The Localization of Function in the Root of an insect Segmental Nerve

1963 ◽  
Vol 40 (3) ◽  
pp. 553-562
Author(s):  
ANN FIELDEN

1. The roots of the segmental nerves in nymphs of Anax imperator originate from separate dorsal and ventral tracts in the ganglionic neuropile. 2. Axons forming the dorsal part of the nerve root can sometimes be traced to ganglion cells and tend to be large and thick-walled compared with the ventral axons which are smaller and thin-walled. 3. In the roots of the fifth nerves of the last ganglion the two parts can be separated by dissection. Recording from each part under various conditions of stimulation shows that sensory activity occurs predominantly in the ventral part of the nerve root whilst motor spikes are recorded almost entirely from the dorsal part. 4. It is concluded that there is a functional localization of motor and sensory fibres in the root of an insect nerve comparable to that in the dorsal and ventral roots of vertebrate nerves.

1966 ◽  
Vol 14 (3) ◽  
pp. 277 ◽  
Author(s):  
K Periasamy

The median dorsal strand is the first to differentiate in Cocos, Phoenix, and Caryota. It traverses the terminal abaxial ridge of the plications, to end at the apex of the non-plicate margin of the lamina wing. The series of strands that afterwards differentiate tangentially on either side of it form the first vasculature of the adaxial ridges of the plications, and are termed "primary strands". In Borassus, the median dorsal strand differentiates only after 5-10 pairs of primary strands are differentiated. In Cocos and Borassus, each primary strand traverses one adaxial ridge; hence the primary strands are more or less equal in number to the pinnae in Cocos and the segments in Borassus. In Phoenix, each primary strand executes an almost right-angled, adaxial curve at its tip and branches dichotomously into two to four branches, each traversing a line parallel to an adaxial ridge, in the "haut" formed by the fusion of the adaxial ridges with each other. Therefore the primary strands are characteristically fewer than the pinnae. In addition to the branches that vascularize the haut, the primary strands make connections later with some of the strands of the pinnae that differentiate in the lamina. When the haut is shed, those parts of the branches of the primary strands situated in the haut are lost, leaving the primary strands connected to the laminar strands alone. In Borassus, during dissection of the palmate lamina, those parts of the primary strands situated in the apical halves of the adaxial ridges are constricted, along with the surrounding ridge, and shed. In the basal half of the adaxial ridge, the primary strand makes connections with other neighbouring strands of the lamina. In Caryota, the primary strands are comparatively few, since the primary plications are few. The strands formed adaxial and abaxial to the tangential row of primary strands are irregularly disposed, and are termed the adaxiai and abaxial complexes respectively. These strands vascularize the rest of the lamina, and also the adaxial ridges. The strands of the adaxial complex of Cocos are inversely oriented. The primary strands extend to the thin ventral part of the sheathing base in Cocos, Borassus, and Caryota, but are confined to the thick dorsal part in Phoenix. The oblique courses of the strands on the two sides of the median ventral line of the sheath as mirror images of one another, and their spatial and temporal sequence of differentiation along two different transverse depths, account for their remarkable interlocking as "warps and wefts" along the median ventral line. The primary strands differentiate acropetally. The adaxial and the abaxial strands show acropetal, basipetal, or discontinuous differentiation in different parts of the leaf. Although the basic pattern of vasculature seen in the younger stages does not change, the vasculature of the mature leaf becomes very complex by the formation of numerous additional bundles and branches, and their anastomoses, especially in the sheath and rachis.


