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The paraldehyde fuchsin positive material in corpora cardiaca of Pimpla turionellae L. (Hymenoptera:Ichneumonidae) during egg maturation

Year 2011, Volume: 70 Issue: 1, 19 - 25, 03.06.2011

Abstract

The purpose of this study is to examine the effects of the neurosecretory material in corpus cardiacum (CC) on the reproduction of endoparasitic Pimpla turionellae L. For this purpose, the egg maturation and amount of the neurosecretory material in corpus cardiacum of the insects were examined by the serial cross sections. Egg maturation was determined by measuring the terminal oocyte length in the serial cross sections of the ovariole. The egg growth which has observed on the 3rd day, reached the maximum on 15th day and after that day the egg laying was observed. The sections of insect brains were stained by paraldehyde fuchsin. The amount of the paraldehyde fuchsin positive neurosecretory (PF+NS) material in CC was at a certain level in the first day of egg development. While terminal oocyte was reaching the maximum length, the amount of the PF+NS material in CC decreased to the minimum level. During the egg laying phase, the amount of the PF+NS material in CC reached the maximum level. These observations give us the idea that the neurosecretory material in corpus cardiacum of this insect may be related to the egg development.

References

  • Acle’ D., Brookes, V.J., Pratt G.E. and Rene’ F. R. (1990) Activity of the corpora allata of adult female Leucophaea maderae: Effects of mating and feding. Archives of Insect Biochemistry and Physiology, 14(3): 121129.
  • Adams T.S., Hintz M.M. and Pomonis J.G. (1968) Oostatic Hormone Production in Houseflies, Musca domestica, with Developing Ovaries. Journal of Insect Physiology, 14: 983-993.
  • Adams T.S., Grugel S., Ittycherian P.I., Olstad G. and Caldwell J.M. (1975) Interactions of the ring gland, ovaries, and juvenile hormone with brain neurosecretory cells in Musca domestica. Journal of Insect Physiology, 21: 1027-1043.
  • Adams T.S. (1976) The ovaries, ring gland, after neurosecretion during the second gonotrophic cycle in the housefly, Musca domestica. General and Comperative Endocrinology, 30: 69-76.
  • Bell W.J., and Barth R.H. (1971) Inititation of yolk deposition by juvenile hormone. Nature, New Biology, 230, 220-221.
  • Bonetti A.M., Siquieroli A.C., Santana F.A., Vieira C.U., Bezerra M., Pereira G.B., Simões Z.L. and Cruz-Landim C. (2006) Effect of juvenile hormone III on the ultrastructure of the corpora allata in Melipona quadrifasciata (Hymenoptera, Apidae, Meliponını). Brazilian Journal of Morphological Science, 23(3-4): 393-400.
  • Briegel, H. (1990) Metabolic relationship between female body size, reserves and fecundity of Aedes aegypti. Journal of Insect Physiology, 36(3): 165-172.
  • Bronskill J.F. (1961) A cage to simplify the rearing of the greater wax moth, Galleria mellonella (Pyralidae). Journal of Lepidopteran Society, 102-104.
  • De Wilde J. (1964) Reproduction-Endocrine Control. Physiology of Insecta (Ed. by. Rockstein, M). 1: 59-88.
  • Engelmann F. (1968) Endocrine control of reproduction in insects. Annual Review of Entomology, 13: 1-26.
  • Ewen A.B. (1962) An improved aldehyde fuchsin staining technique for neurosecretory products in insects. Transmission American Microscopy Society, 81: 94-96.
  • Fisher R.A. (1948) Statical tables for biological agricultural and medical research. 3. ed. Oliver and Boyd. Ltd. Edinburg.
  • Gilbert I.L. and Dia J. (1993) An ultrastructural and developmental analysis of the corpus allatum of juvenile hormone deficient mutants of Drosophila melanogaster. Roux's Archieves of Developmental Biology, 202: 85-94.
  • Greenplate J.T., Glaser R.L. and Hagedorn H.H. (1985) The role of factors from the head in the regulation of egg development in the mosquito Aedes aegypti. Journal of Insect Physiology. 31: 325-329.
  • Huerta C. and Martinez M.I. (2008) Morphological changes in reproductive organs and neuroendocrine centers related to nesting, mating, and larvicide behavior in Eurysternus mexicanus harold (Scarabaeinae: Eurysternini). The Coleopterists Bulletin, 62(1): 123-132.
