 · see citing works
Compton, A. A., Hirsch, V. M., & Emerman, M. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2011.11.010 · Cited by 102 · see citing works
“Despite sharing a recent common ancestor 1–3 million years ago (Perelman et al., 2011; Wertheim and Worobey, 2007), each subspecies is naturally infected with a distinct subtype of SIV, aptly named after the specific host it infects: SIVagm.”
Hybridization in human evolution: Insights from other organisms
Ackermann, R., Arnold, M. L., Baiz, M. D., Cahill, J. A., Cortés‐Ortiz, L., Evans, B. J., Grant, B. R., Grant, P. R., Hallgrímsson, B., Humphreys, R. A., et al. (2019) · Evolutionary Anthropology Issues News and Reviews · doi:10.1002/evan.21787 · Cited by 101 · see citing works
“penicillata.(74,75) Experimental interspecific crosses revealed different levels”
Self-citationThe genome of the vervet (<i>Chlorocebus aethiops sabaeus</i>)
Warren, W. C., Jasinska, A. J., García-Pérez, R., Svardal, H., Tomlinson, C., Rocchi, M., Archidiacono, N., Capozzi, O., Minx, P., Montague, M. J., et al. (2015) · Genome Research · doi:10.1101/gr.192922.115 · Cited by 123 · see citing works
“…vervet provides a different kind of model for studying chromosome stability since the fission events are likely more recent, having occurred since the split between Cercopithecini and other members of Cercopi-thecinae ∼ 11.5 – 14.1 million years ago (Mya) (Perelman et al. 2011; Pozzi et al. 2014).”
BackgroundResultInfluentialConvergent evolution of escape from hepaciviral antagonism in primates
Patel, M. R., Loo, Y.-M., Horner, S. M., Gale, M., & Malik, H. S. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001282 · Cited by 95 · see citing works
“(A) dN/dS ratios for the MAVS gene, calculated using freeratio model in PAML, are shown on a phylogeny [26] along with common and scientific names of the primate species represented.”
MethodResultInfluentialSpecial issue: Comparative biogeography of Neotropical primates
Alfaro, J. W. L., Cortés‐Ortiz, L., Fiore, A. D., & Boubli, J. P. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.09.027 · Cited by 100 · see citing works
“In the case of Alouatta, the genus as a whole is relatively old, with the initial cis- and trans-Andean split estimated, using different kinds of molecular markers, variously as 6.8 Ma (Cortés-Ortiz et al., 2003), 6.0 Ma (Perelman et al., 2011) or 3.7 Ma (Springer et al., 2012).”
BackgroundMethodInfluentialThe Genetic and Evolutionary Drives behind Primate Color Vision
Carvalho, L. S., Pessoa, D. M. A., Mountford, J. K., Davies, W. I. L., & Hunt, D. M. (2017) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2017.00034 · Cited by 100 · see citing works
“Atelidae, and Pitheciidae (Perelman et al., 2011), trichromacy appears to have followed the same evolutionary process seen in the Cebinae family (Riba-Hernandez et al.”
BackgroundInfluential
- Authors
- Perelman, P., Johnson, W. E., Roos, C., Seuánez, H. N., Horvath, J. E., Moreira, M. A. M., Kessing, B., Pontius, J., Roelke, M., Rumpler, Y., Schneider, M. P. C., Silva, A., O'Brien, S. J., & Pecon-Slattery, J.
- Affiliations
- Frederick National Laboratory for Cancer Research (US)
- National Cancer Institute (US)
- German Primate Center (DE)
- Universidade Federal do Rio de Janeiro (BR)
- Duke University (US)
- Université de Strasbourg (FR)
- Universidade Federal do Pará (BR)
- ORCID
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2011-03-17
- Volume
- 7
- Issue
- 3
- Pages
- e1001342
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC3060065
- OpenAlex
- W2144820135
- Semantic Scholar
- fe3c21d27cf4a3bb815467dcde063248e497b923
- Cited by
- 1,414
- References
- 89
- Citations by year
- 2026: 43 · 2025: 53 · 2024: 53 · 2023: 62 · 2022: 91 · 2021: 79 · 2020: 132 · 2019: 81 · 2018: 157 · 2017: 120 · 2016: 111 · 2015: 94 · 2014: 127 · 2013: 99 · 2012: 82
- FWCI
- 74.43
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Genetics (publishedVersion, public-domain)
- PubMed Central (publishedVersion, public-domain)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- GoeScholar The Publication Server of the Georg-August-Universität Göttingen (Georg-August-Universität Göttingen) (submittedVersion, cc-by)
- Funders
- U.S. Department of Health and Human Services (N01-CO-12400)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- National Institutes of Health (n01co12400-79-0-22, N01-CO-12400)
- National Cancer Institute (CO-12400, N01CO12400, N01-CO-012400)
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Social Sciences › Psychology › Social Psychology › Primate Behavior and Ecology
- Keywords
- primate phylogeny, comparative genomics, primate taxonomy, human evolution, primate genomics, Dermoptera, tree shrew, lagomorphs, reticulate evolution, speciation, zoonotic emergence, endangered species conservation
- MeSH terms
- Animals, Female, Male, Phylogeny, Primates, Genetic Variation, Genome, Computational Biology
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.
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