The DOI matches its Crossref record; 76 of the 78 references it cites were found in a registry or an index; none of the 27 sources its claims cite is checked for support yet.
Clades reach highest morphological disparity early in their evolution
Open accessAbstract
There are few putative macroevolutionary trends or rules that withstand scrutiny. Here, we test and verify the purported tendency for animal clades to reach their maximum morphological variety relatively early in their evolutionary histories (early high disparity). We present a meta-analysis of 98 metazoan clades radiating throughout the Phanerozoic. The disparity profiles of groups through time are summarized in terms of their center of gravity (CG), with values above and below 0.50 indicating top- and bottom-heaviness, respectively. Clades that terminate at one of the “big five” mass extinction events tend to have truncated trajectories, with a significantly top-heavy CG distribution overall. The remaining 63 clades show the opposite tendency, with a significantly bottom-heavy mean CG (relatively early high disparity). Resampling tests are used to identify groups with a CG significantly above or below 0.50; clades not terminating at a mass extinction are three times more likely to be significantly bottom-heavy than top-heavy. Overall, there is no clear temporal trend in disparity profile shapes from the Cambrian to the Recent, and early high disparity is the predominant pattern throughout the Phanerozoic. Our results do not allow us to distinguish between ecological and developmental explanations for this phenomenon. To the extent that ecology has a role, however, the paucity of bottom-heavy clades radiating in the immediate wake of mass extinctions suggests that early high disparity more probably results from the evolution of key apomorphies at the base of clades rather than from physical drivers or catastrophic ecospace clearing.
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A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Likelihood ratio tests also confirmed that the relative frequencies of top-and bottom-heavy clades terminating at mass extinctions and at other times were different, whether including all clades (G = 7.648, P = 0.006) or only those with significant skew (G = 13.022,P < 0.001).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The only temporal pattern in disparity profile shapes detected in our data was the significant tendency toward top-heaviness in those clades terminating coincident with a mass extinction [which predominantly result from physical drivers (59)].”
§ Clades reach highest morphological disparity early in their evolution > Why Do Clades Have Early High Disparity?
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Over half of our study clades had disparity profiles that were neither significantly top-nor bottom-heavy.”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The remaining 63 clades show the opposite tendency, with a significantly bottom-heavy mean CG (relatively early high disparity).”
- Also stated in: § Results and Discussion · plain
“Therefore, clades that do not terminate at a mass extinction do indeed tend to reach their highest levels of disparity relatively early in their evolutionary histories (20).”
- Also stated in: § Results and Discussion · plain
“Of these, the proportion (two-thirds) that were either significantly bottom-heavy or showed early saturation (two mutually compatible conceptions of early high disparity) was significantly greater than the proportion that were either significantly top-heavy or showed late saturation (late high disparity) (two-sample test for equality of proportions; χ 2 = 4.613, P = 0.016).”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 98 sampled clades are representative of metazoan clades across the Phanerozoic.
- Rests on an assumption: The 63 clades not terminating at a mass extinction were free-evolving and not otherwise truncated.
- Also stated in: § Results and Discussion · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“For 29 of the 54 symmetrical groups, we were unable to reject this null.”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, comparison across four time bins [Early Paleozoic (Cambrian/ Ordovician), Late Paleozoic, Mesozoic, and Cenozoic] revealed no significant differences in the frequencies (log likelihood ratio test; G = 2.298, P = 0.513).”
- Also stated in: § Results and Discussion · plain
“Again, there were no significant differences in the relative frequencies of significantly top-and bottom-heavy clades across the four time bins (G = 3.558, P = 0.313).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Also stated in: § Results and Discussion · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, there is no clear temporal trend in disparity profile shapes from the Cambrian to the Recent”
- Also stated in: § Results and Discussion · plain
“Finally, a plot of clade CG against the time of clade origin revealed no systemic trends throughout the Phanerozoic (Fig. 2).”
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Also stated in: § Results and Discussion · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Resampling tests are used to identify groups with a CG significantly above or below 0.50; clades not terminating at a mass extinction are three times more likely to be significantly bottomheavy than top-heavy.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“early high disparity is the predominant pattern throughout the Phanerozoic.”
- Also stated in: § Results and Discussion · plain
“Moreover, this tendency occurs throughout the Phanerozoic.”
