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j *@ - Sociedade Brasileira de Psicologia

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V ISUA L SYSTEM O F TH E BEE: LAM INA M O NO PO LA R CELLS<br />

JOHN MANUEL DE SOUZA<br />

Universida<strong>de</strong> <strong>de</strong> Sâo Paulo<br />

The monopolar cels (MC) of the lnmina gansionaris of the optic lobe of the<br />

honeybee constitute the msl'n neural pathway for the relay of visual information from<br />

the photoreceptors to the medula and must play an important role in the codification<br />

of color and other asm cts of vkslnl processing. The importance of the MCs is evi<strong>de</strong>nt<br />

from the neuroanatomy of the 1st optic lobe as <strong>de</strong>scribed by Ribi (1978 , 198 1) using<br />

mas staining teclmiques. The bodies of these MCs are located just proximal to the<br />

basement membrane which separates the retina from the lamina and their axons join<br />

the receptor axon bundles to form the so-caled cartridges which projed into the<br />

medula. n e short visual fibers (blue- and green-sensitive photoreceptors), terminate<br />

witbin the lamina, where their ramifications probably synapse with spines of the MCs.<br />

The three long (UV sensitive) visual fibers also have spines in the lamina but continue<br />

across the outer chinsma to terminate in the distal layeys of the medplla together with<br />

the lamina MCs. ,<br />

Ribi first <strong>de</strong>scribed six different types of lamina MCs (Ribi, 1975) but later<br />

reduced this number to four (Ribi, 1981); a1l four types seem to be present in each<br />

Ortridge.<br />

Nltmerom other neural fibers, tangential, centrifugal and some inœrta sedis<br />

cells, also run between the lamina and the medulla but their configurations su%est<br />

secondary m odulatory or freedback functions. None of these, nor the amacrine cells,<br />

which remain within the lamina, have yet been recor<strong>de</strong>d from as far as is known.<br />

A proper knowledge of the role of the k Cs in codi f y in gan'<br />

d transmitiing<br />

visual signals is thus fundamental to our un<strong>de</strong>rstanding of functioning of the whole<br />

visual system of the honeybee. Due, however, to their slen<strong>de</strong>r axons and to their<br />

relative inaccm sibility, it has been much more difficult to record respom es from MCs<br />

in the bmina than from cels in the retina and in other regions of the optic lobe - the<br />

medula and the lobula. Menzel (1974) recor<strong>de</strong>d with consi<strong>de</strong>rable difficulty from MCs<br />

probably of one type, but was unable to mark them individually perhaps because the<br />

very fi ne ti ps<br />

of the electro<strong>de</strong>s, necessary to penetrate the cels without <strong>de</strong>stroying<br />

them, did not permit succesful injection of the did. Working in his laboratory for 10<br />

weeks in . 1986 l was able to mark and record from some 20 cels (So1zm , Hertel,<br />

Menzel, Venttlra, 1987) using electro<strong>de</strong>s puled on a Cnmp<strong>de</strong>n puler; these electro<strong>de</strong>s<br />

had very rme strongly tapered tips with m uch lower resistances than those pulled on<br />

conventional pulers, thus facilitating die injection. Unfortunately the work, which was<br />

14l

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