It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
5.4.2 Selection for Geotaxis with and without Gene Flow
Soans, et al. (1974) used houseflies to test Pimentel's model of speciation. This model posits that speciation requires two steps. The first is the formation of races in subpopulations. This is followed by the establishment of reproductive isolation. Houseflies were subjected to intense divergent selection on the basis of positive and negative geotaxis. In some treatments no gene flow was allowed, while in others there was 30% gene flow. Selection was imposed by placing 1000 flies into the center of a 108 cm vertical tube. The first 50 flies that reached the top and the first 50 flies that reached the bottom were used to found positively and negatively geotactic populations. Four populations were established:
Population A + geotaxis, no gene flow
Population B - geotaxis, no gene flow
Population C + geotaxis, 30% gene flow
Population D - geotaxis, 30% gene flow
Selection was repeated within these populations each generations. After 38 generations the time to collect 50 flies had dropped from 6 hours to 2 hours in Pop A, from 4 hours to 4 minutes in Pop B, from 6 hours to 2 hours in Pop C and from 4 hours to 45 minutes in Pop D. Mate choice tests were performed. Positive assortative mating was found in all crosses. They concluded that reproductive isolation occurred under both allopatric and sympatric conditions when very strong selection was present.
Hurd and Eisenberg (1975) performed a similar experiment on houseflies using 50% gene flow and got the same results.
A List of Speciation References
Weiberg, James R.. Starczak, Victoria R.. Jorg, Daniele. Evidence for rapid speciation following a founder event in the laboratory. Evolution. V46. P1214(7) August, 1992.
Kluger, Jeffrey. Go fish. (rapid fish speciation in African lakes). Discover. V13. P18(1) March, 1992.
Hauffe, Heidi C.. Searle, Jeremy B.. A disappearing speciation event? (response to J.A. Coyne, Nature, vol. 355, p. 511, 1992). Nature. V357. P26(1) May 7, 1992.
Abstract:
Analysis of contact between two chromosomal races of house mice in northern Italy show that natural selection will produce alleles that bar interracial matings if the resulting offspring are unfit hybrids. This is an important exception to the general rule that intermixing races will not tend to become separate species because the constant sharing of genes minimizes the genetic diversity requisite for speciation.
Barrowclough, George F.. Speciation and Geographic Variation in Black-tailed Gnatcatchers. (book reviews) The Condor. V94. P555(2) May, 1992.
Rabe, Eric W.. Haufler, Christopher H.. Incipient polyploid speciation in the maidenhair fern (Adiantum pedatum; Adiantaceae)? The American Journal of Botany. V79. P701(7) June, 1992.
Nores, Manuel. Bird speciation in subtropical South America in relation to forest expansion and retraction. The Auk. V109. P346(12) April, 1992.
Abstract:
The climatic and geographic history of the Pleistocene and Holocene periods modified the distribution of the bird population in the South American forests. Forest birds are found dispersed in the Yungas and Paranese areas with only minimal infiltration of the Chaco woodland, indicating an atmospheric change during the interglacial periods. In the Chaco lowlands, the interactions between non-forest birds reveal the existence of presence of a forest belt along the Bermejo and Pilcomayo rivers.
Kondrashov, Alexey S.. Jablonka, Eva. Lamb, Marion J.. Species and speciation. (response to J.A. Coyne, Nature, vol. 355, p. 511, 1992). Nature. V356. P752(1) April 30, 1992.
Abstract:
J.A. Coyne wrongly asserted that neodarwinism includes allopatric evolution but not sympatric evolution. Allopatric evolution occurs among geographically isolated populations, whereas sympatric evolution occurs within one species' entire population. Both are neodarwinian since each results from natural selection of genetic variation. Also, Coyne failed to recognize that the molecular models used to illustrate how genetic changes bring on speciation are most useful when researchers acknowledge that both inherited epigenetic and genetic changes affect speciation.
Spooner, David M.. Sytsma, Kenneth J.. Smith, James F.. A molecular reexamination of diploid hybrid speciation of Solanum raphanifolium. Evolution. V45. P757(8) May, 1991.
Orr, H. Allen. Is single-gene speciation possible?. Evolution. V45. P764(6) May, 1991.
Miller, Julie Ann. Pathogens and speciation. (Research Update). BioScience. V40. P714(1) Nov, 1990.
Barton, N.H. Hewitt, G.M. Adaptation, speciation and hybrid zones; many species are divided into a mosaic of genetically distinct populations, separated by narrow zones of hybridization. Studies of hybrid zones allow us to quantify the genetic differences responsible for speciation, to measure the diffusion of genes between diverging taxa, and to understand the spread of alternative adaptations. (includes related information) Nature. V341. P497(7) Oct 12, 1989.
Wright, Karen. A breed apart; finicky flies lend credence to a theory of speciation. Scientific American. V260. P22(2) Feb, 1989.
Coyne, Jerry A. Orr, H. Allen. Patterns of speciation in Drosophila. Evolution. V43. P362(20) March, 1989.
Feder, Jeffrey L. Bush, Guy L. 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. V43. P1813(7) Dec, 1989.
Soltis, Douglas E. Soltis, Pamela S. Allopolyploid speciation in Tragopogon: insights from chloroplast DNA. The American Journal of Botany. V76. P1119(6) August, 1989.
Coyne, J.A. Barton, N.H. What do we know about speciation?. Nature. V331. P485(2) Feb 11, 1988.
Barton, N.H. Jones, J.S. Mallet, J. No barriers to speciation. (morphological evolution). Nature. V336. P13(2) Nov 3, 1988.
Kaneshiro, Kenneth Y. Speciation in the Hawaiian drosophila: sexual selection appears to play an important role. BioScience. V38. P258(6) April, 1988.
Analysis of contact between two chromosomal races of house mice in northern Italy show that natural selection will produce alleles that bar interracial matings if the resulting offspring are unfit hybrids. This is an important exception to the general rule that intermixing races will not tend to become separate species because the constant sharing of genes minimizes the genetic diversity requisite for speciation.
So is this like saying that a species similar to a human mated with an ape and created humanity
Originally posted by Equinox99
It seems as though animals evolve to gain an advantage to their environment, and this is a continuous process. But now you have to think could there be a force somewhere that changes the animals DNA for the better? That question is an essential one for evolution and religion.
How do animals adapt so quick to changes to their environment? What manipulates affects their DNA so their children are born with the traits?
Originally posted by Myollinir
reply to post by madnessinmysoul
So this proves how humans came to being?
I don't understand how this thread relates to creationism still.
I posed a final question on my first posting here and until that question is ultimately answered, these facts about evolution and speciation only prove their existence and do not dispute creationism in any way.
Have you ever fancied an idea that a creator could have fabricated the motion for evolution to make the universe diverse? Or can it only happen with no creator?
"This Just In: Genetic funnels of flies prove God doesn't exist!!! Score one for science!"
..more or less
Originally posted by uva3021
reply to post by madnessinmysoul
This is just microevolution. I mean its still a fly, just a better version of the same fly. When it gets to the point where the fly has changed a little too much, god will step in and make sure it remains a fly.
This does not prove macroevolution.