The pattern of evolution in Pleistocene human brain size.
Abstract
With a sample of 94 Pleistocene cranial capacities between the time period of 1.8 Ma and 50 Ka now known, we consider the evolution of cranial capacity in Homo, with the null hypothesis that the changes over time are a result of one process. We employ a new method that uses a resampling approach to address the limitations imposed on the methods of previous studies. To test the null hypothesis, we examine the distribution of changes in adjacent temporal samples and ask whether there are differences between earlier and later samples. Our analyses do not reject the hypothesis of a single process of brain size change, but they are incompatible with an interpretation of punctuated equilibrium during this period. The results of this paper are difficult to reconcile with the case for cladogenesis in the Homo lineage during the Pleistocene.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
Adjacent basins can show different redox histories, and the oxic chemocline often shoaled during sea-level transgressions.
“Adjacent basins can show different redox histories, and the oxic chemocline often shoaled during sea-level transgressions (75,80).”
From Integrated records of environmental change and evolution challenge the Cambrian Explosion (2019) · cites this paper as [75]
Extensive ocean oxygenation occurred coincident with the end of the Shuram event, ca. 560-551 Ma.
“Extensive ocean oxygenation is argued to have occurred coincident with the end of the Shuram event, ca. 560-551 Ma (see review of 75).”
From Integrated records of environmental change and evolution challenge the Cambrian Explosion (2019) · cites this paper as [75]
Records from the open oceanic Laurentian margin (632-540 Ma), the Nama Group (~550-538 Ma), and the variably restricted Yangtze Block (635-520 Ma), all show continued redox instability after the first fossil evidence for (probable) metazoans.
“Records from the open oceanic Laurentian margin (632-540 Ma), the Nama Group (~550-538 Ma), and the variably restricted Yangtze Block (635-520 Ma), all show continued redox instability after the first fossil evidence for (probable) metazoans (see review of 75).”
From Integrated records of environmental change and evolution challenge the Cambrian Explosion (2019) · cites this paper as [75]
There is growing evidence for the existence of Oxygen Minimum Zones (OMZs) in early Cambrian basins.
“There is growing evidence for the existence of OMZs in early Cambrian basins (75-77).”
From Integrated records of environmental change and evolution challenge the Cambrian Explosion (2019) · cites this paper as [75]
Individual marine basins continued to record unstable redox conditions over short timescales well into the Cambrian, with dominantly ferruginous and even euxinic conditions particularly in shelf and slope environments.
“Individual marine basins continued to record unstable redox conditions over short timescales well into the Cambrian, with dominantly ferruginous and even euxinic conditions particularly in shelf and slope environments (e.g. 40,75,76,80).”
From Integrated records of environmental change and evolution challenge the Cambrian Explosion (2019) · cites this paper as [75]
A steady increase in brain size independent of body size followed the second changepoint and lasted through the Pleistocene.
“A steady increase in brain size-independent of body size-followed and lasted through the Pleistocene (Ruff et al., 1997;Lee and Wolpoff, 2003;Rightmire, 2004;Hawks, 2011).”
From When and Why Did Human Brains Decrease in Size? A New Change-Point Analysis and Insights From Brain Evolution in Ants (2021) · cites this paper as Lee and Wolpoff, 2003
The most basal node in Cetacea included in the phylogeny was probably predominantly aquatic but capable of some terrestrial locomotion.
“The most basal node in Cetacea included in our phylogeny (node 2) was probably predominantly aquatic but, like Dalanistes and Rodhocetus (Gingerich 2003), capable of some terrestrial locomotion.”
From THE EVOLUTIONARY HISTORY OF CETACEAN BRAIN AND BODY SIZE: CETACEAN BRAIN EVOLUTION (2013) · cites this paper as Gingerich 2003
Comparison of Mistaken Point communities with modern deep-sea benthic slope metazoan communities found that they exhibited similar levels of ecosystem complexity in terms of species richness, abundance, diversity values and spatial patterns.
