de-evolution?

[wgasa]

The evolution train’s a-comin’

 

by Carl Wieland

 

The atmosphere in the crowded lecture theatre foyer was alive with curious anticipation. It was the late 1970s, the heady early days of the creation movement in South Australia. The creation/evolution debate I was about to take part in, before some 40 science teachers and involving a prominent academic evolutionist, was a first for the region.

 

As the words of an animated conversation drifted across to me, I realized that my opponent-to-be was only a few metres to my left. A senior lecturer (associate professor in US terms) in population biology, he was holding forth to a small group of supporters, clearly unaware that his creationist protagonist was within earshot.

 

‘This is really frustrating’, I heard him say. ‘I feel like an astronaut who’s come back from the moon, seen the spherical Earth, and now he’s supposed to debate with someone who tries to tell people it’s flat. In my job we see evolution happening in front of our eyes.’

 

Back then, before creationist arguments had had a good airing, it was understandable for him to think like that. Biology teachers could perhaps be excused for perpetuating such a naïve belief. They simply assumed that the easily observable genetic changes in many types of living populations were an obvious demonstration that evolution from microbes to man was fact. Just give it enough time, and voilà, such ‘micro’ changes would accumulate, continually filtered and guided by natural selection. It seemed obvious and logical to expect these ‘little steps’ to keep adding up so as to lead to the ‘macro’ changes—the really big jumps, frog-to-prince, fish-to-philosopher, that type of thing. (As we will show later in this article, though, the very opposite is true.)

 

In that light, this biology lecturer’s perplexed frustration can be readily understood, because he thought that he was often seeing a small bit of what would in time become a large chunk of change. We need to understand that most evolutionists, even today, still think this way. Which is, frankly, why the usual answers given by most Bible-believers, when challenged on the subject of biological change, are inadequate.

 

For instance, a challenger might say, ‘Mosquitoes have evolved resistance to DDT in just 40 years. If that’s not evolution happening before our eyes, what is?’ Most Christian responses focus on the amount of change. For instance, they will say, ‘Well, that’s just variation within a kind.’ Or they reply, ‘But the mosquito’s still a mosquito, isn’t it? It hasn’t turned into anything else.’

 

Both of these replies are true. But they are inadequate and seldom impress the challenger, who thinks, ‘Well, that’s just a copout for the Christians. Evolution takes millions of years, and here we have all this change in only 40 years. So, give it a million years and imagine what sort of change we’ll have then!’

 

The analogy I have for many years used in explaining this in public lectures is that of a railway train. Imagine you see a train pulling out of a station in, say, Miami, Florida, headed north to Chicago.1 The distance you see it travel is only a few hundred metres. But you can reasonably presume that, given enough time, it will end up in Chicago. You have seen sound evidence to indicate that it is in principle capable of making the whole journey, you don’t need to see it make the whole trip. This is just how evolutionists see the little changes (often called ‘microevolution’, but see aside below) happening all around us. If a mosquito has changed a little in 40 years, you don’t need to see it turning into an elephant—it has shown that it is in principle capable of making a similarly radical journey.

 

What we need to be aware of, and focus on in our answers, I tell audiences, is not the amount of change, but the type or direction of change. It is not just that the train has not gone far enough, but that it is headed in the wrong direction. The types of changes observed today, though they can be accommodated within an evolutionary framework, are, we will see, precisely and demonstrably the opposite of the ones which evolutionists really need in order to give some semblance of credibility to their belief system.

 

So while you may be seeing the train pulling out of the station at Miami, if the reality is that it is not heading north, up to Chicago, but is headed in the opposite direction, downwards to where the line (if there was one) would end in the deep blue ocean, then it will never get to Chicago. Time will not solve the problem, since it is in principle an impossibility to reach Chicago by train in that downward direction. Just so, once we can point out to people that the ‘evolution train’ (really the train of biological change) is headed downwards, not upwards, then the more time there is, the less likely the whole evolution scenario becomes.

 

Before explaining what I mean by biological changes having a ‘direction’, I will share what triggered this article. It was a book review2 by well-known evolutionary biologist Dr Jerry Coyne, of the University of Chicago, who could not resist an opportunity to lash out at the creationists.3 Amazingly, Coyne uses the train journey analogy himself, reinforcing my point of how evolutionists see the issue. Though his intention is to mock creationists, he unwittingly provides a great opportunity to show how misplaced this common reasoning is.

