ON WING-VEIN NOMENCLATURE

1906 ◽  
Vol 38 (8) ◽  
pp. 285-285
Author(s):  
John. A. Grossbeck

It will be noticed that in the preceding paper on Geometridæ, I have used the Comstockian terms of designating wing-veins. Heretofore these have not been used by any writers on this family of moths; in act, they have been very little used by writers in any family. The reason for this is, not that the system is not a good one, but because it is comparatively new. Most of the older writers have become used to the number system, having employed it in all their previous work, and therefore retain it to preserve uniformity, and perhaps make no effort to familarize themselves with the new dispensation.

1993 ◽  
Vol 125 (2) ◽  
pp. 181-258 ◽  
Author(s):  
Jarmila Kukalová-Peck ◽  
John F. Lawrence

AbstractA survey is made of the major features of the venation, articulation, and folding in the hind wings of Coleoptera. The documentation is based upon examination of 108 Coleoptera families and 200 specimens, and shown in 101 published figures. Wing veins and articular sclerites are homologized with elements of the neopteran wing groundplan, resulting in wing vein terminology that differs substantially from that generally used by coleopterists. We tabulate the differences between currently used venational nomenclature and the all-pterygote homologous symbols. The use of the neopteran groundplan, combined with the knowledge of the way in which veins evolved, provides many strong characters linked to the early evolutionary radiation of Coleoptera. The order originated with the development of the apical folding of the hind wings under the elytra executed by the radial and medial loop. The loops, which are very complex venational structures, further diversified in four distinctly different ways which mark the highest (suborder) taxa. The remaining venation and the wing articulation have changed with the loops, which formed additional synapomorphies and autapomorphies at the suborder, superfamily, and sometimes even family and tribe levels. Relationships among the four currently recognized suborders of Coleoptera are reexamined using hind wing characters. The number of wing-related apomorphies are 16 in Coleoptera, seven in Archostemata + Adephaga–Myxophaga, four in Adephaga–Myxophaga, seven in Myxophaga, nine in Archostemata, and five in Polyphaga. The following phylogenetic scheme is suggested: Polyphaga [Archostemata (Adephaga + Myxophaga)]. Venational evidence is given to define two major lineages (the hydrophiloid and the eucinetoid) within the suborder Polyphaga. The unique apical wing folding mechanism of beetles is described. Derived types of wing folding are discussed, based mainly on a survey of recent literature. A sister group relationship between Coleoptera and Strepsiptera is supported by hind wing evidence.


Development ◽  
1995 ◽  
Vol 121 (3) ◽  
pp. 785-801 ◽  
Author(s):  
M.A. Sturtevant ◽  
E. Bier

The Drosophila rhomboid (rho) and Egf-r genes are members of a small group of genes required for the differentiation of various specific embryonic and adult structures. During larval and early pupal development expression of rho in longitudinal vein primordia mediates the localized formation of wing veins. In this paper we investigate the genetic hierarchy guiding vein development, by testing for genetic interactions between rho alleles and a wide variety of wing vein mutations and by examining the pattern of rho expression in mutant developing wing primordia. We identify a small group of wing vein mutants that interact strongly with rho. Examination of rho expression in these and other key vein mutants reveals when vein development first becomes abnormal. Based on these data and on previous genetic analyses of vein formation we present a sequential model for establishment and differentiation of wing veins.


2021 ◽  
Author(s):  
Noah Meier ◽  
Anina Wacker ◽  
Seraina Klopfstein

Darwin wasps (Ichneumonidae) are one of the most species-rich insect families, but also one of the most understudied ones, both in terms of their extant and extinct diversity. We here use morphometrics of wing veins and an integrative Bayesian analysis to place a new rock fossil species from the Danish Fur Formation (~54 Ma) in the tree of Darwin wasps. The new species, Pherhombus parvulus n. sp., is placed firmly in Pherhombinae, an extinct subfamily so far only known from Baltic and Rovno-Ukranian ambers, which are estimated to be 34-48 Ma and 34-38 Ma, respectively. Our phylogenetic analysis recovers a subfamily clade within the higher Ophioniformes formed by Pherhombinae, Townesitinae and Hybrizontinae, in accordance with previous suggestions. Due to the placement of the new species as sister to the remaining members of Pherhombinae, we argue that our finding is not at odds with a much younger, late Eocene age (~34-41 Ma) of Baltic amber and instead demonstrates that Pherhombus existed over a much longer period than previously thought. Our results also exemplify the power of wing vein morphometrics and integrative phylogenetic analyses in resolving the placement even of poorly preserved fossil specimens.


