In each compound eye, each ommatidia consists basically of a system
of lenses that collect and focus the luminance rays; and a sensorial
portion that transforms the luminance energy into an electric
signal. The optical portion of the ommatidia has two elements,
the cornea and the crystalline cone. In a superficial view,
these lenses are seen to be packed to form a typical hexagonal
pattern. the cornea is a biconcave transparent and colorless
cuticular lens, which is produced by the corneagenous cells.
Later on, these cells are displaced to the sides of the ommatidia to
form the primary pigmenting cells. Under the cornea are for
Semper cells. In the eyes with eucone shape, which are present
in the majority of the insects, these cells produce a true
intercellular crystalline cone. In the eyes with acone shape,
the Semper cells do not produce a crystalline cone, but the clear
cytoplasm of these cells take on the role of the lens. The
crystalline cone, or the place occupied by the Semper cells, is
laterally surrounded by the primary pigmenting cells. Under
the crystalline cone of each ommatidia, is found the retinula, which
is usually made up of eight retinular cells.
The rhabdom is the photosensitive portion of each ommatidia.
The rhabdom is formed by the microscopic hairs which are packed
densely and correspond to each retinular cell. These hairs are
located on the internal face of each retinular cell, in the 90
degree angle with relation to the longitudinal axis of the cell.
In the majority of insects, the rhabdomeres of the neighboring cells
are placed in a tight position and interlaced to form a "fused
rhabdom;" while the Diptera, Dermaptera, Hemiptera and other
Coleoptera are separate, forming an "open rhabdom." In the
majority of compound eyes, the retinular cells of each ommatidia are
surrounded by 12-18 secondary pigmented cells. These cells,
just like the primary pigmented cells, contain screen pigments.
The compound eyes can be grouped basically into two big categories:
eyes of apposition and eyes of superposition. In the eyes of
apposition, each ommatidia is optically isolated from its neighbors,
meaning that each rhabdom receives only the rays that enter through
its own focus system, while the rays that enter through the
neighboring facets are absorbed by the pigments of the secondary
pigmenting cells. In the eyes of superposition there is not
such optical isolation. The rays that enter through the
corresponding lenses to its different ommatidia are focused in a
unique rhabdom. This is possible because these eyes have
a "clear zone," free of pigmentation, between the crystalline cone
and the rhabdom; and because the rhabdom is restrained from the
proximal portion of the retinular cells.
As a general rule, we can say that the eyes of apposition are common
in the arthropods that are active in very illuminated environments.
The eyes of superposition, typically, are found on the insects and
crustaceans of nocturnal habits; or on those that live in poorly
illuminated environments. However, both cases have more than
few exceptions.
Both types of eyes present variations in structure as well as in the
size of the components of the ommatidia. This has given room
for a great diversity of designs for compound eyes: of simple
apposition, open rhabdom, afocal, with neural superposition, of
refraction superposition, reflection and parabolic.
The term adaptation, in a broad sense, denotes those events that
through a change in the structure, form, function or behavior of
organisms, result in a better adjustment to the environmental
conditions. These adjustments, besides happening in an
evolutionary sense, happen in individual organisms. The annual
rhythms of migration, Diapause, etc are adaptations to the cycles of
weather variations; while the daily rhythms are examples of the
adaptation phenomena that happen in a few hours. But the
environmental conditions can change in much shorter periods and are
unpredictable. The sensory organs are capable of adapting very
quickly to the changing conditions of the environment.
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