The embryology of Dacus tryoni (Diptera). 3. Origins of imaginal rudiments other than the principal discs

Development ◽  
1964 ◽  
Vol 12 (1) ◽  
pp. 65-75
Author(s):  
D. T. Anderson

In addition to the principal imaginal discs (cephalic, labial, wing, haltere, leg and genital), the larva in Cyclorrhapha carries as discrete components the rudiments of the imaginal segmental abdominal hypodermis, salivary glands, fore-, mid- and hind-gut, lateral cerebral ganglia and segmental tracheal system (Snodgrass, 1924; Bodenstein, 1950; Shatoury, 1956b; Anderson, 1964, etc.). The embryonic origins of these rudiments have never been firmly established. The present paper describes their origins in the embryo and larva of Dacus tryoni (Frogg.) (Trypetidae), taking a further step in the elucidation of the developmental relationship between the cyclorrhaphan larva and adult. Material and Methods The embryonic origins of the rudiments in question were traced in serial sections of embryos and larvae prepared by the methods described by Anderson (1962a, 1963b). The reader is referred to these papers for details of the methods employed.


Development ◽  
1963 ◽  
Vol 11 (2) ◽  
pp. 339-351
Author(s):  
D. T. Anderson

The cephalic, labial, wing, haltere, leg and genital imaginal discs of Cyclorrhapha are histologically distinct in the late embryo or early larva (Weismann, 1864; Pratt, 1900; Auerbach, 1936; Kaliss, 1939; Poulson, 1950). Experimental investigation of Drosophila melanogaster further suggests that the determined rudiments of the discs are present in the blastoderm of the early embryo (e.g. Geigy, 1932; Howland and Child, 1935; Howland, 1941; Gloor, 1947). Almost no attempt has been made, however, to describe the embryonic origins of the discs or to follow their development before hatching. Investigation of this matter in Dacus tryoni (Frogg) (Diptera, Trypetidae) has clarified the developmental relationship between the cyclorrhaphan larva and adult. The origin and development of imaginal discs in the embryo of D. tryoni was followed from serial sections prepared in connection with a previous paper (Anderson, 1962). Living embryos were also further examined by the method given in that account.



2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Surman Arya ◽  
Suneel Kumar Singh

The digestive and tracheal system of a poultry shaft louse, Menopon gallinae (Phthiraptera: Amblycera) has been studied in greater details. Alimentary canal of louse was dissected out along with crop under stereozoom binocular microscope. Entire alimentary canal of M. gallinae was found more or less straight and has three basic parts (fore-gut, mid-gut and hind-gut) while crop-teeth was present in the crop. The posterior end of crop contains 20-30 well developed crop-teeth arranged in a single arced plate, in comb-like fashion. Mid-gut was found as simple tube and contributes nearly one half of the total length, while the hind-gut was marked by the opening of Malpighian tubules in alimentary canal. The heart of M. gallinae is of simplest kind, one chambered bulbous structure having three pairs of laterally placed ostia and supported by four pairs of alary muscles. In the tracheal system there were seven pairs of spiracles occurred on the terga of M. gallinae. The first pair of spiracle was found located close to legs while remaining six abdominal spiracles occur from segment 3rd to 8th. The degree of tracheation of various visceral organs has also been noted.



Development ◽  
1957 ◽  
Vol 5 (2) ◽  
pp. 134-142
Author(s):  
H. H. El Shatoury ◽  
C. H. Waddington

This paper is concerned with certain aspects of the development of the mid-gut (stomach), hind-gut, and salivary glands of Drosophila larvae. Attention will be particularly concentrated on two types of phenomenon, firstly, on periodic processes of hypertrophy and regression which affect certain of the larval tissues comprising these organs, and, secondly, on the development of groups of imaginal cells which, at metamorphosis, produce the tissues from which the adult organs are built up. There is evidence that in the control of both these processes an important part is played by the lymph glands. This evidence is derived primarily from the study of certain lethal mutant types which will be described in a later communication (Shatoury & Waddington, 1957b). In these lethals it is found that abnormality of the lymph glands is associated with and appears to be the cause of excessive hypertrophy of the larval cells composing the gut.



