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Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson (1995)

Chapter: Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic

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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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3
Disparate Rates, Differing Fates: Tempo and Mode of Evolutionm Changed from the Precambrian to the Phanerozoic

J. William SchopfCHOPF

When G. G. Simpson wrote Tempo and Mode (Simpson, 1944), fossil evidence of the history of life consisted solely of that known from sediments of the Phanerozoic eon, the most recent 550 million years (Ma) of geologic time (Figure 1). Thus, Simpson's views of the evolutionary process were based necessarily on Phanerozoic life—the familiar progression from seaweeds to flowering plants, from trilobites to humans—a history of relatively rapidly evolving, sexually reproducing plants and animals successful because of their specialized organ systems (flowers, leaves, teeth, limbs) used to partition and exploit particular environments. In short, Simpson elucidated "normal evolution" played by the "normal rules" of the game—speciation, specialization, extinction.

Although certainly applicable to the megascopic eukaryotes of the Phanerozoic, there is reason to question whether these well-entrenched rules apply with equal force to the earlier and very much longer Precambrian phase of microbe-dominated evolutionary history (Figure 1). In place of sexual multicellular plants and animals, the biota throughout much of the Precambrian was dominated by simple nonsexual prokaryotes. Rather than evolving rapidly, many Precambrian microbes evidently evolved at an astonishingly slow pace. And instead



J. William Schopf is professor of paleobiology in the Department of Earth and Space Sciences and director of the Center for the Study of Evolution and the Origin of Life at the University of California, Los Angeles.

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Figure 1 Comparison of the Phanerozoic and Precambrian histories of life.

of having specialized organ systems for exploitation of specific ecologic niches, members of the most successful group of these early-evolving microorganisms—photoautotrophic cyanobacteria—were ecologic generalists, able to withstand the rigors of a wide range of environments. In contrast with normal evolution, the "primitive rules" of prokaryotic evolution appear to have been speciation, generalization, and exceptionally long-term survival.

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

That there is a distinction in evolutionary tempo and mode between the Phanerozoic and Precambrian histories of life is not a new idea (Schopf, 1978), but it is one that has recently received additional impetus (Schopf, 1992a) and therefore deserves careful scrutiny. However, evaluation of this generalization hinges critically on the quality and quantity of the fossil evidence available, and because active studies of the Precambrian fossil record have been carried out for little more than a quarter century (Schopf, 1992b) a thorough comparison of the early history of life with that of later geologic time is not yet possible. Therefore, as a first approximation, the approach used here is to analyze the known fossil record of Precambrian cyanobacteria: well-studied, widespread, abundant, commonly distinctive, and evidently dominant members of the early prokaryotic biota. Microscopic fossils regarded as members of other prokaryotic groups are also known from the Precambrian (Schopf, 1992c, 1992d), but their documented record is minuscule. Hence, conclusions drawn here about the early fossil record apply strictly to free-living cyanobacteria, the evolutionary history of which may or may not be representative of prokaryotes in general. To evaluate the generalization, two central questions must be addressed. First, was the tempo of Precambrian cyanobacterial evolution markedly slower than that typical of Phanerozoic eukaryotes? Second, if so, how can this difference be explained?

Tempos of Evolution

In Tempo and Mode, Simpson coined terms for three decidedly different rate distributions in evolution, inferred from morphological comparisons of Phanerozoic and living taxa: tachytelic, for "fast"-evolving lineages; horotelic, the standard rate distribution, typical of most Phanerozoic animals; and bradytelic, for "slow" morphological evolution (Simpson, 1944). Included among the bradytelic lineages are so-called living fossils (such as linguloid brachiopods, horseshoe crabs, coelacanth fish, crocodilians, opossums), "groups that survive today and show relatively little change since the very remote time when they first appeared in the fossil record" (Simpson, 1944, p. 125). Simpson's bradytely closely approximates Ruedemann's earlier developed concept of "arrested evolution'' (Ruedemann, 1918, 1922a, 1922b), both based on comparison of modern taxa with fossil forms that are virtually indistinguishable in morphology but are 100 Ma or more older.

