Insight into the reproductive biology of euryhaline cyclopoid copepods Apocyclops dengizicus and Apocyclops royi
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The present research work aimed to investigate the unexplored information about mating strategies and reproductive potential of two euryhaline cyclopoid species Apocyclops dengizicus and A. royi. Laboratory experiments on mating strategy and reproductive aspects such as the efficacy of females under different mating conditions, the reproductive potential of males, mating frequency, and the effect of starvation on survival and reproductive potential, were conducted and documented. The once-mated female and females pairing continuously with males favored higher reproductive potential. In the present study, the mate-pursuing males prefers to copulate with mature virgin females. The older female was unable to produce eggs even after the sperm discharge. The lifespan of both the Apocyclops species under different states of mating and unmated conditions showed considerable variation. Apocyclops dengizicus produced 7.92±0.57 pairs of spermatophores, while A. royi extruded 13.32±0.99 pairs of spermatophores during its lifespan. The results were analyzed and inferred; thus, high throughput was applied to reveal the understudied topics of these Apocyclops species to add considerable knowledge about its reproductive biology.
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Abdullahi B.A. (1900). The effect of temperature on reproduction in three species of cylopoid copepods. Hydrobiology, 196: 101-109.
Blades-Eckelbarger P.I. (1977). Mating behavior of Centropages typicus (Copepoda: Calanoida). Marine Biology, 40: 57-64.
Botelho M.J.C. (1999). Revisao do genero Apocyclops Lindberg, 1942 (Copepoda: Cyclopoida). PhD, dissertation, Instituto de Biociencias, Universidade de Sao Paulo, Sao Paulo.
Burris Z.P., Dam H.G. (2015). Female mating status affects mating and male mate-choice in the copepod genus Acartia. Journal of Plankton Research, 37(1): 183-196.
Checkley D.R.Jr. (1980). The egg production of a marine copepod in relation to its food supply: laboratory studies. Limnology and Oceanography, 25: 430-446.
Cheng S.H., Chen H.C., Su M.S., Ho J.S. (1999). Effects of temperature and salinity on the maturation in Apocyclops royi (Cyclopidae, Cyclopoida). In: The 7th International Conference on Copepoda. Curitiba, Brazil, 25-31 July 1999. Chetumal, Mexico: World Association of Copepodologists. 80 p.
Chow-Fraser P., Maly E.J. (1991). Factors governing clutch size in two species of Diaptomus (Copepoda: Calanoida), Canadian Journal of Fisheries and Aquatic Sciences, 48: 364-370.
Dagg M. (1977). Some effects of patchy food environments on copepods, Limnology and Oceanography, 22: 99-107.
Defaye D., Cuoc C., Barthelemy R.M. (2003). A new imterpretation of the female genitalia in Macrocyclops albidus (Copepoda, Cyclopidae). Acta Zoologica, 84: 25-31.
Ederington M.C., McManus G.B., Harvey H.R. (1995). Trophic transfer of fatty acids, sterols, and a triterpenoid alcohol between bacteria, a ciliate and the copepod Acartia tonsa. Limnology and Oceanography, 40: 860-867.
Fleminger A. (1967). Taxonomy, distribution and polymorphism in the Labidocera jollae group with remarks on evolution within the group (Copepoda: Calanoida). Proceedings of the United States National Museum, 120: 1-61.
Foltz K. (1995). Sperm-binding proteins, International Review of Cytology, 163: 249-303.
Hill L.L., Coker R.E. (1930). Observations on mating habits of Cyclops. Journal of the Elisha Mitchell Scientific Society, 45: 206-220.
Ianora A., Carlo B.S., Mascellaro P. (1989). Reproductive biology of the planktonic copepod Temora stylifera. Marine Biology, 101: 187-194.
Jacobs J. (1961). Laboratory cultivation of the marine copepod Pseudodiaptomus coronatus. Limnology and Oceanography, 6: 443-446.
Jayanthi M. (2001). The impact of food quality and selective feeding on the growth and development of Heliodiaptomus viduus. Verhandlungen des Internationalen Verein Limnologie, 27: 3682-3685.
Kiørboe T. (2006). Sex, sex-ratios, and the dynamics of pelagic copepod populations. Oecologia, 148: 40-50.
Lee C.M. (1972). Structure and function of the spermatophore and its coupling device in the Centropagidae (Copepoda, Calanoida). Bulletin of Marine Ecology, 8: 1-20.
