Contents of the exocrine glands of the ant subfamily Cerapachyinae

The chemistry of the exocrine glands of three species of the small and little-known ant subfamily Cerapachyinae has been examined for the first time. The mandibular glands of Cerapachys jacobsoni contained acetophenone and skatole, but some individuals contained, in addition, 4-methyl-3-heptanone and 3-octanol. The mandibular glands of the new species, presently known as Cerapachys sp. 15 of FI contained 4-methyl-3-heptanone, as the major substance but also 4-methyl-3-heptanol, methyl 6-ethylsalicylate, and traces of 4,5-dimethyl-4-hexen-3-one and homomanicone. The Dufour glands of C. jacobsoni contained a mixture of higher aldehydes, acetates and other esters, with a small amount of hydrocarbons, all in the range C₁₁–C₂₀. The Dufour glands of Cylindromyrmex whymperi contained a mixture of long-chain epoxides, the second ant species to display them. The sternal glands of C. whymperi contain a recruitment pheromone, but only partial identification of the contents was possible. The venom glands of all three species were devoid of volatile material. The Dufour glands of Cerapachys sp. 15 of FI and the mandibular glands of C. whymperi had no detectable volatile contents.     

Foraging Area Marking in Two Related Tetramorium Ant Species (Hymenoptera: Formicidae)

The related ants Tetramorium caespitum and T. impurum mark their foraging area in a species-specific, home range and short-lasting manner. Indeed, ants reaching a new area have a slow linear speed which increases during the marking. Conspecific ants are arrested and attracted by marked areas, while heterospecific ants are reluctant to visit them. However, when the latter do visit marked areas, they move more quickly and less sinuously than conspecific ants and do not stay on the areas. The marking is performed in about 3 min by T. caespitum and in 3 to 6 min by T. impurum. If not reinforced, the marking vanishes in the same time intervals. Neither poison gland nor last sternite extracts reproduce the activity of naturally marked areas, whereas a Dufour gland extract does exactly that. Foraging ants touch the ground with the tip of their gaster. Consequently, we can postulate that the workers mark their foraging area with the contents of this gland, which is associated with the sting apparatus, and that they deposit with the extremity of the gaster. Alien conspecific ants are seldom aggressive to one another, even on marked areas. When encountering each other on unmarked areas, heterospecific ants present some aggressive reactions. On marked areas, their aggressiveness is enhanced and intruder ants are restless, while resident ones walk freely. On ground marked by T. impurum, ants of this species are more aggressive than antagonistic T. caespitum workers. The marking of foraging areas thus induces defense against heterospecifics but not against conspecific ants.     

Comparative study of the dufour gland secretions of workers of four species of Myrmica ants

The Dufour gland secretions of myrmica rubra, M. ruginodis, M. sabuleti and M. scabrinodis have been studied. The most volatile portions of the secretion of workers of all four species were found to be similar, containing C₂C₄ oxygenated compounds. The less volatile portion consists of a mixture of hydrocarbons. In M. ruginodis this is chiefly a mixture of linear saturated and mono-unsaturated hydrocarbons, similar in composition to that of M. rubra, while in M. sabuleti it consists of (Z,E)-α-farnesene and its homologues, homofarnesene, bishomofarnesene and trishomofarnesene, similar in composition to that of M. scabrinodis. Workers of each species studied were attracted to the Dufour gland volatiles of all four species, these substances chiefly causing an increase in running speed, with the workers not distinguishing between conspecific and allospecific secretions, though small quantitative differences could be demonstrated between the speed and orientation reaction of workers of each species. The less volatile fraction of the Dufour gland secretion is used for territorial marking by foraging workers. This marking is specific for each species except between M. rubra and M. ruginodis.     

Identification of the alkaloidal venoms of some Monomorium ants of Saudi Arabia

The major volatile compounds in the poison glands of two Monomorium ant species from Saudi Arabia have been identified. Monomorium niloticum and Monomorium najrane both contain mixtures of alkyl- and alkenyl-pyrrolidines and -pyrrolines in their venom glands but no Dufour gland volatile compounds were detected. Monomorium mayri showed neither Dufour gland compounds nor venom components detectable by gas chromatography.     

Mechanobiology of low-density lipoprotein transport within an arterial wall—Impact of hyperthermia and coupling effects

The effects of hyperthermia, coupling attributes and property variations on Low-density lipoprotein (LDL) transport within a multi-layered wall while accounting for the fluid structure interaction (FSI) is analyzed in this work. To understand the potential impact of the hyperthermia process, thermo-induced attributes are incorporated, accounting for the plasma flow, mass transfer, as well as the elastic wall structure. The coupling effect of osmotic pressure, Soret and Dufour diffusion is discussed and their influence on LDL transport is examined, demonstrating that only the Soret effect needs to be accounted for. The effect of thermal expansion on changing the behavior of flow, mass transport, and elastic structure is illustrated and analyzed while incorporating the variations in the effective LDL diffusivity and consumption rate, as well as other dominating parameters. It is shown that hyperthermia results in an enhancement in LDL transport by increasing the concentration levels within the arterial wall.     

