CSIRO Publishing Home Books & CDs Journals About Us Shopping Cart
Invertebrate Systematics
  Continuing Invertebrate Taxonomy
You are here: Journals > Invertebrate Systematics   
Search
 
 
  Advanced Search
   
Journal Home
General Information
Scope
Editorial Board
Editorial Contacts
Print Publication Dates
Online Content
For Authors
For Referees
How to Order

 Most Read
Visit our Most Read page regularly to keep up-to-date with the most downloaded papers in this journal.

 Early Alert
Subscribe to our email Early Alert or RSS feeds for the latest journal papers.

 

Acarinaria in associations of apid bees (Hymenoptera) and chaetodactylid mites (Acari)

Pavel B. Klimov A C, S. Bradleigh Vinson B and Barry M. OConnor A

A University of Michigan, Museum of Zoology, 1109 Geddes Avenue, Ann Arbor, MI 48109-1079, USA.
B Department of Entomology, Texas A&M University, TAMU 2475, College Station, TX 77843-2475, USA.
C Corresponding author. Email: pklimov@umich.edu


Abstract

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.

Invertebrate Systematics 21(2) 109–136    doi:10.1071/IS06019
Submitted: 2 June 2006    Accepted: 23 February 2007    Published: 21 May 2007





   
Subscriber Login
Username:
Password:  

 View
Issue Contents
PDF (1 MB) $40
Export Citation
 Tools
Print
Email this page
    


 
Top  Email this page
 


Legal & Privacy | Sitemap | Contact Us | Help

CSIRO

© CSIRO 1996-2010