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Colour
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cones do?
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1.
Colour vision and communication in aquatic environments
"Even
more mysterious are the 'double cones' - and the puzzle they present is
particularly irritating to the curious investigator because they are so
very widespread among vertebrates" Walls 1942.
a.
The mysterious function of the most abundant daytime photoreceptor: What
do double cones do?
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Vertebrate
retinae are often called 'duplex'
because they consist of two types of photoreceptor cells, rods
and cones.
In
general, cones are used for vision in daytime and rods for vision
at night. Cones can be further subdivided into two types based
on anatomy and/or physiology: single cones
and double cones.
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Double
cones are found
in most vertebrate groups, with the exception of placental mammals
(including humans), sharks and catfish, and are frequently the
most abundant cone type in their retinae. In many reef fish, for
example, double cones make up over 75% of the retina. Their function
in any animal is, however, still as 'mysterious' as it was in
1942. Using a model system of reef fish we aim to clarify the
function or functions of double cones in fish and other vertebrates.
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Examples
of three different types of photoreceptor mosaic from
reef fish.
The
first retina (left) is dominated by rods, whereas the
other two are dominated by double cones as typically seen
in fish.
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Sixty
years after the exasperation expressed by Walls, the function
or functions of double cones still remains elusive. Solving the
problem of double cone function would represent a significant
advance in our understanding of the vertebrate retina, from both
a functional and evolutionary perspective. Discovering why they
are so important in fish will also allow us to understand why
placental mammals have lost them, what has taken their place functionally
in mammals and why the other large fish group, the elasmobranchs
(sharks and allies) lack double cones.
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The
retinae of reef fish are dominated by double cones. Why
is this the case when they are not evident in the other
large marine fish group (elasmobranchs) or placental mammals
such as humans?
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Our
aim will be achieved by testing the following hypotheses:
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- Is there a single function for double
cones in all species, e.g. luminance vision, or do double
cones have different functions in different species, e.g.
luminance vision in fish A as opposed to colour vision in
fish B?
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Do double cones have multiple / parallel functions within
the same animal, e.g. colour discrimination and luminance
vision in fish C, and if so how does the neural wiring function
to achieve this?
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Are the spatial arrays or 'mosaics', of double cones related
to function , e.g. polarisation sensitivity or luminance vision?
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Are the specific functions of double cones determined by /
adapted to the visual environment? Different eye regions frequently
possess different types and densities of double cone mosaic
suggesting this is likely but nothing is proven.
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Does the nature of photoreceptor coupling, horizontal cell
connections, ganglion cell density and other post-photoreceptor
processing vary with double and single cone complement and
the spatial organization of double cones in the retina.
To
read more about the project click
here.
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Last
updated: March 2007 by Janine
Bertler
Vision
Touch and Hearing Research Centre
School of Biomedical Sciences
University of Queensland
Brisbane
Queensland 4072 Australia
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