Dufour gland of the digger wasp<Emphasis Type="Italic"> Liris niger:</Emphasis> structure and developmental and biochemical aspects

The tubiform Dufour gland in the digger wasp species Liris niger is about 1.0 mm long ( 0.15 mm). An alternating arrangement of longitudinal and circumferential bundles of striated muscle fibers surrounds the gland. The Dufour gland, together with the venom gland, enters the sting base and terminates in the sting. The glandular epithelium is monolayered. Glands about 3 day after imaginal ecdysis have an empty lumen but a thick lining epithelium. The gland cells are characterized by a well-developed vesicular smooth endoplasmic reticulum, sparse rough ER and numerous free ribosomes. They also exhibit several electron-lucent vesicles and autophagic vacuoles. Secretion of electron-dense material via the gland cuticle into the gland lumen is apparent. Glands more than 20 days after imaginal ecdysis display a large lumen and a thin epithelium. The cells show signs of degeneration with numerous cytolytic inclusions. Dufour gland liquid contains numerous polypeptides of molecular weights ranging from 14 to about 200 kDa. In addition the secretion consists predominantly of straight-chain hydrocarbons, accompanied by small amounts of esters. The major hydrocarbons are pentadecane and (Z)-8-heptadecene. Dufour gland secretion may have several functions: (1) the polypeptides might be involved in the gluing process of the eggs, while (2) the hydrocarbon oils may function as lubricants for the lancets and (3) might soften the secretion, thus allowing easier application of the glue. The lipophilic volatile material (4) might also be involved in pheromonal signaling.     

Alkaloid secretion inhibited by antibiotics in Aphaenogaster ants

Although alkaloids are frequent in the poison glands of ants of the genus Aphaenogaster, this is not the case for A. iberica. Hypothesizing that in the genus Aphaenogaster, alkaloids are produced by symbiotic bacteria, except for A. iberica, we treated an experimental lot of both A. iberica and a ‘classical’ Aphaenogaster species, A. senilis, with an antibiotic. Compared to workers from a control lot, this treatment reduced considerably alkaloid production in A. senilis, whereas A. iberica did not react to the treatment. Furthermore, the treatment induced an increase in cuticular hydrocarbon quantities in A. senilis, but not in A. iberica. An analysis of the ant microbiota will be the next step to confirm our hypothesis.     

Contents of Dufour glands in some formicine ants: queens and workers of Camponotus aethiops and a re-examination of Lasius fuliginosus

The Dufour gland secretions of both virgin queens and workers of Camponotus aethiops are similar and consist of straight chain hydrocarbons ranging from C₁₀–C₁₅ with C₁₁ the major compound. The difference between the two castes is that C₁₅ appears only as a trace in queens, and the total amount of secretion is smaller in queens than in workers.In Lasius fuliginosus, the Dufour gland secretion contains a series of straight chain hydrocarbons (C₁₀–C₁₇) with undecane the major compound, and a series of 2-alkanones ranging from C₁₃ to C₁₉.

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Résumé Les sécrétions des glandes de Dufour sont toutes semblables et comprennent, chez les reines et les ouvrières de C. aethiops, une chaîne linéaire d'hydrocarbures de C₁₀ à C₁₅, avec C₁₁ comme constituant principal. Les différences entre les castes se traduisent chez la reine, par une teneur totale en sécrétions plus faible et l'existence de C₁₅ uniquement sous forme de traces.Chez L. fuliginosus, la sécrétion de la glande de Dufour comprend une série de chaînes linéaires d'hydrocarbures (C₁₀–C₁₇) avec l'undécane comme constituant principal, et une série de 2-alkanones allant de C₁₃ à C₁₉.

     

Unusual structural and chemical characteristics of the Dufour gland in the ant Meranoplus diversus

Abstract The Dufour gland of both queens and workers of Meranoplus diversus is very large. The reservoir is lined with flat epithelial cells, which usually contain smooth endoplasmic reticulum but also show the unusual accumulation of electron‐dense inclusions. Chemically, the gland contains an unusual mixture of long‐chain fatty acids and their derivatives, including hydrocarbons, ketones and amines with long‐chain substituents, hydroquinone, and sugars. Some of the substances identified are already known as insect defensive compounds against other arthropods.