1998 ◽  
Vol 96 (2) ◽  
pp. 185-190 ◽  
Author(s):  
Jørgen Drasbæk Schiønning ◽  
Jytte Overgaard Larsen ◽  
Rune Eide

2019 ◽  
Author(s):  
Alice Ciofini ◽  
Luca Mercatelli ◽  
Yumi Yamahama ◽  
Takahiko Hariyama ◽  
Alberto Ugolini

AbstractThe crustacean Talitrus saltator is known to use many celestial cues during its orientation along the sea-land axis of sandy shores. In this paper, we investigated the existence of the eye regionalization by morphological, electrophysiological and behavioural experiments. Each ommatidium possesses five radially arranged retinular cells producing a square fused rhabdom by R1-R4 cells; the smaller R5 exist between R1 and R4. The size of R5 rhabdomere is largest in dorsal part and becomes gradually smaller in median and ventral part of the eye. Spectral-sensitivity measurements were recorded from either dorsal or ventral parts of the compound eye to clarify the chromatic difference. Results show that the dorsal part is green and UV-blue dichromatic, whereas the ventral part is UV (390 nm) with a substantial population of 450 nm receptors with the responses in the longer wavelength region. To evaluate the orienting behaviour of individuals, their eyes were black painted either in the dorsal or ventral part, under natural sky or a blue filter with or without the vision of the sun. Results show that animals painted on the dorsal part of their eyes tested under the screened sun were more dispersed and in certain cases their directions deflected than other groups of individuals. Furthermore, sandhoppers subjected to the obscuring of this area met in any case high difficulties in their directional choices. Therefore, our present work indicates the existence of a regionalization of the compound eye of T. saltator.Summary statementThis work provides evidences of the morphological and electrophysiological regionalization of the compound eye and the visual capabilities for behaviour involved in the recognition of the celestial compass orienting factors in crustaceans.


Zootaxa ◽  
2021 ◽  
Vol 4933 (2) ◽  
pp. 277-288
Author(s):  
MAURICE KOTTELAT

‘Nemacheilus’ argyrogaster, new species, is described from the Xe Kong, Mekong drainage, in Attapeu and Xe Kong provinces, southern Laos. It is distinguished from all other Nemacheilidae in Southeast Asia by its unique colour pattern made of a bold black midlateral stripe separating the yellowish brown dorsal part of the body from the silvery whitish ventral part and a middorsal row of 14–19 thin saddles. Besides, the male has a globulous suborbital flap with tubercles along its free, posterior edge, and the pectoral fin with thickened anterior ray and branched rays 1–4 and unculiferous pads behind them covered by small tubercles; lips thin, lower lip continuous with a narrow median notch. It was found in moderate to fast flowing water, over pebble to stone bottom. ‘Nemacheilus’ argyrogaster, was earlier misidentified as N. longistriatus; it is provisionally placed in the genus Nemacheilus. 


The stellate ganglion of cephalopods is sharply divided into a ventral part containing only large cells and a dorsal part where there are also microneurons (amacrine cells). Axons proceed from the larger cells of the ganglion to the stellar nerves in distinct dorsal and ventral roots, which join as they leave the ganglion. The ventral roots contain only large motor fibres, one arising from each of the 30000 ventral cells. The input to this part is from less than 2000 large fibres of the pallial nerve. These fibres branch abundantly in the ventral neuropil. After severing the pallial nerve massive degeneration occurs there, producing shrinkage of the whole ganglion. There is also degeneration in the dorsal neuropil, which therefore also has input from the pallial nerve. The dorsal roots contain some large fibres, being the axons of the larger dorsal cells. In addition, they contain numerous small fibres. These include efferent chromatophore fibres, which degenerate after severing the pallial nerve and therefore pass through the ganglion presumably without synapse. There are also afferent fibres from the periphery in the dorsal roots and, after severing stellar nerves, degeneration appears in the outer layers of the dorsal neuropil and in the pallial nerve. No degeneration occurs in the central stumps of the ventral roots after this operation. The trunks of the small cells of the dorsal part form characteristic bundles of fine fibres in the outer dorsal neuropil and dorsal roots. These bundles carry varicosities and make plexuses in the bases of the dorsal roots, intertwined with collaterals of the outgoing large fibres and branches of the incoming afferents from the periphery. Probably these microneurons terminate within the ganglion and are concerned with reflex modulation of the output of the dorsal neuropil. The arrangement of the dorsal and ventral divisions of the ganglion and roots of the stellar nerves is similar in Sepia and Loligo to that in Octopus. There are more numerous large terminal knobs in the neuropils of these decapods and these endings are also found within the cell layers, especially in the hind part of the dorsal region. The course of degeneration within the ganglion was followed after section of the pallial and stellar nerves in all three species, more in detail in Octopus. Degeneration of terminations is already advanced 15 h after severing the pallial nerve (at about 24 °C); break-up within the nerve trunks comes later. Degeneration granules have mostly disappeared 3 days after the lesion. Severed stellar nerves of Octopus show very abundant sprouting from the central stump, the fibres turning back to invade the ganglion and form terminal knobs in the neuropil and throughout the cell layers.


