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A dating success story: genomes and fossils converge on placental mammal origins
EvoDevovolume 3, Article number: 18 (2012)
The timing of the placental mammal radiation has been a source of contention for decades. The fossil record of mammals extends over 200 million years, but no confirmed placental mammal fossils are known prior to 64 million years ago, which is approximately 1.5 million years after the Cretaceous-Paleogene (K-Pg) mass extinction that saw the end of non-avian dinosaurs. Thus, it came as a great surprise when the first published molecular clock studies suggested that placental mammals originated instead far back in the Cretaceous, in some cases doubling divergence estimates based on fossils. In the last few decades, more than a hundred new genera of Mesozoic mammals have been discovered, and molecular divergence studies have grown from simple clock-like models applied to a few genes to sophisticated analyses of entire genomes. Yet, molecular and fossil-based divergence estimates for placental mammal origins have remained remote, with knock-on effects for macro-scale reconstructions of mammal evolution. A few recent molecular studies have begun to converge with fossil-based estimates, and a new phylogenomic study in particular shows that the palaeontological record was mostly correct; most placental mammal orders diversified after the K-Pg mass extinction. While a small gap still remains for Late Cretaceous supraordinal divergences, this study has significantly improved the congruence between molecular and palaeontological data and heralds a broader integration of these fields of evolutionary science.
As George Gaylord Simpson  detailed in his ground-breaking volume, one of the main contributions of the fossil record to the modern synthesis is primary data on the tempo of evolution. In recent decades, this aspect of fossil data has been leveraged for calibrating molecular estimates of clade divergence times. Concurrently, there has been expanding use of molecular data in palaeobiological studies (for example, ), and linking of fossils and embryos in studies of evolutionary development (for example, ). Yet, these examples of integration between fields of evolutionary science are still rare, and fossils are often excluded from macroevolutionary analyses beyond palaeobiology because of the complexities associated with including extinct taxa of uncertain phylogenetic affinity or with incorporating incomplete data. It has also been suggested that fossil data will likely have little impact on reconstructions of evolution in extant lineages (for example, [4, 5]), despite extensive evidence to the contrary (for example, [6, 7]). One of the most persistent question marks concerning the quality of fossil data has come from molecular dating studies themselves, which can differ from fossil-based divergence time estimates by tens to hundreds of millions of years and are regarded by many as showing the poor quality of the fossil record .
For this reason, many palaeobiologists were pleased when a recent study  using a vast genomic dataset to reconstruct divergence dates for major placental mammal clades, found extensive congruence with the fossil record. Indeed it appears that most placental mammal orders originated and diversified after the demise of the non-avian dinosaurs during the Cretaceous-Paleogene (K-Pg) mass extinction 65.5 million years ago (mya), as palaeomammalogists have long maintained. The timing of this radiation has been a contentious issue since the first published molecular clock studies of placentals pushed the divergence times for many clades deep into the Cretaceous [10–12], in some cases nearly doubling the time between molecular origins and first appearance in the fossil record.
Accurate dating is crucial for understanding the last mass extinction
Resolving the timing of the placental mammal radiation is crucial for understanding the magnitude and selectivity of the K-Pg mass extinction, as well as factors that shaped the evolution of mammals and, more generally, the modern biota. Most molecular divergence studies until now have favored a ‘Short Fuse Model’, in which the major clades originated and diversified long before the K-Pg boundary, with some even suggesting that the extinction of non-avian dinosaurs had little to no effect on the evolution of extant clades . Others have supported a ‘Long Fuse Model’, in which major clades originated long before their first appearance in the fossil record, but did not diversify extensively until after the K-Pg extinction cleared valuable niche space for mammals to occupy . The palaeontological evidence has been consistently in support of an ‘Explosive Model’, wherein the major clades originated and diversified near the K-Pg boundary [14, 15]. However, as stem members of several placental orders can be identified within a few million years of the K-Pg boundary, most palaeontologists accept that some placental lineages may well extend into the Late Cretaceous, as suggested by the Long Fuse Model . Over the last few years, molecular divergence estimates have been steadily moving closer to those supported by palaeontological data [17, 18]. Another recent analysis of a molecular supermatrix also reconstructed most intraordinal divergences near the Cretaceous-Paleogene (K-Pg) boundary , but the dos Reis et al. study goes further still in closing the long-standing gap between molecular data and fossils (Figure 1).
