Abstract
Macroevolution deals with large-scale and complex changes such as the rise of species, mass extinctions, and evolutionary trends. Microevolution describes evolutionary change within a species with changes in allele or genotype frequencies over short time periods. The separation of the two processes is somewhat arbitrary however, as macroevolution is the accumulation of a number of microevolutionary changes leading over time to large-scale changes. As a consequence, understanding macroevolution requires understanding microevolutionary processes. In this chapter we discuss this link between macro- and micro-evolution using the example of the evolution of sexual reproduction. Explaining the evolution of sexual reproduction is one of the most puzzling problems in evolutionary biology and despite ongoing research a general explanation for the evolution and maintenance of sex has not yet been widely confirmed. Sexual reproduction has been suggested to have evolved only once from asexual reproduction during the early stages of the eukaryote evolution. Today, we find that almost all animals and plants reproduce sexually rather than asexually, suggesting that sex is advantageous. There are, however, exemptions from the macroevolutionary observation of the ubiquity of sexual reproduction: asexual taxa are found across almost the whole phylogenetic tree in a twig-like pattern, and these asexual taxa are found in habitats where related sexual taxa are often absent. The evolution of sex, with all its superlatives such as ‘the queen of evolutionary problems’ and the ‘evolutionary scandals’ of the ancient asexuals, is probably one of the fields in evolutionary biology, where already early on macroevolutionary patterns were directly related to microevolutionary processes. Examples of the literature are reviewed here with an emphasis on the link between macro- and microevolution.
Keywords
- Evolution of sex
- Geographic parthenogenesis
- Phylogenetic distribution
- Origin of sexual reproduction
- Maintenance of sexual reproduction
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Abugov R (1986) Is there a cost for meiosis in life-history? J Theor Biol 116:613–623
Agrawal AF (2006) Evolution of sex: why do organisms shuffle their genotypes? Curr Biol 16:R696–R704
Agrawal AF (2009) Spatial heterogeneity and the evolution of sex in diploids. Am Nat 174:S54–S70
Agren J Ericson L (1996) Population structure and morph-specific fitness differences in tristylous Lythrum salicaria. Evolution 50(1):126–139
Allen DE, Lynch M (2008) Both costs and benefits of sex correlate with relative frequency of asexual reproduction in cyclically parthenogenic Daphnia pulicaria populations. Genetics 179:1497–1502
Arkhipova I, Meselson M (2000) Transposable elements in sexual and ancient asexual taxa. Proc Natl Acad Sci USA 97:14473–14477
Baker HG, Stebbins GL (1965) The genetics of colonizing species. Academic Press, New York
Barata C, Hontoria F et al (1996) Competition between sexual and parthenogenetic Artemia: temperature and strain effects. J Exp Mar Biol Ecol 196:313–328
Barton NH (1995a) A general-model for the evolution of recombination. Genet Res 65:123–144
Barton NH (1995b) Linkage and the limits to natural selection. Genetics 140:821–841
Becks L, Agrawal AF (2010) Higher rates of sex evolve in spatially heterogeneous environments. Nature 468:89–92
Becks L, Agrawal AF (2011) The effect of sex on the mean and variance of fitness in facultatively sexual rotifers. J Evol Biol 24:656–664
Becks L, Agrawal AF (2012) The evolution of sex is favoured during adaptation to new environments. PLoS Biol 10
Becks L, Agrawal AF (2013) Higher rates of sex evolve under K-selection. J Evol Biol 26:900–905
Bell G (1982) The masterpiece of nature: the evolution and genetics of sexuality. University of California Press, Berkeley