Hypobradytely. Recently, a fourth term—hypobradytely—has been added to this list of rate distributions (Schopf, 1987) "to refer to the exceptionally low rate of evolutionary change exhibited by cyanobacte-

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

rial taxa, morphospecies that show little or no evident morphological change over many hundreds of millions of years and commonly over more than one or even two thousand million years" (Schopf, 1992e, p. 596). Following Simpson's lead, hypobradytely is based strictly on morphological comparison of living and fossil taxa. Other data, such as chemical biomarkers (Schopf, 1992e), carbon isotopic compositions (Schidlowski et al., 1983), and environmental distributions (Knoll and Golubic, 1992), can provide insight on the paleophysiology of fossil cyanobacteria, but the concept of hypobradytely does not necessarily imply genomic, biochemical, or physiological identity between modern and fossil taxa. The concept can be applied to cyanobacteria because the morphologic descriptors and patterns of cell division used to differentiate taxa at various levels of the taxonomic hierarchy are preservable in ancient sediments (Golubic, 1976a; Schopf, 1992d, 1992e); as emphasized by Knoll and Golubic (1992, p. 453), "Essentially all of the salient morphological features used in the taxonomic classification of living cyanobacteria can be observed in well-preserved microfossils."

Interpreted as evidencing exceptional "morphological evolutionary conservatism," detailed genus- and species-level similarities between Precambrian and extant cyanobacteria, both for filamentous (oscillatoriacean) and spheroidal (chroococcacean) taxa, were documented more than 25 years ago (Schopf, 1968). Since that time, such similarities have been recognized repeatedly. Indeed, it has become common practice for Precambrian paleobiologists to coin generic names intended to denote similarity or inferred identity between ancient cyanobacterium-like fossils and their modern morphological analogs by adding appropriate prefixes (palaeo-, eo-) or suffixes (-opsis, -ites) to the names of living cyanobacterial genera (Table 1). The validity of such comparisons is variable, and although more than 40 such fossil namesakes have been proposed (for genera referred to diverse cyanobacterial families; Table 1), their use does not in and of itself constitute compelling evidence of hypobradytely.

Caveats. Application of the concept of hypobradytely is not without potential pitfalls, three of which deserve particular mention. First, because of the enormous span of Precambrian time (Figure 1), and despite the notable paleontological progress of recent years (Schopf, 1992b), early biotic history is as yet very incompletely documented. In comparison with the vastly better documented record of Phanerozoic organisms—and even in geologic units of the Proterozoic (2500–550 Ma in age), by far the most studied portion of the Precambrian—the known cyanobacterial fossil record is scanty (for filamentous species amounting to 21 taxonomic occurrences per 50-Ma-long interval and, for spheroi-

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

TABLE 1 Precambrian generic namesakes, coined by various authors to suggest similarity to modern cyanobacterial genera (Mendelson and Schopf, 1992a)

Modern genus

Precambrian genus; author(s)

No. of species

Year published

Country of author(s)

Family Oscillatoriaceae

Lyngbya

Palaeolyngbya; Schopf

11

1968

USA

Lyngbya

cf. Lyngbya; Schopf, Xu, Xu, and Hsu

1

1984

USA, China

Microcoleus

Eomicrocoleus; Horodyski and Donaldson

1

1980

USA, Canada

Oscillatoria

Archaeoscillatoriopsis; Schopf

3

1993

USA

Oscillatoria

Oscillatoriopsis; Schopf

22

1968

USA

Oscillatoria

Oscillatorites; Schepeleva

1

1960

Russia

Oscillatoria

cf. Oscillatoria; Schopf and Sovietov

1

1976

USA, Russia

Phormidium

Eophormidium; Xu

3

1984

China

Schizothrix

Schizothrix; Edhorn

1

1973

Canada

Schizothrix

Schizothropsis; Xu

1

1984

China

Spirulina

Palaeospirulina; Edhorn

2

1973

Canada

Spirulina

Spirillinema; Shimron and Horowitz

1

1972

Israel

Spirulina

aff. Spirulina; Schopf and Blacic

1

1971

USA

Family Chroococcaceae

Anacystis

Palaeoanacystis; Schopf

8

1968

USA

Aphanocapsa

Aphanocapsaopsis; Maithy and Shukla

2

1977

India

Aphanocapsa

Eoaphanocapsa; Nyberg and Schopf

1

1984

USA

Aphanothece

Eoaphanothece; Xu

1

1984

China

Chroococcus

Chroococcus-like; Mendelson and Schopf

1

1982

USA

Eucapsis

Eucapsamorpha; Golovenoc and Belova

1

1985

Russia

Eucapsis

Eucapsis?; Licari, Cloud, and Smith

1

1969

USA

Gloeocapsa

Eogloeocapasa; Golovenoc and Belova

1

1984

Russia

Gloeocapsa

Gloeocapsa-like; Zhang

1

1985

China

Merismopedia

cf. Merismopedia; Schopf and Fairchild

1

1973

USA, Brazil

Microcystis

Eomicrocystis; Maithy

2

1975

India

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Modern genus

Precambrian genus; author(s)

No. of species

Year published

Country of author(s)

Family Chroococcaceae (continued)