Development ◽  
1957 ◽  
Vol 5 (2) ◽  
pp. 143-152
Author(s):  
H. H. El Shatoury ◽  
C. H. Waddington

It has been shown that in the normal development of wild-type Drosophila larvae, a process of hypertrophy or proliferation leading to the formation of groups of non-nucleated cellular masses occurs in the mid-gut (stomach) and at the imaginal primordia of the hind-gut and the salivary glands in both the first and second instars (Shatoury & Waddington, 1957b). The process takes place just at the time when the lymph glands hypertrophy and release cells into the body-cavity and the excessive growths of the organs of the alimentary tract regress and are resorbed as soon as the lymph glands become regenerated. The appearances strongly suggest that there is a causal connexion between the proliferation of the lymph glands cells and the hypertrophy which occurs in the gut and salivary glands.



1985 ◽  
Vol 108 (1) ◽  
pp. 130-134 ◽  
Author(s):  
Seiki Ito ◽  
Toshimitsu Suzuki ◽  
Takeshi Momotsu ◽  
Satoko Isemura ◽  
Eiichi Saitoh ◽  
...  

Abstract. An indirect immunofluorescence technique using antisera aganist salivary peptide P-C and against salivary Protein C was carried out on the laryngeal, tracheal and bronchial glands to examine whether salivary peptide P-C-like immunoreactivity, recently demonstrated in the serous cells of the human salivary glands, was also present in those of laryngeal, tracheal and bronchial glands and to ascertain whether salivary peptide P-C is a fragment of salivary Protein C or not. Salivary peptide P-C-like immunoreactivity was present in the serous cells of the human laryngeal, tracheal and bronchial glands. Observation of serial sections immunostained with two kinds of antisera revealed that cells reacting with antisera against salivary peptide P-C were identical to those reacting with antisera against salivary Protein C pre-incubated with salivary peptide P-C. The finding implied that salivary peptide P-C and salivary Protein C, originally isolated from human saliva, were also present in the serous cells of tissues other than the salivary glands. Furthermore, analysis of the primary structure of salivary peptide P-C and salivary Protein C together with the present morphological finding suggests that salivary peptide P-C is a COOH-terminal fragment of salivary Protein C. Thus, salivary Protein C and salivary peptide P-C may play some role in the function of the serous cells of the salivary and laryngo-tracheobronchial glands.



Parasitology ◽  
1924 ◽  
Vol 16 (2) ◽  
pp. 164-213 ◽  
Author(s):  
Leslie G. Saunders