“Comparison of Mistaken Point communities with modern deep-sea benthic slope metazoan communities found that they exhibited similar levels of ecosystem complexity (in terms of species richness, abundance, diversity values and spatial patterns; Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Variability in community composition is significantly lower within individual surfaces than between surfaces.
“Bray-Curtis similarity analysis has further shown that variability in community composition is significantly lower within individual surfaces (e.g. three different outcrops of the 'E' Surface) than between surfaces (Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Analysis of thin sections through the studied bedding planes revealed no variability in sedimentological texture or composition, and a purely taphonomic explanation for observed community composition can be refuted by PCA, DCA, and NMDS ordinations.
“Analysis of thin sections through the studied bedding planes revealed no variability in sedimentological texture or composition (Clapham et al., 2003), whilst a purely taphonomic explanation for observed community composition can be refuted by principal components analysis (PCA), detrended correspondence analysis (DCA), and non-metric multidimensional scaling (NMDS) ordinations (Clapham et al., 2”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Evidence for lateral competition is limited, with only 2 out of 32 possible pairs of taxa at Mistaken Point showing signs of spatial segregation, and only two taxa showing intraspecific spatial segregation.
“In contrast to the vertical tiering, evidence for lateral competition is limited, with only 2 out of 32 possible pairs of taxa at Mistaken Point showing signs of spatial segregation, and only two taxa showing intraspecific spatial segregation (Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Observed differences in community composition were interpreted to result from ecological and environmental variability, with variability between bedding plane communities taken to reflect different stages along an ecological succession.
“Observed differences in community composition were thus interpreted to result from ecological and environmental variability (Clapham et al., 2003;Clapham, 2011), with variability between bedding plane communities taken to reflect different stages along an ecological succession; frondpoor communities such as the 'D' Surface are interpreted as early succession communities, diverse communities with”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Evolutionary effects are considered to have had only a small impact on community structure, since a broad but weak correlation with stratigraphic position has been determined.
“Furthermore, evolutionary effects are considered to have had only a small impact on community structure, since a broad but weak correlation with stratigraphic position has been determined (Clapham et al., 2003;Clapham, 2011).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The quality of preservation directly correlates with observed fossil densities.
“Those authors did, however, demonstrate that the quality of preservation directly correlates with observed fossil densities, and therefore surfaces exhibiting higher-quality preservation are preferred for paleoecological studies.”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Differences in community composition are smaller between outcrops from the same horizon than between different horizons.
“These biases do not necessarily preclude paleoecological analysis, because differences in community composition have been shown to be smaller between outcrops from the same horizon than between different horizons (Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The dataset collected by Clapham et al. (2003) from the Mistaken Point Ecological Reserve is the most comprehensive currently available from Avalonian sites.
“This dataset is the most comprehensive currently available from Avalonian sites.”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
In Avalonia, preservational fidelity varies markedly between bedding planes and geological units, and even across individual bedding surfaces.
“In Avalonia, taphonomic biases are also introduced by the quality of preservational fidelity, which varies markedly between bedding planes and geological units, and even across individual bedding surfaces (cf.Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The Mistaken Point 'E' Surface is considered to be amongst the best global assemblages of Ediacaran macrofossils, with species-area curves and species size distributions indicating that the vast majority of macroorganisms on these surfaces have likely been preserved and documented.
“The Mistaken Point 'E' Surface is considered to be amongst the best global assemblages of Ediacaran macrofossils, with both speciesarea curves (Clapham et al., 2003) and species size distributions (Darroch et al., 2013) indicating that the vast majority of macroorganisms on these surfaces have likely been preserved and documented.”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The two beds showing the highest fossil densities in the study of Mistaken Point fossil assemblages (beds BC and E) also exhibit the highest fidelity of preservation, with morphological features of <0.5 mm resolution preserved.
“The two beds showing the highest fossil densities in the study of Mistaken Point fossil assemblages (Clapham et al., 2003, beds BC and E) also exhibit the highest fidelity of preservation, with morphological features of b0.5 mm resolution being preserved (Clapham et al., 2003).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The range of Shannon diversity values stated to characterise modern marine benthic animal communities encompasses the vast majority of values obtainable from any community with a species richness below 30, regardless of the biological affinities of its constituent organisms.
