Skip to main content
Log in

Spatial and temporal distribution of benthic stages of Cyclops vicinus and Chaoborus flavicans in relation to abiotic factors and benthic fauna

  • Published:
Hydrobiologia Aims and scope Submit manuscript

Abstract

The horizontal distributions of the benthic stages of Chaoborus flavicans and Cyclops vicinus were studied in a eutrophic stratified lake in the Massif-Central (France) over one year, at 5 stations from the shore to the centre of the lake. Their distribution was investigated in relation to temperature, dissolved oxygen, sediment grain-size and other benthic organisms. The dominant taxa of the benthic fauna of Lake Aydat were dipterans, crustaceans and oligochaetes and their distributions were independent of the grain size. In contrast to chironomids which preferentially inhabited the sublittoral zone, chaoborids and crustaceans were more numerous in the profundal zone. The sediment-dwelling oligochaetes remained numerous in both zones, according to the season. The fourth copepodite stages of Cyclops and Tubifex are tolerant to low oxygen concentrations in contrast to the fourth instar larvae of Chaoborus whose distribution was positively correlated with oxygen. The guts of these dipteran larvae were found to be empty and we assumed that, in contrast to the chironomids and oligochaetes, the resting stages of Cyclops vicinus and the benthic stages of Chaoborus flavicans did not use benthic resources. The former are activated at the autumn overturn, while the latter escape from the bottom at the start of the spring oxygen depletion. This suggests that physical factors are largely responsible for their reactivation. Both animals suffered of the effects of starvation and probably lost weight. The reactivation of the copepod at the autumn overturn would be facilitated by fluid mechanical disturbance. In addition, after the spring overturn, a small increase in temperature near 4 °C would be a reliable environmental signal for the dipteran. Food limitation does not occur, invertebrate predation pressure seems to be negligible and the predation by fish on the macrobenthic fauna and by chance on the meiofauna, clearly remains limited in both space and time.

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

References

  • A. F. NOR., 1990. Normes X 31–101 & 31–107. In Association Française de Normalisation (ed.). Recueil des normes.

  • Azam, F., T. Fenchel, J. G. Field, J. S. Gray, L. A. Meyer-Reil & F. Thingstad, 1983. The ecological role of water-column microbes in the sea. Mar. Ecol. Prog. Ser. 10: 257–263.

    Google Scholar 

  • Buchanan, J. B., 1984. Sediment analysis. In N.A. Holme & A.D. McIntyre (eds), Methods for the Study of Marine Benthos. Blackwell Scientific Publications; Oxford: 41–65.

    Google Scholar 

  • Campy, M. & M. Meybeck, 1995. Les sédiments lacustres. In R. Pourriot & M. Meybeck (eds), Limnologie Générale. Masson, Paris: 185–226.

    Google Scholar 

  • Dahms, H. U., 1995. Dormancy in the Copepoda-an overview. Hydrobiologia 306: 199–211.

    Article  Google Scholar 

  • Dawidowicz, P., J. Pijanowska & K. Ciechomski, 1990. Vertical migration of Chaoborus larvae induced by the presence of fish. Limnol. Oceanogr. 35: 1631–1637.

    Google Scholar 

  • Depiereux, E., 1988. Multivariate analysis in the description of community structure: principal component and cluster analysis. In M. Hermy & A. Wilmotte (eds), Multivariate Analysis of Biological Data. Bull. Soc. Roy. Belg.: 127–158.

  • Durieu, M., 1995. Cycle biologique de Chaoborus flavicans (Diptera: Chaoboridae), valorisation de la production de biomasse en bassin de lagunage et optimisation en condition expérimentales. Doctorat d'Université, Université Paul Sabatier, Toulouse, France, 325 pp.

    Google Scholar 

  • Eaton, K. A., 1983. The life-history and production of Chaoborus punctipennis (Diptera: Chaoboridae) in lake Norman, North Carolina, USA. Hydrobiologia 106: 247–252.