Microcystis

Microcystopsis; Xu

1

1984

China

Microcystis

Palaeomicrocystis; Maithy

2

1975

India

Synechococcus

Eosynechococcus; Hofmann

13

1976

Canada

Family Entophysalidaceae

Entophysalis

Eoentophysalis; Hofmann

6

1976

Canada

Family Pleurocapsaceae

Hyella

Eohyella; Zhang and Golubic

4

1987

China, USA

Myxosarcina

cf. Myxosarcina; Schopf and Fairchild

1

1973

USA, Brazil

Pleurocapsa

Eopleurocapsa; Liu

1

1982

China

Pleurocapsa

Palaeopleurocapsa; Knoll, Barghoorn, and Golubic

6

1975

USA

Family Nostocaceae

Anabaena

Anabaenidium; Schopf

4

1968

USA

Aphanizomenon

Palaeoaphanizomenon; Mikhailova

1

1986

Russia

Isocystis

Palaeoisocystis; Xu

2

1984

China

Nostoc

Nostocomorpha; Sin and Liu

1

1978

China

Nostoc

Palaeonostoc; Nautiyal

1

1980

India

Nostoc

Veteronostocale; Schopf

2

1968

USA

Family Rivulariaceae

Calothrix

Palaeocalothrix; Xu

2

1984

China

Rivularia

Primorivularia; Edhorn

3

1973

Canada

Family Scytonemataceae

Plectonema

Eoplectonema; Liu

1

1984

China

Scytonema

Palaeoscytonema; Edhorn

5

1973

Canada

dal species, 46 occurrences; Schopf, 1992c; Mendelson and Schopf, 1992a). Second, assignment of some Precambrian microbial fossils (evidently <10%) to the cyanobacteria can be quite uncertain, a problem that applies especially to minute morphologically simple forms (atypically small-diameter oscillatoriaceans and chroococcaceans, for example), which in the fossil state are essentially indistinguishable from various noncyanobacterial prokaryotes (Schopf, 1992d). Third, lack of change in the external form of morphologically simple prokaryotes may not necessarily reflect evolutionary stasis of their internal physiological

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

machinery (the so-called Volkswagen syndrome; Schopf et al., 1983). This last problem is especially difficult to evaluate, but it may not be of overriding importance—from early in the Proterozoic to the present, the same cyanobacterial families and many of the same (morphologically defined) genera and even species appear to have inhabited the same or closely similar environments, patterns of distribution that "provide proxy information on physiological attributes" (Knoll and Golubic, 1992, p. 451).

Cyanobacterial Hypobradytely

Are cyanobacteria hypobradytelic? Data bearing on this question fall into two classes. First, a large amount of evidence indicates that the proposition is plausible, in fact likely to be correct, but, because of a lack of accompanying relevant (chiefly environmental) information, this evidence is not fully compelling. Second, a small number of in-depth studies firmly support the proposition, but because of their limited number and restricted taxonomic scope these studies do not establish the proposition generally. Considered together, however, the two classes of data present a strong case.

Evidence of Plausibility. Shown in Figure 2 are paired examples of morphologically comparable Proterozoic and living cyanobacteria including specimens illustrating the rather commonly cited (Schopf, 1968; Schopf and Blacic, 1971; Golubic and Campbell, 1979; Campbell, 1979) similarity between fossil Palaeolyngbya (Figure 2B) and Lyngbya (Figure 2A), its modern morphological counterpart. Numerous other genus and species-level comparisons have been drawn [for example, between 850-Ma-old Cephalophytarion grande and the modern oscillatoriacean Microcoleus vaginatus (Schopf, 1968; Campbell, 1979); and between 2-billion year (Ga)-old Eosynechococcus moorei and the living chroococcacean Gloeothece coerulea (Gloeobacter violaceus) (Golubic and Campbell, 1979)]. Examples such as these—and the fact that over the past quarter century such similarities have been noted repeatedly and regarded as biologically and taxonomically significant by a large number of workers in many countries (Table 1)—provide a powerful argument for the plausibility of cyanobacterial hypobradytely.