“However, the range of Shannon diversity values stated to characterise modern marine benthic animal communities (0.05-3.7 = extreme, 0.8-2.5 = typical; Clapham et al., 2003) encompasses the vast majority of values obtainable from any community with a species richness of b 30 (Fig. 8), regardless of the biological affinities of its constituent organisms.”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Fossil densities on the Mistaken Point 'E' Surface varied from 31.9 individuals per m2 at Watern Cove to 39.7-56.5 individuals per m2 on the 'Yale' and 'Queens' surfaces, ranging up to 150 ind./m2 where preservation is best.
“Those authors noted that fossil densities on the Mistaken Point 'E' Surface varied from 31.9 individuals per m 2 at Watern Cove (where preservation is relatively poor and variable across the surface), to 39.7-56.5 individuals per m 2 on the 'Yale' and 'Queens' surfaces respectively (where preservation is best and can range up to 150 ind./m 2 ).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
The highest fossil density values quoted for the 'E' Surface and Bristy Cove are considerably higher than those seen in the cited modern animal communities, undermining comparisons of Ediacaran fossil density with modern continental slope communities.
“However, the quoted highest values on that surface (as well as those at Bristy Cove) are considerably higher than those seen in the cited animal communities (e.g.Clapham et al., 2003, p. 541), thus undermining such comparisons.”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Cumulative sampling curves comparing species richness to randomly sub-sampled areas suggest most Mistaken Point bedding surfaces were fully sampled.
“Cumulative sampling curves comparing species richness to randomly sub-sampled areas suggest most Mistaken Point bedding surfaces were fully sampled (Clapham et al., 2003, fig. 3;Droser et al., 2006, fig.4A).”
From Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota (2015) · cites this paper as Clapham et al., 2003
Cites
Phylogenies and the Comparative Method
Felsenstein, J. (1985) · The American Naturalist · doi:10.1086/284325 · Cited by 9,793 · see citing works
Hutchinson, G. E. (1957) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1957.022.01.039 · Cited by 6,228 · see citing works
Carbon Isotopes in Photosynthesis
O'Leary, M. H. (1988) · BioScience · doi:10.2307/1310735 · Cited by 2,475 · see citing works
Romanek, C. S., Grossman, E. L., & Morse, J. W. (1992) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(92)90142-6 · Cited by 1,215 · see citing works
The Mesozoic marine revolution: evidence from snails, predators and grazers
Vermeij, G. J. (1977) · Paleobiology · doi:10.1017/s0094837300005352 · Cited by 1,043 · see citing works
Body mass and encephalization in Pleistocene Homo.
Ruff, C. B., Trinkaus, E., & Holliday, T. W. (1997) · Nature · doi:10.1038/387173a0 · Cited by 896 · see citing works
Climatic patterns and the distribution of C4 grasses in North America
Teeri, J. A., & Stowe, L. G. (1976) · Oecologia · doi:10.1007/bf00351210 · Cited by 749 · see citing works
Two feathered dinosaurs from northeastern China
Qiang, J., Currie, P. J., Norell, M. A., & Shu-An, J. (1998) · Nature · doi:10.1038/31635 · Cited by 580 · see citing works
Biomat-related lifestyles in the Precambrian