 

The book he was reviewing4 uses familiar examples of rapid human-induced biological changes (antibiotic resistance in bacteria, pesticide resistance in insects, changes in growth rate of fish from overfishing) to get people to ‘consent’ to the bigger idea of microbes-to-man evolution.

 

Coyne deplores the fact that the book’s examples will probably not change the minds of creationist advocates, who have already accepted such changes as ‘adaptation within a species’ (‘variation within a kind’ would have been more precise). He says that creationists argue that ‘such small changes cannot explain the evolution of new groups of plants and animals’, and goes on to say: ‘This argument defies common sense. When, after a Christmas visit, we [presumably his family in Chicago—CW] watch grandma leave on the train to Miami, we assume that the rest of her journey will be an extrapolation of that quarter-mile.’ Thus, says Coyne, a ‘creationist unwilling to extrapolate from micro- to macroevolution’ is being ‘irrational’.

 

Reason vs rhetoric

Why can one say with confidence, concerning the biological changes observable today (man-induced or otherwise) that the train is headed in the wrong direction? Why is it that when evolutionists use this ‘grandma’s train’ extrapolation argument, it can be turned around to make the opposite point? Because the real issue in biological change is all about what happens at the DNA level, which concerns information.5 The information carried on the DNA, the molecule of heredity, is like a recipe, a set of instructions for the manufacture of certain items.

 

Evolutionists teach that one-celled organisms6 (e.g. protozoa) have given rise to pelicans, pomegranates, people and ponies. In each case, the DNA ‘recipe’ has had to undergo a massive net increase of information during the alleged millions of years. A one-celled organism does not have the instructions for how to manufacture eyes, ears, blood, skin, hooves, brains, etc. which ponies need. So for protozoa to have given rise to ponies, there would have to be some mechanism that gives rise to new information.

 

Evolutionists hail natural selection as if it were a creative goddess, but the reality (which they invariably concede when pressed) is that selection on its own always gets rid of information, never the opposite.7 To have a way to add information, the ‘only game in town’ for evolution’s true believers is genetic copying mistakes or accidents, i.e. random mutations (which can then be ‘filtered’ by selection).8 However, the problem is that if mutations were capable of adding the information required, we should see hundreds of examples all around us, considering that there are many thousands of mutations happening continually. But whenever we study mutations, they invariably turn out to have lost or degraded the information. This is so even in those rare instances when the mutational defect gives a survival advantage—e.g. the loss of wings on beetles on windy islands.9

 

What’s in a word? Micro vs macro

Many creationists will say, ‘We accept microevolution, but not macroevolution.’ As our main article points out, the ‘micro’ changes (i.e. observed genetic variation) are not capable of accumulating into macro ones, anyway.

 

We suggest, however, that it would be wiser to avoid the use of the term ‘microevolution’. To most people, it sounds as if you are conceding that there is a ‘little bit of evolution’ going on. I.e. a little bit of the same process that, given enough time, will turn microbes into millipedes, magnolias and microbiologists. Thus, you will be seen as churlish or, as in Dr Coyne’s inverted ‘train’ example, as irrational for putting what they see as an arbitrary distinction between the ‘micro’ and ‘macro’.

 

If the use of such potentially misleading terminology is unavoidable, always take the opportunity to point out that the changes often labelled ‘microevolution’ cannot be the same process as the hypothetical ‘goo-to-you’ belief. They are all information-losing processes, which thus depend on there being a store of information to begin with.

 

 

As creatures diversify, gene pools become increasingly thinned out. The more organisms adapt to their surroundings by selection, i.e. the more specialized they become, the smaller the fraction they carry of the original storehouse of created information for their kind. Thus, there is less information available on which natural selection can act in the future to ‘readapt’ the population should circumstances change. Less flexible, less adaptable populations are obviously heading closer to extinction, not evolving.

 

We see that, just like with the train pulling out from Miami and headed south, if the sorts of changes we see today are extrapolated over time, they lead to extinction, not onwards evolution.

