Mandibular muscle troponin of the Florida carpenter ant Camponotus floridanus: extending our insights into invertebrate Ca2+ regulation

Author(s):  
Yun Shi ◽  
Julia P. Bethea ◽  
Hannah L. Hetzel-Ebben ◽  
Maicon Landim-Vieira ◽  
Ross J. Mayper ◽  
...  
2012 ◽  
Vol 23 (3) ◽  
pp. 486-496 ◽  
Author(s):  
D. F. Simola ◽  
C. Ye ◽  
N. S. Mutti ◽  
K. Dolezal ◽  
R. Bonasio ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (8) ◽  
pp. e43036 ◽  
Author(s):  
Carolin Ratzka ◽  
Frank Förster ◽  
Chunguang Liang ◽  
Maria Kupper ◽  
Thomas Dandekar ◽  
...  

2007 ◽  
Vol 193 (9) ◽  
pp. 993-1000 ◽  
Author(s):  
Sara Diana Leonhardt ◽  
Andreas Simon Brandstaetter ◽  
Christoph Johannes Kleineidam

1988 ◽  
Vol 22 (3) ◽  
pp. 175-183 ◽  
Author(s):  
Laurence Morel ◽  
Robert K. Vander Meer ◽  
Barry K. Lavine

EDIS ◽  
1969 ◽  
Vol 2004 (4) ◽  
Author(s):  
John Warner ◽  
Rudolf H. Scheffrahn

The compact carpenter ant, Camponotus planatus (Roger), although primarily an arboreal species, is increasingly becoming recognized as a structural pest in Florida. This common name is still unofficial. A smaller, more "compact" and close relative of the Florida carpenter ant complex (Camponotus floridanus and C. tortuganus) and often found living in close proximity with them, the compact carpenter ant is the subject of numerous inquiries to pest control operators in the South Florida area. This document is EENY-189, one of a series of Featured Creatures from the Entomology and Nematology Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Published: January 2001. EENY189/IN346: Compact Carpenter Ant (proposed common name),Camponotus planatus (Roger) (Insecta: Hymenoptera: Formicidae) (ufl.edu)


2002 ◽  
Vol 68 (9) ◽  
pp. 4187-4193 ◽  
Author(s):  
Christina Sauer ◽  
Dieter Dudaczek ◽  
Bert Hölldobler ◽  
Roy Gross

ABSTRACT The distribution of endosymbiotic bacteria in different tissues of queens, males, and workers of the carpenter ant Camponotus floridanus was investigated by light and electron microscopy and by in situ hybridization. A large number of bacteria could be detected in bacteriocytes within the midguts of workers, young virgin queens, and males. Large amounts of bacteria were also found in the oocytes of workers and queens. In contrast, bacteria were not present in oocyte-associated cells or in the spermathecae of mature queens, although occasionally a small number of bacteria could be detected in the testis follicles of males. Interestingly, the number of bacteriocytes in mature queens was strongly reduced and the bacteriocytes contained only very few or no bacteria at all, although the endosymbionts were present in huge amounts in the ovaries of the same animals. During embryogenesis of the deposited egg, the bacteria were concentrated in a ring of endodermal tissue destined to become the midgut in later developmental stages. However, during larval development, bacteria could also be detected in other tissues although to a lesser extent. Only in the last-instar larvae were bacteria found exclusively in the midgut tissue within typical bacteriocytes. Tetracycline and rifampin efficiently cleansed C. floridanus workers of their symbionts and the bacteriocytes of these animals still remained empty several months after treatment had ceased. Despite the lack of their endosymbionts, these adult animals were able to survive without any obvious negative effect under normal cultivation conditions.


2010 ◽  
Vol 10 (1) ◽  
pp. 308 ◽  
Author(s):  
Sascha Stoll ◽  
Heike Feldhaar ◽  
Martin J Fraunholz ◽  
Roy Gross

2015 ◽  
Vol 14 (3) ◽  
pp. 1504-1514 ◽  
Author(s):  
Franziska Schmitt ◽  
Jens T. Vanselow ◽  
Andreas Schlosser ◽  
Jörg Kahnt ◽  
Wolfgang Rössler ◽  
...  

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