“…The original description and the figures correspond to Vitzthum's species and I think that it is a synonym of the latter. Vitzthum, 1941Sennertiafrontalis Vitzthum, 1941 (Fig. 1 Remarks: This species is distinguished from S. queenslandica and S.monicae by the structure of the cuticular striations, thick and punctate, and by the shape of the dorsal shield which is much wider posteriorly.…”
“…Legs IV short with very short tarsus bearing a very short ventral seta. Type species: Sennertia frontalis Vitzthum, 1941. There are two other species in this subgenus. Distribution: Neotropical and Nearctic.…”
The genus Sennertia Oudemans, 1905 (Acari, Chaetodactylidae) is revised. Up to now, 49 species have been described in this genus, almost all from their hypopial stage. Adults are known only for four species. The adults live in the nests of bees, mainly Xylocopidae, and their heteromorphic deutonymphs (= hypopi) are phoretic on the bees. The parasitic role of these mites is not known but they probably feed on the bee larvae as do the members of the allied genus Chaetodactylus wich are parasitic in the nests of Megachilidae. The holotypes or lectotypes of 35 species have been examined and most of them are redescribed and redepicted. Four species have been placed in synonymy: S. moandensis with S. morstatti Vitzthum, 1914 S. xylocopae (Donnadieu, 1868) with S. cerambycina (Scopoli, 1763); S. sumatrensis Oudemans, 1924 with S. horrida (Vitzthum, 1912 S. donaldi Turk, 1948 with S. argentina Vitzthum, 1941. The genus Sennertia is redefined from the hypopial stage and four new subgenera (Afrosennertia, Asiosennertia, Amsennertia and Spinosennertia) and two new species S. (Asiosennertia) vitzthumi and S. (Asiosennertia) delfinadoae) are described. A key to the species is given.
“…The original description and the figures correspond to Vitzthum's species and I think that it is a synonym of the latter. Vitzthum, 1941Sennertiafrontalis Vitzthum, 1941 (Fig. 1 Remarks: This species is distinguished from S. queenslandica and S.monicae by the structure of the cuticular striations, thick and punctate, and by the shape of the dorsal shield which is much wider posteriorly.…”
“…Legs IV short with very short tarsus bearing a very short ventral seta. Type species: Sennertia frontalis Vitzthum, 1941. There are two other species in this subgenus. Distribution: Neotropical and Nearctic.…”
The genus Sennertia Oudemans, 1905 (Acari, Chaetodactylidae) is revised. Up to now, 49 species have been described in this genus, almost all from their hypopial stage. Adults are known only for four species. The adults live in the nests of bees, mainly Xylocopidae, and their heteromorphic deutonymphs (= hypopi) are phoretic on the bees. The parasitic role of these mites is not known but they probably feed on the bee larvae as do the members of the allied genus Chaetodactylus wich are parasitic in the nests of Megachilidae. The holotypes or lectotypes of 35 species have been examined and most of them are redescribed and redepicted. Four species have been placed in synonymy: S. moandensis with S. morstatti Vitzthum, 1914 S. xylocopae (Donnadieu, 1868) with S. cerambycina (Scopoli, 1763); S. sumatrensis Oudemans, 1924 with S. horrida (Vitzthum, 1912 S. donaldi Turk, 1948 with S. argentina Vitzthum, 1941. The genus Sennertia is redefined from the hypopial stage and four new subgenera (Afrosennertia, Asiosennertia, Amsennertia and Spinosennertia) and two new species S. (Asiosennertia) vitzthumi and S. (Asiosennertia) delfinadoae) are described. A key to the species is given.
Acarinaria are specialised structures on the bodies of insects that harbour dispersing mites, providing a secure attachment place for the mites. The structures are best known among bees and wasps. Their presence remains enigmatic, however, since the associated mites often have negative or neutral effects on their hosts. A new hypothesis explaining the origin of the acarinarium as a specialised defence mechanism is proposed. In nests with partitions (as constructed by many bees and wasps), parasitic or cleptoparasitic mites are rarely found in all cells. They negatively interact only with host larvae developing in infested cells and apparently cannot disperse within the nest to attack others in the developing brood before bee emergence. Only when emerging bees break the partitions can the mites reach other hosts. We propose that acarinaria serve to concentrate unwanted mites, reducing the chance that they will disperse to other members of the brood as the infested host leaves the nest. Development of special mite pouches (acarinaria) by hymenopteran hosts presumably increases the likelihood that all mites will stay with the individual(s) with reduced fitness, thereby reducing their effect on other bees in the brood. This paper reviews the associations between chaetodactylid mites and long-tongued bees (Apidae and Megachilidae). Only apid bees (Apidae) have acarinaria; megachilid bees, which harbour species of Chaetodactylus that usually kill the bee larvae, do not possess acarinaria. The following associations involving previously undescribed acarinaria or mite species are reported: Achaetodactylus ceratinae (axillar acarinarium on Ceratina nigriceps); Roubikia latebrosa, sp. nov. (metasomal acarinarium on Tetrapedia sp.), Sennertia argentina (genital acarinarium on Xylocopa fimbriata), Sennertia devincta, sp. nov., Sennertia sayutara, sp. nov. (metasomal acarinaria on Ceratina (Zadontomerus) spp.), Sennertia lauta, sp. nov. and Sennertia ratiocinator, sp. nov. (incipient scutellar–metanotal acarinarium on Xylocopa (Zonohirsuta) spp.). In the latter case, the mites display a remarkable difference in the attachment sites between male and female hosts. In females, the mites are phoretic in a groove between the scutellum and metanotum (scutellar–metanotal acarinarium), whereas on males, mites attach to the hairs of the anterior scutum.
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