Bernstein H, Byerly HC et al (1985) Genetic damage, mutation, and the evolution of sex. Science 229:1277–1281
Bernstein H, Hopf FA et al (1987) The molecular basis of the evolution of sex. Adv Genet Mol Genet Med 24:323–370
Beukeboom LW, Vrijenhoek RC (1998) Evolutionary genetics and ecology of sperm-dependent parthenogenesis. J Evol Biol 11:755–782
Bierzychudek P (1985) Patterns in plant parthenogenesis. Experientia 41:1255–1264
Bruggeman J, Debets AJM et al (2003) Sex slows down the accumulation of deleterious mutations in the homothallic fungus Aspergillus nidulans. Genetics 164:479–485
Castagnone-Sereno P, Danchin EGJ (2014) Parasitic success without sex—the nematode experience. J Evol Biol 27:1323–1333
Cavalier-Smith T (2002) Origins of the machinery of recombination and sex. Heredity 88:125–141
Charlesworth B (1993) Directional selection and the evolution of sex and recombination. Genet Res 61:205–224
Charlesworth B, Charlesworth D (1975) Experiment on recombination load in Drosophila melanogaster. Genet Res 25:267–274
Charlesworth D, Morgan MT et al (1993) Mutation accumulation in finite outbreeding and inbreeding populations. Genet Res 61:39–56
Colegrave N (2002) Sex releases the speed limit on evolution. Nature 420:664–666
Colegrave N, Kaltz O et al (2002) The ecology and genetics of fitness in Chlamydomonas. VIII. The dynamics of adaptation to novel environments after a single episode of sex. Evolution 56:14–21
Cooper TF, Lenski RE et al (2005) Parasites and mutational load: an experimental test of a pluralistic theory for the evolution of sex. Proc R Soc B Biol Sci 272:311–317
Cutter AD, Payseur BA (2003) Rates of deleterious mutation and the evolution of sex in Caenorhabditis. J Evol Biol 16:812–822
DaSilva J, Bell G (1996) The ecology and genetics of fitness in Chlamydomonas 7. The effect of sex on the variance in fitness and mean fitness. Evolution 50:1705–1713
de Visser JAGM, Elena SF (2007) The evolution of sex: empirical insights into the roles of epistasis and drift. Nat Rev Genet 8:139–149
Decaestecker E, Gaba S et al. (2007). Host-parasite ‘Red Queen’ dynamics archived in pond sediment. Nature 450:870–U816
Doncaster CP, Pound GE et al (2003) Dynamics of regional coexistence for more or less equal competitors. J Anim Ecol 72:116–126
Doolittle WF, Sapienza C (1980) Selfish genes, the phenotype paradigm and genome evolution. Nature 284:601–603
Dufresne F, Hebert PDN (1995) Polyploidy and clonal diversity in an arctic cladoceran. Heredity 75:45–53
Elzinga JA, Chevasco V et al (2012) Low parasitism rates in parthenogenetic bagworm moths do not support the parasitoid hypothesis for sex. J Evol Biol 25:2547–2558
Engelmoer DJP, Rozen DE (2011) Competence increases survival during stress in Streptococcus pneumoniae. Evolution 65:3475–3485
Felsenstein J (1965) Effect of linkage on directional selection. Genetics 52:349–363
Felsenstein J (1974) Evolutionary advantage of recombination. Genetics 78:737–756
Finnegan DJ (1989) Eukaryotic transposable elements and genome evolution. Trends Genet 5:103–107
Finnegan DJ (1992) Transposable elements. Curr Opin Genet Dev 2:861–867
Fisher RA (1930) The genetical theory of natural selection. Clarendon Press, Oxford (reprinted by Dover 1958)
Flot J-F, Hespeels B et al (2013) Genomic evidence for ameiotic evolution in the bdelloid rotifer Adineta vaga. Nature 500:453–457
Gandon S, Otto SP (2007) The evolution of sex and recombination in response to abiotic or coevolutionary fluctuations in epistasis. Genetics 175:1835–1853
Ghiselin MT (1974) The economy of nature and the evolution of sex. University of California Press, Berkeley
Glesener RR, Tilman D (1978) Sexuality and components of environmental uncertainty: clues from geographic parthenogenesis in terrestrial animals. Am Nat 112:659–673
Goddard MR, Godfray HCJ et al (2005) Sex increases the efficacy of natural selection in experimental yeast populations. Nature 434:636–640