Mind the gap
Many hypotheses have been suggested for the persistent discrepancy between molecular and fossil-based estimates, and a primary one is incomplete sampling in the fossil record. Rock availability and collection effort can drive apparent patterns of taxonomic diversity [21, 22], but statistical models suggest that preservation alone is unlikely to explain the difference in divergence estimates for placental mammals . The relatively poor sampling of Mesozoic mammal fossils from the large southern continents may be a confounding factor, but current data offer little support for a southern ‘Garden of Eden’ for placental mammals [14, 15]; but see . On the molecular side, the effects of body size, population fluctuations, overlapping generations and other life history and ecological factors have been shown to affect estimates of substitution rates, potentially misleading divergence estimates [26, 27].
The new study by dos Reis et al. suggests that previous molecular clock studies were misled by inadequate molecular data, poor quality control and treatment of fossil calibrations, and overly simplistic treatment of the variation in molecular data. The immense amount of data (36 nuclear genomes and 274 mitochondrial genomes) used in this study was certainly the most obvious improvement, representing an increase of multiple orders of magnitude (in terms of genes sampled) over previous studies. Perhaps even more important was the use of more accurate fossil data, following the increasing participation of palaeobiologists in establishing calibration dates (for example, [9, 28, 29]), as well as a more realistic use of those dates as ‘soft’ bounds or probability distributions, and not as invariant minima . Indeed, much of the offset in previous studies may have been due to inappropriate treatment of fossil data, such as using single calibrations from poorly sampled intervals  or incorrectly assuming that Cretaceous eutherians represent extant clades . In addition, methodological innovations in the approach used by dos Reis et al. allowed for better treatment of branch length and rate variance, which will be even more important as next-generation sequencing continues to expand the use of genomic data in phylogenetic and other evolutionary analyses.
Fossils are more than calibration points
The utility of fossils extends beyond their use as first appearance events. Some studies have attempted to model clade origins based on present and past diversity, as well as sampling intensity, with one such analysis concluding that Primates likely originated in the Cretaceous . Quantifying rates of phenotypic character change across fossil-dominated phylogenetic trees for placentals has also suggested that there is no significant change immediately before and after the K-Pg boundary . However, analyses of this nature are preliminary and limited by the accuracy of available phylogenies, which, in the case of mammals, usually focus either on Cretaceous or more recent Cenozoic taxa. Perhaps the most problematic aspect of these approaches at present is that placental mammals from the Paleocene (the ten-million year interval immediately following the K-Pg extinction) are phylogenetically poorly resolved and thus excluded in most studies. Ongoing work should eventually resolve early Cenozoic mammal relationships, allowing for integration of a broader range of fossil data into studies of mammalian evolutionary rates and clade origins.