 

Remember, evolutionary belief teaches that once upon a time, there were living things, but no lungs—lungs had not evolved yet, so there was no DNA information coding for lung manufacture. Somehow this program had to be written. New information had to arise that did not previously exist, anywhere.

 

Later, there were lungs, but no feathers anywhere in the world, thus no genetic information for feathers. Real-world observation has overwhelmingly shown mutation to be totally unable to feed the required new information into the system.10 In fact, mutations overall hasten the downward trend by adding genetic load in the form of harmful mutations, of which we have all accumulated hundreds over the generations of our ancestry.11

 

In other words, populations can change and adapt because they have a lot of information (variety) in their DNA ‘recipe’. But unless mutations can feed in new information, each time there is variation/adaptation, the total information decreases (as selection gets rid of the unadapted portions of the population, some information is lost in that population). Thus, given a fixed amount of information, the more adaptation we see, the less the potential for future adaptation. The train is definitely headed downhill, destined to fall off the jetty of extinction.

 

The supreme irony is that, of all the examples lauded by Dr Coyne as ‘evolution’, whether antibiotic resistance12 or changes in fish growth rates, not one single one supports his ‘train’ analogy, but rather the reverse. Not one involves a gain of information; all show the opposite, a net loss. Pondering all this, I feel a sense of the same sort of frustration (only in reverse) that my evolutionist opponent was airing all those years ago, which he could have paraphrased as: ‘Why can’t they see it? It’s obvious, isn’t it?’

 

Who knows, perhaps somehow this article will get into Dr Coyne’s hands. Maybe it will give him, and some other evolutionist apologists, food for thought the next time they put one of their grandmothers on a train.

 

 

heres the site.

http://www.answersingenesis.org/creation/v24/i2/evolution_train.asp#aside

[ecoli]

please don't just copy and paste text from websites without adding any of your own ideas.

[wgasa]

damn, sorry for the tripple post, slow computer.

[NeonBlack]

De-evolution?

You didn't watch the Mario Brother movie did you?

[rakuenso]

suggesting de-evolution implies that evolution is supposed to lead to somewhere

 

but remember, there is no point to evolution.

[bascule]

Creationists sure like to play the out of sight, out of mind game when it comes to evidence for speciation, don't they? If we pretend it doesn't exist, then we can just ignore it, right?

 

Well, science has the following to say about the matter, in the form of observed speciation events. Yes, macroevolution really does happen, and we do have evidence for it. Lots of it.

 

General

1. M Nei and J Zhang, Evolution: molecular origin of species. Science 282: 1428-1429, Nov. 20, 1998. Primary article is: CT Ting, SC Tsaur, ML We, and CE Wu, A rapidly evolving homeobox at the site of a hybrid sterility gene. Science 282: 1501-1504, Nov. 20, 1998. As the title implies, has found the genes that actually change during reproductive isolation.

2. M Turelli, The causes of Haldane's rule. Science 282: 889-891, Oct.30, 1998. Haldane's rule describes a phase every population goes thru during speciation: production of inviable and sterile hybrids. Haldane's rule states "When in the F1 [first generation] offspring of two different animal races one sex is absent, rare, or sterile, that sex is the heterozygous [heterogemetic; XY, XO, or ZW] sex."Two leading explanations are fast-male and dominance. Both get supported. X-linked incompatibilities would affect heterozygous gender more because only one gene."

3. Barton, N. H., J. S. Jones and J. Mallet. 1988. No barriers to speciation. Nature. 336:13-14.

4. Baum, D. 1992. Phylogenetic species concepts. Trends in Ecology and Evolution. 7:1-3.

5. Rice, W. R. 1985. Disruptive selection on habitat preference and the evolution of reproductive isolation: an exploratory experiment. Evolution. 39:645-646.

6. Ringo, J., D. Wood, R. Rockwell, and H. Dowse. 1989. An experiment testing two hypotheses of speciation. The American Naturalist. 126:642-661.

7. Schluter, D. and L. M. Nagel. 1995. Parallel speciation by natural selection. American Naturalist. 146:292-301.

8. Callaghan, C. A. 1987. Instances of observed speciation. The American Biology Teacher. 49:3436.

9. Cracraft, J. 1989. Speciation and its ontology: the empirical consequences of alternative species concepts for understanding patterns and processes of differentiation. In Otte, E. and J. A. Endler [eds.] Speciation and its consequences. Sinauer Associates, Sunderland, MA. pp. 28-59.

