Spiracular Plate of Nymphal and Adult Hard Ticks (Acarina: Ixodidae): Morphology and Cuticular Ultrastructure

1997 ◽  
Vol 116 (4) ◽  
pp. 341 ◽  
Author(s):  
Gerald T. Baker
Keyword(s):  
2021 ◽  
Author(s):  
Alberto A. Guglielmone ◽  
Santiago Nava ◽  
Richard G. Robbins
Keyword(s):  

Author(s):  
Richard C. Pacheco ◽  
Thiago F. Martins ◽  
Thiago B. F. Semedo ◽  
Drausio H. Morais ◽  
Herbert S. Soares ◽  
...  

2021 ◽  
pp. 101692
Author(s):  
Jiří Černý ◽  
Buyantogtokh Buyannemekh ◽  
Tersia Needham ◽  
Gantulga Gankhuyag ◽  
Dashzeveg Oyuntsetseg
Keyword(s):  

1983 ◽  
Vol 9 (12) ◽  
pp. 1543-1549 ◽  
Author(s):  
Robert M. Silverstein ◽  
Janet R. West ◽  
Daniel E. Sonenshine ◽  
Galila M. Khalil

1967 ◽  
Vol 15 (5) ◽  
pp. 941 ◽  
Author(s):  
HE Hinton

The structures of the nymphal and adult spiracles of the tick, Boophilus microplus, have been examined by means of serial sections and a stereoscan electron microscope. Contrary to the views of recent writers, the functional openings of the spiracle have been found to be holes or aeropyles in the peripheral part of the spiracular plate of the adult tick. The ostium of previous writers is shown to be the ecdysial tube, which is present only in the spiracles of adult ixodid ticks. After the nymphal-adult ecdysis, the ecdysial tube is closed. There is thus no ostium in this stage, as has been claimed by previous writers who supposed that the chief or only route for gas exchanges between the atrium of the spiracle and the ambient air was through the so-called ostium. The ecdysial process of the spiracles of ticks is shown to be basically similar to the ecdysial process of the spiracles of certain insects such as scarabaeid larvae and the larvae of some Diptera-Cyclorrhapha.


2018 ◽  
Vol 9 (3) ◽  
pp. 471-478 ◽  
Author(s):  
Brooke Storey-Lewis ◽  
Ann Mitrovic ◽  
Brent McParland

Parasitology ◽  
2003 ◽  
Vol 126 (1) ◽  
pp. 11-20 ◽  
Author(s):  
K. HANINCOVÁ ◽  
S. M. SCHÄFER ◽  
S. ETTI ◽  
H.-S. SEWELL ◽  
V. TARAGELOVÁ ◽  
...  

Borrelia burgdorferi sensu lato (s.l.) is maintained in nature by complex zoonotic transmission cycles, involving a large variety of vertebrates as hosts and hard ticks of the genus Ixodes as vectors. Recent studies suggest that the genospecies of B. burgdorferi s.l. and sometimes their subtypes are propagated by different spectra of hosts, mainly birds and rodents. In order to test the concept of host-association, we analysed the relationships between Borrelia genospecies, rodent hosts and I. ricinus ticks in an endemic focus of Lyme borreliosis in western Slovakia. Rodents and questing ticks were collected at a forested lowland locality near Bratislava. Tick infestation levels on rodents were determined, and spirochaete infections in ticks and in ear punch biopsies were analysed by PCR followed by genotyping. Mice were more heavily infested with ticks than bank voles, and a higher proportion of mice was infected with spirochaetes than voles. However, the infectivity of voles was much higher than that of mice. The vast majority of infections detected in the skin and in ticks feeding on the rodents represented B. afzelii. In contrast, more than half of all infections in questing ticks collected in the same region of Slovakia were identified as B. valaisiana and B. garinii. In conclusion, whilst the study reveals that mice and voles play different quantitative roles in the ecology of Lyme borreliosis, it demonstrates that B. afzelii is specifically maintained by European rodents, validating the concept of host-association of B. burgdorferi s.l.


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