Literature DB >> 16388145

Structure and function of the spermathecal complex in the phlebotomine sandfly Phlebotomus papatasi Scopoli (Diptera: Psychodidae): I. ultrastructure and histology.

K Ilango1.   

Abstract

Females of phlebotomine sandflies (Diptera: Psychodidae) possess highly variable spermathecae that present several important taxonomic characters. The cause of this diversity remains a neglected field of sandfly biology, but may possibly be due to female post-mating sexual selection. To understand this diversity, a detailed study of the structure and function of the spermathecal complex in at least one of the species was a prerequisite. Using scanning and transmission electron microscopy, described here is ultrastructure of the spermathecal complex in the sand fly, Phlebotomus papatasi Scopoli. The spermathecal complexes are paired; each consists of a long spermathecal duct, a cylindrical spermathecal body, and a spherical spermathecal gland. Muscle fibres, nerves, tracheoles, and vascular sinuses connect the spermathecal body and duct through the epithelial layers. Spermathecal gland is formed by a typical insect epidermis and consisting of an epithelial layer of class-1 epidermal cells and elaborate glandular cells of class-3 epidermal cells, each having both receiving and conducting ductules (i.e. "end apparatus") and a "cytological apodeme", which is a newly described cell structure. The spermathecal body and duct are lined by class-1 epidermal cells and a cuticle, and are enveloped by a super-contracting visceral muscular system. The cuticle consists of rubber-like resilin, and its fibrillar arrangement and chemical nature are described. A well-developed neuromuscular junction exists between the spermathecal gland and the spermathecal body, which are connected to each other by a nerve and a muscle. The spermathecal complexes of the sandfly are compared with those of other insect species. The physiological role and possible evolutionary significance of the different parts of spermathecal complex in the sandfly are inferred from the morphology and behaviour. Post-mating sexual selection may be responsible for the structural uniqueness of the spermathecal complex in phlebotomine sandflies.

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Year:  2005        PMID: 16388145     DOI: 10.1007/BF02703571

Source DB:  PubMed          Journal:  J Biosci        ISSN: 0250-5991            Impact factor:   1.826


  16 in total

1.  Criteria for demonstrating female sperm choice.

Authors:  S Pitnick; W D Brown
Journal:  Evolution       Date:  2000-06       Impact factor: 3.694

2.  Scanning electron microscopy of the spermatheca in Sitophilus granarius (L.).

Authors:  A S Tombes; R M Roppel
Journal:  Tissue Cell       Date:  1971       Impact factor: 2.466

3.  Ultrastructure of sperm penetration of house fly eggs.

Authors:  M E Degrugillier; R A Leopold
Journal:  J Ultrastruct Res       Date:  1976-09

4.  PERSPECTIVE: CHASE-AWAY SEXUAL SELECTION: ANTAGONISTIC SEDUCTION VERSUS RESISTANCE.

Authors:  Brett Holland; William R Rice
Journal:  Evolution       Date:  1998-02       Impact factor: 3.694

Review 5.  The fine structure of membranes and intercellular communication in insects.

Authors:  P Satir; N B Gilula
Journal:  Annu Rev Entomol       Date:  1973       Impact factor: 19.686

6.  The fine structure of the spermathecae and their ducts in the mosquito Aedes aegypti.

Authors:  A N Clements; S A Potter
Journal:  J Insect Physiol       Date:  1967-12       Impact factor: 2.354

7.  Coadaptation of male aedeagal filaments and female spermathecal ducts of the old world phlebotomine sand flies (Diptera: Psychodidae).

Authors:  K Ilango; R P Lane
Journal:  J Med Entomol       Date:  2000-09       Impact factor: 2.278

8.  Structure and function of the spermathecal complex in the phlebotomine sandfly Phlebotomus papatasi Scopoli (Diptera: Psychodidae): II. post-copulatory histophysiological changes during the gonotrophic cycle.

Authors:  K Ilango
Journal:  J Biosci       Date:  2005-12       Impact factor: 1.826

9.  EVOLUTION OF MULTIPLE KINDS OF FEMALE SPERM-STORAGE ORGANS IN DROSOPHILA.

Authors:  Scott Pitnick; Therese Marrow; Greg S Spicer
Journal:  Evolution       Date:  1999-12       Impact factor: 3.694

10.  Supercontracting and non-supercontracting visceral muscles in the tsetse fly, Glossina austeni.

Authors:  M J Rice
Journal:  J Insect Physiol       Date:  1970-06       Impact factor: 2.354

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  5 in total

1.  Spermatheca of the scorpionfly Sinopanorpa tincta (Navás, 1931) (Mecoptera: Panorpidae).

Authors:  Lu-Yao Yang; Bao-Zhen Hua
Journal:  Protoplasma       Date:  2020-11-09       Impact factor: 3.356

2.  Structure and function of the spermathecal complex in the phlebotomine sandfly Phlebotomus papatasi Scopoli (Diptera: Psychodidae): II. post-copulatory histophysiological changes during the gonotrophic cycle.

Authors:  K Ilango
Journal:  J Biosci       Date:  2005-12       Impact factor: 1.826

3.  Morphology of ovary and spermathecae of the parasitoid Eibesfeldtphora tonhascai Brown (Diptera: Phoridae).

Authors:  Cliver Fernandes Farder-Gomes; Helen Cristina Pinto Santos; Marco Antonio Oliveira; José Cola Zanuncio; José Eduardo Serrão
Journal:  Protoplasma       Date:  2018-06-16       Impact factor: 3.356

4.  Unlocking the "Black box": internal female genitalia in Sepsidae (Diptera) evolve fast and are species-specific.

Authors:  Nalini Puniamoorthy; Marion Kotrba; Rudolf Meier
Journal:  BMC Evol Biol       Date:  2010-09-10       Impact factor: 3.260

5.  Fine structure of the male reproductive system and reproductive behavior of Lutzomyia longipalpis sandflies (Diptera: Psychodidae: Phlebotominae).

Authors:  Carolina N Spiegel; Jorge A C Bretas; Alexandre A Peixoto; Felipe M Vigoder; Rafaela V Bruno; Maurilio J Soares
Journal:  PLoS One       Date:  2013-09-13       Impact factor: 3.240

  5 in total

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