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Author Topic:   Should the term species be used?
RAZD
Member (Idle past 1434 days)
Posts: 20714
From: the other end of the sidewalk
Joined: 03-14-2004


Message 3 of 24 (598065)
12-27-2010 6:05 PM
Reply to: Message 1 by wolfwing
12-27-2010 2:03 PM


Hi wolfwing
The term species works, but in reality looking at long time, it doesn't exist. We've found many fossils of various animals, and call some species like T-rex, triceratops and so on, but in reality what were seeing is a snapshot of a continual line of animals. We have species today, but what were seeing is a snapshot of the animal lines that exist today.
One of the things to consider is the difference between species identified by speciation events - where a parent population divides into two or more daughter populations that have become reporductively isolated - and species identified by arbitrary comparison of traits - as in the gradual change of species along a lineage.
Or even a line, say mine all the way back to the common ancestor of chimps ...
That would be a speciation event that divide the populations between chimp ancestors and human ancestors.
... and us, taking a section of the timeline you could say this was say aferensis, and this section past it is the next species.
That would be the arbitrary speciation designations along a lineage.
A good visual example of this difference is found in Pelycodus evolution:
A Smooth Fossil Transition: Pelycodus
quote:
The dashed lines show the overall trend. The species at the bottom is Pelycodus ralstoni, but at the top we find two species, Notharctus nunienus and Notharctus venticolus. The two species later became even more distinct, and the descendants of nunienus are now labeled as genus Smilodectes instead of genus Notharctus.
As you look from bottom to top, you will see that each group has some overlap with what came before. There are no major breaks or sudden jumps. And the form of the creatures was changing steadily.
The division shown is a speciation event, and as you look at the lineage you will see several arbitrary speciation designations to differentiate the morphological changes (including size) as they trend from the bottom to the top.
You will also see that the overall trend from Pelycodus ralstoni at the bottom to Notharctus venticolus at the top right has a gradual "trendency" of increasing size with time, but that the divergence of Notharctus nunienus from that trendency occurs at a greater rate of change. This likely occurs for two reasons: (1) the original ecological niche of Pelycodus ralstoni still exists, providing an open opportunity for a smaller species, and (2) the separation in habitat\ecology is necessary to reduce competition between the daughter species (without it one species will likely drive the other to extinction or being reabsorbed - as you can see occurred between Pelycodus trigonodus and Pelycodus jarrovii when an earlier shift to the left shows up, then dissappears).
Reason I say this is that as we keep finding with animals alive now, there really isn't any easily defined definition of species even using animals alive, what many would consider a species, like lions/leopards/tigers can still interbreed and ocasionally produce reproductive capable offspring.
There is a difference between animals that can be made to interbreed in captivity, and what animals chose to do in the wild. If the mating signals are all wrong between daughter populations, they will not chose to mate whether they are capable of doing so or not.
A good example of this is the ring species, the Asian Greenish Warbler:
Greenish warblers
quote:
Greenish warblers (Phylloscopus trochiloides) inhabit forests across much of northern and central Asia. In central Siberia, two distinct forms of greenish warbler coexist without interbreeding, and therefore these forms can be considered distinct species. The two forms are connected by a long chain of populations encircling the Tibetan Plateau to the south, and traits change gradually through this ring of populations. There is no place where there is an obvious species boundary along the southern side of the ring. Hence the two distinct 'species' in Siberia are apparently connected by gene flow. By studying geographic variation in the ring of populations, we can study how speciation has occurred. This unusual situation has been termed a 'circular overlap' or 'ring species'.
The mating songs and the plumage are sufficiently different at the overlap that the two populations remain reproductively isolated, yet the hybrid zones between each of the pairs of varieties as you go around the ring from one end to the other show that in these zones the mating songs and the plumage do not prevent or inhibit interbreeding, because they are still recognized as being potential mate material.
Also see Definition of Species
Plus it gets hung up on the creationists term Kind and get into semantic arguments.
In my humble (or not so much) opinion, the best comparison with the creationist "kind" is with clade, from cladistics, as all descendants are members of the same clade\kind.
Species is useful in clarifying what we are talking about, but should also be taken with a grain of salt.
Enjoy.

we are limited in our ability to understand
by our ability to understand
Rebel American Zen Deist
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This message is a reply to:
 Message 1 by wolfwing, posted 12-27-2010 2:03 PM wolfwing has seen this message but not replied

Replies to this message:
 Message 12 by New Cat's Eye, posted 12-28-2010 3:00 PM RAZD has replied

  
RAZD
Member (Idle past 1434 days)
Posts: 20714
From: the other end of the sidewalk
Joined: 03-14-2004


Message 24 of 24 (599697)
01-09-2011 9:04 PM
Reply to: Message 12 by New Cat's Eye
12-28-2010 3:00 PM


Hi Catholic Scientist,
To me, it looks like the smaller version was "trying" to split off a few times over and over again and then finally found a niche where it worked.
Any ideas on what could be driving that? Doesn't look very random...
I agree that there are several instances here that can at first glance appear to be populations "trying" to evolve.
Think of evolution as the change in frequency of hereditary traits in breeding populations from generation to generation in response to ecological opportunities.
There appears to be an ecological opportunity for the evolution of gradually larger individuals within the breeding population (see Cope's rule)*, but that a broad spectrum of sizes, extending back to the original size, cannot be supported (perhaps the smallest survive quite well, but have low reproductive success).
This gradual trend for larger individuals leaves behind an opportunity for a smaller population, and several excursions are made, along with a staggering back and forth in size in the overall trendency, but it is not until that smaller population can become reproductively isolated from the larger population that the branching allows both survival and breeding success for the smaller population.
Enjoy.
* Cope's rule is named after E.D. Cope, and interestingly (to me) there is another reference with this graphic of the same fossil graphic with additional data:
Here you will see fossils of the smaller Copelemur genus that appears to have paralleled or branched off from Pelycodus, with Copelemur named for Cope. Ironically, the Copelemur get smaller here.
Edited by RAZD, : ...

we are limited in our ability to understand
by our ability to understand
Rebel American Zen Deist
... to learn ... to think ... to live ... to laugh ...
to share.


Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click)

This message is a reply to:
 Message 12 by New Cat's Eye, posted 12-28-2010 3:00 PM New Cat's Eye has not replied

  
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