No. There is only proof of micro-evolution. A dog changing fur color is not the same as it sprouting an entirely new limb or something of the like (which has yet to be observed).
Animals sprout extra limbs all the time in nature. Some snakes are born with two heads, some cows are born with deformed heads, dual heads, extra eyes, one eye fruit flies can grow extra wings, no wings, a mouth where it's ass should be an ass where it's mouth should be etc etc. Even the Stickleback fish I linked is able to grow and lose a portion of it's body merely by deleting a string of DNA. So yes, a dog changing fur color is the same as it sprouting an extra limb. They're due to some kind of genes being turned off or on or the combination and absorption of twins during the gestation period.
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I get what you're trying to say only because it's the same thing Bored38 was trying to use in earlier arguments in a different way. You're trying to make a point for microevolution and macroevolution being different and they are to an extent. That extent is that macroevoulution to my knowledge and anyone with cited proof can make me look stupid if I'm wrong is the culmination of all the microevoulations of a species until it becomes unable to breed with it's previous incarnation. Meaning it takes thousands of microevolutions over thousands if not millions of years to get to that point where a population is unable to breed with a separate population. Apple Maggot fly is going through the process now. It's broken away from the Hawthorn fly. It no longer shares a common environment, feeds on a separate food source, breeds earlier in the year and it's offspring mature quicker to meet the demands of the Apple trees maturing earlier then the Hawthorns. Most breeding due to environmental crossover is a non-factor and they have to be brought together in a lab to mate. Similar process going on with the Nicaraguan crater lake cichlid fish. I mentioned these two earlier but they were mostly ignored. I also mentioned an example of specialization/macroevoution through chromosome change in plants. This was mostly ignored as well.
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Digby (1912) crossed the primrose species Primula verticillata and Primula floribunda to produce a sterile hybrid. Polyploidization occurred in a few of these plants to produce fertile offspring. The new species was named Primula kewensis. Newton and Pellew (1929) note that spontaneous hybrids of Primula verticillata and Primula floribunda set tetraploid seed on at least three occasions. These happened in 1905, 1923 and 1926.
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Later studies showed that at least one of his elementary species was a tetraploid (see below) and it established itself as a new species in self-fertilizing evening primrose.
All of this is directed at both of the users who are making a case against microevoultion and macroevolution without any citation.