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Ergo Proxy wrote:The reason that they both have prominent dorsal fins is because of convergent evolution. The dorsal fin is absolutely necessary for (large) sea creatures for stability
Net Traveller wrote:What I mean to say is although dolphins and sharks look alike they are not very closely related, one is a fish one is a mammal. I am just curious as to how both wound up with prominent dorsal fins. I mean when I look at drawings of the dolphins ancestors, they had arms, legs and a tal so you can clearly where fins came from, i.e. they evolved from the arms but there is nothing on the animals back that could be considered homologous to a fin. I an just curious.
Ubjon wrote:Your God is just a pair of lucky underpants.
Net Traveller wrote:What I mean to say is although dolphins and sharks look alike they are not very closely related, one is a fish one is a mammal. I am just curious as to how both wound up with prominent dorsal fins. I mean when I look at drawings of the dolphins ancestors, they had arms, legs and a tal so you can clearly where fins came from, i.e. they evolved from the arms but there is nothing on the animals back that could be considered homologous to a fin. I an just curious.
susu.exp wrote:Ergo Proxy wrote:The reason that they both have prominent dorsal fins is because of convergent evolution. The dorsal fin is absolutely necessary for (large) sea creatures for stability
Ever looked at a beluga? Bowhead whale? Northern or Southern right whale dolphin? The Finless porpoise? Narwhal? North Pacific right whale?
Dahn et al, 2007 wrote:The genetic mechanisms regulating tetrapod limb development are well characterized, but how they were assembled during evolution and their function in basal vertebrates is poorly understood. Initial studies report that chondrichthyans, the most primitive extant vertebrates with paired appendages, differ from ray-finned fish and tetrapods in having Sonic hedgehog (Shh)-independent patterning of the appendage skeleton1. Here we demonstrate that chondrichthyans share patterns of appendage Shh expression, Shh appendage-specific regulatory DNA, and Shh function with rayfinned fish and tetrapods2–10. These studies demonstrate that some aspects of Shh function are deeply conserved in vertebrate phylogeny, but also highlight how the evolution of Shh regulation may underlie major morphological changes during appendage evolution.
Coates & Cohn, 1998 wrote:Summary
Current phylogenies show that paired fins and limbs are unique to jawed vertebrates and their immediate ancestry. Such fins evolved first as a single pair extending from an anterior location, and later stabilized as two pairs at pectoral and pelvic levels. Fin number, identity, and position are therefore key issues in vertebrate developmental evolution. Localization of the AP levels at which developmental signals initiate outgrowth from the body wall may be determined by Hox gene expression patterns along the lateral plate mesoderm. This regionalization appears to be regulated independently of that in the paraxial mesoderm and axial skeleton. When combined with current hypotheses of Hox gene phylogenetic and functional diversity, these data suggest a new model of fin/limb developmental evolution. This coordinates body wall regions of outgrowth with primitive boundaries
established in the gut, as well as the fundamental nonequivalence of pectoral and pelvic structures.
Abstract
Detailed examples of how hierarchical assemblages of modules change over time are few. We found broadly conserved phylogenetic patterns in the directions of development within the median fins of fishes. From these, we identify four modules involved in their positioning and patterning. The evolutionary sequence of their hierarchical assembly and secondary dissociation is described. The changes in these modules during the evolution of fishes appear to be produced through dissociation, duplication and divergence, and co-option. Although the relationship between identified median fin modules and underlying mechanisms is unclear, Hox addresses may be correlated. Comparing homologous gene expression and function in various fishes may test these predictions.
The earliest actinopterygians likely had dorsal and anal fins that were symmetrically positioned via a positioning module. The common patterning (differentiation) of skeletal elements within the dorsal and anal fins may have been set into motion by linkage to this positioning module. Frequent evolutionary changes in dorsal and anal fin position indicate a high level of dissociability of the positioning module from the patterning module. In contrast, the patterning of the dorsal and anal fins remains linked: In nearly all fishes, the endo- and exoskeletal elements of the two fins co-differentiate. In all fishes, the exoskeletal fin rays differentiate in the same directions as the endoskeletal supports, indicating complete developmental integration. In acanthopterygians, a new first dorsal fin module evolved via duplication and divergence. The median fins provide an example of how basic modularity is maintained over 400 million years of evolution.
Jehannum wrote:"Convergent evolution" is not satisfactory. It sounds like a shitty answer because it is a shitty answer, as bad as creationist jargon. Anyone who IS satisfied with that as an explanation should be ashamed.
Jehannum wrote:"Convergent evolution" is not satisfactory. It sounds like a shitty answer because it is a shitty answer, as bad as creationist jargon. Anyone who IS satisfied with that as an explanation should be ashamed.
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