- Also stated in: § Why Do Clades Have Early High Disparity? · hedged
“Moreover, it seems to apply throughout the Phanerozoic, and not merely at times of global diversification (e.g., the early Paleozoic).”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 98 sampled clades are representative of metazoan clades across the Phanerozoic.
- Also stated in: § Results and Discussion · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although clade disparity profiles had a mean CG indistinguishable from 0.5, there was a marked and significant difference in CG between those clades terminating coincident with a mass extinction event and those becoming extinct at other times (Fig. 3).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- It may state two separate claims as one. 18
- Probably not a substantial claim. 14
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Time-averaged indices masked some apparent differences in clade disparity profiles within and between eras; most notably, there were more bottom-heavy (CG <0.5) clades in the Late Paleozoic than top-heavy (CG >0.5) clades, with the opposite pattern in the Mesozoic.”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These extant clades (truncated by the present) had a median CG significantly greater than 0.500 (V = 1,150, P < 0.001) but indistinguishable from that for fossil clades terminating at a mass extinction (W = 924, P = 0.980).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although late saturation was observed in 32 symmetrical clades, 12 of these also ended at a mass extinction (and were therefore likely to have been prematurely truncated).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Across our sample of 98 clades (including those terminating coincident with a mass extinction), we found a mean disparity profile of CG of 0.495, with a median CG (0.501) indistinguishable from 0.5 (V = 2,429, P = 0.992).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Clades that terminate at one of the”
- Also stated in: § Results and Discussion · plain
“By contrast, the 35 clades ending at mass extinctions had a mean CG significantly greater than 0.500 (t = 3.901, P < 0.001).”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Also stated in: § Results and Discussion · plain
In the paper
“Moreover, only one of these studies (44) focused on extinction selectivity per se; all others investigated the subsequent evolution of extinction survivors.”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
What the sources say
- Not checked yetcites [44] source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Extant clades are more likely to have”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“New species can only arise from the fission of existing ones (clades initially diversify from a single species and therefore a single point in morphospace), whereas extinctions can be random with respect to this same tree (34).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
What the sources say
- Not checked yetcites [34] source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Second, the manner in which these data have been analyzed is equally variable, although most studies implement some form of data reduction and ordination (10,12).”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Third, there are many possible indices of morphological disparity, and these are known to describe different aspects of morphospace occupation (34).”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
What the sources say
- Not checked yetcites [34] source
Strength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Early high patterns inevitably imply an unsampled period of cladogenesis (or the existence of ghost ranges) at the base of the clade, but this either occurs too fast for the available stratigraphic resolution or is not fossilized (11,50).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Mass extinctions have undoubtedly influenced the manner in which clades have explored morphospaces (42), but this phenomenon received little”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
What the sources say
- Not checked yetcites [42] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“First, the type of data used is highly variable (outlines, landmarks, and discrete characters), as is the information that these data are intended to convey (shape, form, or homologous characters of the entire organism or of particular organ systems).”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“More generally it is likely that global shifts in climate, sea level, and ocean chemistry [coupled with the elevated rates of extinction and turnover that these phenomena engender (56-58)] affected the availability of ecospace throughout the Phanerozoic.”
§ Clades reach highest morphological disparity early in their evolution > Why Do Clades Have Early High Disparity?
What the sources say
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“We avoided taxonomically overlapping cases or datasets obviously derivative of others.”
§ Clades reach highest morphological disparity early in their evolution > Materials and Methods
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“which predominantly result from physical drivers (59)”
§ Clades reach highest morphological disparity early in their evolution > Why Do Clades Have Early High Disparity?
What the sources say
- Not checked yetcites [59] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, clades terminating at a mass extinction event might be similarly truncated and are likely to have higher CGs for similar reasons.”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds. It may state two separate claims as one.
In the paper
“However, mass extinctions need not increase the subsequent availability of ecospace but may actually cause its collapse (60).”
§ Clades reach highest morphological disparity early in their evolution > Why Do Clades Have Early High Disparity?
What the sources say
- Not checked yetcites [60] source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Many studies have recently followed similar protocols (27,(36)(37)(38), and we adopted these methods here as a unifying approach.”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Morphological change under these circumstances may be rapid either because transitions are unusually large or because rates of cladogenesis are unusually high (even with”
§ Clades reach highest morphological disparity early in their evolution > Why Do Clades Have Early High Disparity?