Plausibility of the concept is similarly indicated by quantitative studies recently carried out on large assemblages of modern and Precambrian microbes. Morphometric data (for such attributes as cell size, shape, and range of variability; colony form; sheath thickness and structure) were compiled for 615 species and varieties of living cyanobacteria (Schopf, 1992d) as well as for an extensive worldwide sample of Proterozoic

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Figure 2 Comparison of living and Precambrian cyanobacteria. Living examples (A, C, E, and G) are from mat-building stromatolitic communities of northern Mexico. (A) Lyngbya (Oscillatoriaceae), encompassed by a cylindrical mucilaginous sheath (arrow). (B) Palaeolyngbya, similarly ensheathed (arrows), FIGURE 2 (Continued) from the 950-Ma-old Lakhanda Formation of eastern Siberia. (C) Spirulina (Oscillatoriaceae). (D) Heliconema, a Spirulina-like cyanobacterium from the 850-Ma-old Miroedikha Formation of eastern Siberia. (E) Gloeocapsa (Chroococcaceae), a four-celled colony having a thick distinct encompassing sheath (arrow). (F) Gloeodiniopsis, a similarly sheath-enclosed (arrow) Gloeocapsa-like cyanobacterium, from the 1550-Ma-old Satka Formation of southern Bashkiria. (G) Entophysalis (Entophysalidaceae). (H) Eoentophysalis, an Entophysalis-like colonial cyanobacterium from the 2-Ga-old Belcher Group of Northwest Territories, Canada (Golubic and Hofmann, 1976).

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

cyanobacterium-like microfossils (Mendelson and Schopf, 1922a), both filamentous (650 taxonomic occurrences in 160 geologic formations) and spheroidal (1400 occurrences in 259 formations). To avoid confusion stemming from variations in taxonomic practice, fossils having the same or similar morphology (regardless of their binomial designations) were grouped together as informal species-level morphotypes designed to have ranges of morphologic variability comparable to those exhibited by living cyanobacterial species (Schopf, 1992c). Of the 143 informal species of filamentous microfossils thus recognized, 37% are essentially indistinguishable in morphology from established species of living (oscillatoriacean) cyanobacteria (Schopf, 1992c). Similarly, 25% of the 120 informal taxa of spheroidal fossil species have modern species-level (largely chroococcacean) morphological counterparts (Schopf, 1992c). Virtually all of the fossil morphotypes are referable to living genera of cyanobacteria, and the patterns and ranges of size distribution exhibited by taxa of cylindrical sheath-like Proterozoic fossils are essentially identical to those of the tubular sheaths that encompass trichomes of modern oscillatoriacean species (Figure 3).

About half of the 2000 fossil occurrences included in this morphometric study were reported from cherty carbonate stromatolites, with the remainder from clastic shales and siltstones. Data regarding the specific environmental settings represented by these lithologies are available for very few of the >300 fossiliferous geologic units considered. With varying degrees of uncertainty (but almost always without firm evidence), most of these strata have been assumed to represent relatively shallow water coastal marine facies, ranging from sabkhas and lagoons to mud flats and intertidal carbonate platforms. In such environments today, mat-building oscillatoriaceans (predominantly Oscillatoria, Lyngbya, Phormidium, Spirulina, Microcoleus, and Schizothrix ) and subsidiary chroococcaceans (such as Chroococcus, Aphanocapsa, Aphanothece, and Synechococcus) are common (Golubic, 1976a, 1976b; Pierson et al., 1992). As is shown in Figure 4, these same two families, as well as

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Figure 3 Comparison of patterns and ranges of size distribution of cylindrical sheath-like Precambrian fossils with those of the tubular sheaths of living oscillatoriacean cyanobacteria (Schopf, 1992d).

morphotypes referable to most of the same genera, are similarly common among the fossil taxa having living species-level counterparts.

In view of these data, it is difficult not to conclude that "the biological constitution of [Proterozoic] microbial mat communities was probably quite similar to that of modern communities in comparable environments" (Knoll, 1985, p. 411).

In-Depth Studies. In addition to studies of cellular morphology and likely (but not firmly established) broad-scope environmental comparisons, what is needed to move the hypobradytelic hypothesis from the plausible to the compelling are supporting data on the paleoenvironment and taphonomy of the fossils in question (Knoll and Golubic, 1992). A number of such in-depth studies have been carried out (Knoll et al. , 1975; Golubic and Hofmann, 1976; Knoll and Golubic, 1979; Green et al., 1987; Green et al., 1988), focusing on fossil representatives of two cyanobacterial families, the Entophysalidaceae and the Pleurocapsaceae, members of which are decidedly more distinctive morphologically than are the oscillatoriaceans and chroococcaceans discussed above. Golubic and Hofmann (1976) compared 2-Ga-old Eoentophysalis belcherensis (Figure 2H) with two modern entophysalidaceans (Entophysalis major and Entophysalis granulosa). They showed that not only are the fossil and modern species morphologically comparable (in cell shape and in form and arrangement of originally mucilaginous cellular envelopes) and that

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Figure 4 Distribution among modern oscillatoriacean and chroococcacean genera of Precambrian species-level morphotypes having living morphological counterparts (Schopf, 1992c, 1992d).