Gorelick R, Heng HHQ (2011) Sex reduces genetic variation: a multidisciplinary review. Evolution 65:1088–1098
Greig D, Borts RH et al (1998) The effect of sex on adaptation to high temperature in heterozygous and homozygous yeast. Proc R Soc B Biol Sci 265:1017–1023
Haag CR, Ebert D (2004) A new hypothesis to explain geographic parthenogenesis. Ann Zool Fenn 41:539–544
Hamilton WD (1980) Sex versus non-sex versus parasite. Oikos 35:282–290
Hamilton WD, Axelrod R et al (1990) Sexual reproduction as an adaptation to resist parasites (a review). Proc Natl Acad Sci USA 87:3566–3573
Hartfield M, Keightley PD (2012) Current hypotheses for the evolution of sex and recombination. Integr Zool 7:192–209
Henry L, Schwander T et al (2012) Deleterious mutation accumulation in asexual Timema stick insects. Mol Biol Evol 29:401–408
Hickey DA (1982) Selfish DNA—a sexually-transmitted nuclear parasite. Genetics 101:519–531
Hill WG, Robertson A (1966) Effects of linkage on limits to artificial selection. Genet Res 8:269–294
Howard RS, Lively CM (1998) The maintenance of sex by parasitism and mutation accumulation under epistatic fitness functions. Evolution 52(2):604–610
Hörandl E (2008) Evolutionary implications of self-compatibility and reproductive fitness in the apomicitc Ranunculus auricomus polyplid complex (Ranunculaceae). Int J Plant Sci 169:1219–1228
Hörandl E (2009) Geographical parthenogenesis: opportunities for asexuality. In: Schon I, Martens K, VanDijk P (eds) Lost sex: the evolutionary biology of parthenogenesis. Springer, Dordrecht, pp 161–186
Hsu WS (1956) Oogenesis in the Bdelloidea rotifer Philodina roseola Ehrenberg. Cellule 59:281–296
Jaenike J (1978) An hypothesis to account for the maintenance of sex within populations. Evol Theory 3:191–194
Janko K, Drozd P et al (2011) Do clones degenerate over time? Explaining the genetic variability of asexuals through population genetic models. Biol Direct 6(1):17
Janko K, Drozd P et al (2008) Clonal turnover versus clonal decay: a null model for observed patterns of asexual longevity, diversity and distribution. Evolution 62:1264–1270
Johnson SG (2006) Geographic ranges, population structure, and ages of sexual and parthenogenetic snail lineages. Evolution 60:1417–1426
Johnson SG Bragg E (1999) Age and polyphyletic origins of hybrid and spontaneous parthenogenetic Campeloma (Gastropoda: Viviparidae) from the southeastern United States. Evolution 53(6):1769–1781
Jokela J, Lively CM (1995) Spatial variation in infection by digenetic trematodes in a population of fresh-water snails (Potamopyrgus antipodarum). Oecologia 103:509–517
Jokela J, Lively CM et al (1997) Evidence for a cost of sex in the freshwater snail Potamopyrgus antipodarum. Ecology 78:452–460
Kaltz O, Bell G (2002) The ecology and genetics of fitness in Chlamydomonas. XII. Repeated sexual episodes increase rates of adaptation to novel environments. Evolution 56:1743–1753
Kearney M, Shine R (2004) Morphological and physiological correlates of hybrid parthenogenesis. Am Nat 164:803–813
Kearney MR (2003) Why is sex so unpopular in the Australian desert? Trends Ecol Evol 18(12):605–607
Kelley SE, Antonovics J et al (1988) A test of the short-term advantage of sexual reproduction. Nature 331:714–716
Kerstes NAG, Berenos C et al (2012) Antagonistic experimental coevolution with a parasite increases host recombination frequency. BMC Evol Biol 12
Killick SC, Carlsson AM et al (2006) Testing the pluralist approach to sex: the influence of environment on synergistic interactions between mutation load and parasitism in Daphnia magna. J Evol Biol 19:1603–1611
King KC, Delph LF et al (2009) The geographic mosaic of sex and the Red Queen. Curr Biol 19:1438–1441
Koivisto RKK, Braig HR (2003) Microorganisms and parthenogenesis. Biological Journal of the Linnean Society 79:43–45
Kondrashov AS (1992) Classification of hypotheses on the advantage of amphimixis. In: Symposium on the evolution of sex, Blacksburg, Va