New methods will require good fossil data, and in the intervening 14 years since the publication of the first extensive molecular clock estimates of mammal divergence times , more than 100 new genera of Mesozoic mammals have been discovered . Although none of these taxa are currently well-supported as stem representatives of extant placental lineages [14, 15]; but see [25, 35], they provide important data on the effect of the K-Pg extinction on mammals and cast doubt on extant-only based reconstructions, which suggest that at least 43 placental lineages survived that event . Fossil evidence demonstrates that there was a diverse mammalian fauna leading up to the K-Pg extinction, which included eutherians and metatherians (the clades that include placentals and marsupials, respectively), as well as the taxonomically-depauperate, but still extant egg-laying monotremes. In addition, the latest Cretaceous saw cosmopolitan dryolestoids and multituberculates, as well as gondwanatheres and other clades with southern or more restricted distributions. Most of these clades survive the K-Pg extinction, but in limited numbers. Other than the extant clades, only multituberculates recovered or maintained, according to , high levels of diversity in the Paleogene. Between Eutheria and Metatheria, only five lineages (Herpetotheriidae, Cimolestidae, Adapisoriculidae, Leptictidae [+Gypsonictops, and Protungulatum) are known to have survived the K-Pg extinction, while many others perished [14, 15, 37]. The dos Reis et al. study  adds another dozen or so lineages to the list of survivors, but it is clear that evidence from fossils and molecules are converging on a model where a small number of mammalian lineages survive the K-Pg extinction and diversify soon afterwards.
The fuse remains cryptic
Although the gap has closed substantially, disagreement between the most recent molecular divergence time estimates and the fossil record persists. Intraordinal divergence estimates now nearly replicate the fossil record of placental mammals, but the oldest interordinal divergences continue to predate the first fossil occurrences by approximately 20 million years. The fuse, relative to the fossil record, is almost 50 million years shorter than in the first molecular clock studies, and may change further. At the moment, however, this suggests that nearly 25% of placental mammal history remains unrepresented in the fossil record, if none of the known Cretaceous eutherians fall along the crown’s Mesozoic fuse. This remaining gap emphasizes a continuing need for palaeontological exploration, as was highlighted by the recent discovery of an approximately 160 million-year-old eutherian . The fossil record and molecular divergence studies have both improved dramatically in recent years and continue to demonstrate that there is much more to learn about mammal evolution.
The great strides that have been made in resolving the timing of placental mammal origin may also bode well for the many other contentious gaps between molecular divergence estimates and the fossil record. The timing of origin for eukaryotes is a notable area of ongoing debate, with some molecular estimates and fossil-based estimates differing by more than a billion years, (but see ). The origin of animals (Metazoa) is no less controversial, with some molecular dates predating the fossil evidence for a ‘Cambrian Explosion’ by 800 million years, although most studies find the gap to be a mere 100 million years [40, 41]. Studies such as the one by dos Reis et al. demonstrate that better integration of molecular and palaeontological data is essential for a more accurate understanding of the patterns and processes underlying organismal evolution. Hopefully, this progress in divergence time estimates will encourage further synthesis of the diverse sources of data available to evolutionary biologists. It is long overdue.
Simpson GG: Tempo and mode in evolution. 1944, New York: Columbia University Press
Asher R, Müller J: (Eds): From clone to bone: the synergy of morphological and molecular tools in palaeobiology. 2012, Cambridge: Cambridge University Press
Sánchez-Villagra MR: Embryos in deep time: the rock record of biological development. 2012, Berkeley: University of California Press
Bininda-Emonds ORP, Cardillo M, Jones KE, MacPhee RDE, Beck RMD, Grenyer R, Price SA, Vos RA, Gittleman JL, Purvis A: The delayed rise of present-day mammals. Nature. 2007, 446: 507-512. 10.1038/nature05634.
Venditti C, Meade A, Pagel M: Multiple routes to mammalian diversity. Nature. 2011, 479: 393-396. 10.1038/nature10516.
Finarelli JA, Flynn JJ: Ancestral state reconstruction of body size in the Caniformia (Carnivora, Mammalia): the effects of incorporating data from the fossil record. Syst Biol. 2006, 55: 301-313. 10.1080/10635150500541698.
Quental TB, Marshall CR: Diversity dynamics: molecular phylogenies need the fossil record. Trends Ecol Evol. 2010, 25: 434-441. 10.1016/j.tree.2010.05.002.