they exhibit similar frequency distributions of dividing cells and essentially identical patterns of cellular development (resulting from cell division in three perpendicular planes), but also that both taxa form microtexturally similar stromatolitic structures in comparable intertidal to shallow marine environmental settings, that they undergo similar postmortem degradation sequences, and that they occur in microbial communities that are comparable in both species composition and biological diversity. In a subsequent detailed study, Knoll and Golubic compared the morphology, cell division patterns, ecology, and postmortem degradation sequences of a second Precambrian entophysalidacean (850-Ma-old Eoentophysalis cumulus) with those of modern E. granulosa and concluded that the fossil "microorganism is identical in all its salient characteristics to members of the extant [cyanobacterial] genus" (Knoll and Golubic, 1979, p. 125).

Several species of fossil and living pleurocapsaceans have also been compared in detail. Polybessurus bipartitus, first reported from 770-Ma-old stromatolites of South Australia (Fairchild, 1975; Schopf, 1977), is a morphologically distinctive, gregarious, cylindrical fossil pleurocapsacean composed of stacked cup-shaped envelopes often extended into long tubes oriented predominantly perpendicular to the substrate. Specimens of this taxon occurring in rocks of about the same age in East Greenland were interpreted by Green et al. to be "a

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

close morphological, reproductive, and behavioral counterpart" to populations of a species of the pleurocapsacean Cyanostylon present "in Bahamian environments similar to those in which the Proterozoic fossils occur" (Green et al., 1987, p. 928). A second fossil pleurocapsacean described from the 770-Ma-old Australian deposit (Palaeopleurocapsa wopfnerii) has been compared by Knoll et al. with its living morphological and ecological analog (Pleurocapsa fuliginosa) and regarded as "further evidence of the evolutionary conservatism of [cyanobacteria]" (Knoll et al., 1975, p. 2492). Two other species of morphologically distinctive fossil pleurocapsaceans (the endolithic taxa Eohyella dichotoma and Eohyella rectroclada), cited as ''compelling examples of the close resemblance between Proterozoic prokaryotes and their modern counterparts" (Knoll et al., 1986, p. 857), have been described by Green et al. from the East Greenland geologic sequence as being "morphologically, developmentally, and behaviorally indistinguishable" from living Hyella species of the Bahama Banks (Green et al., 1988, pp. 837–838).

These in-depth studies of entophysalidaceans and pleurocapsaceans—involving analyses of environment, taphonomy, development, and behavior, in addition to cellular morphology—provide particularly convincing evidence of species-specific fossil-modern similarities.

Cyanobacteria are Hypobradytelic. Thus, numerous workers worldwide have noted and regarded as significant the detailed similarities in cellular morphology between Precambrian and extant cyanobacteria (Table 1; Figure 2). A substantial fraction of known Proterozoic oscillatoriacean and chroococcacean cyanobacteria have living species-level morphological counterparts (Figure 4), and almost all such fossils are referable to living cyanobacterial genera. And in-depth studies of several fossil-modern species pairs of morphologically distinctive entophysalidaceans and pleurocapsaceans permit detailed comparison of morphology, development, population structure, environment, and taphonomy, all of which show that for at least these taxa, ancient and modern cyanobacteria are essentially indistinguishable in salient characteristics.

Taken together, these observations support an obvious conclusion—the morphology (and evidently the physiology as well) of diverse taxa belonging to major cyanobacterial families evolved little or not at all over hundreds of millions, indeed thousands of millions of years. In comparison with the later history of life, this widespread hypobradytely is surprising. In Phanerozoic evolution, bradytelic stasis is notable principally because of its rarity (Simpson, 1944; Ruedemann, 1918, 1922a,

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

1922b), but in the Precambrian it seems to have been a general phenomenon characteristic of a group of prokaryotic microorganisms that dominated the Earth's biota, possibly even as early as 3.5 Ga ago (Schopf, 1993). Why have cyanobacteria evidently changed so little over their exceedingly long evolutionary history?

Survival of the Ecologically Unspecialized

To understand the underlying causes of cyanobacterial hypobradytely, it is instructive to review Simpson's thoughtful analysis in Tempo and Mode, for although he was unaware of the Precambrian prokaryotic fossil record, Simpson was much interested in slowly evolving (bradytelic) Phanerozoic lineages. In addition to noting (but dismissing) the possibility that "asexual reproduction (as inhibiting genetic variability)" might be conducive to slow evolution (Simpson, 1944, p. 137), he singled out two principal factors: large population size, and ecologic versatility, an exceptional degree of adaptation "to some ecological position or zone with broad … selective limits … a particular, continuously available environment" (Simpson, 1944, pp. 138, 140, 141). Because unusually slow evolution involves "not only exceptionally low rates of [evolutionary change] but also survival for extraordinarily long periods of time" (p. 138), and because "more specialized phyla tend to become extinct before less specialized," Simpson proposed ''the rule of the survival of the relatively unspecialized" (Simpson, 1944, pp. 138, 143).