1970 ◽  
Vol 48 (2) ◽  
pp. 293-295 ◽  
Author(s):  
Susan McIver ◽  
Christel Charlton

Four structures are found on the maxillary palps of female culicine mosquitoes: microtrichia, scales, sensilla chaetica, and thin-walled, bulb-shaped organs. The bulb organs are localized on the distal half of the ventral part of palpal segment 4, have perforated walls, are carbon dioxide receptors (Kellogg, in press), and vary in number among the species from 29/palp on Aedes aegypti to 89/palp on Culex restuans. An explanation for observed behavioral responses to carbon dioxide is given.


To describe the ganglion-cells of the Mammalian spinal cord as confined to the grey substance of the cord is not quite strictly correct. Beisso was the first to draw attention to the fact, that apart from axis-cylinder processes which pass into the ventral roots from cells of the ventral cornu, there project also from those cells of the cornu which lie next the white column other branches to mingle with the fibres of the bundles of the ventral nerve-roots. The ganglion-cells of the grey matter often, by one or more of their processes, jut partially into the white matter. The descriptions of Beisso, Pick, and Schiefferdecker have further shown that in certain situations in the anterior and lateral columns, ganglion-cells lie outside the grey substance in the surrounding white matter. Since Gaskell, in 1885, drew attention to the ganglion-cells in the cord of Alligator, lying at the periphery of the antero-lateral column, and, of course, quite removed from the central grey matter, I have often searched in the cord of the Mammalia for evidence of similarly situated cells; always, however, without success. The search has, however, persuaded me that isolated ganglion-cells are no infrequent constituents of the white columns. The cords examined by me have been chiefly those of Man, the Monkey (Bonnet, Jew, and Rhesus), and the Dog. A number of sections have also been prepared from the Cat, Lion, Calf, Bat, Mouse, Rabbit, and Guinea-pig. The out-lying ganglion-cells in the white matter may conveniently be considered in three sections, according as their situation is within the anterior (ventral), the lateral, or the posterior (dorsal) white column respectively.


2006 ◽  
Vol 60 (1-2) ◽  
pp. 107-114
Author(s):  
Slavca Hristov ◽  
Sreten Mitrovic ◽  
Mirjana Todorovic ◽  
Vladan Djermanovic ◽  
Ivica Cvetkovic

The paper examined the incidence of different forms of feather loss and cannibalism in laying hens aged 74 weeks following moulting and in laying hens following exploitation for a period of one year. The forms of feather loss were considered in detail through a repeated examination of video recordings and they were sorted according to localization - to feather loss on the ventral part of the neck, on the dorsal part of the neck, and on the back between the wings. Feather loss on the ventral part of the neck was established in 47.9% hens, and in the dorsal part in 16.77% hens of the 167 laying hens aged 74 weeks following moulting. The group of 129 laying hens that were observed following one-year exploitation exhibited considerably more frequent feather loss, in 96.90% hens it was localized on the ventral part of the neck, in 60.47% hens on the dorsal part of the neck, and in 20.16% hens it was localized on the back between the wings. A comparison of the results of the incidence of co localized forms of feather loss in the one and the other group of laying hens using the t-test showed statistically very significant differences. A detailed consideration of the video recordings using the method of sequence analysis did not reveal any cannibalism in either group of laying hens.


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