Kondrashov AS (1993) Classification of hypotheses on the advantage of amphimixis. J Hered 84:372–387
Koskella B, Lively CM (2009) Evidence for negative frequency-dependent selection during experimental coevolution of a freshwater snail and a sterilizing trematode. Evolution 63:2213–2221
Kumpulainen T, Grapputo A et al (2004) Parasites and sexual reproduction in psychid moths. Evolution 58:1511–1520
Lachapelle J, Bell G (2012) Evolutionary rescue of sexual and asexual populations in a deteriorating environment. Evolution 66:3508–3518
Law JH, Crespi BJ (2002) Recent and ancient asexuality in Timema walkingsticks. Evolution 56:1711–1717
Lehtonen J, Jennions MD et al (2012) The many costs of sex. Trends Ecol Evol 27:172–178
Levin DA (1983) Polyploidy and novelty in flowering plants. Am Nat 122:1–25
Lively CM (1987) Evidence from a New Zealand snail for the maintenance of sex by parasitism. Nature 328:519–521
Lively CM (2010) Parasite virulence, host life history, and the cost and benefits of sex. Ecology 91
Lively CM, Lyons EJ et al (1998) Environmental stress and the maintenance of sex in a freshwater snail. Evolution 52:1482–1486
Lomnicki A (2001) Carrying capacity, competition and maintenance of sexuality. Evol Ecol Res 3:603–610
Lynch M, Deng HW (1994) Genetic slippage in response to sex. Am Nat 144:242–261
Mallet J (2007) Hybrid speciation. Nature 446:279–283
Moritz C,m Heideman A (1993) The origin and evolution of parthenogenesis in Heteronotia binoei (Gekkonidae)—Reciprocal origins and diverse mitrochondrial DNA in western populations. Syst Biol 42(3):293–306
Pongratz N, Storhas M et al (2003) Phylogeography of competing sexual and parthenogenetic forms of a freshwater flatworm: patterns and explanations. BMC Evolutionary Biology 3
Welch DM, Meselson M (2000) Evidence for the evolution of bdelloid rotifers without sexual reproduction or genetic exchange. Science 288:1211–1215
Smith JM (1978). The evolution of sex. Cambridge University Press, Cambridge
Smith JM (1988) Selection for recombination in a polygenic model—the mechanism. Genet Res 51:59–63
Smith JM, Szathmary E (1995) The major transitions in evolution. Nature 374:227–232
McDonald JF (1993) Evolution and consequences of transposable elements. Curr Opin Genet Dev 3:855–864
Meirmans S, Meirmans PG et al (2012) The costs of sex: facing real-world complexities. Q Rev Biol 87:19–40
Melters DP, Paliulis LV et al (2012) Holocentric chromosomes: convergent evolution, meiotic adaptations, and genomic analysis. Chromosome Res 20:579–593
Morran LT, Schmidt OG et al (2011) Running with the red queen: host-parasite coevolution selects for biparental sex. Science 333:216–218
Muller HJ (1932) Some genetic aspects of sex. Am Nat 66:118–138
Muller HJ (1964) The relation of recombination to mutational advance. Mutat Res 1:2–9
Nei M (1967) Modification of linkage intensity by natural selection. Genetics 57:625
Neiman M, Hehman G et al (2010) Accelerated mutation accumulation in asexual lineages of a freshwater snail. Mol Biol Evol 27:954–963
Neiman M, Meirmans S et al (2009) What can asexual lineage age tell us about the maintenance of sex? In: Schlichting CD, Mousseau TA (eds) Year in evolutionary biology 2009, vol 1168. New York Academy of Sciences, New York, pp 185–200
Normark BB, Moran NA (2000) Testing for the accumulation of deleterious mutations in asexual eukaryote genomes using molecular sequences. J Nat Hist 34:1719–1729
Olofsson H, Lundberg P (2007) The twofold cost of sex unfolded. Evol Ecol Res 9:1119–1129
Otto SP (2009) The Evolutionary enigma of sex. Am Nat 174:S1–S14
Otto SP, Lenormand T (2002) Resolving the paradox of sex and recombination. Nat Rev Genet 3:252–261
Paland S, Lynch M (2006) Transitions to asexuality result in excess amino acid substitutions. Science 311:990–992