Although intended by Simpson to apply to Phanerozoic organisms, chiefly animals, these same considerations (with the addition of asexual reproduction) apply to Precambrian cyanobacteria. First, with regard to reproduction, cyanobacteria are strictly asexual, lacking even the parasexual processes known to occur in some other prokaryotes. Given the remarkable longevity of the cyanobacterial lineage and moderate or even low rates of mutation, however, the absence of sexually generated genetic variability cannot be the sole explanation for their hypobradytely. Second, like virtually all free-living microorganisms, cyanobacteria typically occur in local populations of large size. Coupled with their ease of dispersal (via water currents, wind, and hurricanes, for example) and for many species a resulting very wide (essentially cosmopolitan) geographic distribution, their large populations can also be presumed to have played a role in their evolutionary stasis (Figure 1). Third, and probably most important, however, is the ecologic versatility of the group.

Summarized in Table 2 are known ranges of survivability (and of growth under natural conditions) for modern oscillatoriaceans and

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Table 2 Survival [and growth under natural conditions (boldface)] of oscillatoriacean and chroococcacean cyanobacteria*

Light intensity

1–5 µE·s-1·m-2

50–60 µE·s-1·m-2

>2000 µE·s-1·m-2

 

Conditions

Cultures

Optimum growth

Intertidal zone

 

Genera

1C; 2E, F

1, 2

1, 2

 

Total salinity

<0.001–0.1%

3.5%

27.5%

100–200%

Conditions

Freshwater

Marine

Great Salt Lake

Salterns

Genera

1, 2

1, 2

2D

1B–D, F; 2F

Acidity/basicity

pH 4

pH 7–10

pH 10–11

 

Conditions

Hot springs

Optimum growth

Alkaline lakes

 

Genera

2F

1, 2

1F; 2E

 

High temperature

55–70°C

74°C

111°C

112°C

Conditions

Hot springs

Hot springs

Dried

Dried

Genera

1C, D, F; 2C, F

2F

1E

1B

Low temperature

-269°C

-196°C

-55°C

-2° to +4°C

Conditions

Liquid He

Liquid H2

Freeze-dried

Antarctic lakes

Genera

1C

1 D, E

1A

1 C, D

Desiccation

88

82 yr

Absence of rainfall

 

Conditions

Dried

Dried

Atacama Desert

 

Genera

1C

2E

1E; 2B, D

 

Oxygen

<0.01%

1%

20%

100%

Conditions

Anoxic lakes

Blooms, muds

Ambient O2

Cultures

Genera

1, 2

1, 2

1, 2

2B

Carbon dioxide

0.001%

0.035%

3.5%

40%

Conditions

Cultures

Ambient CO2

Cultures

Cultures

Genera

2B

1, 2

1E; 2A, B, D, F

2B

Radiation

Ultraviolet

X-rays

γ-rays

Highly ionizing

Conditions

290–400 nma

200 krb

2560 krc

Thermonuclear explosion

Genera

1A, E; 2C

1C

1B

1 B, E

Oscillatoriacean genera: 1A, Lyngbya; 1B, Microcoleus; 1C, Oscillatoria ; 1D, Phormidium; 1E, Schizothrix; 1F, Spirulina. Chroococcacean genera: 2A, Agmenellum; 2B, Anacystis; 2C, Aphanocapsa; 2D, Coccochloris ; 2E, Microcystis; 2F, Synechococcus.

a Absorbed by scytonemin pigment in encompassing sheaths.

b Twice as resistant as eukaryotic microalgae.

c Ten times as resistant as eukaryotic microalgae.

* Table from Abeliovich and Shilo, 1972; Brock, 1978; Cameron, 1963; Castenholz, 1969; Ciferri, 1983; Davis, 1972; Davison, 1991; Desikachary, 1959; Drouet, 1968; Drouet and Daily, 1973; Flowers and Evans, 1966; Fogg, 1973; Fogg et al., 1973; Forest and Weston, 1966; Frémy, 1972; Fuhs, 1968; Garcia-Pichel and Castenholz, 1991; Godward, 1962; Grant and Tindall, 1986; Knoll and Bauld, 1989; Langworthy, 1978; Lloyd et al., 1977; Mizutani and Wada, 1982; Pardue et al., 1976; Parker et al., 1981; Schopf, 1974; Shields and Drouet, 1962; Vallentyne, 1963; Vincent et al., 1993.

