The sensilla on the terminal antennomere of selected Hydradephagans (Coleoptera) are modified in several distinct ways as compared to the sensilla on the terminal antennomere of Geadephagans (Coleoptera). There are no long sensilla of any type on antennae of Hydradephagans, the sensilla are either short, peg-like sensilla that may be recessed in the antennal surface or they are multiporous plate-like sensilla. Multiporous plate-like sensilla have not been found on the antennae of Geadephagans. A pit sensillum occurs on the antennae of one family, Gyrinidae, in the Hydradephaga whereas it is found on the antennae of several species from the families of Geadephaga. The sensilla on the terminal antennomere of Hydradephaga are often grouped into sensory fields that could be located on a particular area of the antennomere. Sensory fields are also located on the apices of the maxillary and labial palps and the most unique sensory fields occur in the Noteridae. The maxillary palpal apex of Hydrocanthus oblongus (Noteridae) is bifurcate and a sensory field with several types of sensilla is at the apex of each branch. The terminal labial palpomere is greatly enlarged and has a long, slender sensory field at the apex and a secondary sensory field on a thumb-like projection. The sensilla on the palpal apices are more diverse and complex in form as compared to the sensilla on the palps of Geadephaga. The most complex sensillum has a cuticular collar and a dome that is divided into six or seven triangular sections. The dome may be opened or closed and a peg-like sensillum with a very wide apical pore is situated beneath the dome.
When given a choice of cotton (host) and ground cherry (non host) in a close range situation, Heliothis virescens (F.), the tobacco budworm, depends primarily on contact chemoreception and mechanoreception, and not olfaction or vision, to discriminate between these two plant species for oviposition. Further, in the presence of a certain level of hairiness (the non‐host plant, ground cherry, has short capitate hairs), the females are capable of discriminating between these two plants based on contact chemosensory cues, if at least one pair of tarsi is intact. The contact chemosensilla on the ovipositor do not seem to be important for this purpose. These results are discussed in relation to the sensory cues and receptors for oviposition in other Lepidoptera, especially moths.
Résumé
Signaux et récepteurs sensoriels intervenant dans la ponte d'Heliothis virescens
Les différentes récepteurs sensoriels (chimique, mécanique et visuel) des femelles d'H. virescens ont été rendus inactifs par traitement à l'acide, anten‐notectomie ou peinture des yeux avec un enduit noir du type vernis à ongles, pour étudier le déterminisme sensoriel de la sélection des hǒtes lors de la ponte; les papillons avaient le choix entre le coton (Gossypium hirsutum), sur lequel ils pondent normalement, et Physalis angulata sur lequel on n'observe pas de pontes dans la nature. Au laboratoire, à faible distance, le choix de H. virescens dépendait en premier lieu des mécanorécepteurs et des récepteurs chimiques dits de contact (gustatifs), et non de la vision ou de l'olfaction. En présence d'un certain niveau de pilosité (P. angulata possède de courts poils capités), les femelles choisissent les plantes en fonction de la perception chimique dite de contact (gustation) tant qu'une paire de tarses reste intacte. Les sensilles chimiques de l'ovitube ne semblent pas jouer un rǒle important à cet égard. La discussion a examiné ces résultats à la lumière des processus sensoriels utilisés par d'autres papillons.
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