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Gas chromatographic-mass spectrometric analysis of whole body extracts of Platynothrus peltifer, a desmonomatan oribatid mite that belongs to the family Camisiidae, exhibited a basic profile of seven compounds, comprising the monoterpenes neral, geranial, and nerylformate; the aromatics 3-hydroxybenzene-1,2-dicarbaldehyde (= gamma-acaridial) and 2-formyl-3-hydroxybenzyl formate (= rhizoglyphinyl formate), and two unsaturated Cl7-hydrocarbons, 6,9-heptadecadiene and 8-heptadecene. Neryl formate, gamma-acaridial, and rhizoglyphinyl formate were the main components and amounted to 80% of the extracts. With the exception of y-acaridial (relative abundance varied considerably among samples), this chemical profile was consistently present in extracts of P. peltifer from nine different localities in SE-Austria. In addition, two further components, 2,3-dihydroxy benzaldehyde and 7-hydroxyphthalide, both probably of non-oil gland origin, infrequently were detected in the extracts. The aromatic compound rhizoglyphinyl formate, also known from Astigmata, was found for the first time in extracts of Oribatida, whereas all other compounds have already been reported from other oribatid species. The hydrocarbons are generally considered to represent plesiomorphic characters of mite oil gland secretions, whereas the monoterpenes and y-acaridial form a part of the so-called "astigmatid compounds" that are thought to be characteristic for middlederivative Mixonomata and all more highly derived oribatid groups (including Astigmata).

Chemical and behavioural studies indicated that the oil glands of the Oribatida represented a central organ for protection and semiochemical communication.The hitherto unknown mode of action of these glands and their microscopic anatomy have been investigated in Collohmannia gigantea by histological and SEM techniques. The paired oil glands are located dorsolaterally in the hysterosoma and mainly comprise large intima-lined and sac-like reservoirs which are surrounded by glandular tissue. The reservoirs consist of a single-layered flat epithelium and probably serve for storage of the oil gland secretion only, but not for its production. Each reservoir opens to the body outside via a single pore. Externally, the pores appear as oval-shaped rings of smooth cuticle, moderately projecting from the surface of the notogaster. The pore orifices are supplied with trapdoor-like closing mechanisms, consisting of cuticular flaps which permit reservoir opening by muscles attaching to the posterior part of the reservoir and the inner side of the notogaster. These morphological data, especially the large intimalined reservoirs along with closing mechanisms under muscular control, are consistent with supposed biological roles of oil glands as defensive or alarm pheromonal organs.

As a first example for the chemistry of oil gland secretions in the Hermannioidea (one of the three superfamilies of desmonomatan Oribatida), the oil gland secretion of Hermannia convexa was investigated by gas chromatography-mass spectrometry. Hexane extracts of all juvenile stages showed a multicomponent chromatographic pattern, mainly consisting of well-known oil gland secretion components such as neral, geranial, gamma-acaridial and the unsaturated C17-hydrocarbons, 6,9-heptadecadiene and 8-heptadecene. The secretion profiles of juveniles varied slightly between samples of two different collections, namely in the presence of gamma-acaridial and 8-heptadecene. Furthermore, a minor component, identified as 1,8-cineole (= eucalyptol) and hitherto not known from oil gland secretions of other species, was recorded in both juvenile and adult extracts. In adult profiles, 1,8-cineole, in low amounts, represented the only detectable component; thus, their profiles fundamentally differed from those of juveniles. A subsequent histological investigation revealed well developed oil glands in all juvenile stages, but degenerated oil glands in adults, consistent with the chemical data. So far, apart from H. convexa, degeneration of oil glands in the course of ontogenetic development is only known from a brachypylid species; on the other hand, chemical oil gland-polymorphism between juveniles and adults may occur in closely related Nothridae while it does not occur in oil glands of early- and middle-derivative Oribatida (Parhyposomata, Mixonomata, trhypochthoniid Desmonomata), nor in astigmatid mites.

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