(1) Forcipomyia is one of the few genera of the Ceratopogoninae (Chironomidae) whose larvae are not aquatic. They retain, however, the apneustic condition typical of the entire family, and are therefore compelled to live in moist places such as beneath the rotting bark of fallen trees, in the hollow tap roots of dead plants, in wounds and rot holes in trees, in drying horse and cow manure, in decaying fungi, and in the nests of ants. The immature forms are strongly gregarious.(2) The larvae pass through four stages, each lasting about a week; the successive changes in chaetotaxy at each moult is recorded in the discussion of F. picea. All known European species of this genus hibernate as third or fourth stage larvae. The duration of the pupal stage is about one week; the length of life of the adult has not been determined. There are usually three generations per annum. The adults are known to suck the blood of other insects.(3) The larvae are eucephalous, more or less cylindrical, 3–6 mm. long, with eleven clearly denned segments (three thoracic and eight abdominal, the eighth divided into two apparent segments). Progression is achieved by means of a retractable, biramous, prothoracic pseudopod, and a ventral hook-studded ridge on the ultimate abdominal segment, with the occasional aid of the mandibles.(4) The head and body bear numerous lanceolate and simple hairs of great specific importance.(5) The mouth-parts consist of a fleshy labrum, a pair of small premandibles, a pair of long, slender mandibles working in the sagittal plane on either side of the labrum, a pair of reduced maxillae of fleshy nature with chitinous internal supports, and a simple untoothed labium. Within the head there is a complicated chitinous structure, the hypopharynx; this is figured and described in full detail and its action in comminuting the food is revealed for the first time.(6) No investigation has hitherto been made of the internal anatomy. The alimentary canal, consisting of buccal cavity, hypopharynx, oesophagus, mid-gut, and hind-gut, is quite simple in structure, without nodules or caecal chambers. It is only slightly longer than the body, a loop occurring in the hind-gut when the larva contracts.(7) The malpighian tubules are either two or three in number, the latter condition being unique among insects. The third is ventral, passing into the posterior part of the body only.(8) The salivary glands are a pair of S-shaped bodies closely adhering to the walls of the anterior portion of the mid-gut; they are chiefly composed of large binucleate cells.(9) The circulatory system consists of a dorsal vessel extending throughout the body and passing between the lobes of the brain above the oesophagus into the head. In the eighth abdominal segment it enlarges slightly to form the heart, with one pair of ostia or valves situated on its posterior extremity.(10) The nephrocytes are arranged segmentally, four to each abdominal segment and a single mass in the thorax, all attached to the dorsal vessel. The excretory function of these cells was demonstrated by injection of ammonia-carmine into the body cavity.(11) The nervous system is only very slightly cephalised, there being seven ganglia for the eight abdominal segments and three in the thorax; the normal bilobed brain is situated in the thorax in all larval stages. The sympathetic system is described, and differs somewhat from that of its close relative, Chironomus.(12) Despite the absence of spiracles there is a well-developed tracheal system in the form of two main trunks with transverse connections, branch tracheae, and subcutaneous plexuses.(13) The muscular system, oenocytes, fat-body, and gonads have also been studied in detail.(14) The larval skin is retained upon the last four or five abdominal segments of the pupa.(15) The characters used for determining the species, in their order of importance, are as follows: Larva: chaetotaxy, prothoracic pseudopod, markings of the head, anal blood-gills. Pupa: cuticular spines, prothoracic horns.(16) The larvae and pupae of nine species of Forcipomyia are described with particular reference to their specific characters. Descriptions of the adults of two new species, F. radidcola and F. pulchrithorax, by Mr F. W. Edwards, are appended.(17) Closely related forms are Euforcipomyia and other exotic subgenera not yet named, and the genus Atrichopogon (now including Kempia). Dasyhelea belongs to this group of hairy-winged flies, but its larvae partly resemble those of the bare-winged Ceratopogonines in that they have lost the pro-thoracic pseudopod and macrochaetae, but retain the anal hooks.