 

Chromosome numbers in various species

http://www.kean.edu/~breid/chrom2.htm

 

Speciation in Insects

1. G Kilias, SN Alahiotis, and M Pelecanos. A multifactorial genetic investigation of speciation theory using drosophila melanogaster Evolution 34:730-737, 1980. Got new species of fruit flies in the lab after 5 years on different diets and temperatures. Also confirmation of natural selection in the process. Lots of references to other studies that saw speciation.

2. JM Thoday, Disruptive selection. Proc. Royal Soc. London B. 182: 109-143, 1972.

Lots of references in this one to other speciation.

3. KF Koopman, Natural selection for reproductive isolation between Drosophila pseudobscura and Drosophila persimilis. Evolution 4: 135-148, 1950. Using artificial mixed poulations of D. pseudoobscura and D. persimilis, it has been possible to show,over a period of several generations, a very rapid increase in the amount of reproductive isolation between the species as a result of natural selection.

4. LE Hurd and RM Eisenberg, Divergent selection for geotactic response and evolution of reproductive isolation in sympatric and allopatric populations of houseflies. American Naturalist 109: 353-358, 1975.

5. Coyne, Jerry A. Orr, H. Allen. Patterns of speciation in Drosophila. Evolution. V43. P362(20) March, 1989.

6. Dobzhansky and Pavlovsky, 1957 An incipient species of Drosophila, Nature 23: 289- 292.

7. Ahearn, J. N. 1980. Evolution of behavioral reproductive isolation in a laboratory stock of Drosophila silvestris. Experientia. 36:63-64.

8. 10. Breeuwer, J. A. J. and J. H. Werren. 1990. Microorganisms associated with chromosome destruction and reproductive isolation between two insect species. Nature. 346:558-560.

9. Powell, J. R. 1978. The founder-flush speciation theory: an experimental approach. Evolution. 32:465-474.

10. Dodd, D. M. B. and J. R. Powell. 1985. Founder-flush speciation: an update of experimental results with Drosophila. Evolution 39:1388-1392. 37. Dobzhansky, T. 1951. Genetics and the origin of species (3rd edition). Columbia University Press, New York.

11. Dobzhansky, T. and O. Pavlovsky. 1971. Experimentally created incipient species of Drosophila. Nature. 230:289-292.

12. Dobzhansky, T. 1972. Species of Drosophila: new excitement in an old field. Science. 177:664-669.

13. Dodd, D. M. B. 1989. Reproductive isolation as a consequence of adaptive divergence in Drosophila melanogaster. Evolution 43:1308-1311.

14. de Oliveira, A. K. and A. R. Cordeiro. 1980. Adaptation of Drosophila willistoni experimental populations to extreme pH medium. II. Development of incipient reproductive isolation. Heredity. 44:123-130.15. 29. Rice, W. R. and G. W. Salt. 1988. Speciation via disruptive selection on habitat preference: experimental evidence. The American Naturalist. 131:911-917.

30. Rice, W. R. and G. W. Salt. 1990. The evolution of reproductive isolation as a correlated character under sympatric conditions: experimental evidence. Evolution. 44:1140-1152.

31. del Solar, E. 1966. Sexual isolation caused by selection for positive and negative phototaxis and geotaxis in Drosophila pseudoobscura. Proceedings of the National Academy of Sciences (US). 56:484-487.

32. Weinberg, J. R., V. R. Starczak and P. Jora. 1992. Evidence for rapid speciation following a founder event in the laboratory. Evolution. 46:1214-1220.

33. V Morell, Earth's unbounded beetlemania explained. Science 281:501-503, July 24, 1998. Evolution explains the 330,000 odd beetlespecies. Exploitation of newly evolved flowering plants.

34. B Wuethrich, Speciation: Mexican pairs show geography's role. Science 285: 1190, Aug. 20, 1999. Discusses allopatric speciation. Debate with ecological speciation on which is most prevalent.

 

Speciation in Plants

1. Speciation in action Science 72:700-701, 1996 A great laboratory study of the evolution of a hybrid plant species. Scientists did it in the lab, but the genetic data says it happened the same way in nature.