    Article  Google Scholar 

  • Fedorenko, A. Y., 1975. Feeding characteristics and predation impact of Chaoborus (Diptera: Chaoboridae) larvae in small lake. Limnol. Oceanogr. 20: 250–258.

    Google Scholar 

  • George, D. G., 1976. Life cycle and production of Cyclops vicinus in a shallow eutrophic reservoir. Oikos 27: 101–110.

    Google Scholar 

  • Gerdeaux, D., J. Guillard & J. L. Jamet, 1989. Abundance estimation of Chaoborus larvae and fishes in Lake Aydat by echo-integration. Proc. I. O. A. 11: 231–237.

    Google Scholar 

  • Giani, N. & H. Laville, 1995. Réseau trophique benthique. In R. Pourriot & M. Meybeck (eds), Limnologie générale. Masson; Paris: 565–587.

    Google Scholar 

  • Hansen, A. M. & B. Santer, 1995. The influence of food resources on the development, survival and reproduction of the two cyclopoid copepods: Cyclops vicinus and Mesocyclops leuckarti. J. Plankton Res. 17: 631–646.

    Google Scholar 

  • Hartmann, H. J., H. Taleb, L. Aleya & N. Lair, 1993. Predation on ciliates by the suspension-feeding calanoid copepod Acanthodiaptomus denticornis. Can. J. Fish. aquatic. Sci. 50: 1382–1393.

    Article  Google Scholar 

  • Heinis, F. & T. Crommentuijn, 1992. Behavioural responses to changing oxygen concentrations of deposit feeding chironomid larvae (Diptera) of littoral and profundal habitats. Arch. Hydrobiol. 124: 173–185.

    Google Scholar 

  • Hillbricht-Ilkowska, A., Z. Kajak, J. Ejsmont-Karabin, A. Karabin & J. Rybak, 1975. Ecosystem of the Mikolajskie lake. The utilization of the consumers production by invertebrate predators in pelagic and profundal zone. Pol. Arch. Hydrobiol. 22: 53–64.

    Google Scholar 

  • Howmiller, R. P., 1977. On abundance of Tubificidae (Annelida: Oligochaeta) in the profundal benthos of some Wisconsin lakes. Am. Midl. Nat. 97: 211–215.

    Article  Google Scholar 

  • Jamet, J. L., 1991. Importance de la faune ichtyologique dans le lac d'Aydat, milieu eutrophe de la zone tempérée Nord, ses relations trophiques avec les autres composants de l'écosystème. Doctorat d'Université, Université Blaise Pascal, Clermont-Ferrand, France, 263 pp.

    Google Scholar 

  • Jønasson, P. M., 1955. The efficiency of sieving techniques for sampling freshwater bottom fauna. Oikos 6: 183–207.

    Google Scholar 

  • Jønasson, P. M., 1972. Ecology and production of the profundal benthos in relation to phytoplankton in Lake Esrom. Oikos (suppl.) 14: 139 pp.

  • Jønasson, P. M., 1996. Limits for life in the lake ecosystem. Verh. int. Ver. Limnol. 26: 1–33.

    Google Scholar 

  • Kajak, Z. & B. Ranke-Rybicka, 1970. Feeding and production efficiency of Chaoborus flavicans MEIGEN (Diptera; Culicidae) larvae in eutrophic and dystrophic lake. Pol. Arch. Hydrobiol. 30: 225–232.

    Google Scholar 

  • Kajak, Z., J. Rybak & B. Ranke-Rybicka, 1978. Fluctuations in numbers and changes in the distribution of Chaoborus flavicans (Meigen) (Diptera, Chaoboridae) in the eutrophic Mikolajskie lake and dystrophic lake Flosek. Ekol. pol. 26: 259–272.

    Google Scholar 

  • Kajak, Z. & J. Rybak, 1979. The feeding of Chaoborus flavicans MEIGEN (Diptera: Chaoboridae) and its predation on lake zooplankton. Int. Rev. ges. Hydrobiol. 64: 361–378.

