Skip to main content
Log in

Ultrastructural and cytochemical studies on the germarium of Dicrocoelium dendriticum (Plathelminthes, Digenea)

  • Published:
Zoomorphology Aims and scope Submit manuscript

Summary

The unpaired germarium of Dicrocoelium dendriticum contains many female germ cells at different stages of maturation and is enveloped by a fibrous basal lamina-like structure and a multilayered cytoplasmic sheath whose origins and functions are discussed. The maturation process of primary oocytes occurs completely within the prophase of the first meiotic division. It has been divided into three stages, as previously suggested for monogeneans. Stage I corresponds to oogonia and early oocytes which are located in the distal germinative area of the gonad. These cells are characterized by a high nucleo/cytoplasmic ratio and a poorly differentiated cytoplasm. Stage II corresponds to maturing oocytes grouped in the central area of the gonad and exhibiting long synaptonemal complexes and a prominent nucleolus. The main feature of cytoplasmic differentiation is the increase in the number of RER and Golgi complex which are involved in the production of small electron-dense granules. Stage III corresponds to mature oocytes located in the proximal area of the germarium near the origin of the oviduct. In this stage, the granules become regularly distributed in a monolayer in the peripheral ooplasm and make contact with the oolemma. They show a distinctive complex structure, are composed of proteins and glycoproteins and do not contain polyphenols. Their possible role as cortical granules is discussed in relation to chemical composition and previous studies on other Plathelminthes. Neither yolk globules nor glycogen are present in the oocytes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

I :

oogonium and early oocyte

II :

growing oocyte

III :

mature oocyte

cg :

cortical granule

cs :

cytoplasmic sheath

db :

dense body

ecm :

extra cellular matrix

ER :

endoplasmic reticulum

fl :

fibrous extracellular layer

gc :

Golgi complex

m :

mitochondria

N :

nucleus

nu :

nucleolus

RER :

rough endoplasmic reticulum

sc :

synaptonemal complex

References

  • Anderson A, André J (1968) The extraction of some cell components with pronase and pepsin from thin sections of tissue embedded in an Epon-Araldite mixture. J Microscopie 7:343–345

    Google Scholar 

  • Awad AH, Probert J (1990) Scanning and transmission electron microscopy of the female reproductive system of Schistosoma margrebowiei Le Roux, 1933. Parasitology 73:13–23

    Google Scholar 

  • Ax P (1987) The phylogenetic system. The systematization of organisms on the basis of their phylogenesis. Wiley, Chichester, pp 1–340

    Google Scholar 

  • Bjorkman N, Thorsell W (1964) On the ultrastructure of the ovary of the liver fluke Fasciola hepatica L. Z Zellforsch 63:538–549

    Google Scholar 

  • Davies RE, Roberts LS (1983) Platyhelminthes-Eucestoda. In: Adiyodi KG, Adiyodi RG (eds) Reproductive biology of invertebrates, vol I Oogenesis, oviposition and oosorption. Wiley, Chichester, pp 109–233

    Google Scholar 

  • Domenici L, Galleni L, Gremigni V (1975) Electron microscopical and cytochemical study of egg-shell globules in Notoplana alcinoi (Turbellaria, Polycladida). J Submicrosc Cytol 7:239–247

    Google Scholar 

  • Eddy EM (1975) Germ plasm and the differentiation of the germ cell line. Int Rev Cytol 43:229–280

    Google Scholar 

  • Ehlers U (1985) Das phylogenetischeSystem der Plathelminthes. G Fischer, Stuttgart New York, pp 1–317

    Google Scholar 

  • Erasmus DA (1973) A comparative study of the reproductive system of mature, immature and ‘unisexual’ female Schistosoma mansoni. Parasitology 67:165–183

    Google Scholar 

  • Falleni A, Gremigni V (1989) Egg covering formation in the acoel Convoluta psammophila (Platyhelminthes, Turbellaria): an ultrastructural and cytochemical investigation. Acta Embryol Morphol Exper ns 10:105–112

    Google Scholar 

  • Falleni A, Gremigni V (1990) Ultrastructural study of oogenesis in the acoel turbellarian Convoluta. Tissue Cell 22:301–310

    Google Scholar 

  • Falleni A, Gremigni V (1992) An ultrastructural study of growing oocytes in Nematoplana riegeri (Platyhelminthes). J Submicrosc Cytol Pathol 24:51–59