2. Hybrid speciation in peonies http://www.pnas.org/cgi/content/full/061288698v1#B1

3. http://www.holysmoke.org/new-species.htm new species of groundsel by hybridization

4. Butters, F. K. 1941. Hybrid Woodsias in Minnesota. Amer. Fern. J. 31:15-21.

5. Butters, F. K. and R. M. Tryon, jr. 1948. A fertile mutant of a Woodsia hybrid. American Journal of Botany. 35:138.

6. Toxic Tailings and Tolerant Grass by RE Cook in Natural History, 90(3): 28-38, 1981 discusses selection pressure of grasses growing on mine tailings that are rich in toxic heavy metals. "When wind borne pollen carrying nontolerant genes crosses the border [between prairie and tailings] and fertilizes the gametes of tolerant females, the resultant offspring show a range of tolerances. The movement of genes from the pasture to the mine would, therefore, tend to dilute the tolerance level of seedlings. Only fully tolerant individuals survive to reproduce, however. This selective mortality, which eliminates variants, counteracts the dilution and molds a toatally tolerant population. The pasture and mine populations evolve distinctive adaptations because selective factors are dominant over the homogenizing influence of foreign genes."

7. Clausen, J., D. D. Keck and W. M. Hiesey. 1945. Experimental studies on the nature of species. II. Plant evolution through amphiploidy and autoploidy, with examples from the Madiinae. Carnegie Institute Washington Publication, 564:1-174.

8. Cronquist, A. 1988. The evolution and classification of flowering plants (2nd edition). The New York Botanical Garden, Bronx, NY.

9. P. H. Raven, R. F. Evert, S. E. Eichorn, Biology of Plants (Worth, New York,ed. 6, 1999).

10. M. Ownbey, Am. J. Bot. 37, 487 (1950).

11. M. Ownbey and G. D. McCollum, Am. J. Bot. 40, 788 (1953).

12. S. J. Novak, D. E. Soltis, P. S. Soltis, Am. J. Bot. 78, 1586 (1991).

13. P. S. Soltis, G. M. Plunkett, S. J. Novak, D. E. Soltis, Am. J. Bot. 82,1329 (1995).

14. Digby, L. 1912. The cytology of Primula kewensis and of other related Primula hybrids. Ann. Bot. 26:357-388.

15. Owenby, M. 1950. Natural hybridization and amphiploidy in the genus Tragopogon. Am. J. Bot. 37:487-499.

16. Pasterniani, E. 1969. Selection for reproductive isolation between two populations of maize, Zea mays L. Evolution. 23:534-547.

 

Speciation in microorganisms

1. Canine parovirus, a lethal disease of dogs, evolved from feline parovirus in the 1970s.

2. Budd, A. F. and B. D. Mishler. 1990. Species and evolution in clonal organisms -- a summary and discussion. Systematic Botany 15:166-171.

3. Bullini, L. and G. Nascetti. 1990. Speciation by hybridization in phasmids and other insects. Canadian Journal of Zoology. 68:1747-1760.

4. Boraas, M. E. 1983. Predator induced evolution in chemostat culture. EOS. Transactions of the American Geophysical Union. 64:1102.

5. Brock, T. D. and M. T. Madigan. 1988. Biology of Microorganisms (5th edition). Prentice Hall, Englewood, NJ.

6. Castenholz, R. W. 1992. Species usage, concept, and evolution in the cyanobacteria (blue-green algae). Journal of Phycology 28:737-745.

7. Boraas, M. E. The speciation of algal clusters by flagellate predation. EOS. Transactions of the American Geophysical Union. 64:1102.

8. Castenholz, R. W. 1992. Speciation, usage, concept, and evolution in the cyanobacteria (blue-green algae). Journal of Phycology 28:737-745.

9. Shikano, S., L. S. Luckinbill and Y. Kurihara. 1990. Changes of traits in a bacterial population associated with protozoal predation. Microbial Ecology. 20:75-84.

 

New Genus

1. Muntzig, A, Triticale Results and Problems, Parey, Berlin, 1979. Describes whole new *genus* of plants, Triticosecale, of several species, formed by artificial selection. These plants are important in agriculture.