  • Juberthie C. and Caussanel C. (1980) Release of Brain Neurosecretory Products from the Neurohaemal Part of the Aorta During EggLaying and Egg-Care in Labidura riparia, (Insecta: Dermaptera). Journal of Insect Physiology, 26: 427-429.
  • Khan M.A., Romberg-Privee H.M. and Schooneveld H. (1984) Innervation of the corpus allatum in the Colorado Potato Beetle as revealed by retrograde diffusion with horseradish peroxidase. General and Comperative Endocrinology, 55: 66-73.
  • Kim S.K., Seung K. and Rulifson E.J. (2004) Conserved mechanisms of glucose sensing and regulation by Drosophila corpora cardiaca cells. Nature, 16.431: 316-320.
  • King R.C., Aggarwal S.K. and Bodenstein D. (2005) The comparative submicroscopic cytology of the corpus allatum-corpus cardiacum complex of wild type and fes adult female Drosophila melanogaster. Journal of Experimental Zoology, 161(2): 151-175.
  • Lea A.O. and Thomsen E. (1969) Size idependent secretion by the corpus ailatum of Calliphora erythrocephala. Journal of Insect Physiology, 15: 477-482.
  • Leob M.J. and Hayes D.K. (1980) Neurosecretion during diapause and diapause development in brains of mature embryos of the gypsy moth, Laymantria dispar. Annual Entomological Society of American, 73: 432-436.
  • Meola R. and Lea A.O. (1971) Independence of paraldehyde-fuchsin staining of the corpus cardiacci and the presence of the neurosecretory hormone required for egg development in mosquito. General and Comperative Endocrinology, 16: 105-111.
  • Meola A. R., Lea A.O. and Meola R. (1970) Corpus cardiacum: Induced Fluctuation in Paraldehyde-Fuchsin Material in Aedes sollicitans Transactions of the American Microscopical Society . Vol. 89, No. 3: 418423.
  • Özlük A. (1991) The cerebral neurosecretory system and the diversity of the neurosecretory cell types in Pimpla turionellae L. (Hymenoptera: Ichneumonidae). Communications. Fac. Sic. Univ. Ank. Ser: C., 9: 33-47.
  • Panov A.A. (1980) Demonstration of neurosecretory cells in the insect central nervous system. In “Neuroanatomical Techniques” Ed by NJ Strausfeld, TA Miller, Springer-Verlag, New York, 25–50.
  • Park Y.I. and Ramaswamy S.B. (1998) Role of Brain, Ventral Nerve Cord, and Corpora Cardiaca-Corpora Allata Complex in the Reproductive Behavior of Female Tobacco budworm (Lepidoptera: Noctuidae). Annual Entomological Society of America. 91(3): 329-334.
  • Pratt G.E. and Davey K.G. (1972) The corpus allatum and oogenesis in Rhodnius prolixus (STAL.) I. The effects of allatectomy. Journal of Experimental Biology. 56: 215222.
  • Pearse A.G.E. (1961) Histochemistry, Theoretical and Applied, 2 nd. ed. J. and A. Curchii Ltd. London.
  • Rohdendorf E.B. and Watson J.A.L. (1969) The Control of Reproductive Cycles in the Female Firebrat, Lepismodes inquilinus. Journal of Insect Physiology, 2085-2101.
  • Sefiani M (1987) Regulation of Egg Laying and in Vitro Oviducal Contractions in Gryllus bimaculatus. Journal of Insect Physiology, 3(4): 215-222.
  • Siew Y.S. (1965) The Endocrine Control of Adult Reproductive Diapause in the Chrysomelid Beetle, Galeruca tanaceti (L.), III. Journal of Insect Physiology, 2: 973981.
  • Tabakoğlu A. (1988) Neurosecretory cell types and "C - cysteine incorporation in adult female Calliphora vicina. ROB. - DESV. (ERYTH-ROCEPHALA MEIG.) Istanbul Universitesi Fen Fakültesi Biyoloji Dergisi, 53: 45-64.
  • Tombes A. and Smith D.S. (2005) Ultrastructural studies on the corpora cardiaca-allata complex of the adult alfalfa weevil, Hypera postica. Journal of Morphology, 132(2): 137-147.
  • Toyoda I., Numata H. and Sakiko S. (1999) Role of the Median Neurosecretory Cells in the Ovarian Development of the Blow Fly Protophormia terraenovae. Zoological Science, 16(2): 187-199.
  • Ulrich G.M., Schlagintwelt B., Eder J. and Rembold H. (1985) Elimination of the allatotrophic activity in locust by microsurgical and immunological methods: Evidence for humoral control of the corpora allata, haemolymph proteins, and ovary development. General and Comperative Endocrinology, 59: 120-129.