    Google Scholar 

  • Falleni A, Lucchesi P (1992) Ultrastructural and cytochemical aspects of oogenesis in Castrada viridis (Platyhelminthes, Rhabdocoela). J Morphol 213:241–250

    Google Scholar 

  • Grant WC, Harkema R, Muse KE (1977) Ultrastructure of Pharyngostomoides procyonis Harkema, 1942 (Diplostomatidae). II. The female reproductive system. J Parasitol 63:1019–1030

    Google Scholar 

  • Gremigni V (1969) Ricerche istochimiche e ultrastrutturali sull'ovogenesi dei Tricladi. II. Inclusi citoplasmatici in Planaria torva, Dendrocoelum lacteum e Polycelis nigra. Accad Naz Lincei 47:397–404

    Google Scholar 

  • Gremigni V (1976) Genesis and structure of the so-called “Balbiani body” or “yolk nucleus” in the oocyte of Dugesia dorotocephala (Turbellaria, Tricladida). J Morphol 149:265–277

    Google Scholar 

  • Gremigni V (1983) Platyhelminthes-Turbellaria. In: Adiyodi KG, Adiyodi RG (eds) Reproductive biology of invertebrates, vol I Oogenesis, oviposition and ooresoption. Wiley, Chichester, pp 67–107

    Google Scholar 

  • Gremigni V (1988) A comparative ultrastructural study of homocellular and heterocellular female gonads in free-living Platyhelminthes-Turbellaria. Fortschr Zool 36:245–261

    Google Scholar 

  • Gremigni V, Domenici L (1975) Genesis, composition and fate of cortical granules in the eggs of Polycelis nigra (Turbellaria, Tricladida). J Ultrastruct Res 50:277–283

    Google Scholar 

  • Gremigni V, Falleni A (1992) Mechanisms of shell-granule and yolk production in oocytes and vitellocytes of Platyhelminthes-Turbellaria. Anim Biol 1:29–37

    Google Scholar 

  • Gremigni V, Falleni A, Lucchesi P (1987) An ultrastructural study of oogenesis in the turbellarian Macrostomum. Acta Embryol Morphol Experns 8:257–262

    Google Scholar 

  • Gremigni V, Nigro M (1983) An ultrastructural study of oogenesis in a marine triclad. Tissue Cell 15:405–415

    Google Scholar 

  • Gremigni V, Nigro M (1984) Ultrastructural study of oogenesis in Monocelis lineata (Turbellaria, Proseriata). Int J Invert Repr Dev 7:105–118

    Google Scholar 

  • Gremigni V, Nigro M, Settembrini MS (1986) Ultrastructural features of oogenesis in some marine neoophoran turbellarians. Hydrobiologia 132:145–150

    Google Scholar 

  • Gresson RA (1964) Oogenesis in the hermaphroditic Digenea (Trematoda). Parasitology 54:409–421

    Google Scholar 

  • Guraya SS, parshad VR (1988) Platyhelminthes. In: Adiyodi KG, Adiyodi RG (eds) Reproductive biology of invertebrates, vol III Accessory sex glands. Wiley, Chichester, pp 1–49

    Google Scholar 

  • Halton DW, Stranock SD, Hardcastle A (1976) Fine structural observations on oocyte development in monogeneans. Parasitology 73:13–23

    Google Scholar 

  • Hathaway RP (1979) The morphology of crystalline inclusions in primary oocytes of Aspidogaster conchicola von Baer, 1827 (Trematoda: Aspidobothria). Proc Helminth Soc Wash 46:201–206

    Google Scholar 

  • Holy JM, Wittrock DD (1986) Ultrastructure of the female reproductive organs (ovary, vitellaria, and Mehli'sgland) of Halipegus eccentricus (Trematoda:Derogenidae). Can J Zool 64:2203–2212

    Google Scholar 

  • Hori I (1982) An ultrastructural study of the chromatoid body in planarian regenerative cells. J Electron Microsc 31:63–72

    Google Scholar 

  • Irwin SW, Threagold LT (1972) Electron microscope studies of Fasciola hepatica. X Egg formation. Exp Parasitol 31:321–331