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

chroococcaceans, the most primitive (Giovannoni et al., 1988) and commonly occurring (Schopf, 1992d) Precambrian cyanobacterial families. Similar tolerance is also exhibited by members of other cyanobacterial families. For example, a nostocacean was revived after more than a century of storage in a dried state (Davis, 1972) and a scytonematacean is reported to have maintained growth at pH 13 (Vallentyne, 1963). Thus, cyanobacteria exhibit notable ecologic flexibility, and even though no single oscillatoriacean or chroococcacean species is known to be capable of tolerating the total range of observed growth conditions (for example, thermophiles dominant in 70°C waters rarely grow below 50°C, and species adapted to highly alkaline lakes do not occur in acid hot springs), both groups include impressive ecologic generalists, able to thrive in virtually all present-day widespread environments (Table 2). Moreover, many of the oscillatoriacean and chroococcacean genera for which wide ecologic tolerance has been demonstrated (Table 2) are the same as those having species-level Precambrian-extant counterparts (Figure 4). Finally, numerous cyanobacteria, including both oscillatoriaceans and chroococcaceans (Stewart, 1980), are capable of fixing atmospheric nitrogen; provided with light, CO2, a source of electrons (H2, H2S, H2O), and a few trace elements, such cyanobacteria are highly effective colonizers, able to invade and flourish in a wide range of habitats.

The wide ecologic tolerance of cyanobacteria is almost certainly a product of their early evolutionary history. Fossil evidence suggests that oscillatoriaceans (Schopf, 1993) and chroococcaceans (Schopf and Packer, 1987) were extant as early as 3.5 Ga ago. If so, they must have originated and initially diversified in an oxygen-deficient environment, one lacking an effective UV-absorbing ozone layer. In such an environment, the ability to photosynthesize at low light intensities (Table 2) coupled with the presence of gas vesicles to control buoyancy (Jensen, 1993) would have permitted planktonic cyanobacteria to avoid deleterious UV by inhabiting the deep oceanic photic zone, just as Synechococcus does today. Similarly, numerous characteristics of living benthic mat-building cyanobacteria—effective DNA repair mechanisms, synthesis of UV-absorbing scytonemin, secretion of copious extracellular mucilage, phototactic motility, adherence to substrates, stromatolitic mat formation—initially may have been adaptations to cope with a high UV flux in near-shore shallow water settings. Adaptive radiation in an early oxygen-deficient environment is also suggested by the ability of cyanobacteria to live in either the presence or absence of oxygen (Table 2), their capability to switch between oxygenic and anoxygenic photosynthesis (Olson and Pierson, 1987), the occurrence of oxygen-sensitive nitrogenase in many taxa (Stewart, 1980), and the restriction of nitroge-

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

nase-protecting heterocysts to late-evolving members of the group (Giovannoni et al., 1988). In addition, both the low affinity of cyanobacterial ribulose-bisphosphate carboxylase for CO2 and the presence of intracellular CO2-concentrating mechanisms (Badger, 1987) may reflect initial adaptation of the lineage to a CO2-rich primordial environment (Kasting, 1992).

Finally, the remarkable hardiness of cyanobacteria—their ability to survive wide ranges of light intensity, salinity, temperature, and pH as well as prolonged desiccation and intense radiation (Table 2)—may be a product of their marked success in competing for photosynthetic space with other early-evolving microbes. Unlike the oxygen-producing photosynthesis based on chlorophyll a in cyanobacteria, that in all other photoautotrophic prokaryotes is anoxygenic and bacteriochlorophyll-based. Because biosynthesis of bacteriochlorophyll is inhibited by molecular oxygen (Olson and Pierson, 1987), oxygen-producing cyanobacteria would have rapidly supplanted oxygen-sensitive anoxygenic photoautotrophs throughout much of the global photic zone. As a result of the ease of their global dispersal and their success in competing for photosynthetic space, cyanobacteria presumably expanded into a broad range of habitable niches during an early, evidently rapid phase of adaptive radiation (Giovannoni et al., 1988), evolving to become exceptional ecologic generalists. Thus, the ecologic versatility of cyanobacteria appears to hark back to an early stage of planetary history when they established themselves as the dominant primary producers of the Precambrian ecosystem.

In view of their evolutionary history, it is perhaps not surprising that Simpson's rule of survival of the (ecologically) relatively unspecialized is applicable to cyanobacteria, numerous taxa of which qualify as so-called living fossils. According to Stanley (1984, p. 280), such extraordinarily long-lived organisms "are simply champions at warding off extinction." If so, as has been previously suggested (Schopf, 1992e, p. 598), the "grand champions," over all of geologic time, must be the hypobradytelic cyanobacteria!