Pimpla turionellae L.’nin (Hymenoptera:Ichneumonidae) yumurta gelişimi sırasında Korpora Kardiaka’sındaki paraldehit fuksin pozitif materyal

Year 2011, Volume: 70 Issue: 1, 19 - 25, 03.06.2011

Abstract

Bu çalışmanın amacı, bir dış parazit olan Pimpla turionellae’nin korpus kardiacum(CC)’undaki nörosekresyon maddesinin üreme üzerine olan etkisini incelemektir. Bu amaçla, seri kesitlerde, böceğin yumurta gelişimi ve korpus kardiacum’undaki nörosekresyon maddesi gözlenmiştir.Böceğin beyin kesitleri paraldehit fuksin ile boyanmıştır. Yumurta gelişimi, yumurtalık kesitlerindeki terminal oosit boyu ölçülerek belirlenmiştir. 3. günde gözlenen yumurta büyümesi, 15. günde en yüksek seviyesine ulaşmış ve bu günden sonra yumurta bırakma gözlenmiştir. CC’deki paraldehit fuksin pozitif (PF+ NS) maddenin miktarı, yumurta gelişiminin ilk günlerinde belirli bir seviyedeydi. Terminal oositler en uzun boylarına ulaşırken, CC’deki PF+ NS maddenin seviyesi en aza indi. Yumurta bırakma evresinde ise bu seviye, en yüksek değerine ulaştı. Bu gözlemler bize, bu böceğin korpora kardiaka’sındaki nörosekresyon maddesinin yumurta gelişimi ile ilişkisi olabileceği fikrini vermiştir

