The (Paleo)Geography of Evolution: Making Sense of Changing Biology and Changing Continents
© Springer Science+Business Media, LLC 2012
Published: 18 April 2012
During the voyage of the H.M.S. Beagle, Charles Darwin quickly realized that geographic isolation led to significant changes in the adaptation of local flora and fauna (Darwin 1859). Genetic isolation is one of the well-known mechanisms by which adaptation (allopatric speciation) can occur (Palumbi, Annu Rev Ecol Syst 25:547–72, 1994; Ricklefs, J Avian Biol 33:207–11, 2002; Burns et al., Evolution 56:1240–52, 2002; Hendry et al., Science 290:516–8, 2009). Evolutionary changes can also occur when landmasses converge or are “bridged.” An important and relatively recent (Pliocene Epoch) example known as the “Great American Biotic Interchange” allowed for the migration of previously isolated species into new ecological niches between North and South America (Webb 1985, Ann Mo Bot Gard 93:245–57, 2006; Kirby and MacFadden, Palaeogeogr Palaeoclimatol Palaeoecol 228:193–202, 2005). Geographic isolation (vicariance) or geographic merging (geodispersal) can occur for a variety of reasons (sea level rise, splitting of continents, mountain building). In addition, the growth of a large supercontinent (or breakup) may change the climatic zonation on the globe and form a different type of barrier for species migration. This short review paper focuses on changing paleogeography throughout the Phanerozoic and the close ties between paleogeography and the evolutionary history of life on Earth.
KeywordsEvolution Paleogeography Tectonics
Paleogeomagnetism and Paleogeography
Sedimentary rocks may acquire a memory of the ancient field in several ways. One important mechanism of remanence acquisition occurs as a grain of magnetite or hematite (rust) settles to the bottom of the ocean or lake. In the upper parts of the water column, the particles are influenced by the Earth's magnetic field, but perturbations in the water column prevent alignment. As the particles reach the quieter interface between the water column and the sediments, they will align themselves with the magnetic field and “lock in” the direction of the field. This is the primary mode of remanence acquisition in sandstones, siltstones and clays, and is called “detrital remanent magnetizaton” and is shown in Fig. 2b. In other sedimentary rocks, magnetic minerals may form via chemical processes and acquire a memory of the field as they grow to a critical size. This method is called “chemical remanent magnetization.” As long as the chemical event producing the magnetization in the rocks takes place close to the time of deposition, it can be reliably used to reconstruct the continents.
The magnetic directions locked into the rocks can be studied by collecting oriented samples in the field and then measuring the directions recorded in those rocks back in the laboratory. In practice, paleomagnetists will sample several layers of sedimentary rock or many flows of igneous rocks to assure averaging to the GAD field.
Biogeography and Paleogeography: Some Examples
In general, reconstructions of the globe back to about 150 million years ago can be reliably obtained by studying the pattern of ocean floor magnetic anomalies along with paleomagnetic data from the continents. Attempts to reconstruct the globe prior to 150 million years ago require integration of various types of data in addition to paleomagnetism in order to reliably produce paleogeographic maps. In the following sections, I show how paleogeography has influenced thinking about evolutionary changes and vice-versa for selected time slices of the Phanerozoic. The paper briefly examines the paleogeography/biogeography at the end of the Cretaceous Period (85 million years ago), the end of the Paleozoic (~260 million years ago) and the Ediacaran–Cambrian transition (~570–530 million years ago) as examples of the interplays between evolutionary history and paleogeography.
Late Cretaceous—85 Million Years Ago
The Middle Cretaceous (from about 120–100 million years ago) was an interval of major changes in atmospheric chemistry, the pace of sea-floor spreading was high, the magnetic field was in a stable normal polarity “superchron,” and average global temperatures were on the rise. By the late Cretaceous, the globe was ice free and a greenhouse climate resulted in elevated sea levels and further isolation of the splitting continents.
