Role of water temperature in formation of the silver carp Carassius gibelio (Bloch 1782) spawning phenology in the reservoirs of natural preserve "Dnieper-Orelsky"

Authors

  • M. P. Fedyushko Bogdan Khmelnitsky Melitopol State Pedagogical University image/svg+xml
  • D. L. Bondarev Dnepr-Oril Nature Reserve , Природний заповідник «Дніпровсько-Орільський»

DOI:

https://doi.org/10.31548/bio2019.03.011

Keywords:

spawning, carp silver, temperature, phenology, global warming

Abstract

The patterns are established phenology spawning goldfish Carassius gibelio (Bloch, 1782) on the water temperature in a natural reserve "Dneprovsko-Orelsky". Materials, which formed the basis of work, have been collected in the reserve area in 1997-2018 gg. Information on the spawning fish are collected in four locations: ponds system Nicholas ledge river system reservoirs. Inst and Obukhovskaya floodplain of the Dnieper river bed, water system Taromske ledge. Water temperature The measurement was performed at the time of locking start of spawning appropriate species of fish in the pond. water temperature measurement was conducted in 12-13 hours of the day. These water temperature measurements were compared with the data about the average air temperature according to the weather station (g Dnepr). There are dependencies between the air temperature and water temperature, that have their own characteristics in different types of reservoirs. These relationships are described logistic equation. Spawning of Carassius gibelio in 95% of cases occur in the 113-139 hours each year (on average takes 125 day). Spawning Carassius gibelio in 95% of cases starts at 11.5-15.5ºS. This figure is subject to a non-linear trend in time with a local minimum in the period of 2008-2010. The non-linear nature of time changes during the study period as the temperature of the onset of spawning and cumulative temperature for spawning indicates that the likely impact of global warming is not a major factor in the dynamics of the silver carp spawning phenology. Spawning of Carassius gibelio in 95% of cases occur in the 113-139 hours each year (on average takes 125 day). Spawning Carassius gibelio in 95% of cases starts at 11.5-15.5ºS. This figure is subject to a non-linear trend in time with a local minimum in the period of 2008-2010. The non-linear nature of time changes during the study period as the temperature of the onset of spawning and cumulative temperature for spawning indicates that the likely impact of global warming is not a major factor in the dynamics of the silver carp spawning phenology. Spawning of Carassius gibelio in 95% of cases occur in the 113-139 hours each year (on average takes 125 day). Spawning Carassius gibelio in 95% of cases starts at 11.5-15.5ºS. This figure is subject to a non-linear trend in time with a local minimum in the period of 2008-2010. The non-linear nature of time changes during the study period as the temperature of the onset of spawning and cumulative temperature for spawning indicates that the likely impact of global warming is not a major factor in the dynamics of the silver carp spawning phenology.

References

Alavi, S.M.H., Cosson, J. (2005). Sperm motility in fishes. I. Effects of temperature and pH: A review. Cell Biology International, 29 (2), 101-110.

https://doi.org/10.1016/j.cellbi.2004.11.021

Baker, J.R. (1938). The evolution of breeding seasons. In: de Beer GR, editor. Evolution: Essays on Aspects of Evolutionary Biology. Oxford, UK: Clarendon Press. 161-177.

Billard, R., Breton, B., Fostier, A., Jalabert, B., Weil, C. (1978). Endocrine control of the teleos reproductive cycle and its relation to external factors: salmonid and cyprinid models. In: P. J. Gaillard, H. H. Boer (eds), Comparative Endocrinology. Elsevier/North Holland Biomedical Press, Amsterdam, 37-47.

Blenckner, T.( 2001). Climate Related Impacts on a Lake. From Physics to Biology. Acta Universitatis Upsaliensis. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 674, 37.

Bondarev, D. L., Zhukov, O. V. (2017). Phenology of the white bream (Blicca bjoerkna) spawning in natural reserve "Dnieper-Orylskiy" in dependence from seasonal temperature dynamic. Biosystems Diversity, 25(2), 67-73.

https://doi.org/10.15421/011710

Bondarev, D., Kunah, O., Zhukov, O. (2018). Assessment of the impact of seasonal patterns climatic conditions on spawning events of the white bream Blicca bjoerkna (Linnaeus, 1758) in astronomical and biological time. Acta Biologica Sibirica, 4 (2), 48-64.

https://doi.org/10.14258/abs.v4i2.4125

Bradshaw, W.E., Holzapfel, C.M. (2007). Evolution of animal photoperiodism. Annu. Rev. Ecol. Evol. Syst, 38, 1 -25.

https://doi.org/10.1146/annurev.ecolsys.37.091305.110115

Bradshaw, W.E., Holzapfel, C.M. (2010). Light, time, and the physiology of biotic response to rapid climate change in animals. Annu. Rev. Physiol., 72, 149 -166.

https://doi.org/10.1146/annurev-physiol-021909-135837

Breton, B., Horoszewicz, L., Billard, R., Bieniarz, K. (1980). Temperature and reproduction in tench: Effect of a rise in the annual temperature regime on gonadotropin level, gametogenesis and spawning. I. The male. Reproduction Nutrition Développement, 20 (1A), 105-118.