    Google Scholar 

  • Ishida S, Teshirogi W (1986) Eggshell formation in polyclads (Turbellaria). Hydrobiologia 132:127–135

    Google Scholar 

  • Justine JL, Mattei X (1984) Ultrastructural observations on the spermatozoon, oocyte and fertilization process in Gonapodasmius, a gonochoristic Trematode (Trematoda:Digenea:Didymozoidae). Acta Zool (Stockholm) 65:171–177

    Google Scholar 

  • Justine JL, Mattei X (1986) Ultrastructural observations on fertilization in Dionchus remorae (Platyhelminthes, Monogenea, Dionchidae). Acta Zool (Stockholm). 67:97–101

    Google Scholar 

  • Karling TG (1940) Zur Morphologie und Systematik der Alloecoela cumulata und Rhabdocoela lecithophora (Turbellaria). Acta Zool Fenn 26:1–260

    Google Scholar 

  • Koulish S (1965) Ultrastructure of differentiating oocytes in the trematode Gorgoderina attenuata. I. The ‘nucleolus-like’ cytoplasmic body and some lamellar membrane system. Dev Biol 12:248–268

    Google Scholar 

  • Locke M, Krishnan N (1971) The distribution of polyphenoloxidases and polyphenols during cuticle formation. Tissue Cell 3:103–126

    Google Scholar 

  • Mahendrasingam S, Fairweather I, Halton DW (1990) Oogenesis in the free proglottis of Trilocularia acanthiaevulgaris (Cestoda, Tetraphyllidae). Parasitol Res 76:692–699

    Google Scholar 

  • Martinez-Alos S, Cifrian B, Gremigni V (1993) Ultrastructural investigations on the vitellaria of the digenean Dicrocoelium dendriticum. II. J Submicrosc Cytol Pathol 25

  • Orido Y (1987) Development of the ovary and the female reproductive cells of the lung fluke, Paragonimus ohirai (Trematoda:Troglotrematidae). J Parasitol 73:161–171

    Google Scholar 

  • Rieger RM, Tyler S, Smith III JPS, Rieger GE (1991) Platyhelminthes: Turbellaria. In: Harrison FW, Bogitsh BJ (eds) Microscopic anatomy of invertebrates, vol III Platyhelminthes and Nemertinea. Wiley, New York, pp 7–140

    Google Scholar 

  • Smith JPS, Thomas MB, Chandler R, Zane SF (1988) Granular inclusions in the oocyte of Convoluta sp, Nemertoderma sp, and Nemertinoides elongatus (Turbellaria, Acoelomorpha). Fortsch Zool 36:263–269

    Google Scholar 

  • Smyth JD, Halton DW (1983) The physiology of trematodes. Cambridge Univ Press, Cambridge, pp 1–417

    Google Scholar 

  • Sopott-Ehlers B (1986) Fine-structural characteristics of female and male germ cells in Proseriata Otoplanidae (Platyhelminthes) Hydrobiologia 132:137–144

    Google Scholar 

  • Sopott-Ehlers B (1990) Feinstrukturelle Untersuchungen an Vitellarien und Germarien von Coelogynopora gynocotyla Steinböck, 1924 (Plathelminthes, Proseriata). Microfauna Marina 6:121–138

    Google Scholar 

  • Sopott-Ehlers B (1991) Electron microscopical observations on vitellocytes and germocytes in Nematoplana coelogynoporoides (Plathelminthes, Proseriata). Zoomorphology 110:293–300

    Google Scholar 

  • Spence IM, Silk MH (1971) Ultrastructural studies of the blood fluke Schistosoma mansoni. V. The female reproductive system. A preliminary report. South African J Med Sci 36:41–50

    Google Scholar 

  • Thiery JP (1967) Mise en evidence des polysaccharides sur coupes fines en microscopie electronique. J Microscopie 6:987–1018

    Google Scholar 

  • Wallace RA, Selman K (1990) Ultrastructural aspects of oogenesis and oocyte growth in fish and amphibians. J Electron Microsc Tech 16:175–201

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cifrian, B., Martinez-Alos, S. & Gremigni, V. Ultrastructural and cytochemical studies on the germarium of Dicrocoelium dendriticum (Plathelminthes, Digenea). Zoomorphology 113, 165–171 (1993). https://doi.org/10.1007/BF00394857

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00394857

Keywords

Navigation