In contrast, several lines of biogeographic analysis suggest that there were pathways for faunal transfer between the Gondwana continents even into the Paleocene (Vences et al. 2003; Sereno et al. 2004; Van Bocxlaer et al. 2006; Bossuyt et al. 2006). While isolation and rising sea levels played a large role in creating barriers to biological connections, there must have remained some pathways for significant faunal exchanges (Jacobs et al. 2011). In particular, Jacobs et al. (2011) discuss possibilities of “Noah's Ark,” “Beached Viking Funeral Ships,” and “landspans” across the Gondwana landmasses following the initial work of McKenna (1973). “Noah's Arks” are segments of continental crust that rift away from their larger landmasses and carry with them their biota. The “arks” result in initial isolation of the organisms, but they may also “dock” with a new landmass and introduce their species to a new area.
“Beached Viking Funeral Ships” are similar in that they are also segments of continental crust rifted from one area, but these also may later collide and join new continental regions where the (extinct) biota carried on the funeral ship are now found on a new landmass. Both “Noah's Arks,” “Docked Noah's Arks,” and “Beached Viking Funeral Ships” are expected occurrences during continental rifting and later collision (Jacobs et al. 2011).
India and Madagascar are argued to be good examples of “Noah's Arks” formed during the rifting of Gondwana. India and Madagascar were isolated from Africa and Australo-Antarctica and ultimately from each other during the Cretaceous and Cenozoic. Jacobs et al. (2011) show that India–Madagascar shared the same “Noah's Ark” dinosaur fauna until their split in the Late Cretaceous. India was also argued to be a good example of a “Beached Viking Funeral Ship” due the fact that its older vertebrate fossils now reside on the Asian continent.
Lastly, Jacobs et al. (2011) also propose a possible series of “landspans” between the Gondwana continents that may have allowed for transfers of biota between the various elements of land before significant separation was achieved by continuing drift; opening of the Indian, Atlantic, and Southern Oceans; and falling sea levels. Due to its long journey northward to Asia, it is possible that India interacted with island arcs or other continents before final docking resulting in a more cosmopolitan Cretaceous fauna (Chatterjee and Scotese 1999; Briggs 2003; Chatterjee et al. 2009).
End Paleozoic/Early Mesozoic—260 Million Years
While the Cretaceous was a period of disaggregation of large landmasses, the end of the Paleozoic witnessed the formation of the supercontinent Pangea (Fig. 4). The biogeography of Pangea was influenced by geodispersal, vicariance, and strong climatic zoning. Species were isolated by the uplift of major mountain chains along the suture zones of Pangea and by the lowering of sea level associated with climatic changes in the Permian, but there were also numerous opportunities for dispersal of biota across the large landmass and surrounding Panthalassic and PaleoTethys Oceans (Ross and Ross 1985; Perez-Huerta 2007).
Pangea also extended through a wide range of climatic zones as the continental landmass stretched from pole to pole (Fig. 4). The poles were cold temperate with winter ice. Interiors of the larger continents (West Gondwana and Laurasia) were deserts and normal latitudinal zoning was present elsewhere (see Fig. 4). This strong climatic zoning may also have influenced provinciality as (for example) certain tetrapod fossils appear to be restricted to specific latitudinal zones in the absence of any physical barriers (Sidor et al. 2004; Whiteside et al. 2011).
It is also interesting to consider the relationship between the large and connected supercontinent and the mass extinction that occurred at the close of the Paleozoic (~251 million years ago; Benton and Twitchett 2003). Causative mechanisms for the Permian extinction are diverse and range from the effects associated with the massive volcanic outpouring of the Siberian traps, global warming, global cooling, and ocean anoxia (Benton and Twitchett 2003; Becker et al. 2004). Although the exact cause of the extinction is debated, the changes in oceanic circulation brought about by the assembly of Pangea and the fact that the land surface of the Earth was mostly confined to a single hemisphere should not be underestimated.
Cambrian—542–525 Million Years Ago
Changing paleogeography throughout Earth history played an important role in evolutionary biology. Paleogeographic changes influence evolution in myriad ways including, but not limited to, vicariance, geodispersal, and climatic zonation. Analysis of how flora and fauna are affected by changes in plate tectonic setting and concomitant changes in climate plays an important role in evaluating evolutionary change. This paper briefly reviews three intervals of time and gives examples of how biology and paleogeography are integrated into paleogeographic analyses.