What the sources say
- Not checked yetcites [29]
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Our use of 0.5 as a null is slightly simplistic, therefore, but biased against our principal finding (namely that clades not terminating at a mass extinction event are bottom-heavy on average).”
§ Clades reach highest morphological disparity early in their evolution > Results and Discussion
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Within datasets, strict rules were applied to ensure that sampling was adequately uniform across known operational taxonomic units (OTUs) and through time, amalgamating taxa where necessary (Dataset S1).”
§ Clades reach highest morphological disparity early in their evolution > Materials and Methods
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Fourth, the manner in which trajectories of disparity through time are quantified and classified is also variable.”
§ Clades reach highest morphological disparity early in their evolution > macroevolution | morphological disparity | morphospace | clade shape |
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
None of the sources cited for this claim have been checked yet.
In the paper
“The”
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
The paper relies on this without support.
The early high disparity model had not been tested systematically before this study.
“However, the validity of this early high disparity model has never been tested systematically.”
The paper relies on this without support.
The 98 sampled clades are representative of metazoan clades across the Phanerozoic.
“We compiled published discrete morphological and stratigraphic data for 98 vertebrate and invertebrate clades radiating throughout the Phanerozoic (Dataset S2).”
The paper relies on this without support.
Key innovations can arise at any time.
“key innovations (which can evolve at any time)”
The paper relies on this without support.
The 63 clades not terminating at a mass extinction were free-evolving and not otherwise truncated.
“we again focused on the 63”
Claims other papers make about this one
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In the citing paper
“Early bursts of morphological and taxonomic diversity should be associated with adaptive radiations [5] and many have been identified in the fossil record, ranging from the Cambrian radiation [27] to many invertebrate [28,29] and vertebrate [30,31] clades.”
From Novelty and Innovation in the History of Life (2015) · cites this paper as [29]
Experimental — accuracy not yet measured
Citations
Cites
(1945) · Annals of the Entomological Society of America · doi:10.1093/aesa/38.3.396 · Cited by 1,859
Simpson, G. G. (2005) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-47468-9_7 · Cited by 1,657
Smith, J. M., Burian, R. M., Kauffman, S. A., Alberch, P., Campbell, J., Goodwin, B. C., Lande, R., Raup, D. M., & Wolpert, L. (1985) · The Quarterly Review of Biology · doi:10.1086/414425 · Cited by 1,442
Early animal evolution: emerging views from comparative biology and geology
Knoll, A. H., & Carroll, S. B. (1999) · Science · doi:10.1126/science.284.5423.2129 · Cited by 821
Adaptive radiation: Contrasting theory with data
Gavrilets, S., & Losos, J. B. (2009) · Science · doi:10.1126/science.1157966 · Cited by 750
Benton, M. J. (2009) · Science · doi:10.1126/science.1157719 · Cited by 663
The Evolution of Morphological Diversity
Foote, M. (1997) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.ecolsys.28.1.129 · Cited by 655
(1997) · Choice Reviews Online · doi:10.5860/choice.34-4488 · Cited by 530
The origin of species by natural selection.
Morgan, T. H. (2011) · Princeton University Press eBooks · doi:10.1037/13436-011 · Cited by 422
Evolution since Darwin: the first 150 years
(2011) · Choice Reviews Online · doi:10.5860/choice.48-5062 · Cited by 376
Flagged first, then by citations
2 of the 78 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- SJ Gould Wonderful Life (W. W. Norton, New York, 1989).
- ENK Clarkson Invertebrate Palaeontology & Evolution (Wiley, New York, 1998).