    Google Scholar 

  • Kerfoot, W. C., D. L. Kellogg Jr & J. R. Strickler, 1980. Visual observations of live zooplankters: evasion, escape, and chemical defences. In W. C. Kerfoot (ed.), Evolution and Ecology of Zooplankton Communities. The University Press of New England, Hanover (N.H.); Lond.: 10–27.

    Google Scholar 

  • Lair, N., 1990. Effect of invertebrate predation on seasonal succession of a zooplankton community: a two year study in lake Aydat. Hydrobiologia 198: 1–12.

    Article  Google Scholar 

  • Lair, N. & A. Ayadi, 1989. The seasonal succession of planktonic events in Lake Aydat, France. A comparison with the PEG model. Arch. Hydrobiol. 115: 589–602.

    Google Scholar 

  • Lair, N. & Y. El Ghachtoul, 1989. La diapause de Cyclops vicinus vicinus (Ulianine, 1875) dans un lac eutrophe du Massif-Central Français. SITE Atti 7: 289–295.

    Google Scholar 

  • Leaner, M. A., G. Lochhead & B. D. Hughes, 1978. A review of the biology of British Naididae, with emphasis on the lotic environment. Freshwat. Biol. 8: 357–375.

    Article  Google Scholar 

  • Maier, G., 1989. Variable life cycles in the freshwater copepod Cyclops vicinus (Uljanin, 1875): Support for the predator avoidance hypothesis ? Arch. Hydrobiol. 115: 203–219.

    Google Scholar 

  • Mumm, H. & A. F. Sell, 1995. Estimating the impact of Chaoborus predation on zooplankton: A new design for in situ enclosures studies. Arch. Hydrobiol. 134: 195–206.

    Google Scholar 

  • Neill, W. E., 1981. Impact of Chaoborus predation upon the structure and dynamics of a crustacean zooplankton community. Oecologia 48: 164–177.

    Article  Google Scholar 

  • Neill, W. E., 1990. Induced vertical migration in copepods as a defence against invertebrate predation. Nature 345: 524–526.

    Article  Google Scholar 

  • Nilssen, J. P. & K. Elgmork, 1977. Cyclops abyssorum-Life cycle dynamics and habitat selection. Mem. Ist. ital. Idrobiol. 34: 197–238.

    Google Scholar 

  • Nilssen, J. P., 1978. On the evolution of life histories of limnetic cyclopoid copepods. Mem. Ist. ital. Idrobiol. 36: 193–214.

    Google Scholar 

  • Parma, S., 1971. The morphology of the larval instars of Chaoborus flavicans (Meigen, 1818) (Diptera, Chaoboridae). Beaufortia, 238: 173–181.

    Google Scholar 

  • Santer, B., 1993. Potential importance of algae in the diet of adult Cyclops vicinus. Freshwat. Biol. 30: 269–278.

    Article  Google Scholar 

  • Santer, B. & F. van den Bosch, 1994. Herbivorous nutrition of Cyclops vicinus: the effect of a pure algal diet on feeding, development, reproduction and life cycle. J. Plankton Res. 16: 171–195.

    Google Scholar 

  • Särkkä, J., 1993. Diversity of meiofauna in the lacustrine profundal zone: Bathymetric differences and influence of environmental factors. Aquat. Sci. 55: 197–205.

    Article  Google Scholar 

  • Särkkä, J., 1995. Profundal meiofauna in two large lakes: Influence of pollution and bathymetric differences. Arch. Hydrobiol. 32: 453–493.

    Google Scholar 

  • Sikorowa, A., 1968. The behaviour of Chaoborus LICHT. larvae under unfavorable oxygen conditions. Ekol. pol. A 16: 1–7.

    Google Scholar 

  • Smyly, W. J. P., 1974. The effect of temperature on the development time of the eggs of three freshwater cyclopoid copepods from the English Lake District. Crustaceana 27: 278–284.

    Article  Google Scholar 

  • Stahl, J. B., 1966. The ecology of Chaoborus inMyers lake, Indiana. Limnol. Oceanogr. 11: 177–183.