Seilacher, A. (1999) · PALAIOS · doi:10.2307/3515363 · Cited by 560 · see citing works
The new animal phylogeny: Reliability and implications
Adoutte, A., Balavoine, G., Lartillot, N., Lespinet, O., Prud'homme, B., & de Rosa, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.9.4453 · Cited by 512 · see citing works
Martin, M. W., Grazhdankin, D. V., Bowring, S. A., Evans, D. A. D., Fedonkin, M. A., & Kirschvink, J. L. (2000) · Science · doi:10.1126/science.288.5467.841 · Cited by 386 · see citing works
Mechanistic interpretation of carbon isotope discrimination by marine macroalgae and seagrasses
Raven, J. A., Johnston, A. M., Kübler, J. E., Korb, R., McInroy, S. G., Handley, L. L., Scrimgeour, C. M., Walker, D. I., Beardall, J., Vanderklift, M., et al. (2002) · Australian Journal of Plant Physiology · doi:10.1071/pp01201 · Cited by 360 · see citing works
Large–scale heterogeneity of the fossil record: implications for Phanerozoic biodiversity studies
Smith, A. B. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2000.0768 · Cited by 340 · see citing works
Brain Size, Cranial Morphology, Climate, and Time Machines [and Comments and Reply]
Beals, K. L., Smith, C. L., Dodd, S. M., Angel, J. L., Armstrong, E., Blumenberg, B., Girgis, F. G., Turkel, S., Gibson, K. R., Henneberg, M., et al. (1984) · Current Anthropology · doi:10.1086/203138 · Cited by 332 · see citing works
Onshore-Offshore Patterns in the Evolution of Phanerozoic Shelf Communities
Jablonski, D., Sepkoski, J. J., Bottjer, D. J., & Sheehan, P. M. (1983) · Science · doi:10.1126/science.222.4628.1123 · Cited by 307 · see citing works
Constant extinction, constrained diversification, and uncoordinated stasis in North American mammals
Alroy, J. (1996) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/s0031-0182(96)00100-9 · Cited by 276 · see citing works
Self-citationThe first named Ediacaran body fossil, <i>Aspidella Terranovica</i>
Gehling, J. G., Narbonne, G. M., & Anderson, M. M. (2000) · Palaeontology · doi:10.1111/j.0031-0239.2000.00134.x · Cited by 268 · see citing works
Long expected sponges from the Neoproterozoic Ediacara fauna of South Australia
Gehling, J. G., & Rigby, J. K. (1996) · Journal of Paleontology · doi:10.1017/s0022336000023283 · Cited by 256 · see citing works
Patterns of taxonomic and ecological structure of the shelf benthos during Phanerozoic time
Valentine, J. W. (1969) · Palaeontological Association · doi:10.5281/zenodo.16226412 · Cited by 251 · see citing works
Functional and Ecological Aspects of Ediacaran Assemblages
Jenkins, R. J. F. (1992) · Topics in Geobiology · doi:10.1007/978-1-4899-2427-8_5 · Cited by 197 · see citing works
Dating the Time of Origin of Major Clades: Molecular Clocks and the Fossil Record
Smith, A. B., & Peterson, K. J. (2002) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev.earth.30.091201.140057 · Cited by 193 · see citing works
Self-citationWood, D. A., Dalrymple, R. W., Narbonne, G. M., Gehling, J. G., & Clapham, M. E. (2003) · Canadian Journal of Earth Sciences · doi:10.1139/e03-048 · Cited by 159 · see citing works
Continental drift and Phanerozoic carbonate accumulation in shallow-shelf and deep-marine settings
Walker, L. J., Wilkinson, B. H., & Ivany, L. C. (2002) · The Journal of Geology · doi:10.1086/324318 · Cited by 149 · see citing works
Paleozoic record of morphologica diversity in blastozoan echinoderms.