Donoghue PCJ, Smith P(E): Telling the evolutionary time: molecular clocks and the fossil record. 2004, London: CRC Press
dos Reis M, Inoue J, Hasegawa M, Asher RJ, Donoghue PCJ, Yang Z: Phylogenomic datasets provide both precision and accuracy in estimating the timescale of placental mammal phylogeny. Proc Biol Sci. 2012, 279: 3491-3500. 10.1098/rspb.2012.0683.
Kumar S, Hedges SB: A molecular timescale for vertebrate evolution. Nature. 1998, 392: 917-920. 10.1038/31927.
Springer MS: Molecular clocks and the timing of the placental and marsupial radiations in the relation to the Cretaceous-Tertiary boundary. J Mamm Evol. 1997, 4: 285-302. 10.1023/A:1027378615412.
Hedges SB, Parker PH, Sibley CG, Kumar S: Continental breakup and the ordinal diversification of birds and mammals. Nature. 1996, 381: 226-229. 10.1038/381226a0.
Springer MS, Murphy WJ, Eizirik E, O’Brien SJ: Placental mammal diversification and the Cretaceous-Tertiary boundary. Proc Natl Acad Sci USA. 2003, 100: 1056-1061. 10.1073/pnas.0334222100.
Goswami A, Prasad GVR, Upchurch P, Boyer DM, Seiffert ER, Gheerbrant E, Verma O, Flynn JJ: A radiation of basal arboreal mammals beginning in the late Cretaceous of India. P Natl Acad Sci USA. 2011, 108: 16333-16338. 10.1073/pnas.1108723108.
Wible JR, Rougier GW, Novacek MJ, Asher RJ: Cretaceous eutherians and Laurasian origin for placental mammals near the K/T boundary. Nature. 2007, 447: 1003-1006. 10.1038/nature05854.
Archibald JD, Deutschman DH: Quantitative analysis of the timing of the origin and diversification of extant placental orders. J Mamm Evol. 2001, 8: 107-124. 10.1023/A:1011317930838.
Kitazoe Y, Kishino H, Waddell PJ, Nakajima N, Okabayashi T, Watabe T, Okuhara Y: Robust time estimation reconciles views of the antiquity of placental mammals. PLoS One. 2007, 2: e384-10.1371/journal.pone.0000384.
Hallström BM, Janke A: Resolution among major placental mammal interordinal relationships with genome data imply that speciation influenced their earliest radiations. BMC Evol Biol. 2010, 8: 162-
Meredith RW, Janecka JE, Gatesy J, Ryder OA, Fisher CA, Teeling EC: Impacts of the Cretaceous terrestrial revolution and KPg extinction on mammal diversification. Science. 2011, 334: 521-524. 10.1126/science.1211028.
Hedges SB, Kumar S: Divergence times of eutherian mammals. Science. 1999, 285: 2031a (6 pp.)-
Peters SE, Foote M: Biodiversity in the Phanerozoic: a reinterpretation. Paleobiology. 2001, 27: 583-601. 10.1666/0094-8373(2001)027<0583:BITPAR>2.0.CO;2.
Smith AB: Large scale heterogeneity of the fossil record: implications for biodiversity studies. Philos Trans RSoc B. 2001, 356: 361-367.
Foote M, Hunter JP, Janis CM, Sepkoski JJ: Evolutionary and preservational constraints on origins of biologic groups: divergence times of eutherian mammals. Science. 1999, 283: 1310-1314. 10.1126/science.283.5406.1310.
Hunter JP, Janis CM: Spiny Norman in the Garden of Eden? Dispersal and early biogeography of Placentalia. J Mamm Evol. 2006, 13: 89-123. 10.1007/s10914-006-9006-6.
Smith T, Bast ED, Sigé B: Euarchontan affinity of Paleocene Afro-European adapisoriculid mammals and their origin in the late Cretaceous Deccan Traps of India. Naturwissenschaften. 2010, 97: 417-422. 10.1007/s00114-010-0651-5.
Balloux F, Lehmann L: Substitution rates at neutral genes depend on population size under fluctuating demography and overlapping generations. Evol. 2011, 66: 605-611.
