Abstract
People group and organize entities or observations as a way of understanding the world. We also believe that the structures we generate doing this fundamental taxonomic activity approach the “true” organization of the natural world. Initially few characters, often of a single class, are available for organizing individuals into groups. As new characters, and especially those of a different nature or class, become available, the effectiveness of the original classification is tested and evaluated. An ideal taxonomy results in the same classification regardless of the nature of the characters used. In biology the species level was more effective than higher levels of classification in forming “natural” groups, i.e., those in which different classes of characters resulted in the same or similar groupings. In this century the greater effectiveness of the species level of classification could be rationalized through the gene pool shared by members of this evolutionary unit. Along with this new evolutionary definition of species came the discovery that morphologically similar Drosophila could sometimes be divided into more than one genetic species. These became known as sibling species.
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References
Agatsuma T, Tsukii Y (1980) Genetic control of lactate dehydrogenase isozymes in Paramecium caudatum. Biochem Genet 18:77–85
Allen SL, Byrne BC, Cronkite DL (1971) Intersyngenic variations in the esterases of bacterized Paramecium aurelia. Biochem Genet 5:135–150
Allen SL, Farrow SW, Golembiewski PA (1973) Esterase variations between the 14 syngens of Paramecium aurelia under axenic growth. Genetics 73:561–573
Allen SL, Lau ET, Nerad TA, Rushford CL (1982) Esterase variants in four species of the Paramecium aurelia complex. J Protozool 29:604–611
Allen SL, Nerad TA, Rushford CL (1983a) Intraspecies variability in the esterases and acid phosphatases of four species of the Paramecium aurelia complex. J Protozool 30:131–143
Allen SL, Adams J, Rushford CL (1983b) Interspecies relationships in the Paramecium aurelia complex: acid phosphatase variation. J Protozool 30:143–147
Allen SL, Nerad TA, Rushford CL (1983c) Comparison of the esterases and acid phosphatases in Paramecium multimicronucleatum, syngens 1–5, P. jenningsi, P. caudatum, and the P. aurelia complex. J Protozool 30:148–154
Allen SL, Rushford CL, Nerad TA, Lau ET (1983d) Intraspecies variability in the esterases and acid phosphatases of Paramecium jenningsi and Paramecium multimicronucleatum assignment of unidentified Paramecia; comparison with the P. aurelia complex. J Protozool 30:155–163
Ammermann D (1966) Das Paarungssystem der Ciliaten Paramecium woodruffi and Paramecium trichium. Arch Protistenk 109:139–146
Aufderheide KJ, Daggett P-M, Nerad TA (1983) Paramecium sonneborni n.sp., a new member of the Paramecium aurelia species complex. J Protozool 30:128–131
Beale GH, Knowles JKC (1976) Interspecies transfer of mitochondria in Paramecium aurelia. Mol Gen Genet 143:197–201
Beale GH, Tait A (1981) Mitochondrial genetics of Paramecium aurelia. Int Rev Cytol 71:19–40
Bomford R (1966) The syngens of Paramecium bursaria new mating types and intersyngenic mating reactions. J Protozool 13:497–501
Butzel HM, Jr (1974) Mating type determination and development in Paramecium aurelia. In: Van Wagtendonk WJ (ed) Paramecium, a current survey. Elsevier, Amsterdam, pp 91–130
Cummings DJ (1980) Evolutionary divergence of mitochondrial DNA from Paramecium aurelia. Mol Gen Genet 180:77–84
Cummings DJ, Maki RA, Conlon PJ, Laping J (1980) Anatomy of mitochondrial DNA from Paramecium aurelia. Mol Gen Genet 178:499–510