1934 ◽  
Vol s2-77 (306) ◽  
pp. 273-304
Author(s):  
W. H. THORPE

1. In a previous paper was described the life-history of Cryptochaetum iceryae parasitic on Icerya purchasi, an Australian species introduced into California. It was shown that the genus is highly specialized for life as a parasite, and that it represents a separate and restricted line of evolution of parasitic habits among insects. The present study concerns Cryptochaetum grandicorne which is probably confined to the Mediterranean region, and which is the only species of the genus known to occur in Europe. The two species show notable differences in structure and life-history although both are highly adapted to a parasitic mode of life. 2. The very minute eggs are laid in the haemocoel of the host. The egg hatches to form a short-lived ‘embryo-larva’ at first atracheate and showing no trace of external segmentation. Mouth parts are present although the fore-gut is closed, food materials presumably being absorbed by diffusion from the blood of the host. 3. The second stage larva is tracheate but apneustic. Segmentation is complete. The fore-gut is now open but the hindgut remains closed. The food consists of the blood and fat-body of the host. 4. The third stage larva is omnivorous devouring the internal organs of the host indiscriminately and the hind-gut is open. The tracheal system is amphipneustic. A few days after the commencement of the instar the posterior spiracles pierce the skin of the host and establish connexion with the atmospheric air. The puparium is formed within the dead body of the host. 5. As in Cryptochaetum iceryae the larva is supplied with a pair of long tubular caudal filaments, lobes of the bodywall containing blood and tracheae, which arise from the posterior segment and ramify among the organs of the host. Experiments indicate that they serve to increase the surface area available for respiratory exchange between the larva and the blood of the host. They are also readily permeable to water. 6. Although a large number of eggs may be placed within a single host, only one reaches maturity. 7. The highly specialized ovipositor is described in detail since it appears to be a striking adaptation to a parasitic mode of life, and cannot be derived directly from the rasping ovipositor of the Agromyzidae. 8. In South Italy as in South France there is one generation per year, the life-history of the parasite being closely correlated with that of the host. 9. Special attention is paid to those features in which grandicorne differs from iceryae and the significance of these differences is discussed.



1907 ◽  
Vol s2-51 (203) ◽  
pp. 395-448
Author(s):  
C. GORDON HEWITT

1. The exoskeleton of the head capsule and of the pharynx is described in detail; the relations of the parts in the terms generally employed by dipterologists to the morphological divisions of the insect head capsule are shown. On morphological grounds, the view that the distal portion of the proboscis represents the modified second maxillar or labium is adopted, as opposed to that of a first maxillar derivation put forward by Lowne for the blowfly. 2. After a detailed description of the external and internal skeletal structures of the thorax, the neuration of the wings is described in the terms proposed by Comstock and Needham in their valuable memoir; and to facilitate their more general adoption for the wings of the Muscidas and other Diptera, a comparison is made between their nomenclature and the several systems employed in describing the muscid wing. 3. The abdomen is shown to consist of eight segments in the male and nine in the female, in both cases the first five segments form the visible portion of the abdomen; the external genitalia of the two sexes are described under another section. 4. As the muscular system does not differ from that of Volucella described by Kunckel d'Herculais and the blowfly described by Hammond and Lowne, it is briefly described. The cephalic muscles, however, are fully described in the detailed description of the head (V). 5. The nervous system, which is of the normal muscid type, is described, but for the sake of clearness a very detailed description of the composition of the cephalic ganglion is not given. The structure of the optic tract is similar to that of the blowfly as described by Hickson. The structure of the thoracic nerve-centre is found to differ slightly from that of the blowfly as described by Lowne. 6. The alimentary canal is similar in its structure to those of Stomoxys and Glossina, only differing in a few details. The mesenteric region, which is represented by the ventriculus or chyle, stomach, and proximal intestine, is well developed. The lingual salivary glands, rectal glands, and Malpighiau tubes are described; the function of the rectal glands is believed to be of an excretory nature. 7. As the tracheal systems of the Diptera have not received much attention a detailed account of the tracheal system is given. There are two thoracic spiracles, the first of which supplies the whole of the head, the anterior and median regions of the thorax and the three pairs of legs, and by means of a pair of large abdominal air-sacs a large part of the viscera. The posterior thoracic spiracle supplies the muscles of the median and posterior region of the thorax, especially the large dorsales muscles. There are seven pairs of abdominal spiracles in the male and five pairs in the female all of which are connected with tracheae only. 8. The dorsal vessel or heart is found to consist of five incomplete chambers, each with a pair of ostia. The anterior end is continued forwards along the dorsal side of the ventriculus, and terminates in a glandular mass in the anterior margin of the proventriculus. 9. The reproductive organs of the male are simple, consisting of a pair of testes, vasa deferentia, and common ejaculatory duct; there are no accessory glands such as are found in many other Diptera. The terminal abdominal segments of the male exhibit a sinistral asymmetry. The ovaries of the female, when mature, occupy the greater portion of the abdominal cavity. There are a pair of accessory glands (probably of a "gum" or "glue" nature), three spermatheceæ, and a pair of vesicles used during copulation. The ovipositor is about as long as the abdomen, and is composed of segments six to nine. 10. The musculature of the head is described in detail, and it is found that the House-fly agrees with the blowfly in the number and relations of its cephalic muscles, though in a few cases the attachments are slightly different. In the haustellum and oral lobes of the House-fly no tracheal sacs similar to those described and figured by Lowne for the blowfly occur, but only annulated tracheae are found, and, as these are incapable of distension, the view that the oral lobes are distended by the action of inflated air cannot be held. The extension of the proboscis I believe is due to the inflation of the tracheal sacs of the head and rostrum, and I agree with Kraepelin that the distension of the oral lobes is effected by blood-pressure. Two kinds of gustatory sense-organs are found on the margin of the aboral and on the oral surfaces respectively. The latter were described in the blowfly by Lowue as the openings of the ducts of the labial salivary glands, but Kraepelin's correct description of their structure in the blowfly is confirmed by this study of the House-fly. The labial salivary glands are described in detail. They consist of large cells containing permanent vacuoles, which communicated with intracellular ducts. These open by a pair of pores into the oral pits, the secretions of the glands serving to keep the surface of the oral lobes moist.