Foote, M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.16.7325 · Cited by 145 · see citing works
Dentition and ageing of the hippopotamus
Laws, R. M. (1968) · African Journal of Ecology · doi:10.1111/j.1365-2028.1968.tb00899.x · Cited by 139 · see citing works
Growing up with dinosaurs: molecular dates and the mammalian radiation
Bromham, L., Phillips, M. J., & Penny, D. (1999) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(98)01507-9 · Cited by 127 · see citing works
Why no new phyla after the Cambrian? Genome and ecospace hypotheses revisited
Valentine, J. W. (1995) · PALAIOS · doi:10.2307/3515182 · Cited by 113 · see citing works
Laurie, W. A., Lang, E. M., & Groves, C. P. (1983) · Mammalian Species · doi:10.2307/3504002 · Cited by 74 · see citing works
MISRA, S. B. (1971) · Geological Society of America Bulletin · doi:10.1130/0016-7606(1971)82[979:sadhol]2.0.co;2 · Cited by 38 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Late-Neoproterozoic Deep-Ocean Oxygenation and the Rise of Animal Life
Canfield, D. E., Poulton, S. W., & Narbonne, G. M. (2007) · Science · doi:10.1126/science.1135013 · Cited by 1,000 · see citing works
Self-citationThe Ediacara biota: Neoproterozoic origin of animals and their ecosystems
Narbonne, G. M. (2005) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev.earth.33.092203.122519 · Cited by 714 · see citing works
Self-citationOn the eve of animal radiation: phylogeny, ecology and evolution of the Ediacara biota
Xiao, S., & Laflamme, M. (2009) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2008.07.015 · Cited by 543 · see citing works
PHANEROZOIC BIODIVERSITY MASS EXTINCTIONS
Bambach, R. K. (2006) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev.earth.33.092203.122654 · Cited by 529 · see citing works
Campione, N. E., & Evans, D. C. (2012) · BMC Biology · doi:10.1186/1741-7007-10-60 · Cited by 475 · see citing works
A new time tree reveals Earth history’s imprint on the evolution of modern birds
Claramunt, S., & Cracraft, J. (2015) · Science Advances · doi:10.1126/sciadv.1501005 · Cited by 383 · see citing works
DISPARITY: MORPHOLOGICAL PATTERN AND DEVELOPMENTAL CONTEXT
ERWIN, D. H. (2007) · Palaeontology · doi:10.1111/j.1475-4983.2006.00614.x · Cited by 363 · see citing works
Integrated records of environmental change and evolution challenge the Cambrian Explosion
Wood, R., Liu, A. G., Bowyer, F., Wilby, P. R., Dunn, F. S., Kenchington, C. G., Cuthill, J. F. H., Mitchell, E. G., & Penny, A. (2019) · Nature Ecology & Evolution · doi:10.1038/s41559-019-0821-6 · Cited by 337 · see citing works
The Great Ordovician Biodiversification Event (GOBE): The palaeoecological dimension
Servais, T., Owen, A. W., Harper, D. A. T., Kröger, B., & Munnecke, A. (2010) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2010.05.031 · Cited by 342 · see citing works
Mass extinctions and macroevolution
Jablonski, D. (2005) · Paleobiology · doi:10.1666/0094-8373(2005)031[0192:meam]2.0.co;2 · Cited by 317 · see citing works
The end of the Ediacara biota: Extinction, biotic replacement, or Cheshire Cat?
Laflamme, M., Darroch, S. A. F., Tweedt, S. M., Peterson, K. J., & Erwin, D. H. (2013) · Gondwana Research · doi:10.1016/j.gr.2012.11.004 · Cited by 300 · see citing works
Seilacher, A., Buatois, L. A., & Gabriela Mángano, M. (2005) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2005.06.003 · Cited by 277 · see citing works
Modular Construction of Early Ediacaran Complex Life Forms
Narbonne, G. M. (2004) · Science · doi:10.1126/science.1099727 · Cited by 269 · see citing works
The Ordovician biodiversification: setting an agenda for marine life
Harper, D. A. T. (2006) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2005.07.010 · Cited by 261 · see citing works
The origin of the animals and a 'Savannah' hypothesis for early bilaterian evolution
Budd, G. E., & Jensen, S. (2017) · Biological Reviews · doi:10.1111/brv.12239 · Cited by 240 · see citing works
Growth in small dinosaurs and pterosaurs: The evolution of archosaurian growth strategies.