Peters AD, Lively CM (1999) The Red Queen and fluctuating epistasis: a population genetic analysis of antagonistic coevolution. Am Nat 154:393–405
Peters AD, Lively CM (2007) Short- and long-term benefits and detriments to recombination under antagonistic coevolution. J Evol Biol 20:1206–1217
Pfrender ME, Lynch M (2000) Quantitative genetic variation in Daphnia temporal changes in genetic architecture. Evolution 54:1502–1509
Poon A, Chao L (2004) Drift increases the advantage of sex in RNA bacteriophage Phi 6. Genetics 166:19–24
Pylkov KV, Zhivotovsky LA et al (1998) Migration versus mutation in the evolution of recombination under multilocus selection. Genet Res 71:247–256
Quattro JM, Avise JC et al (1991) Molecular evidence for multiple origins of hybridogenetic fish clones (Peocilidae, Poeciliopsis). Genetics 127:391–398
Redfield RJ (1993) Evolution of natural transformation—testing the DNA-repair hypothesis in Bacillus subtilis and Haemophilus influenzae. Genetics 133:755–761
Roze D (2012) Disentangling the benefits of sex. PLoS Biol 10
Salathe M, Kouyos RD et al (2009) On the causes of selection for recombination underlying the red queen hypothesis. Am Nat 174:S31–S42
Schwander T, Crespi BJ (2009) Twigs on the tree of life? Neutral and selective models for integrating macroevolutionary patterns with microevolutionary processes in the analysis of asexuality. Mol Ecol 18:28–42
Simon JC, Delmotte F et al. (2003) Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals. Biol J Linn Soc 79:151–163
Som C, Reyer HU (2007) Hemiclonal reproduction slows down the speed of Muller’s ratchet in the hybridogenetic frog rana esculenta. J Evol Biol 20:650–660
Stelzer C-P (2011) The cost of sex and competition between cyclical and obligate parthenogenetic rotifers. Am Nat 177:E43–E53
Suomalainen E (1950) Parthenogenesis in animals. Adv Genet 3:193–253
van Dijk PJ (2003) Ecological and evolutionary opportunities of apomixis: insights from Taraxacum and Chondrilla. Philos Trans R Soc London Ser B Biol Sci 358:1113–1120
van Dijk PJ (2007) Potential and realized costs of sex in dandelions, Taraxacum officinale s.l. In: Horandl E, Grossniklaus U, VanDijk PJ Sharbel TF (eds) Apomixis: evolution, mechanisms and perspectives. ARG Gantner Verlag KG, Lichtenstein, pp 215–233
Vandel A (1928) La parthénogénèse géographique contribution a l`étude biologique et cy-tologique de la parthénogénèse naturelle. Bull Biol France Belg 62:164–281
Vellend M, Harmon L et al. (2007) Effects of exotic species on evolutionary diversification. Trends in Ecology Evolution 22(9):481–488
Verhoeven KJF, Biere A (2013) Geographic parthenogenesis and plant-enemy interactions in the common dandelion. BMC Evol Biol 13
Weismann A (1889) The significance of sexual reproduction in the theory of natural selection. In: Poulton SSEB, Shipley AE (eds) Essays upon heredity and kindred biological problems. Clarendon Press, Oxford
Weismann A (1904) The evolution theory. Edward Arnold, London
West SA, Lively CM et al (1999a) A pluralist approach to sex and recombination. J Evol Biol 12:1003–1012
West SA, Lively CM et al (1999b) Sex may need more than one. J Evol Biol 12:1053–1055
Williams GC (1975) Sex and evolution. Princeton University Press, Princeton
Wolf HG, Wohrmann K et al (1987) Experimental-evidence for the adaptive value of sexual reproduction. Genetica 72:151–159
Zeyl C, Bell G (1997) The advantage of sex in evolving yeast populations. Nature 388:465–468
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This work was supported and the German Research Foundation DFG (LB).
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Becks, L., Alavi, Y. (2015). Using Microevolution to Explain the Macroevolutionary Observations for the Evolution of Sex. In: Serrelli, E., Gontier, N. (eds) Macroevolution. Interdisciplinary Evolution Research, vol 2. Springer, Cham. https://doi.org/10.1007/978-3-319-15045-1_8
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