https://doi.org/10.1051/rnd:19800106

Brett, J.R. (1979). Environmental factors and growth. Pp. 599-675. In: Hoar W.S., Randall D.J., Brett J.R. (eds.) Fish physiology. Vol. 8. Bioenergetics and growth. Academic Press, NewYork, NY, USA.

https://doi.org/10.1016/S1546-5098(08)60033-3

Domagała J., Kirczuk L., Pilecka-Rapacz M. (2013). Annual development cycle of gonads of Eurasian ruffe (Gymnocephalus cernuus L.) females from lower Odra River sections differing in the influence of cooling water. Journal of Freshwater Ecology, 28(3): 423-437.

https://doi.org/10.1080/02705060.2013.777855

Edwards, M., Richardson, A.J. (2004). Impact of climate change on marine pelagic phenology and trophic mismatch. Nature, 430, 881-884.

https://doi.org/10.1038/nature02808

Forrest J, Miller-Rushing AJ. (2010). Toward a synthetic understanding of the role of phenology in ecology and evolution. Phil. Trans. R. Soc., B365, 3101-3112.

https://doi.org/10.1098/rstb.2010.0145

Foster, R.G., Kreitzman, L. (2009). Seasons of life: the biological rhythms that enable living things to thrive and survive. New Haven, CT: Yale University Press.

Gwinner, E. (1981). Annual Rhythms: Perspective. In: Aschoff J. (eds) Biological Rhythms. Springer, Boston, MA, 381-389.

https://doi.org/10.1007/978-1-4615-6552-9_20

Helm, B., Ben-Shlomo, R., Sheriff, M.J., Hut, R.A., Foster, R., Barnes, B.M., Dominoni, D. (2013). Annual rhythms that underlie phenology: biological time-keeping meets environmental change. Proc R Soc B, 280, 20130016.

https://doi.org/10.1098/rspb.2013.0016

Herzig, A., Winkler, H. (1986). The influence of temperature on the embryonic development of three cyprinid fishes, Abramis brama,Chalcalburnus chalcoides mentoand Vimba vimba. Journal of Fish Biology, 28 (2), 171-181.

https://doi.org/10.1111/j.1095-8649.1986.tb05155.x

Jafri, S.I.H. (1989). The effects of photoperiod and temperature manipulation on reproduction in the roach Rutilus rutilus (L.) (Teleostei). Pakistan Journal of Zoology, 21 (4), 289-299.

Jobling, M. (2003). The thermal growth coefficient (TGC) model of fish growth: A cautionary note. Aquaculture Research, 34(7), 581-584.

https://doi.org/10.1046/j.1365-2109.2003.00859.x

Kryizhanovskiy, S. G. (1949). Ekologo-morfologicheskie zakonomernosti razvitiya karovyih, vyunovyih i somovyih ryib [Ecological and morphological patterns of development cirque, loaches and catfish fish]. Tr.in-ta morfologii zhivotnyih AN SSSR, 1, 5-332 (in Russian).

Lahnsteiner, F., Mansour, N. (2012). The effect of temperature on sperm motility and enzymatic activity in brown trout Salmo trutta, burbot Lota lota and grayling Thymallus thymallus. Journal of Fish Biology, 81 (1), 197-209.

https://doi.org/10.1111/j.1095-8649.2012.03323.x

Mbungu, W., Ntegeka, V., Kahimba, F.C.; Taye, M.; Willems, P. (2012). Temporal and spatial variations in hydro-climatic extremes in the Lake Victoria basin. Phys. Chem. Earth, 50-52, 24-33.

https://doi.org/10.1016/j.pce.2012.09.002

McCarty, J. (2001). Ecological consequences of recent climate change. Conserv Biol., 15, 320-331.

https://doi.org/10.1046/j.1523-1739.2001.015002320.x

Noges, P., Jarvet, A. (2005). Climate driven changes in the spawning of roach (Rutilus rutilus (L.)) and bream (Abramis brama (L.)) in the Estonian part of the Narva River basin. Boreal Environment Research, 10 (1), 45−55.

Ouarda, T.B.M.J., Charron, C., Kumar, K.N., Marpu, P.R., Ghedira, H., Molini, A., Kayal, I. (2014). Evolution of the rainfall regime in the United Arab Emirates. J. Hydrol., 514, 258-270.

https://doi.org/10.1016/j.jhydrol.2014.04.032

Sandström, O., Neuman, E., Thoresson, G. (1995). Effect of temperature on life history variables in perch. Journal of Fish Biology, 47(4), 652-670.

https://doi.org/10.1111/j.1095-8649.1995.tb01932.x

Schneider, K. N., Newman, R. M., Card, V., Weisberg, S. & Pereira, D. L. (2010). Timing of walleye spawning as an indicator of climate change. Transactions of the American Fisheries Society, 139, 1198-1210.

https://doi.org/10.1577/T09-129.1

Thompson, A. L. (1950). Factors determining the breeding seasons of birds: an introductory review. Ibis, 92, 173-184.

https://doi.org/10.1111/j.1474-919X.1950.tb01748.x

Visser, M.E., Caro, S.P., van Oers, K., Schaper, S.V., Helm, B. (2010). Phenology, seasonal timing and circannual rhythms: towards a unified framework. Phil. Trans. R. Soc. B365, 3113-3127.

https://doi.org/10.1098/rstb

Published

2019-08-23

Issue

Section

Animal husbandry