Padian, K., Horner, J. R., & De Ricqlès, A. (2004) · Journal of Vertebrate Paleontology · doi:10.1671/0272-4634(2004)024[0555:gisdap]2.0.co;2 · Cited by 214 · see citing works
Poriferan paraphyly and its implications for Precambrian palaeobiology
Sperling, E. A., Pisani, D., & Peterson, K. J. (2007) · Geological Society, London, Special Publications · doi:10.1144/sp286.25 · Cited by 206 · see citing works
Patterns of evolution of the Ediacaran soft-bodied biota
Grazhdankin, D. (2014) · Journal of Paleontology · doi:10.1666/13-072 · Cited by 175 · see citing works
Liu, A. G., Mcllroy, D., & Brasier, M. D. (2010) · Geology · doi:10.1130/g30368.1 · Cited by 174 · see citing works
The Rise of Animals in a Changing Environment: Global Ecological Innovation in the Late Ediacaran
Droser, M. L., Tarhan, L. G., & Gehling, J. G. (2017) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev-earth-063016-015645 · Cited by 172 · see citing works
Eagle, R. A., Tütken, T., Martin, T. S., Tripati, A. K., Fricke, H. C., Connely, M., Cifelli, R. L., & Eiler, J. M. (2011) · Science · doi:10.1126/science.1206196 · Cited by 157 · see citing works
Archaeological collagen: why worry about collagen diagenesis?
Dobberstein, R. C., Collins, M. J., Craig, O. E., Taylor, G., Penkman, K. E. H., & Ritz-Timme, S. (2009) · Archaeological and Anthropological Sciences · doi:10.1007/s12520-009-0002-7 · Cited by 157 · see citing works
Stigall, A. L., Edwards, C. T., Freeman, R. L., & Rasmussen, C. M. Ø. (2019) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2019.05.034 · Cited by 160 · see citing works
Biotic replacement and mass extinction of the Ediacara biota
Darroch, S. A. F., Sperling, E. A., Boag, T. H., Racicot, R. A., Mason, S. J., Morgan, A. S., Tweedt, S., Myrow, P., Johnston, D. T., Erwin, D. H., et al. (2015) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2015.1003 · Cited by 160 · see citing works
Wood, D. A., Dalrymple, R. W., Narbonne, G. M., Gehling, J. G., & Clapham, M. E. (2003) · Canadian Journal of Earth Sciences · doi:10.1139/e03-048 · Cited by 159 · see citing works
Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota
Liu, A. G., Kenchington, C. G., & Mitchell, E. G. (2015) · Gondwana Research · doi:10.1016/j.gr.2014.11.002 · Cited by 157 · see citing works
Carbonate-hosted Avalon-type fossils in arctic Siberia
Grazhdankin, D. V., Balthasar, U., Nagovitsin, K. E., & Kochnev, B. B. (2008) · Geology · doi:10.1130/g24946a.1 · Cited by 146 · see citing works
Ediacaran biota on Bonavista Peninsula, Newfoundland, Canada
Hofmann, H. J., O'Brien, S. J., & King, A. F. (2008) · Journal of Paleontology · doi:10.1666/06-087.1 · Cited by 140 · see citing works
Parry, L. A., Smithwick, F., Nordén, K. K., Saitta, E. T., Lozano‐Fernandez, J., Tanner, A. R., Caron, J., Edgecombe, G. D., Briggs, D. E. G., & Vinther, J. (2018) · BioEssays · doi:10.1002/bies.201700167 · Cited by 140 · see citing works
Boag, T. H., Darroch, S. A. F., & Laflamme, M. (2016) · Paleobiology · doi:10.1017/pab.2016.20 · Cited by 136 · see citing works
Dietary characterization of terrestrial mammals
Pineda-Munoz, S., & Alroy, J. (2014) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2014.1173 · Cited by 117 · see citing works
Assemblage palaeoecology of the Ediacara biota: The unabridged edition?