Cited by
Sorted by citations
Items 101–200 of 262
Trait-based diversification shifts reflect differential extinction among fossil taxa
Wagner, P. J., & Estabrook, G. F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406304111 · Cited by 26
López‐Romero, F. A., Stumpf, S., Pfaff, C., Marramà, G., Johanson, Z., & Kriwet, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-69525-7 · Cited by 27
Boivin, S., Saucède, T., Laffont, R., Steimetz, É., & Neige, P. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194575 · Cited by 25
Multiple paths to morphological diversification during the origin of amniotes
Brocklehurst, N., & Benson, R. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-021-01516-x · Cited by 25
Simões, T. R., Kinney-Broderick, G., & Pierce, S. E. (2022) · Communications Biology · doi:10.1038/s42003-022-03144-y · Cited by 25
Discordance between morphological and taxonomic diversity: land snails of oceanic archipelagos
Triantis, K. A., François Rigal, A., Parent, C. E., Cameron, R. A. D., Lenzner, B., Parmakelis, Α., Yeung, N. W., Alonso, M. R., Ibáñez, M., Martins, A. M. D. F., et al. (2016) · Journal of Biogeography · doi:10.1111/jbi.12757 · Cited by 25
Koch, N. M., Ceccarelli, F. S., Ojanguren-Affilastro, A. A., & Ramírez, M. J. (2017) · Journal of Evolutionary Biology · doi:10.1111/jeb.13050 · Cited by 25
Developmental push or environmental pull? The causes of macroevolutionary dynamics
Erwin, D. H. (2017) · History & Philosophy of the Life Sciences · doi:10.1007/s40656-017-0163-0 · Cited by 25
Morphological evolution in a time of phenomics
Goswami, A., & Clavel, J. (2025) · Paleobiology · doi:10.1017/pab.2024.35 · Cited by 27
Ruta, M., & Wills, M. A. (2016) · Palaeontology · doi:10.1111/pala.12227 · Cited by 23
Self-citationLyman, R. L. (2019) · Studies in History and Philosophy of Science Part C Studies in History and Philosophy of Biological and Biomedical Sciences · doi:10.1016/j.shpsc.2019.101178 · Cited by 23
Habitat and developmental constraints drove 330 million years of horseshoe crab evolution
Bicknell, R. D. C., Kimmig, J., Budd, G. E., David, L., Bader, K. S., Haug, C., Kaiser, D., Laibl, L., Tashman, J. N., & Campione, N. E. (2021) · Biological Journal of the Linnean Society · doi:10.1093/biolinnean/blab173 · Cited by 23
Morphological volatility precedes ecological innovation in early echinoderms
Novack‐Gottshall, P. M., Sultan, A., Smith, N. S., Purcell, J. N., Hanson, K. E., Lively, R., Ranjha, I., Collins, C., Parker, R., Sumrall, C. D., et al. (2022) · Nature Ecology & Evolution · doi:10.1038/s41559-021-01656-0 · Cited by 23
Not-so-early bursts and the dynamic nature of morphological diversification
Slater, G. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502204112 · Cited by 24
Slow and steady: the evolution of cranial disparity in fossil and recent turtles
Foth, C., & Joyce, W. G. (2016) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2016.1881 · Cited by 23
Foth, C., Sookias, R. B., & Ezcurra, M. D. (2021) · Frontiers in Earth Science · doi:10.3389/feart.2021.723973 · Cited by 24
Evolutionary contingency in lingulid brachiopods across mass extinctions
Liang, Y., Strotz, L. C., Topper, T. P., Holmer, L. E., Budd, G. E., Chen, Y., Fang, R., Hu, Y., & Zhang, Z. (2023) · Current Biology · doi:10.1016/j.cub.2023.02.038 · Cited by 23
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O'Connor, A., & Wills, M. A. (2016) · Systematic Biology · doi:10.1093/sysbio/syw039 · Cited by 20
Self-citationCavin, L., Piuz, A., Ferrante, C., & Guinot, G. (2021) · Scientific Reports · doi:10.1038/s41598-021-90962-5 · Cited by 22
Romano, M., Brocklehurst, N., & Fröbisch, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-17757-5 · Cited by 22
Sclafani, J. A., Congreve, C. R., Krug, A. Z., & Patzkowsky, M. E. (2018) · Paleobiology · doi:10.1017/pab.2018.24 · Cited by 21
Santos, B. F., Perrard, A., & Brady, S. G. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.2352 · Cited by 20
Hopkins, M. J., & Gerber, S. (2021) · Springer eBooks · doi:10.1007/978-3-319-32979-6_132 · Cited by 20
Self-citationWhy should we compare morphological and molecular disparity?