The author wishes to thank Bruce Lieberman for inviting this contribution and two anonymous reviewers for helpful suggestions that vastly improved the manuscript. Work reported in this paper was supported by grants from the National Science Foundation grants EAR09-10888, EAR04-09101, and EAR05-08597(to JGM).
- Becker L, Poreda R, Basu A, Pope K, Harrison T, Nicholson C, et al. Bedout: a possible end-Permian impact crater offshore of northwestern Australia. Science. 2004;304:1469–76.View ArticleGoogle Scholar
- Benton MJ, Twitchett RJ. How to kill (almost) all life: the end-Permian extinction event. Trends Ecol Evol. 2003;18:358–65.View ArticleGoogle Scholar
- Bossuyt F, Brown KM, Hillis PM, Cannatella DC, Milinkovitch MC. Phylogeny and biogeography of a cosmopolitan frog radiation: late Cretaceous diversification resulted in continent-scale endemism in the Family Ranidae. Syst Biol. 2006;55:579–94.View ArticleGoogle Scholar
- Bowring SA, Erwin DH. A new look at evolutionary rates in deep time: uniting paleontology and high-precision geochronology. GSA Today. 1998;8:2–8.Google Scholar
- Briggs JC. The biogeographic and tectonic history of India. J Biogeogr. 2003;30:381–8.View ArticleGoogle Scholar
- Burns KJ, Hackett SJ, Klein NK. Phylogenetic relationships and morphological diversity in Darwin's finches and their relatives. Evolution. 2002;56:1240–52.View ArticleGoogle Scholar
- Butler RF. Paleomagnetism: magnetic domains to geologic terranes. Cambridge: Cambridge University Press; 1991. 233 pp.Google Scholar
- Chatterjee S, Scotese C. The breakup of Gondwana and the evolution and biogeography of the Indian Plate. Proc Indian Natl Sci Acad. 1999;65:397–425.Google Scholar
- Chatterjee S, Scotese C. The wandering Indian plate and its changing biogeography during the Late Cretaceous–Early Tertiary period. Platinum Jubilee, Indian Statistical Institute, 2009;60–91.Google Scholar
- Cocks LRM, Torsvik TH. Earth geography from 500 to 400 million years ago: a faunal and paleomagnetic review. J Geol Soc London. 2002;159:631–44.View ArticleGoogle Scholar
- Darwin C. On the origin of species by means of natural selection, or the preservation of favoured races in the struggle for life (1st ed.). London; 1859.Google Scholar
- Evans DA. True polar wander, a supercontinental legacy. Earth Planet Sci Lett. 1998;157:1–8.View ArticleGoogle Scholar
- Gheerbrant E, Rage J-C. Paleobiogeography of Africa: how distinct from Gondwana and Laurasia? Palaeogeogr Palaeoclimatol Palaeoecol. 2006;241:224–46.View ArticleGoogle Scholar
- Hedges SB. Afrotheria: plate tectonics meets genomics. Proc Nat Acad Sci. 2001;98:1–2.View ArticleGoogle Scholar
- Hedges SB, Parker PH, Sibley CG, Kumar S. Continental breakup and the ordinal diversification of birds and mammals. Nature. 1996;381:226–29.Google Scholar
- Hendry AP, Wenburg JK, Bentzen P, Volk EC, Quin TP. Rapid evolution of reproductive isolation in the wild: evidence from introduced salmon. Science. 2009;290:516–8.View ArticleGoogle Scholar
- Jacobs L, Strganac C, Scotese C. Plate motions, Gondwana dinosaurs, Noah’s arks, beached viking funeral ships, ghost ships, and landspans. An Acad Bras Cienc. 2011;83:3–22.View ArticleGoogle Scholar
- Kirby MX, MacFadden B. Was southern Central America an archipelago or a peninsula in the middle miocene? A test using land-mammal body size. Palaeogeogr Palaeoclimatol Palaeoecol. 2005;228:193–202.View ArticleGoogle Scholar