 

Invertebrate not insect

1. ME Heliberg, DP Balch, K Roy, Climate-driven range expansion and morphological evolution in a marine gastropod. Science 292: 1707-1710, June1, 2001. Documents mrorphological change due to disruptive selection over time. Northerna and southern populations of A spirata off California from Pleistocene to present.

2. Weinberg, J. R., V. R. Starczak and P. Jora. 1992. Evidence for rapid speciation following a founder event with a polychaete worm. . Evolution. 46:1214-1220.

 

Vertebrate Speciation

1. N Barton Ecology: the rapid origin of reproductive isolation Science 290:462-463, Oct. 20, 2000. http://www.sciencemag.org/cgi/content/full/290/5491/462 Natural selection of reproductive isolation observed in two cases. Full papers are: AP Hendry, JK Wenburg, P Bentzen, EC Volk, TP Quinn, Rapid evolution of reproductive isolation in the wild: evidence from introduced salmon. Science 290: 516-519, Oct. 20, 2000. and M Higgie, S Chenoweth, MWBlows, Natural selection and the reinforcement of mate recognition. Science290: 519-521, Oct. 20, 2000

2. G Vogel, African elephant species splits in two. Science 293: 1414, Aug. 24, 2001. http://www.sciencemag.org/cgi/content/full/293/5534/1414

3. C Vila` , P Savolainen, JE. Maldonado, IR. Amorim, JE. Rice, RL. Honeycutt, KA. Crandall, JLundeberg, RK. Wayne, Multiple and Ancient Origins of the Domestic Dog Science 276: 1687-1689, 13 JUNE 1997. Dogs no longer one species but 4 according to the genetics. http://www.idir.net/~wolf2dog/wayne1.htm

4. Barrowclough, George F.. Speciation and Geographic Variation in Black-tailed Gnatcatchers. (book reviews) The Condor. V94. P555(2) May, 1992

5. Kluger, Jeffrey. Go fish. Rapid fish speciation in African lakes. Discover. V13. P18(1) March, 1992.

Formation of five new species of cichlid fishes which formed since they were isolated from the parent stock, Lake Nagubago. (These fish have complex mating rituals and different coloration.) See also Mayr, E., 1970. _Populations, Species, and Evolution_, Massachusetts, Harvard University Press. p. 348

6. Genus _Rattus_ currently consists of 137 species [1,2] and is known to have

originally developed in Indonesia and Malaysia during and prior to the Middle

Ages[3].

[1] T. Yosida. Cytogenetics of the Black Rat. University Park Press, Baltimore, 1980.

[2] D. Morris. The Mammals. Hodder and Stoughton, London, 1965.

[3] G. H. H. Tate. "Some Muridae of the Indo-Australian region," Bull. Amer. Museum Nat. Hist. 72: 501-728, 1963.

7. Stanley, S., 1979. _Macroevolution: Pattern and Process_, San Francisco,

W.H. Freeman and Company. p. 41

Rapid speciation of the Faeroe Island house mouse, which occurred in less than 250 years after man brought the creature to the island.

 

Speciation in the Fossil Record

1. Paleontological documentation of speciation in cenozoic molluscs from Turkana basin. Williamson, PG, Nature 293:437-443, 1981. Excellent study of "gradual" evolution in an extremely find fossil record.

2. A trilobite odyssey. Niles Eldredge and Michelle J. Eldredge. Natural History 81:53-59, 1972. A discussion of "gradual" evolution of trilobites in one small area and then migration and replacement over a wide area. Is lay discussion of punctuated equilibria, and does not overthrow Darwinian gradual change of form. Describes transitionals

 

Overkill

20. Craig, T. P., J. K. Itami, W. G. Abrahamson and J. D. Horner. 1993. Behavioral evidence for host-race fromation in Eurosta solidaginis. Evolution. 47:1696-1710.

21. Cronquist, A. 1978. Once again, what is a species? Biosystematics in agriculture. Beltsville Symposia in Agricultural Research 2:3-20.

24. de Queiroz, K. and M. Donoghue. 1988. Phylogenetic systematics and the species problem. Cladistics. 4:317-338.