van den Ende, C., Puttick, M. N., Urrutia, A. O., & Wills, M. A. (2023) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.14166 · Cited by 21
Self-citationThe significance of developmental robustness for species diversity
Melzer, R., & Theißen, G. (2016) · Annals of Botany · doi:10.1093/aob/mcw018 · Cited by 20
Wagner, P. J. (2019) · Paleobiology · doi:10.1017/pab.2018.35 · Cited by 18
Prospects for a General Theory of Evolutionary Novelty
Erwin, D. H. (2019) · Journal of Computational Biology · doi:10.1089/cmb.2019.0089 · Cited by 18
Reviewing the bases for a nomenclatural uniformization of the highest taxonomic levels in arthropods
Aria, C. (2019) · Geological Magazine · doi:10.1017/s0016756819000475 · Cited by 18
Climate, competition, and the rise of mosasauroid ecomorphological disparity
Cross, S. R. R., Moon, B. C., Stubbs, T. L., Rayfield, E. J., & Benton, M. J. (2022) · Palaeontology · doi:10.1111/pala.12590 · Cited by 17
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Disparity of cycad leaves dispels the living fossil metaphor
Coiro, M., & Seyfullah, L. J. (2024) · Communications Biology · doi:10.1038/s42003-024-06024-9 · Cited by 16
Ferrón, H. G., Greenwood, J. M., Deline, B., Martínez‐Pérez, C., Botella, H., Sansom, R. S., Ruta, M., & Donoghue, P. C. J. (2020) · Palaeontology · doi:10.1111/pala.12482 · Cited by 16
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Smith, A. J., Rosario, M. V., Eiting, T. P., & Dumont, E. R. (2014) · Evolution · doi:10.1111/evo.12435 · Cited by 16
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Foth, C., Ascarrunz, E., & Joyce, W. G. (2017) · Royal Society Open Science · doi:10.1098/rsos.170899 · Cited by 14
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Wright, A. M., Wagner, P. J., & Wright, D. F. (2020) · doi:10.32942/osf.io/ykzg5 · Cited by 14
Romano, M. (2017) · Historical Biology · doi:10.1080/08912963.2017.1397655 · Cited by 14
Gómez, R. O., & Pérez-Ben, C. M. (2019) · Frontiers in Earth Science · doi:10.3389/feart.2019.00056 · Cited by 13
Holmes, J. D. (2023) · Palaeontology · doi:10.1111/pala.12647 · Cited by 11
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Tajika, A., Landman, N. H., Morimoto, N., Ikuno, K., & Linn, T. (2020) · Palaeontology · doi:10.1111/pala.12490 · Cited by 11
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Whalen, C. D., Hull, P. M., & Briggs, D. E. G. (2020) · Science Advances · doi:10.1126/sciadv.abc2365 · Cited by 11
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Deline, B., & Thomka, J. R. (2017) · Journal of Paleontology · doi:10.1017/jpa.2016.129 · Cited by 10
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Konietzko‐Meier, D., Teschner, E. M., Bodzioch, A., & Sander, P. M. (2020) · Journal of Anatomy · doi:10.1111/joa.13276 · Cited by 7
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Huntsman, S. V., & Leslie, A. B. (2023) · New Phytologist · doi:10.1111/nph.19482 · Cited by 6
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Jiang, H., Szwedo, J., Labandeira, C. C., Chen, J., Moulds, M. S., Mähler, B., Muscente, A. D., Zhuo, D., Nyunt, T. T., Zhang, H., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44446-x · Cited by 6
Multiple phase transitions in an agent-based evolutionary model with neutral fitness
King, D. M., Scott, A. D., & Bahar, S. (2017) · Royal Society Open Science · doi:10.1098/rsos.170005 · Cited by 6
Early Bursts of Disparity and the Reorganization of Character IntegrationPreprint
Wagner, P. J. (2017) · PaleoRxiv (OSF Preprints) · doi:10.31233/osf.io/5jp83 · Cited by 7
Quantifying the configurational complexity of biological systems in multivariate ‘complexity space’
Rock, T., & Wills, M. A. (2025) · Journal of The Royal Society Interface · doi:10.1098/rsif.2024.0558 · Cited by 9
Self-citationGraciotti, R. P., Porto, L. M. V., Gonçalves‐Neto, S., & Quental, T. B. (2025) · Evolution · doi:10.1093/evolut/qpaf113 · Cited by 5