- Kirschvink JL, Ripperdan RL, Evans DA. Evidence for large-scale reorganization of Early Cambrian continental landmasses by inertial interchange true polar wander. Science. 1997;277:541–5.View ArticleGoogle Scholar
- Lieberman BS. Early Cambrian paleogeography and tectonic history: a biogeographic approach. Geology. 1997;25:1039–42.View ArticleGoogle Scholar
- Lieberman BS. Phylogenetic analysis of some early Cambrian trilobites, the biogeographic origins of Eutrilobita and the timing of the Cambrian explosion. J Paleontol. 2002;692–708.Google Scholar
- McKenna MC. Sweepstakes, filters, corridors, Noah's Arks, and beached viking funeral ships in palaeogeography. In: Tarling DH, Runcorn SK, editors. Implications of continental drift to the earth sciences. New York: Academic; 1973. p. 295–308.Google Scholar
- Meert JG. A paleomagnetic analysis of Cambrian true polar wander. Earth Planet Sci Lett. 1999;168:131–44.View ArticleGoogle Scholar
- Meert JG. In GAD we trust. Nature Geoscience. 2009;2:673–4.View ArticleGoogle Scholar
- Meert JG, Lieberman BS. A palaeomagnetic and palaeogeographic perspective on latest Neoproterozoic and early Cambrian tectonic events. J Geol Soc Lond. 2004;161:477–87.View ArticleGoogle Scholar
- Meert JG, Lieberman BS. The Neoproterozoic assembly of Gondwana and its relationship to the Ediacaran–Cambrian radiation. Gondwana Res. 2008;14:5–21.View ArticleGoogle Scholar
- Meert JG, Walderhaug HJ, Torsvik TH, Hendricks BWH. Age and paleomagnetic signature of the Alno carbonatite complex (NE Sweden): additional controversy for the Neoproterozoic paleoposition of Baltica. Precambrian Res. 2007;154:159–74.View ArticleGoogle Scholar
- Palumbi SR. Genetic divergence, reproductive isolation and marine speciation. Annu Rev Ecol Syst. 1994;25:547–72.View ArticleGoogle Scholar
- Perez-Huerta A. First record of post-middle Desmoinesian (Late Carboniferous) brachiopods in the Great Basin USA: Implications for faunal migration in response to Late Paleozoic paleogeography. J Paléo. 2007;81:312–30.Google Scholar
- Ricklefs RE. Splendid isolation: historical ecology of the South American passerine fauna. J Avian Biol. 2002;33:207–11.View ArticleGoogle Scholar
- Ross CA, Ross JRP. Carboniferous and early Permian biogeography. Geology. 1985;13:27–30.View ArticleGoogle Scholar
- Sereno PC, Wilson JA, Conrad JL. New dinosaurs link southern landmasses in the mid-Cretaceous. Proc Roy Soc Lond B. 2004;271:1325–30.View ArticleGoogle Scholar
- Sidor CA, O'Keefe FR, Damiani R, Steyer JS, Smith RMH, Larsson HCE, et al. New dinosaurs link southern landmasses in the Mid-Cretaceous. Proc R Soc Lond B. 2004;271:1325–30.View ArticleGoogle Scholar
- Van Bocxlaer IV, Roelants K, Biju SD, Nagaraju J, Bossuyt F. Late Cretaceous vicariance in Gondwana amphibians. PLoS 1. 2006; e74, doi:https://doi.org/10.1371/journal.pone.0000074
- Van der Voo R. Paleomagnetism of the Atlantic, Tethys and Iapetus Oceans. Cambridge: Cambridge University Press; 1993. 411 pp.Google Scholar
- Vences M, Vieites DR, Glaw F, Brinkmann H, Kosuch J, et al. Multiple overseas dispersal in amphibians. Proc R Soc Lond B. 2003;270:2435–42.View ArticleGoogle Scholar
- Webb SD. In: Stehli F, Webb S, editors. The great American interchange. New York: Plenum Press; 1985. p. 357–86.View ArticleGoogle Scholar
- Webb SD. The great American biotic interchange: patterns and processes. Ann Mo Bot Gard. 2006;93:245–57.View ArticleGoogle Scholar
- Whiteside JH, Grogan DS, Olsen PE, Kent DV. Climatically driven biogeographic provinces of Late Triassic tropical Pangea. PNAS. 2011;108(22):8972–7.View ArticleGoogle Scholar