Re-appraisal of the Australian genus Eutermiphora Lea (Diptera: Phoridae)

1988 ◽  
Vol 19 (4) ◽  
pp. 435-436 ◽  
Author(s):  
R.H.L. Disney

AbstractThe Australian genus Eutermiphora Lea is characterised by a forward cxtension of the anterior dorsal region of the abdomen, which obscures most of the thorax from view. This gave rise to the erroneous statement that both wings and halteres were missing in this genus. An amplified description of E. abdominalis is provided and its correct placement in Schmitz's (1929) key to world genera indicated.

Development ◽  
1998 ◽  
Vol 125 (18) ◽  
pp. 3645-3654 ◽  
Author(s):  
C. Wolff ◽  
R. Schroder ◽  
C. Schulz ◽  
D. Tautz ◽  
M. Klingler

In short germ embryos, the germ rudiment forms at the posterior ventral side of the egg, while the anterior-dorsal region becomes the extra-embryonic serosa. It is difficult to see how an anterior gradient like that of bicoid in Drosophila could in these embryos be directly involved in patterning of the germ rudiment. Moreover, since it has not yet been possible to recover a bicoid homologue from any species outside the diptera, it has been speculated that the anterior bicoid gradient could be a late addition during insect evolution. We addressed this question by analysing the regulation of potential target genes of bicoid in the short germ embryo of Tribolium castaneum. We demonstrate that homologues of caudal and hunchback from Tribolium are regulated by Drosophila bicoid. In Drosophila, maternal caudal RNA is translationally repressed by bicoid. We find that Tribolium caudal RNA is also translationally repressed by bicoid, when it is transferred into Drosophila embryos under a maternal promoter. This strongly suggests that a functional bicoid homologue must exist in Tribolium. The second target gene, hunchback, is transcriptionally activated by bicoid in Drosophila. Transfer of the regulatory region of Tribolium hunchback into Drosophila also results in regulation by early maternal factors, including bicoid, but in a pattern that is more reminiscent of Tribolium hunchback expression, namely in two early blastoderm domains. Using enhancer mapping constructs and footprinting, we show that caudal activates the posterior of these domains via a specific promoter. Our experiments suggest that a major event in the evolutionary transition from short to long germ embryogenesis was the switch from activation of the hunchback gap domain by caudal to direct activation by bicoid. This regulatory switch can explain how this domain shifted from a posterior location in short germ embryos to its anterior position in long germ insects, and it also suggest how an anterior gradient can pattern the germ rudiment in short germ embryos, i.e. by regulating the expression of caudal.


2005 ◽  
Vol 125 (4) ◽  
pp. 337-349 ◽  
Author(s):  
Jörg Fleischer ◽  
Nicole Hass ◽  
Karin Schwarzenbacher ◽  
Stefanie Besser ◽  
Heinz Breer

1985 ◽  
Vol 63 (6) ◽  
pp. 1459-1462
Author(s):  
Michael E. Smith

Naidid species Chaetogaster diaphanus, Chaetogaster diastrophus, Chaetogaster limnaei limnaei, Dero digitata, Dero nivea, Nais communis, Nais simplex, Nais variabilis, Pristina leidyi, Slavina appendiculata, and Stylaria lacustris were observed as paratenic and possibly intermediate hosts for larval mermithid nematodes from field collections. Mermithids were generally found in the anterior, dorsal region of the oligochaetes. Individual naidids were at most infected with two nematodes. No seasonal prevalence patterns could be firmly established owing to the sporadic occurrence of mermithid infections in the naidids.