Bromham L: The genome as a life-history character: why rate of molecular evolution varies between mammal species. Philos Trans R Soc Lond B Biol Sci. 2011, 366: 2503-2513. 10.1098/rstb.2011.0014.
Parham JF, Donoghue PCJ, Bell CJ, Calway TD, Head JJ, Holroyd PA, Inoue JG, Irmis RB, Joyce WG, Ksepka DT: Best practices for justifying fossil calibrations. Syst Biol. 2012, 61: 346-359. 10.1093/sysbio/syr107.
Benton MJ, Donoghue PCJ, Asher RJ: The timetree of life. Calibrating and constraining molecular clocks. Edited by: Hedges SB, Kumar S. 2009, Oxford: Oxford University Press, 35-86.
Yang Z, Rannala B: Bayesian estimation of species divergence times under a molecular clock using multiple fossil calibrations with soft bounds. Mol Biol Evol. 2006, 23: 212-226.
Reisz RR, Müller J: Molecular timescales and the fossil record: a paleontological perspective. Trends Genet. 2004, 20: 237-241. 10.1016/j.tig.2004.03.007.
Tavare S, Marshall CR, Will O, Soligo C, Martin RD: Using the fossil reconrd to estimate the age of the last common ancestor of extant primates. Nature. 2002, 416: 726-729. 10.1038/416726a.
Larsson HCE, Dececchi TA, Harrison LB: From Clone to Bone: the Synergy of Morphological and Molecular Tools in Paleobiology. Morphological largess: can morphology offer more and be modelled as a stochastic evolutionary process?. Edited by: Asher RJ, Mueller J. 2012, Cambridge: University of Cambridge Press, 83-115.
Luo Z-X: Transformation and diversification in early mammal evolution. Nature. 2007, 450: 1011-1019. 10.1038/nature06277.
Archibald JD, Zhang Y, Harper T, Cifelli RL: Protungulatum, confirmed Cretaceous occurrence of an otherwise Paleocene eutherian (placental?) mammal. J Mamm Evol. 2011, 18: 153-161. 10.1007/s10914-011-9162-1.
Wilson GP, Evans AR, Corfe IJ, Smits PD, Fortelius M, Jernvall J: Adaptive radiation of multituberculate mammals before the extinction of dinosaurs. Nature. 2012, 483: 457-460. 10.1038/nature10880.
Horowitz I, Martin T, Bloch J, Ladavèze S, Kurz C, Sánchez-Villagra MR: Cranial anatomy of the earliest marsupials and the origin of opossums. PLoS One. 2009, 4: e8278-10.1371/journal.pone.0008278.
Luo Z-X, Yuan C-X, Meng Q-J, Ji Q: A Jurassic eutherian mammal and divergence of marsupials and placentals. Nature. 2011, 476: 442-445. 10.1038/nature10291.
Wegener Parfrey L, Lahr DJG, Knoll AH, Katz LA: Estimating the timing of early eukaryotic diversification with multigene molecular clocks. P Natl Acad Sci USA. 2011, 108: 13624-13629. 10.1073/pnas.1110633108.
Blair JE: The timetree of life. Animals (Metazoa). Edited by: Hedges SB, Kumar S. 2009, Oxford: Oxford University Press, 223-230.
Edgecombe GD, Giribet G, Dunn CW, Hejnol A, Kristensen RM, Neves RC, Rouse GW, Worsaae K, Sørensen MV: Higher-level metazoan relationships: recent progress and remaining questions. Org Divers Evol. 2011, 11: 151-172. 10.1007/s13127-011-0044-4.
I thank J.A. Finarelli, R.J. Asher, M.E.H. Jones, M. dos Reis, Z. Yang, M. Telford, and the UCL-NHM Vertebrate Palaeobiology journal club for relevant discussions and suggestions on previous drafts of this manuscript.
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