Droser, M. L., Gehling, J. G., & Jensen, S. R. (2006) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2005.12.015 · Cited by 124 · see citing works
Reconstructing the reproductive mode of an Ediacaran macro-organism
Mitchell, E. G., Kenchington, C. G., Liu, A. G., Matthews, J. J., & Butterfield, N. J. (2015) · Nature · doi:10.1038/nature14646 · Cited by 109 · see citing works
THE EVOLUTIONARY HISTORY OF CETACEAN BRAIN AND BODY SIZE: CETACEAN BRAIN EVOLUTION
Montgomery, S. H., Geisler, J. H., McGowen, M. R., Fox, C., Marino, L., & Gatesy, J. (2013) · Evolution · doi:10.1111/evo.12197 · Cited by 106 · see citing works
Jablonski, D. (2005) · Journal of Experimental Zoology Part B: Molecular and Developmental Evolution · doi:10.1002/jez.b.21075 · Cited by 108 · see citing works
SPERLING, E. A., PETERSON, K. J., & LAFLAMME, M. (2011) · Geobiology · doi:10.1111/j.1472-4669.2010.00259.x · Cited by 112 · see citing works
Reconstructing a lost world: Ediacaran rangeomorphs from Spaniard's Bay, Newfoundland
Narbonne, G. M., Laflamme, M., Greentree, C., & Trusler, P. (2009) · Journal of Paleontology · doi:10.1666/08-072r1.1 · Cited by 110 · see citing works
Bicknell, R. D. C., & Paterson, J. R. (2018) · Biological Reviews · doi:10.1111/brv.12365 · Cited by 101 · see citing works
Deep-water Ediacaran fossils from northwestern Canada: taphonomy, ecology, and evolution
Narbonne, G. M., Laflamme, M., Trusler, P. W., Dalrymple, R. W., & Greentree, C. (2014) · Journal of Paleontology · doi:10.1666/13-053 · Cited by 103 · see citing works
Experimental formation of a microbial death mask
DARROCH, S. A. F., LAFLAMME, M., SCHIFFBAUER, J. D., & BRIGGS, D. E. G. (2012) · Palaios · doi:10.2110/palo.2011.p11-059r · Cited by 103 · see citing works
Liu, A. G., Matthews, J. J., Menon, L. R., McIlroy, D., & Brasier, M. D. (2014) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2014.1202 · Cited by 101 · see citing works
Lower Cambrian vendobionts from China and early diploblast evolution
Shu, D.-G., Morris, S. C., Han, J., Li, Y., Zhang, X.-L., Hua, H., Zhang, Z.-F., Liu, J.-N., Guo, J.-F., Yao, Y., et al. (2006) · Science · doi:10.1126/science.1124565 · Cited by 100 · see citing works
Wilby, P. R., Carney, J. N., & Howe, M. P. A. (2011) · Geology · doi:10.1130/g31890.1 · Cited by 93 · see citing works
Sea otters, kelp forests, and the extinction of Steller’s sea cow
Estes, J. A., Burdin, A., & Doak, D. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502552112 · Cited by 91 · see citing works
PETERSON, K. J., SUMMONS, R. E., & DONOGHUE, P. C. J. (2007) · Palaeontology · doi:10.1111/j.1475-4983.2007.00692.x · Cited by 93 · see citing works
Population structure of the oldest known macroscopic communities from Mistaken Point, Newfoundland
Darroch, S. A. F., Laflamme, M., & Clapham, M. E. (2013) · Paleobiology · doi:10.1666/12051 · Cited by 91 · see citing works
Evans, S. D., Tu, C., Rizzo, A., Surprenant, R. L., Boan, P. C., McCandless, H., Marshall, N., Xiao, S., & Droser, M. L. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2207475119 · Cited by 90 · see citing works
DeSilva, J. M., Traniello, J. F. A., Claxton, A. G., & Fannin, L. D. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.742639 · Cited by 86 · see citing works
TARHAN, L. G., DROSER, M. L., & GEHLING, J. G. (2010) · Palaios · doi:10.2110/palo.2010.p10-074r · Cited by 79 · see citing works
Ichaso, A. A., Dalrymple, R. W., & Narbonne, G. M. (2007) · Canadian Journal of Earth Sciences · doi:10.1139/e06-098 · Cited by 75 · see citing works