Darlington CD (1958) Evolution of genetic systems, 2nd edn. Oliver & Boyd, Edinburgh, 265 pp
Dini F (1984) On the evolutionary significance of autogamy in the marine Euplotes. Am Nat 123:151–162
Dippell RV (1954) A preliminary report on the chromosomal constitution of certain variety 4 races of Paramecium aurelia. Caryologia 6(Suppl):1109–1111
Gates MA, Berger J (1976) Morphometric inseparability of Paramecium primaurelia and P. pentaurelia. Trans Am Microsc Soc 95:507–514
Genérmont J, Machelon V, Demar C (1985) The “vannus” group of the genus Euplotes. Sibling species and related forms; evolutionary significance and taxonomic implications. Att Soc Tosc Sci Nat Mem (Ser B) 92:53–65
Gilman LC (1941) Mating types in diverse races of Paramecium caudatum. Biol Bull 80:384–402
Görtz H-D, Fujishima M (1983) Conjugation and meiosis of Paramecium caudatum infected with the micronucleus-specific bacterium Holospora elegans. Eur J Cell Biol 32:86–91
Haga N, Saimi Y, Takahashi M, Kung C (1983) Intra- and interspecific complementation of membrane-inexcitable mutants of Paramecium. J Cell Biol 97:378–382
Haggard B (1974) Interspecies crosses in Paramecium aurelia (syngen 4 by syngen 8). J Protozool 21:152–159
Hairston NG (1958) Observations on the ecology of Paramecium, with comments on the species problem. Evolution 12:440–450
Hairston NG (1967) Studies on the limitation of a natural population of Paramecium aurelia. Ecology 48:904–910
Hairston NG, Kellerman SL (1965) Competition between varieties 2 and 3 of Paramecium aurelia the influence of temperature in a food limited system. Ecology 46:134–139
Hiwatashi K (1949) Studies on the conjugation of Paramecium caudatum. I. Mating types and groups in the races obtained in Japan. Sci Rep Tohoku Univ (4th Ser) 18:137–140
Hiwatashi K (1968) Determination and inheritance of mating type in Paramecium caudatum. Genetics 58:373–386
Khadem N, Gibson I (1985) Enzyme variation in Paramecium caudatum. J Protozool 32:622–626
Komala Z, Przyboś E (1984) Distribution of the Paramecium aurelia species complex in the Carpathian Chain of Poland. Zool Scr 13:161–163
Kroll RJ, Barnett A (1968) The effect of different fission rates on the onset of maturity in Paramecium multimicronucleatum. J Protozool 15(Suppl):10
Landis WG (1981) The ecology, role of the killer trait, and interactions of five species of the Paramecium aurelia complex inhabiting the littoral zone. Can J Zool 59:1734–1743
Landis WG (1982) The spatial and temporal distribution of Paramecium bursaria in the littoral zone. J Protozool 29:159–161
Luporini P, Dini F (1977) The breeding system and genetic relationship between autogamous and non-autogamous sympatric populations of Euplotes crassus. Monitore Zool Ital 11:119–154
Machelon V, Demar C (1984) Electrophoretic variations among the genus Euplotes (Ciliata, Hypotrichida): comparative data for the sibling species complex Euplotes vannus and survey of infrageneric variability. J Protozool 31:74–82
Miwa I (1979a) Specificity of the immaturity substances of Paramecium. J Cell Sci 36:253–260
Miwa I (1979b) Immaturity substances in Paramecium primaurelia and their specificity. J Cell Sci 38:193–199
Miyake A (1968) Induction of conjugation by chemical agents in Paramecium. J Exp Zool 167:359–380
Nanney DL (1980) Experimental ciliatology. John Wiley & Sons, New York, 304 pp
Nyberg D (1974) Breeding systems and resistance to environmental stress in ciliates. Evolution 28:367–380
Nyberg D (1975) Genetic analysis of copper resistance in Paramecium aurelia syngen 4. Genetics 80:463–473
Nyberg D (1978) Genetic analysis of trichocyst discharge of the wild stocks of Paramecium tetraurelia. J Protozool 25:107–112