A Bipartite View of the History of Life

In broadbrush outline, biotic history thus seems divisible into two separate phases (Schopf, 1978, 1992a), each characterized by its own tempo and mode, each by its own set of evolutionary rules (Figure 1).

During the shorter more recent Phanerozoic eon, the history of life was typified by the horotelic evolution of dominantly megascopic, sexual, aerobic, multicellular eukaryotes based on alternating life cycle phases specialized either for reproduction or for nutrient assimilation.

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

Changes in the dominant (commonly diploid) phase resulted chiefly from structural modification of organ systems used to partition and exploit particular environments. In large part as a result of this ecologic specialization, the Phanerozoic was punctuated by recurrent episodes of extinction, each followed by the adaptive radiation of surviving lineages.

In contrast with Phanerozoic evolution, much of the earlier and decidedly longer Precambrian history of life was typified by the hypobradytelic evolution of dominantly microscopic, asexual, metabolically diverse, and commonly ecologically versatile prokaryotes, especially cyanobacteria. Evolutionary innovations were biochemical and intracellular. Once established, lineages exhibited long-term stasis. Extinction occurred rarely among prokaryotic ecologic generalists, evidently becoming a significant evolutionary force only late in the Precambrian and primarily affecting ecologically relatively specialized, large-celled eukaryotic phytoplankters (Mendelson and Schopf, 1992b; Vidal and Knoll, 1982; Schopf, 1992f).

Although as yet incompletely documented, this bipartite interpretation of evolutionary history seems consistent with the fossil record as now known. It remains to be established whether it, like Simpson's Tempo and Mode, will stand the test of time.

Summary

Over the past quarter century, detailed genus- and species-level similarities in cellular morphology between described taxa of Precambrian microfossils and extant cyanobacteria have been noted and regarded as biologically and taxonomically significant by numerous workers worldwide. Such similarities are particularly well documented for members of the Oscillatoriaceae and Chroococcaceae, the two most abundant and widespread Precambrian cyanobacterial families. For species of two additional families, the Entophysalidaceae and Pleurocapsaceae, species-level morphologic similarities are supported by in-depth fossil-modern comparisons of environment, taphonomy, development, and behavior. Morphologically and probably physiologically as well, such cyanobacterial "living fossils" have exhibited an extraordinarily slow (hypobradytelic) rate of evolutionary change, evidently a result of the broad ecologic tolerance characteristic of many members of the group and a striking example of G. G. Simpson's [Simpson, G. G. (1944) Tempo and Mode in Evolution (Columbia Univ. Press, New York)] "rule of the survival of the relatively unspecialized." In both tempo and mode of evolution, much of the Precambrian history of life—that dominated by microscopic cyanobacteria and related prokaryotes—

Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×

appears to have differed markedly from the more recent Phanerozoic evolution of megascopic, horotelic, adaptationally specialized eukaryotes.

For helpful reviews of this manuscript, I thank W. Altermann, J. Bartley, J. Bragin, T. R. Fairchild, A. H. Knoll, D. M. Raup, B. N. Runnegar, E. Schultes, and J. Shen-Miller. This work was supported by National Aeronautics and Space Administration Grant NAGW-2147.

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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
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Page 52
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 53
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 54
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 55
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 56
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 57
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 58
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 59
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 60
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 61
Suggested Citation:"Disparate Rates, Differing Fates: Tempo and Mode of Evolution Changed from the Precambrian to the Phanerozoic." National Academy of Sciences. 1995. Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson. Washington, DC: The National Academies Press. doi: 10.17226/4910.
×
Page 62
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Tempo and Mode in Evolution: Genetics and Paleontology 50 Years After Simpson Get This Book
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Since George Gaylord Simpson published Tempo and Mode in Evolution in 1944, discoveries in paleontology and genetics have abounded. This volume brings together the findings and insights of today's leading experts in the study of evolution, including Ayala, W. Ford Doolittle, and Stephen Jay Gould.

The volume examines early cellular evolution, explores changes in the tempo of evolution between the Precambrian and Phanerozoic periods, and reconstructs the Cambrian evolutionary burst. Long-neglected despite Darwin's interest in it, species extinction is discussed in detail.

Although the absence of data kept Simpson from exploring human evolution in his book, the current volume covers morphological and genetic changes in human populations, contradicting the popular claim that all modern humans descend from a single woman.

This book discusses the role of molecular clocks, the results of evolution in 12 populations of Escherichia coli propagated for 10,000 generations, a physical map of Drosophila chromosomes, and evidence for "hitchhiking" by mutations.

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