1985 ◽  
Vol 224 (1236) ◽  
pp. 287-313 ◽  

Described are all the sensilla and non-innervated hairs observable by scanning electron microscopy on the thorax and wings of the minute (0 .4- 0.8 mm) parasitoid wasp, Trichogramma minutum . Most of the sensilla appear mechanosensory, and occur on the wing veins, around the wing bases and near the spiracles. The number, position and morphological type of the sensilla were constant between individuals. Dorsally, the thorax bears 18 hair sensilla, between 5 and 50 μm long. Around each forewing base are nine hair sensilla, and three unique sensilla less than 1 μm long; two of the latter form bifurcated ‘pronged’ structures. Of the nine, four form the anterior wing base hairplate, and two the basalare hairplate; these probably contact the wing at extreme anterodorsal and anteroventral positions. Each hindwing base is equipped with three hairplates, of either two or three 4-6 μm hairs. Two of these are located appropriately to contact the wing during flight, the third only when the wings are folded. Posterior to the hindwing base are two socketed hairs and an unusual grooved hair 10—12 μm long, all located near the opening of the third thoracic spiracle. Each membranous forewing is surrounded by 110-120 evenly spaced, unsocketed fringe hairs. A parallel secondary row of similar hairs occurs on both dorsal and ventral surfaces. The forewing surfaces also bear numerous hairs, unsocketed marginally, but with increasingly distinct sockets centrally. Dorsally, these hairs mainly occur in rows radiating from the wing vein. Ventrally the surface hairs are only partly arranged in rows, and vary more in form. Transmission electron microscopy shows these hairs to be non-innervated. In contrast, the wing veins bear innervated structures, comprising 19 hair-like, and 22-23 campaniform, sensilla. The rod-like hindwings also bear a fringe of hairs similar to those of the forewing, although longer and confined to the posterior margin. The sensilla of the hind wing comprise four ventral and one dorsal campaniform sensilla, and six hairs. The function of the described structures is discussed in relation to the flight mechanism and its control in these very small insects.


Genetics ◽  
1982 ◽  
Vol 101 (1) ◽  
pp. 71-80
Author(s):  
Anne Fausto-Sterling ◽  
Heidi Smith-Schiess

ABSTRACT In this paper we demonstrate that the severity of the engrailed phenotype is greatly increased when engrailed is combined with the X-linked mutation fused. The secondary sex combs of fu;en flies contain from two to four times more setae than do those of en siblings. The number of transverse rows of bristles on the metatarsus of the metathoracic leg is reduced by a factor of one and a half to two in fu;en flies when compared to their en siblings, while the frequency of reversed bract polarity, bristle abnormalities and misshapen metatarsi increases greatly. In addition, fu;en flies express the en wing phenotype more completely than their siblings and have a much higher frequency of wing vein abnormalities—some of which we have interpreted as triplications of the third and first longitudinal wing veins. We briefly discuss the significance of the fused-engrailed gene interaction.


2018 ◽  
Vol 14 (10) ◽  
pp. 20180496 ◽  
Author(s):  
Penghui Sun ◽  
Natasha Mhatre ◽  
Andrew C. Mason ◽  
Jayne E. Yack

Insects have evolved a diversity of hearing organs specialized to detect sounds critical for survival. We report on a unique structure on butterfly wings that enhances hearing. The Satyrini are a diverse group of butterflies occurring throughout the world. One of their distinguishing features is a conspicuous swelling of their forewing vein, but the functional significance of this structure is unknown. Here, we show that wing vein inflations function in hearing. Using the common wood nymph, Cercyonis pegala , as a model, we show that (i) these butterflies have ears on their forewings that are most sensitive to low frequency sounds (less than 5 kHz); (ii) inflated wing veins are directly connected to the ears; and (iii) when vein inflations are ablated, sensitivity to low frequency sounds is impaired. We propose that inflated veins contribute to low frequency hearing by impedance matching.


2020 ◽  
Vol 1 (9) ◽  
pp. 28-30
Author(s):  
D. M. Zlatopolski

The article describes a number of little-known methods for translating natural numbers from one number system to another. The first is a method for converting large numbers from the decimal system to the binary system, based on multiple divisions of a given number and all intermediate quotients by 64 (or another number equal to 2n ), followed by writing the last quotient and the resulting remainders in binary form. Then two methods of mutual translation of decimal and binary numbers are described, based on the so-called «Horner scheme». An optimal variant of converting numbers into the binary number system by the method of division by 2 is also given. In conclusion, a fragment of a manuscript from the beginning of the late 16th — early 17th centuries is published with translation into the binary system by the method of highlighting the maximum degree of number 2. Assignments for independent work of students are offered.


1960 ◽  
Vol XXXV (II) ◽  
pp. 245-252 ◽  
Author(s):  
G. P. van Rees ◽  
F. J. A. Paesi

ABSTRACT In the experiments reported in this paper the hypothesis that the decrease in the pituitary I. C. S. H.-content, which occurs after administration of steroid sex hormones in gonadectomized animals, is counteracted by a reflex stimulation of the hypophysis initiated by the operation has been investigated. If treatment with a low dose of testosterone propionate (100 μg) was started immediately after castration, the resulting decrease in the pituitary I. C. S. H.-content became more marked if the reflex stimulation of the hypophysis had been prevented. If, however, two months were allowed to elapse before the beginning of treatment, the presence or absence of this reflex was no longer of importance for the effect of testosterone propionate on the pituitary I. C. S. H.-content. And yet, in this case too, the decrease in the pituitary I. C. S. H.-content by testosterone propionate was less than in intact animals (see preceding paper). Hence this decrease appears to be counteracted by two factors: one rapidly occurring and short lasting, resulting from a reflex elicited by gonadectomy; the other gradually increasing in potency and possibly a direct consequence of the continued absence of pituitary inhibiting sex steroids.


Author(s):  
Parinya CHALERMSOOK ◽  
Hiroshi IMAI ◽  
Vorapong SUPPAKITPAISARN

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