1971 ◽  
Vol 69 (3) ◽  
pp. 331-396 ◽  
Author(s):  
Dyrce Lacombe

The Embioptera are rather generalized insects whose internal anatomy is simple and not subject to great modifications. For this reason these insects form an ideal group for elementary anatomical and histological studies (fig. 2). The digestive tract is a long, simple tube without convolutions or diverticulae from the buccal cavity to the rectum. The buccal structures are of the chewing type. The oesophagus and ingluvia are differentiated only by slight dilation of their walls. In nymphs and females the proventriculus is very distinct due to folds which flatten as the structure becomes packed with food. The enteron is the largest in such forms and in both sexes limited caudally by the Malpighian tubules. The proctodeus has six large rectal papillae. The nervous system is complete with only the fifth abdominal segment lacking a ganglion in the metathorax includes the ganglion of the first abdominal segment. The brain exhibits very clear structure in histological sections. The tracheal system includes two pairs of thoracic spiracles and eight abdominal pairs. Only th metathoracic spiracle has an air expiration function; all others serve for inspiration. Various structures in the spiracles protect the atrium. The circulatory system includes a long, simple dorsal vessel which extends forward from the ninth abdominal segment into the cranium. It opens anteriorly near the circumoesophageal connectives. The dorsal vessel has a pair of ostia and valves corresponding to each abdominal and thoracic segment. It lacks the diverticulae or folds commonly found in more highly evolved insects. The excretory system is represented by Malphighian tubules, pericardial cells, and fat-body. The number and disposition of Malpighian tubules is variable within the order. The pericardial cells are localized around the entire dorsal vessel up to the opening of the aorta in the head. The fat-bodies form compact layers in the dorsal and ventral regions of the body. In males they are more developed in the abdominal region. The mandibles, maxillae, and salivary glands are of a simple type with very few cytological modifications. Only the salivary glands which extend into the mesothoracic region show appreciable specialization. The reproductive system is bi-sixual and shows considerable sexual dimorphism. Males have five pair of testes with a metameric disposition, two distinct ducts, two epidymis, and the ejaculatory organs. The accessory glands vary in number and size and open in the anterior portion of the ejaculatory duct. The female reproductive organs are of the panoistic type. The system includes five pairs of ovarioles, two long paired oviducts a small, unpaired oviduct and the spermatheca which opens in the vagina. Reproduction usually involves a union of male and female gametes, and eggs are usually laid in clusters attached to a substrate.



Author(s):  
P.J. Dailey

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.



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