References

  • Acle’ D., Brookes, V.J., Pratt G.E. and Rene’ F. R. (1990) Activity of the corpora allata of adult female Leucophaea maderae: Effects of mating and feding. Archives of Insect Biochemistry and Physiology, 14(3): 121129.
  • Adams T.S., Hintz M.M. and Pomonis J.G. (1968) Oostatic Hormone Production in Houseflies, Musca domestica, with Developing Ovaries. Journal of Insect Physiology, 14: 983-993.
  • Adams T.S., Grugel S., Ittycherian P.I., Olstad G. and Caldwell J.M. (1975) Interactions of the ring gland, ovaries, and juvenile hormone with brain neurosecretory cells in Musca domestica. Journal of Insect Physiology, 21: 1027-1043.
  • Adams T.S. (1976) The ovaries, ring gland, after neurosecretion during the second gonotrophic cycle in the housefly, Musca domestica. General and Comperative Endocrinology, 30: 69-76.
  • Bell W.J., and Barth R.H. (1971) Inititation of yolk deposition by juvenile hormone. Nature, New Biology, 230, 220-221.
  • Bonetti A.M., Siquieroli A.C., Santana F.A., Vieira C.U., Bezerra M., Pereira G.B., Simões Z.L. and Cruz-Landim C. (2006) Effect of juvenile hormone III on the ultrastructure of the corpora allata in Melipona quadrifasciata (Hymenoptera, Apidae, Meliponını). Brazilian Journal of Morphological Science, 23(3-4): 393-400.
  • Briegel, H. (1990) Metabolic relationship between female body size, reserves and fecundity of Aedes aegypti. Journal of Insect Physiology, 36(3): 165-172.
  • Bronskill J.F. (1961) A cage to simplify the rearing of the greater wax moth, Galleria mellonella (Pyralidae). Journal of Lepidopteran Society, 102-104.
  • De Wilde J. (1964) Reproduction-Endocrine Control. Physiology of Insecta (Ed. by. Rockstein, M). 1: 59-88.
  • Engelmann F. (1968) Endocrine control of reproduction in insects. Annual Review of Entomology, 13: 1-26.
  • Ewen A.B. (1962) An improved aldehyde fuchsin staining technique for neurosecretory products in insects. Transmission American Microscopy Society, 81: 94-96.
  • Fisher R.A. (1948) Statical tables for biological agricultural and medical research. 3. ed. Oliver and Boyd. Ltd. Edinburg.
  • Gilbert I.L. and Dia J. (1993) An ultrastructural and developmental analysis of the corpus allatum of juvenile hormone deficient mutants of Drosophila melanogaster. Roux's Archieves of Developmental Biology, 202: 85-94.
  • Greenplate J.T., Glaser R.L. and Hagedorn H.H. (1985) The role of factors from the head in the regulation of egg development in the mosquito Aedes aegypti. Journal of Insect Physiology. 31: 325-329.
  • Huerta C. and Martinez M.I. (2008) Morphological changes in reproductive organs and neuroendocrine centers related to nesting, mating, and larvicide behavior in Eurysternus mexicanus harold (Scarabaeinae: Eurysternini). The Coleopterists Bulletin, 62(1): 123-132.
  • Juberthie C. and Caussanel C. (1980) Release of Brain Neurosecretory Products from the Neurohaemal Part of the Aorta During EggLaying and Egg-Care in Labidura riparia, (Insecta: Dermaptera). Journal of Insect Physiology, 26: 427-429.
  • Khan M.A., Romberg-Privee H.M. and Schooneveld H. (1984) Innervation of the corpus allatum in the Colorado Potato Beetle as revealed by retrograde diffusion with horseradish peroxidase. General and Comperative Endocrinology, 55: 66-73.
  • Kim S.K., Seung K. and Rulifson E.J. (2004) Conserved mechanisms of glucose sensing and regulation by Drosophila corpora cardiaca cells. Nature, 16.431: 316-320.
  • King R.C., Aggarwal S.K. and Bodenstein D. (2005) The comparative submicroscopic cytology of the corpus allatum-corpus cardiacum complex of wild type and fes adult female Drosophila melanogaster. Journal of Experimental Zoology, 161(2): 151-175.
  • Lea A.O. and Thomsen E. (1969) Size idependent secretion by the corpus ailatum of Calliphora erythrocephala. Journal of Insect Physiology, 15: 477-482.
  • Leob M.J. and Hayes D.K. (1980) Neurosecretion during diapause and diapause development in brains of mature embryos of the gypsy moth, Laymantria dispar. Annual Entomological Society of American, 73: 432-436.
  • Meola R. and Lea A.O. (1971) Independence of paraldehyde-fuchsin staining of the corpus cardiacci and the presence of the neurosecretory hormone required for egg development in mosquito. General and Comperative Endocrinology, 16: 105-111.
  • Meola A. R., Lea A.O. and Meola R. (1970) Corpus cardiacum: Induced Fluctuation in Paraldehyde-Fuchsin Material in Aedes sollicitans Transactions of the American Microscopical Society . Vol. 89, No. 3: 418423.
  • Özlük A. (1991) The cerebral neurosecretory system and the diversity of the neurosecretory cell types in Pimpla turionellae L. (Hymenoptera: Ichneumonidae). Communications. Fac. Sic. Univ. Ank. Ser: C., 9: 33-47.
  • Panov A.A. (1980) Demonstration of neurosecretory cells in the insect central nervous system. In “Neuroanatomical Techniques” Ed by NJ Strausfeld, TA Miller, Springer-Verlag, New York, 25–50.
  • Park Y.I. and Ramaswamy S.B. (1998) Role of Brain, Ventral Nerve Cord, and Corpora Cardiaca-Corpora Allata Complex in the Reproductive Behavior of Female Tobacco budworm (Lepidoptera: Noctuidae). Annual Entomological Society of America. 91(3): 329-334.
  • Pratt G.E. and Davey K.G. (1972) The corpus allatum and oogenesis in Rhodnius prolixus (STAL.) I. The effects of allatectomy. Journal of Experimental Biology. 56: 215222.
  • Pearse A.G.E. (1961) Histochemistry, Theoretical and Applied, 2 nd. ed. J. and A. Curchii Ltd. London.
  • Rohdendorf E.B. and Watson J.A.L. (1969) The Control of Reproductive Cycles in the Female Firebrat, Lepismodes inquilinus. Journal of Insect Physiology, 2085-2101.
  • Sefiani M (1987) Regulation of Egg Laying and in Vitro Oviducal Contractions in Gryllus bimaculatus. Journal of Insect Physiology, 3(4): 215-222.
  • Siew Y.S. (1965) The Endocrine Control of Adult Reproductive Diapause in the Chrysomelid Beetle, Galeruca tanaceti (L.), III. Journal of Insect Physiology, 2: 973981.
  • Tabakoğlu A. (1988) Neurosecretory cell types and "C - cysteine incorporation in adult female Calliphora vicina. ROB. - DESV. (ERYTH-ROCEPHALA MEIG.) Istanbul Universitesi Fen Fakültesi Biyoloji Dergisi, 53: 45-64.
  • Tombes A. and Smith D.S. (2005) Ultrastructural studies on the corpora cardiaca-allata complex of the adult alfalfa weevil, Hypera postica. Journal of Morphology, 132(2): 137-147.
  • Toyoda I., Numata H. and Sakiko S. (1999) Role of the Median Neurosecretory Cells in the Ovarian Development of the Blow Fly Protophormia terraenovae. Zoological Science, 16(2): 187-199.
  • Ulrich G.M., Schlagintwelt B., Eder J. and Rembold H. (1985) Elimination of the allatotrophic activity in locust by microsurgical and immunological methods: Evidence for humoral control of the corpora allata, haemolymph proteins, and ovary development. General and Comperative Endocrinology, 59: 120-129.
There are 35 citations in total.

Details

Primary Language English
Journal Section Makaleler
Authors

Aydın Özlük

Nursel Gül This is me

Publication Date June 3, 2011
Submission Date June 3, 2011
Published in Issue Year 2011 Volume: 70 Issue: 1

Cite

AMA Özlük A, Gül N. The paraldehyde fuchsin positive material in corpora cardiaca of Pimpla turionellae L. (Hymenoptera:Ichneumonidae) during egg maturation. Eur J Biol. June 2011;70(1):19-25.