Nyberg D (1982) Sex, recombination, and reproductive fitness: an experimental study using Paramecium. Am Nat 120:198–217
Nyberg D, Bishop P (1983) High levels of phenotypic variability of metal and temperature tolerance in Paramecium. Evolution 37:341–357
Nyberg D, Bogar AE (1986) Genotypic and subgenotypic variation in heavy metal tolerance in Paramecium. Am Nat 127:615–628
Orias E (1959) Mating interaction between varieties 6 and 8 of Tetrahymena pyriformis. J Protozool 6(Suppl):19
Powelson EE, Gates MA, Berger J (1975) A biometrical analysis of 22 stocks of four syngens of Paramecium aurelia. Can J Zool 53:19–32
Pringle CR, Beale GH (1960) Antigenic polymorphism in a wild population of Paramecium aurelia. Genet Res 1:62–68
Przyboś E (1968) The occurrence of syngens of Paramecium aurelia in Rumania. Folia Biol 16:131–136
Przyboś E (1980) Distribution of species of the Paramecium aurelia complex in Spain. Folia Biol 28:405–412
Schlegel M (1985) Comparative study of allozyme variation in eight species of hypotrichous ciliates. Z Zool Syst Evolutionsforsch 23:171–183
Seilhamer JJ, Olsen GJ, Cummings DJ (1984a) Paramecium mitochondrial genes. I. Small subunit rRNA gene sequence and microevolution. J Biol Chem 259:5167–5172
Seilhamer JJ, Gutell RR, Cummings DJ (1984b) Paramecium mitochondrial genes. II. Large subunit rRNA gene sequence and microevolution. J Biol Chem 259:5173–5181
Siegel RW (1958) Hybrid vigor, heterosis, and evolution in Paramecium aurelia. Evolution 12:402–416
Siegel RW (1963) New results on the genetics of mating types in Paramecium bursaria. Genet Res 4:132–142
Simon EM, Meyer EB, Preparata RM (1985) New wild Tetrahymena from southeast Asia, China, and North America, including T. malaccensis, T. asiatica, T. nanneyi, T. caudata, and T. silvana n. spp. J Protozool 32:183–189
Sogin ML, Elwood HJ (1986) Primary structure of the Paramecium tetraurelia small-subunit rRNA coding region: phylogenetic relationships within the ciliophora. J Mol Evol 23:53–60
Sonneborn TM (1937) Sex, sex inheritance and sex determination in Paramecium aurelia. Proc Natl Acad Sci USA 23:378–385
Sonneborn TM (1939) Paramecium aurelia mating types and groups; lethal interactions; determination and inheritance. Am Nat 73:390–413
Sonneborn TM (1957) Breeding systems, reproductive methods, and species problems in protozoa. In: Mayr E (ed) The species problem. AAAS, Washington, DC, pp 155–324
Sonneborn TM (1975) The Paramecium aurelia complex of fourteen sibling species. Trans Am Microsc Soc 94:155–178
Stebbins GL, Jr (1950) Variation and evolution in plants. Columbia Univ Press, New York, 643 pp
Tait A (1970) Enzyme variation between syngens in Paramecium aurelia. Biochem Genet 4:461–470
Takagi Y (1970) Expression of the mating-type trait in the clonal life history after conjugation in Paramecium multimicronucleatum and Paramecium caudatum. Jpn J Genet 45:11–20
Tsukii Y, Hiwatashi K (1983) Genes controlling mating type specificity in Paramecium caudatum three loci revealed by intersyngenic crosses. Genetics 104:41–62
Tsukii Y, Hiwatashi K (1985) Meiotic nondisjunction and aneuploids in intersyngenic hybrids of Paramecium caudatum. Genetics 111:779–794
Vivier E (1974) Morphology, taxonomy and general biology of the genus Paramecium. In: Van Wagtendonk WJ (ed) Paramecium, a current survey. Elsevier, Amsterdam, pp 1–89
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Nyberg, D. (1988). The Species Concept and Breeding Systems. In: Görtz, HD. (eds) Paramecium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73086-3_3
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DOI: https://doi.org/10.1007/978-3-642-73086-3_3
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