Literature DB >> 8041691

Disparate rates, differing fates: tempo and mode of evolution changed from the Precambrian to the Phanerozoic.

J W Schopf1.   

Abstract

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

Keywords:  NASA Discipline Exobiology; Non-NASA Center

Mesh:

Year:  1994        PMID: 8041691      PMCID: PMC44277          DOI: 10.1073/pnas.91.15.6735

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  22 in total

1.  Microfossils from oolites and pisolites of the Upper Proterozoic Eleonore Bay Group, Central East Greenland.

Authors:  J W Green; A H Knoll; K Swett
Journal:  J Paleontol       Date:  1988       Impact factor: 1.471

2.  Early Archean (3.3-billion to 3.5-billion-year-old) microfossils from Warrawoona Group, Australia.

Authors:  J W Schopf; B M Packer
Journal:  Science       Date:  1987-07-03       Impact factor: 47.728

3.  The evolution of ecological tolerance in prokaryotes.

Authors:  A H Knoll; J Bauld
Journal:  Trans R Soc Edinb Earth Sci       Date:  1989

4.  Organically preserved microbial endoliths from the late Proterozoic of East Greenland.

Authors:  A H Knoll; S Golubic; J Green; K Swett
Journal:  Nature       Date:  1986-06-26       Impact factor: 49.962

5.  Paleobiology of distinctive benthic microfossils from the upper Proterozoic Limestone-Dolomite "Series," central East Greenland.

Authors:  J W Green; A H Knoll; S Golubic; K Swett
Journal:  Am J Bot       Date:  1987       Impact factor: 3.844

6.  Environmental biophysics and microbial ubiquity.

Authors:  J R VALLENTYNE
Journal:  Ann N Y Acad Sci       Date:  1963-06-29       Impact factor: 5.691

7.  Archean microfossils showing cell division from the swaziland system of South Africa.

Authors:  A H Knoll; E S Barghoorn
Journal:  Science       Date:  1977-10-28       Impact factor: 47.728

Review 8.  Some aspects of structure and function in N2-fixing cyanobacteria.

Authors:  W D Stewart
Journal:  Annu Rev Microbiol       Date:  1980       Impact factor: 15.500

9.  The development and diversification of Precambrian life.

Authors:  J W Schopf
Journal:  Orig Life       Date:  1974 Jan-Apr

Review 10.  Spirulina, the edible microorganism.

Authors:  O Ciferri
Journal:  Microbiol Rev       Date:  1983-12
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  20 in total

Review 1.  A fresh look at the fossil evidence for early Archaean cellular life.

Authors:  Martin Brasier; Nicola McLoughlin; Owen Green; David Wacey
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-06-29       Impact factor: 6.237

2.  Sulfur-cycling fossil bacteria from the 1.8-Ga Duck Creek Formation provide promising evidence of evolution's null hypothesis.

Authors:  J William Schopf; Anatoliy B Kudryavtsev; Malcolm R Walter; Martin J Van Kranendonk; Kenneth H Williford; Reinhard Kozdon; John W Valley; Victor A Gallardo; Carola Espinoza; David T Flannery
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-02       Impact factor: 11.205

Review 3.  Molecular phylogeny of Metazoa (animals): monophyletic origin.

Authors:  W E Müller
Journal:  Naturwissenschaften       Date:  1995-07

Review 4.  Protein phylogenies and signature sequences: A reappraisal of evolutionary relationships among archaebacteria, eubacteria, and eukaryotes.

Authors:  R S Gupta
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

5.  Molecular evolution of viruses: an interim summary.

Authors:  Y Becker
Journal:  Virus Genes       Date:  1995       Impact factor: 2.332

Review 6.  Evolvability.

Authors:  M Kirschner; J Gerhart
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

Review 7.  Solar ultraviolet and the evolutionary history of cyanobacteria.

Authors:  F Garcia-Pichel
Journal:  Orig Life Evol Biosph       Date:  1998-06       Impact factor: 1.950

8.  Putative extremely long evolutionary stasis in bacteria might be explained by serial convergence.

Authors:  Petr Dvořák; Dale A Casamatta; Petr Hašler; Aloisie Poulíčková
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-20       Impact factor: 11.205

9.  Information transmission in microbial and fungal communication: from classical to quantum.

Authors:  Sarangam Majumdar; Sukla Pal
Journal:  J Cell Commun Signal       Date:  2018-02-23       Impact factor: 5.782

Review 10.  Tempo, mode, the progenote, and the universal root.

Authors:  W F Doolittle; J R Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

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