Development ◽  
1973 ◽  
Vol 29 (3) ◽  
pp. 549-558
Author(s):  
F. S. Billett ◽  
T. H. Courtenay

A stereoscan electron microscope has been used to survey the epidermis of axolotl embryos as it becomes ciliated. The observations are consistent with much earlier ones that ciliated cells first occur on the surface of the epidermis at about the time of the closure of the neural folds. The cells are located first in the anterior dorsal region of the embryo at about the one-somite stage. After this they rapidly increase in number and by the three- to six-somite stage ciliated cells, which are isolated from one another, are scattered over the entire surface of the embryo in numbers which approach those of much later stages (18 somites). At the earlier stage, however, most of the ciliated cells lie below the general surface of the epidermis, occupying pit-like depressions. This is in contrast to the later stage when they are raised above the surface. The observations support the view that the precursors of the ciliated cells lie beneath the outer epidermal layer of cells and that the ciliation of the embryonic surface occurs when they move into the outer layer as they complete their differentiation.


2021 ◽  
pp. 1-16
Author(s):  
Arymathéia Santos Franco ◽  
Rodrigo Temp Müller ◽  
Agustín G. Martinelli ◽  
Carolina A. Hoffmann ◽  
Leonardo Kerber

Abstract Traversodontidae is a group of Triassic herbivorous/omnivorous cynodonts that represents the most diversified lineage within Cynognathia. In southern Brazil, a rich fossil record of late Middle/mid-Late Triassic cynodonts has been documented, with Exaeretodon riograndensis Abdala, Barberena, and Dornelles, 2002 and Siriusgnathus niemeyerorum Pavanatto et al., 2018 representing two abundant and well-documented traversodontids. The present study provides a comparative analysis of the morphology of the nasal cavity, nasal recesses, nasolacrimal duct, and maxillary canals of both species using computed tomography, highlighting the changes that occurred in parallel to the origin of mammaliaforms. Our results show that there were no ossified turbinals or a cribriform plate delimiting the posterior end of the nasal cavity, suggesting these structures were probably cartilaginous as in nonmammaliaform cynodonts. Both species show lateral ridges on the internal surface of the roof of the nasal cavity, but the median ridge for the attachment of a nasal septum is absent. Exaeretodon riograndensis and S. niemeyerorum show recesses on the dorsal region of the nasal cavity, which increase the volume of the nasal cavity, potentially enhancing the olfactory chamber and contributing to the sense of smell. On the lateral sides of the nasal cavity, the analyzed taxa show a well-developed maxillary recess. Although E. riograndensis and S. niemeyerorum have roughly similar nasal cavities, in the former taxon, the space between the left and right dorsal recesses of the nasal cavity is uniform along its entire extension, whereas this space narrows posteriorly in S. niemeyerorum. Finally, the nasolacrimal duct of S. niemeyerorum is more inclined anteroposteriorly than in E. riograndensis.


1980 ◽  
Vol 58 (11) ◽  
pp. 2105-2115 ◽  
Author(s):  
Jean Percy ◽  
J. A. MacDonald ◽  
J. Weatherston

The three dorsal abdominal glands in larvae of Apateticus bracteatus (Pentatomidae) secrete a mixture of compounds. Major volatile constituents of the secretion are identified, herein, as tridecane and 2-octenal. There are also trace amounts of 2-hexenal and two other unidentified compounds.Each of the glands has paired orifices that are located between tergites 3/4, 4/5, and 5/6, but only the most anterior gland is paired. In anterior glands of midinstar larvae, glandular cells associated with ducts, and interstitial glandular cells are distributed along the ventral walls of the reservoirs. In posterior glands, columnar glandular cells are located in the anterior dorsal wall of the reservoirs; secretory cells associated with ducts, and nonglandular interstitial cells are distributed throughout the ventral and posterior walls of the reservoirs. The interstitial glandular cells of the anterior gland and the columnar glandular cells of the middle and posterior glands contain cytoplasmic organelles characteristic of lipid-producing cells. In all glands the secretory cells associated with ducts secrete lipids. Evidence indicating the importance of Golgi and ER in secretion synthesis is presented. The reservoirs and ducts have a thin cuticular lining.The bearing of the results on present ideas of gland function in Heteroptera is discussed.


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