25. de Queiroz, K. and M. Donoghue. 1990. Phylogenetic systematics and species revisited. Cladistics. 6:83-90.

26. de Vries, H. 1905. Species and varieties, their origin by mutation.

27. de Wet, J. M. J. 1971. Polyploidy and evolution in plants. Taxon. 20:29-35.

28. Rice, W. R. and E. E. Hostert. 1993. Laboratory experiments on speciation: What have we learned in forty years? Evolution. 47:1637-1653.

 

42. Du Rietz, G. E. 1930. The fundamental units of biological taxonomy. Svensk. Bot. Tidskr. 24:333-428.

43. Ehrman, E. 1971. Natural selection for the origin of reproductive isolation. The American Naturalist. 105:479-483.

44. Ehrman, E. 1973. More on natural selection for the origin of reproductive isolation. The American Naturalist. 107:318-319.

45. Feder, J. L., C. A. Chilcote and G. L. Bush. 1988. Genetic differentiation between sympatric host races of the apple maggot fly, Rhagoletis pomonella. Nature. 336:61-64.

46. Feder, J. L. and G. L. Bush. 1989. A field test of differential host-plant usage between two sibling species of Rhagoletis pomonella fruit flies (Diptera:Tephritidae) and its consequences for sympatric models of speciation. Evolution 43:1813-1819.

47. Frandsen, K. J. 1943. The experimental formation of Brassica juncea Czern. et Coss. Dansk. Bot. Arkiv., No. 4, 11:1-17.

48. Frandsen, K. J. 1947. The experimental formation of Brassica napus L. var. oleifera DC and Brassica carinata Braun. Dansk. Bot. Arkiv., No. 7, 12:1-16.

49. Galiana, A., A. Moya and F. J. Alaya. 1993. Founder-flush speciation in Drosophila pseudoobscura: a large scale experiment. Evolution. 47432-444.

50. Gottleib, L. D. 1973. Genetic differentiation, sympatric speciation, and the origin of a diploid species of Stephanomeira. American Journal of Botany. 60: 545-553.

51. Halliburton, R. and G. A. E. Gall. 1981. Disruptive selection and assortative mating in Tribolium castaneum. Evolution. 35:829-843.

52. Karpchenko, G. D. 1927. Polyploid hybrids of Raphanus sativus L. X Brassica oleraceae L. Bull. Appl. Botany. 17:305-408.

53. Karpchenko, G. D. 1928. Polyploid hybrids of Raphanus sativus L. X Brassica oleraceae L. Z. Indukt. Abstami-a Verenbungsi. 48:1-85.

54. Knight, G. R., A. Robertson and C. H. Waddington. 1956. Selection for sexual isolation within a species. Evolution. 10:14-22.

55. Levin, D. A. 1979. The nature of plant species. Science 204:381-384.

56. Lokki, J. and A. Saura. 1980. Polyploidy in insect evolution. In: W. H. Lewis (ed.) Polyploidy: Biological Relevance. Plenum Press, New York.

57. Macnair, M. R. and P. Christie. 1983. Reproductive isolation as a pleiotropic effect of copper tolerance in Mimulus guttatus. Heredity. 50:295-302.

58. Manhart, J. R. and R. M. McCourt. 1992. Molecular data and species concepts in the algae. Journal of Phycology. 28:730-737.

59. Mayr, E. 1942. Systematics and the origin of species from the viewpoint of a zoologist. Columbia University Press, New York.

60. Mayr, E. 1982. The growth of biological thought: diversity, evolution and inheritance. Harvard University Press, Cambridge, MA. McCourt, R. M. and R. W. Hoshaw. 1990. Noncorrespondence of breeding groups, morphology and monophyletic groups in Spirogyra (Zygnemataceae; Chlorophyta) and the application of species concepts. Systematic Botany. 15:69-78.

61. McPheron, B. A., D. C. Smith and S. H. Berlocher. 1988. Genetic differentiation between host races of Rhagoletis pomonella. Nature. 336:64-66.

62. Muntzing, A. 1932. Cytogenetic investigations on the synthetic Galeopsis tetrahit. Hereditas. 16:105-154.

63. Newton, W. C. F. and C. Pellew. 1929. Primula kewensis and its derivatives. J. Genetics. 20:405-467.

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