Disparification and extinction trade-offs shaped the evolution of Permian to Jurassic Odonata
Deregnaucourt, I., Bardin, J., Villier, L., Julliard, R., & Béthoux, O. (2023) · iScience · doi:10.1016/j.isci.2023.107420 · Cited by 6
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Luo, Y., Li, H.-T., Lu, L., Davey, A. H., Zhang, M.-Y., Ying, Y., Jiang, W., He, H.-J., Tao, Z.-B., Yang, L.-E., et al. (2026) · Nature Communications · doi:10.1038/s41467-025-68253-8 · Cited by 6
Multiple paths to recovery after the Permian-Triassic mass extinction
Liu, X., Song, H., Chu, D., Dai, X., Tian, L., Wu, Y., Wang, F., & Silvestro, D. (2026) · Current Biology · doi:10.1016/j.cub.2025.11.065 · Cited by 5
Pimiento, C., Tang, K. L., Zamora, S., Klug, C., & Sánchez-Villagra, M. R. (2018) · PeerJ · doi:10.7717/peerj.4899 · Cited by 4
Chornelia, A., & Hughes, A. C. (2022) · Journal of Systematics and Evolution · doi:10.1111/jse.12924 · Cited by 5
Ecomorphological datasets: comment on Hopkins (2022)
Esteve, J., & Suárez, M. G. (2023) · Lethaia · doi:10.18261/let.56.2.2 · Cited by 4
Body size correlates with discrete-character morphological proxies
Brougham, T., & Campione, N. E. (2020) · Paleobiology · doi:10.1017/pab.2020.23 · Cited by 4
Using Introduced Species of Anolis Lizards to Test Adaptive Radiation Theory
Stroud, J. T. (2018) · doi:10.25148/etd.fidc006576 · Cited by 3
Koch, N. M., & Thompson, J. R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.13.947796 · Cited by 4
Toman, J., & Jaroslav Flegr, A. (2018) · Evolutionary Biology · doi:10.1007/s11692-018-9462-y · Cited by 3
DeLorenzo, L., & Powder, K. E. (2023) · Evolution & Development · doi:10.1111/ede.12461 · Cited by 3
Evolutionary constraints on disparity of ericaceous pollen grains
Yu, Y., Schneider, H., Li, D.-Z., & Wang, H. (2018) · Annals of Botany · doi:10.1093/aob/mcy212 · Cited by 3
Aubry, M. (2025) · Minerals · doi:10.3390/min15030322 · Cited by 2
Bringing dinosaurs to life: A scientific revolution in palaeobiological methods
Benton, M. J., & Rayfield, E. J. (2026) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2026.113684 · Cited by 2
The global pattern of epiphytic liverwort disparity: insights from Frullania
Yu, Y., Fan, M., Zhou, H., & Song, Y. (2024) · BMC Ecology and Evolution · doi:10.1186/s12862-024-02254-x · Cited by 2
Phenotypic Change in Experimental Lineages
Gingerich, P. D. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316711644.008 · Cited by 1
Temporal Scaling and Evolutionary Mode
Gingerich, P. D. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316711644.006 · Cited by 1
��, Ï., ��, �., ��, �., ��, �., & ��, �. (2019) · SCIENTIA SINICA Terrae · doi:10.1360/sste-2019-0183 · Cited by 1
Metadata
- Authors
- Hughes, M., Gerber, S., & Wills, M. A.
- Affiliations
- University of Bath (GB)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2013-07-24
- Volume
- 110
- Issue
- 34
- Pages
- 13875-13879
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3752257
- OpenAlex
- W2040344633
- Cited by
- 262
- References
- 78
- Citations by year
- 2026: 14 · 2025: 18 · 2024: 10 · 2023: 19 · 2022: 13 · 2021: 23 · 2020: 24 · 2019: 38 · 2018: 26 · 2017: 24 · 2016: 23 · 2015: 17 · 2014: 11 · 2013: 2
- FWCI
- 11.97
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Leverhulme Trust (F/00 351/Z)
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Morphological variations and asymmetry
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Evolutionary Biology
- Keywords
- morphological disparity, macroevolutionary trends, center of gravity, mass extinction, Phanerozoic, apomorphies, developmental constraints
- MeSH terms
- Anatomy, Comparative, Biological Evolution, Models, Biological, Phylogeny, Species Specificity
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