    Google Scholar 

  • Strayer, D., 1985. The benthic micrometazoans of Mirror Lake, New Hampshire. Arch. Hydrobiol. (Suppl.) 72: 287–426.

    Google Scholar 

  • Strayer, D., 1991. Perspectives on the size structure of lacustrine zoobenthos, its causes and its consequences. J. n. am. benthol. Soc. 10: 210–221.

    Article  Google Scholar 

  • Strommer, J. L. & L. A. Smock, 1989. Vertical distribution and abundance of invertebrates within the sandy substrate of a low gradient headwater stream. Freshwat. Biol.: 22, 263–274.

    Article  Google Scholar 

  • Swift, M. C. & A. Y. Fedorenko, 1975. Some aspect of the prey capture by Chaoborus larvae. Limnol. Oceanogr. 20: 418–425.

    Google Scholar 

  • Swüste, H. F. J., R. Cremer & S. Parma, 1973. Selective predation by larvae of Chaoborus flavicans (Diptera, Chaoboridae). Verh. int. Ver. Limnol. 18: 1559–1563.

    Google Scholar 

  • Taleb, H., N. Lair & J. L. Jamet, 1992. Estival diel vertical migration of Acanthodiaptomus denticornis (Wierzejski, 1887) (Calanoïda: Copepoda) in a eutrophic lake of the temperate zone as a mean of predator avoidance. Ann. Nat. Zool. 13: 149–156.

    Google Scholar 

  • Taleb, H., N. Lair, P. Reyes-Marchant & J. L. Jamet, 1993. Observations on vertical migrations of zooplankton at four different stations of a small, eutrophic, temperate zone lake, in relation to their predators. Arch. Hydrobiol. Beih. 39: 199–216.

    Google Scholar 

  • Ten Winkel, E. H. & C. Davids, 1987. Population dynamics aspects of chironomid larvae of the littoral zone of Lake Maarsseveeb I. Hydrobiol. Bull. 21: 81–94.

    Article  Google Scholar 

  • Tinson, S. & J. Laybourn-Parry, 1986. The distribution and abundance of benthic cyclopoid copepods in Esthwaite Water, Cumbria. Hydrobiologia 131: 225–234.

    Article  Google Scholar 

  • Traunspurger, W., 1996. Distribution of benthic nematodes in the littoral of an oligotrophic lake (Königssee, National Park Berchtesgaden, FRG). Arch. Hydrobiol. 135: 393–412.

    Google Scholar 

  • Van de Bund, W. J. & D. Groenendijk, 1994. Seasonal dynamics and burrowing of littoral chironomid larvae in relation to competition and predation. Arch. Hydrobiol. 132: 213–225.

    Google Scholar 

  • Walter, R. A., 1985. Benthic macroinvertebrates. In G.E. Lickens (ed.), An Ecosystem Approach to Aquatic Ecology: Mirror Lake and its Environment. Springer Verlag, New York: 204–228

    Google Scholar 

  • Wyngaard, G. A., B. E. Taylor & D. L. Mahoney, 1991. Emergence and dynamics of cyclopoid copepods in an unpredictable environment. Freshwat. Biol. 25: 219–232.

    Article  Google Scholar 

  • Yan, N. D., W Keller, H. J. Mac Isaac & L. J. Mac Eachern, 1991. Regulation of zooplanktonic community structure of an acidified lake by Chaoborus. Ecol. Appl. 1: 52–65.

    Google Scholar 

  • Yurista, P. M., 1997. Bythotrephes cederstroemi diapausing egg distribution and abundance in Lake Michigan and the environmental cues for breaking diapause. J. Great Lakes Res. 23: 202–209.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rabette, C., Lair, N. Spatial and temporal distribution of benthic stages of Cyclops vicinus and Chaoborus flavicans in relation to abiotic factors and benthic fauna. Hydrobiologia 390, 61–72 (1998). https://doi.org/10.1023/A:1003559832628

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1003559832628

Navigation