Environmental disturbance, resource availability, and biologic turnover at the dawn of animal life
Muscente, A. D., Boag, T. H., Bykova, N., & Schiffbauer, J. D. (2018) · Earth-Science Reviews · doi:10.1016/j.earscirev.2017.11.019 · Cited by 72 · see citing works
A new assemblage of juvenile Ediacaran fronds from the Drook Formation, Newfoundland
Liu, A. G., McIlroy, D., Matthews, J. J., & Brasier, M. D. (2012) · Journal of the Geological Society · doi:10.1144/0016-76492011-094 · Cited by 69 · see citing works
Dynamic patterns of latest Proterozoic‐Palaeozoic‐early Mesozoic marine biodiversity in South China
Jiayu, R., Junxuan, F., Miller, A. I., & Guoxiang, L. (2007) · Geological Journal · doi:10.1002/gj.1073 · Cited by 71 · see citing works
Self-citationGhisalberti, M., Gold, D. A., Laflamme, M., Clapham, M. E., Narbonne, G. M., Summons, R. E., Johnston, D. T., & Jacobs, D. K. (2014) · Current Biology · doi:10.1016/j.cub.2013.12.017 · Cited by 70 · see citing works
BAILEY, J. V., CORSETTI, F. A., BOTTJER, D. J., & MARENCO, K. N. (2006) · Palaios · doi:10.2110/palo.2005-p05-51e · Cited by 65 · see citing works
The utility of height for the Ediacaran organisms of Mistaken Point
Mitchell, E. G., & Kenchington, C. G. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-018-0591-6 · Cited by 60 · see citing works
Patterns of craniofacial integration in extantHomo,Pan, andGorilla
Polanski, J. M., & Franciscus, R. G. (2006) · American Journal of Physical Anthropology · doi:10.1002/ajpa.20421 · Cited by 54 · see citing works
Laflamme, M., Flude, L. I., & Narbonne, G. M. (2012) · Journal of Paleontology · doi:10.1666/11-044.1 · Cited by 51 · see citing works
The palatal dentition of tetrapods and its functional significance
Matsumoto, R., & Evans, S. E. (2017) · Journal of Anatomy · doi:10.1111/joa.12534 · Cited by 44 · see citing works
Selection for smaller brains in Holocene human evolution
Hawks, J. (2011) · arXiv · doi:10.48550/arxiv.1102.5604 · Cited by 45 · see citing works
LIU, A. G., MCILROY, D., MATTHEWS, J. J., & BRASIER, M. D. (2014) · Palaios · doi:10.2110/palo.2014.011 · Cited by 45 · see citing works
Nardin, E., & Lefebvre, B. (2010) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2010.01.005 · Cited by 38 · see citing works
Oxygen and Early Animal Evolution
Xiao, S. (2014) · Treatise on Geochemistry · doi:10.1016/b978-0-08-095975-7.01310-3 · Cited by 31 · see citing works
Kröger, B., & Lintulaakso, K. (2017) · Palaeontologia Electronica · doi:10.26879/729 · Cited by 21 · see citing works
- Authors
- Lee, S.-H., & Wolpoff, M. H.
- Venue
- Paleobiology
- Publisher
- Cambridge University Press (CUP)
- Published
- 2003-06
- Volume
- 29
- Issue
- 2
- Pages
- 186-196
- ISSN
- 0094-8373 (ISSN-L)
- 1938-5331
- OpenAlex
- W4244458236
- Cited by
- 27
- References
- 29
- Citations by year
- 2021: 1 · 2020: 4 · 2019: 2 · 2018: 1 · 2017: 3 · 2016: 2 · 2015: 2 · 2014: 3 · 2013: 2 · 2012: 2
- FWCI
- 1.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Paleobiology (publishedVersion)
- Topics
- Social Sciences › Anthropology › Pleistocene-Era Hominins and Archaeology
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Physical Sciences › Mathematics › Geometry and Topology › Morphological variations and asymmetry
- Keywords
- Pleistocene, cranial capacity, Homo, brain evolution, punctuated equilibrium, cladogenesis, null hypothesis testing, hominin evolution
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review