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Re: post brought back here in expectation of deletion for no reason

By: Cactus Flower in ALEA | Recommend this post (0)
Fri, 16 Nov 12 10:03 PM | 53 view(s)
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Msg. 11790 of 54959
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very interesting and burgess shaly.

but there you also have the reason i use wings.




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The above is a reply to the following message:
Re: post brought back here in expectation of deletion for no reason
By: DigSpace
in ALEA
Fri, 16 Nov 12 9:57 PM
Msg. 11789 of 54959

For those so inclined:

http://jhered.oxfordjournals.org/content/96/3/171.full.pdf+html

and from a different source (wiki)http://en.wikipedia.org/wiki/Evolution_of_the_eye:

it starts here:

The earliest predecessors of the eye were photoreceptor proteins that sense light, found even in unicellular organisms, called "eyespots". Eyespots can only sense ambient brightness: they can distinguish light from dark, sufficient for photoperiodism and daily synchronization of circadian rhythms. They are insufficient for vision, as they cannot distinguish shapes or determine the direction light is coming from. Eyespots are found in nearly all major animal groups, and are common among unicellular organisms, including euglena. The euglena's eyespot, called a stigma, is located at its anterior end. It is a small splotch of red pigment which shades a collection of light sensitive crystals. Together with the leading flagellum, the eyespot allows the organism to move in response to light, often toward the light to assist in photosynthesis,[17] and to predict day and night, the primary function of circadian rhythms. Visual pigments are located in the brains of more complex organisms, and are thought to have a role in synchronising spawning with lunar cycles. By detecting the subtle changes in night-time illumination, organisms could synchronise the release of sperm and eggs to maximise the probability of fertilisation.[citation needed]
Vision itself relies on a basic biochemistry which is common to all eyes. However, how this biochemical toolkit is used to interpret an organism's environment varies widely: eyes have a wide range of structures and forms, all of which have evolved quite late relative to the underlying proteins and molecules.[17]
At a cellular level, there appear to be two main "designs" of eyes, one possessed by the protostomes (molluscs, annelid worms and arthropods), the other by the deuterostomes (chordates and echinoderms).[17]
The functional unit of the eye is the receptor cell, which contains the opsin proteins and responds to light by initiating a nerve impulse. The light sensitive opsins are borne on a hairy layer, to maximise the surface area. The nature of these "hairs" differs, with two basic forms underlying photoreceptor structure: microvilli and cilia.[18] In the protostomes, they are microvilli: extensions or protrusions of the cellular membrane. But in the deuterostomes, they are derived from cilia, which are separate structures.[17] The actual derivation may be more complicated, as some microvilli contain traces of cilia — but other observations appear to support a fundamental difference between protostomes and deuterostomes.[17] These considerations centre on the response of the cells to light – some use sodium to cause the electric signal that will form a nerve impulse, and others use potassium; further, protostomes on the whole construct a signal by allowing more sodium to pass through their cell walls, whereas deuterostomes allow less through.[17]
This suggests that when the two lineages diverged in the Precambrian, they had only very primitive light receptors, which developed into more complex eyes independently.


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