Leeuwen V.H.C., Maly E.J. (1991). Changes in swimming behaviour of male Diaptomus leptopus (Copepoda: Calanoida) in response to gravid females. Limnology and Oceanography, 36: 1188-1195.
Lonsdale D.J., Frey M.A., Snell T.W. (1998). The role of chemical signals in copepod reproduction. Journal of Marine Systems, 15: 1-12.
Maier G. (1992). The reproductive biology of Cyclops vicinus. Journal of Plankton Research, 14(1): 127-135.
Marshall S.M., Orr A.P. (1972). The biology of a marine copepod, Calanus finmarchicus (Gunnerus). Springer-Verlag Berlin Heidelberg Gmbh. 195 p.
Marshall S.M., Orr A.P. (1958). On the biology of Calanus finmarchicus X. Seasonal changes in oxygen consumption. Journal of Marine Biological Association of United Kingdom, 37: 459-472.
Muthupriya P., Sivakumar K., Altaff K. (2004). Egg production in Mesocyclops thermocyclopoides and Thermocyclops decipines with reference to mating. Journal of Aquatic Biology, 19(1): 31-36.
Nival S., Pagona M., Nival P. (1990). Laboratory study of the spawning rate of the calanoid copepod Centropages typicus: effect of fluctuating food supply. Journal of Plankton Research, 12: 535-547.
Pandian T.J. (1994). Arthropoda-Crustacea. In: K.G. Adiyodi, R.G. Adiyodi (Eds.), Reproductive biology of invertebrates. Oxford IBH Publishing Company Private Limited Delhi. pp: 39-166.
Preetha P.E., Altaff K. (1996). Fecundity in relation to different types of food composition Sinodiaptomus (Rhinediaptomus) indicus (Copepoda: Calanoida). Proceedings of the Indian National Science Academy, B 62(3): 191-198.
Reid J.W., Hamilton R, Duffield R.M. (2002). First confirmed New World Record of Apocylcops dengizicus (Lepeschkin), with a key to the species of Apocylcops North America and the Carribean region (Crustacea: Copepoda: Cyclopidae), Jeffersoniana, 10: 1-25.
Runge J.A. (1985) Relationship of egg production of Calanus pacificusto seasonal changes in phytoplankton availability in Puget Sound, Washington. Limnology and Oceanography, 30: 382-396.
Schaller B. (1980). Significance of sperm transfer and formation of spermatophores in an arthropod phylogeny. In: A.P. Gupta (Ed.), Arthropod Physiology. Van Nostrand-Reinhold, New York.
Sciandra A., Gouze J., Nival P. (1990). Modelling the reproduction of Centropages typicus (Copepoda: Calanoida) in a fluctuating food supply: effect of adaptation. Journal of Plankton Research, 12(3): 549-572.
Sichlau M.H., Kiorboe T. (2011). Age and size dependent mating performance and fertility in a pelagic copepod, Temora longicornis. Marine Ecology Progress Series, 442: 123-132.
Subramoniam T. (1993). Spermatophores and sperm transfer in marine crustaceans. Advances in Marine Biology, 29: 129-214.
Uchima M., Murano M. (1988). Mating behavior of the marine copepod. Oithona davisae. Marine Biology, 99: 39-45.
Uchima M., Hirano R. (1988). Swimming behaviour of the marine copepod Oithona davisae: internal control and search from environment. Marine Biology, 99: 47-56.
Uchima M. (1985). Copulation in the marine copepod Oithona davisae Ferrari and Orsi. I. Mate discrimination. Bulletin of the Plankton Society of Japan, 32: 23-30.
Vacquier V.D., Swanson W.J, Hellberg M.E. (1995). What have we learned about sea urchin sperm binding? Development, Growth and Differentiation, 37: 1-10.
Watras C.J. (1983). Mate location by diaptomid copepods. Journal of Plankton Research, 5: 417-423.
Willey R.L., Cantrell P.A., Threlkeld S.T. (1990). Epibiotic euglenoid flagellates increase the susceptibility of some zooplankton to fish predation. Limnology and Oceanography, 35: 952-959.
Williamson C.E., Butler N.M. (1987). Temperature, food and mate limitation of copepod reproductive rates: separating the effects of multiple hypothesis. Journal of Plankton Research, 9(5): 821-836.
Wyngaard G.A., Chinnappa C.C. (1982). General biology and cytology of cyclopoids. In: F.W. Harrison, R.R. Cowden (Eds.), Developmental biology of freshwater invertebrates. Alan R. Liss, Inc. New York. pp. 485-533.
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